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<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The Microbiologist conducts validation and feasibility testing for quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Performs validation testing to analyze samples to determine an accurate microbiological procedure for the following analyses: Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity).</li>
<li>Performs Disinfectant Efficacy testing for clients facilities utilizing specific disinfectants, surfaces, and organisms determined by the clients.</li>
<li>Perform feasibility work with guidance from USP and BA SOPs. Being able to work independently with little to no guidance to figure out and apply test methods to different products and materials.</li>
<li>Documents work in a clear and organized manner.</li>
<li>Revises procedures and ELNs under close supervision.</li>
<li>Writes validation reports and client protocols for QC Micro to follow for routine testing.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
<li>Under close supervision confers with Microbiologists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>
<li>Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts.</li>
<li>Performs data generation and problem solving with a minimal rework.</li>
<li>Works under close supervision to ensure all work performed is executed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a BA or BS degree in Microbiology or related science discipline with 0-2 years of related experience is required. Knowledge of cGMP and related compliance regulations and guidances is preferred.
 
SHIFT
WED-SAT 1ST SHIFT

MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>
<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Microbiologist I, VD

<h3>Job Description</h3>
Job Description
Principal Biostatistician
Statistics &amp; Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.
Job Location: AZ/MA/NC
Job Summary
Apply a high level of technical expertise to help guide and develop the more junior biostatistics staff members. Serve as a lead statistician on clinical studies and provide senior level peer review of work being accomplished by other biostatisticians in the department. Maintain the statistical and analytical integrity of clinical trials analyzed by SDC. Actively participate in writing statistical sections of protocols, preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, writing statistical sections of clinical study reports, and participating in meetings with drug regulatory agencies as required. Support business development and project management with strategic planning, proposals, pricing, and timeline planning.
Primary Responsibilities
• Serve as an internal consultant for biostatistics analysis tools and methods
• Serve as a subject matter expert during client and vendor meetings for biostatistics analysis support
• Actively support business development in capabilities presentations to prospective and current clients
• Effectively manage assigned clinical study budgets for biostatistics analysis support
• Develop, coach and mentor junior biostatistics department personnel
• Act as the lead statistician on clinical research projects and help with SAS programming
• Provide statistical expertise for study design of clinical trial protocols
• Write statistical methods section of the study protocol, as needed
• Write statistical analysis plans ensuring appropriate regulatory requirements and study objectives defined in the study protocol are followed
• Review CRFs to ensure consistency with protocol and statistical analysis plan (SAP)
• Program summary tables, data listings and graphical representations of clinical trials data
• Perform all analyses defined in the statistical analysis plan as well as any post-hoc analyses and relevant exploratory analyses of clinical trial data
• Prepare/review key sections of clinical study reports and various regulatory documents
• Perform statistical QC of all department outputs including analyses and clinical study reports
• Provide statistical support to answer questions from external clients (such as FDA, Investigators)
• Contribute to the development, maintenance, and training of standard operating procedures (SOPs)
• Represent the biostatistics department at regulatory meetings, sponsor meetings, and any other multifunctional meetings, as needed
• Manage biostatistics timelines, budgets, and client expectations
• Adhere to all aspects of the Statistics &amp; Data Corporation’s quality system
• Comply with Statistics &amp; Data Corporation’s data integrity &amp; business ethics requirements
• Perform other related duties incidental to the work described herein
• Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements
The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.
Requirements
Required Skills
• Effective leadership, budget forecast and implementation skills
• Excellent analytical skills, with the ability to process scientific and medical data
• Able to work independently and in teams
• Project management abilities including analytical evaluation, organization, delegation, flexible team management, negotiating and resource management skills
• Excellent knowledge of statistical programming
• Expertise in manipulating and analyzing SAS data
• Able to identify data issues, present problems, and implement solutions.
• Capable of communicating technical concepts clearly, concisely, and understandably to non-statistical colleagues and clients
• Excellent organizational and time management skills, with the ability to multi-task
• Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP)
• Strong interpersonal communication and presentation skills
• Able to effectively collaborate across cross-functional teams
• Focus on quality at all times and in all situations
Education or Equivalent Experience
• A Master’s degree in biostatistics, statistics or other related, scientific field and at least eight years of relevant professional experience or a combination of education and experience.
Benefits
Why SDC
SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances, positive work/life balance and 401k matching (US), we are able to attract some of the most talented people in the industry. 
•We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits. 
•We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment. 
•We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.
•We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry. 
•With a proven track record, SDC has been successfully executing client clinical programs since 2005.
Take a look at how you can join our team!
#LI-Hybrid

Principal Biostatistician

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Prepares and analyzes samples to determine microbiological quality through the following analyses: Microbial enumeration methods, absence of specified microorganisms, Sterility, endotoxin, and water quality analysis (bioburden, TOC, Conductivity).</li>
<li>Documents work in a clear and organized manner.</li>
<li>Revises procedures and ELNs under close supervision.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
<li>Under close supervision confers with Microbiologists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>
<li>Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts.</li>
<li>Performs routine data generation and problem solving with a minimal rework.</li>
<li>Works under close supervision to ensure all work performed is executed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a BA or BS degree in Microbiology or related science discipline with 0-2 years of related experience is required. Knowledge of cGMP and related compliance regulations and guidances is preferred.
 
SHIFT
Sunday-Wednesday, 1st shift.
 
MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>
<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Microbiologist QC I

<h3>Job Description</h3>
Job Description
Who We Are: 
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented and diverse workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview:
The Scientist I - Process Research &amp; Development (PRD) is responsible for conducting small to large scale chemical reactions to optimize synthetic routes of active pharmaceutical ingredients (APIs) under the direction of project technical leads to deliver projects on target with quantity, quality, time, and within budget.
Core Responsibilities: 
<ul>
<li>Delivers experimental output with a high scientific integrity, both on time and target, and of high quality with guidance. </li>
<li>Exhibits safety awareness, safely conducts lab and other operations and hold themselves accountable for safe behavior in the work environment. </li>
<li>Maintains technical equipment and services.</li>
<li>Acts on feedback and show continuous commitment to learning and development.</li>
<li>Lead technical and operational areas and support troubleshooting for complex scientific issues under minimal guidance.</li>
<li>Expertly shares knowledge, skills and experience, communicating internally and externally. May lead focused projects as key contact. </li>
<li>Keeps accurate, legible and complete records of all experiments, observations, and equipment. </li>
<li>Writes high quality reports and delivers presentations to customers and management with some guidance in alignment with project milestones.</li>
<li>Contributes to sustaining good customer relations and identifies new commercial opportunities.</li>
<li>Actively contributes to the technical development of the department and company.</li>
<li>Accomplishes additional duties within the employee’s skills and abilities per reasonable request.</li>
</ul>
Qualifications: 
Required
<ul>
<li>PhD degree (or equivalent experience) in a chemistry related discipline.</li>
<li>2+ years hand on experience with PhD; 5+ years hand-on experience if Master's degree.</li>
<li>Proficiency with relevant lab and analytical techniques.</li>
<li>Previous industry experience in relevant areas.</li>
<li>Proficiency with relevant analytical techniques within an industry environment.</li>
<li>Ability to write clear and concise technical reports.</li>
<li>Good understanding of Microsoft Office and other relevant technical software platforms</li>
<li>Skilled in written and spoken communication and proven ability to effectively interact with management. </li>
<li>Demonstrates good judgment, quick decision-making skills, and the ability to work independently and in a team environment.</li>
</ul>
Physical Demands &amp; Work Environment:
<ul>
<li>Stand, walk, and manually operate objects, tools, or controls; reach with hands or arms; climb, balance, stoop, kneel, or crouch when necessary for the job activity.</li>
<li>Lift and/or move up to 50 pounds.</li>
<li>Specific vision abilities include near, distance, peripheral, color perception, and the ability to adjust focus.</li>
<li>Regularly work with moving mechanical parts and may work with toxic or caustic chemicals. </li>
<li>The work may be performed in humid areas with low or high temperatures. </li>
<li>This work may need to work with a respirator or operate with full-body Tyvek suits and supplied air or PAPR.</li>
</ul>
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a mission to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit <a href="http://www.veranova.com" target="_blank">www.veranova.com</a> to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. 
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. 
If you are a veteran, first responder, or in the process of transitioning from service member to civilian life, we encourage you to apply. Your experience brings invaluable skills and insights that can contribute to our team.
For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to <a href="mailto:talentacquisition@veranova.com" target="_blank">talentacquisition@veranova.com</a> in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship.
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
Important Notice Regarding Recruitment Scams: Veranova is committed to providing a professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.
<ul>
<li>Legitimate communications from Veranova will only come from official email addresses using our domain: @veranova.com.</li>
<li>Legitimate LinkedIn communications will only come from active Veranova employees.</li>
<li>Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number).</li>
<li>Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks).</li>
</ul>
If you have any doubts or concerns about the authenticity of a job posting, please reach out to our HR department: <a href="mailto:pharm.hr@veranova.com" target="_blank">pharm.hr@veranova.com</a> (US) or <a href="mailto:UKHR@veranova.com" target="_blank">UKHR@veranova.com</a> (UK).
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

Scientist - Process Research & Development

<h3>Job Description</h3>
Job Description
Xometry (NASDAQ: XMTR) powers the industries of today and tomorrow by connecting the people with big ideas to the manufacturers who can bring them to life. Xometry's digital marketplace gives manufacturers the critical resources they need to grow their business while also making it easy for buyers at Fortune 1000 companies to tap into global manufacturing capacity.
Xometry is seeking a Principal Data &amp; ML Scientist to join our Generative AI team. The ideal candidate will have a passion for advancing machine learning and generative AI capabilities, particularly for fine-tuning generative and language models, multimodal document understanding, and structured data extraction. This person will leverage their expertise in generative models and data science to develop and optimize innovative AI-driven solutions that enhance Xometry's service offerings.
Responsibilities:
<ul>
<li>Provide technical leadership to the Generative AI team, setting technical direction, defining best practices, and ensuring the team follows industry standards in AI and ML development.</li>
<li>Lead strategic planning and roadmap development for generative AI initiatives, identifying high-impact projects and aligning them with Xometry's business objectives.</li>
<li>Develop and deploy generative AI models and large language models (LLMs) for multimodal document processing, focusing on extracting structured data from technical drawings, purchasing orders, and other complex documents.</li>
<li>Lead the exploration and development of innovative text and image-based data processing solutions, including training and fine-tuning generative and language models.</li>
<li>Design and implement efficient workflows for data preparation, cleaning, and augmentation to support the training of generative AI models.</li>
<li>Utilize cloud platforms (e.g., Amazon Web Services) for large-scale data processing, model training, and deployment.</li>
<li>Collaborate with cross-functional teams, including engineering and business teams, to align generative AI solutions with business needs and drive impactful applications.</li>
<li>Mentor and guide team members on advanced machine learning techniques, model architecture design, and problem-solving strategies to elevate the team's technical capabilities.</li>
<li>Continuously experiment and iterate on model performance, tuning architectures and parameters to improve accuracy and efficiency in a fast-paced, agile environment.</li>
<li>Stay updated with the latest research in generative AI, deep learning, and multimodal data processing, incorporating best practices and advancements into model development.</li>
</ul>
Qualifications:
<ul>
<li>A bachelor's degree is required, but an advanced degree (M.S. or PhD) in computer science, machine learning, AI, or a related field is highly preferred.</li>
<li>7+ years of experience in data science and machine learning, focusing on generative models, LLMs, or computer vision.</li>
<li>Expertise in large-scale language and vision models (e.g., Transformers, GPT, VLMs).</li>
<li>Experience with multimodal data processing (e.g., combining text, image, and 3D data).</li>
<li>Proficient in Python, including key libraries such as PyTorch, TensorFlow, pandas, and numpy.</li>
<li>Strong background in probability, statistics, and optimization techniques relevant to generative modeling.</li>
<li>Familiarity with cloud computing resources and tools for model training and deployment (e.g., AWS SageMaker).</li>
<li>Familiar with software engineering principles, including version control, reproducibility, and continuous integration.</li>
<li>Experience in the manufacturing, supply chain, or similar industries is a plus.</li>
</ul>
#LI-Hybrid
Xometry is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
For US based roles: Xometry participates in E-Verify and after a job offer is accepted, will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Principal Machine Learning Data Scientist, Gen AI

<h3>Job Description</h3>
Job Description
Summary:
As a senior member of NCF’s Department of Ecological Research, Stewardship and Restoration, the Coastal Wetlands Research Ecologist is responsible for executing the Coastal and Wetland Ecology Research Program. They oversee research on the ecology of wetlands and coastal habitats related to restoration, habitat quality, ecosystem function, and resilience. Broad project topics include but are not limited to baseline coastal wetland habitat health, effectiveness of nature-based responses to climate change impacts, understanding impacts of climate change on coastal habitats, habitat restoration for function and improved resilience, and broad ecological research within the Program focus. 
Under the direction of the Vice President of Science and Stewardship, the Coastal Wetlands Research Ecologist is responsible for developing targeted inventory, monitoring and research projects related to their Program’s areas of interest (as described above) as well as overseeing and participating in the successful execution of these projects. They provide oversight, planning, and logistical support to NCF’s year-round Coastal Research Technician and related seasonal field staff. They also oversee and may participate in related research conducted by outside research partners working on NCF properties, work cooperatively on joint projects with other local and regional conservation organizations, and represent NCF on key committees, working groups and the like related to their program’s areas of expertise. 
The Coastal Wetlands Research Ecologist serves as a key senior member of the NCF Department of Ecological Research, Stewardship and Restoration, working closely and coordinating with senior level staff from the Wildlife Ecology, Plant Ecology and Botany, and Land Management and Stewardship Programs. Furthermore, they coordinate education, mentoring and outreach programming relevant to coastal wetland ecology in partnership with NCF’s Interpretive Education staff, contribute content to NCF’s social media, website, newsletters, annual reports, and other publications and provide team-oriented support for the successful implementation of NCF’s overall mission. 
Specific Responsibilities:
Staff Management
1. Supervise the Coastal Research Technician; assists in supervising seasonal field assistant(s) and volunteers working on coastal and wetland ecology related projects.
Coastal and Wetland Ecology Research
In coordination with the Vice President of Science and Stewardship, oversee all aspects of the Coastal and Wetlands Ecology Program of the NCF Department of Ecological Research, Stewardship and Restoration, including but not limited to the following: 
1. Provide leadership and strategic planning for current and future goals and projects related to the Program.
2. Develop and oversee the implementation of research, restoration and monitoring projects related to coastal and wetlands ecology and potential coastal resilience initiatives on NCF properties, including:
o Project design, field work, data collection and analysis, and interpretation and presentation of results in reports, scientific publications, and professional presentations.
o Staff oversight, delegation and support for all aspects of project implementation needed for success.
o Relevant grant opportunity identification and application for funding as opportunities arise.
3. Identify and target potential partnerships with academic and research institutions that complement the focus of the Coastal and Wetland Ecology Program, as well as the vision, mission and strategic goals of the overall department.
4. Represent NCF’s wetland ecology interests and coastal resilience initiatives at appropriate local and regional committees, working groups, professional networks and the like when appropriate.
5. Provide oversight and participate as appropriate in research conducted by outside investigators working on Foundation properties.
Stewardship, Land Management and Restoration
1. Play a leadership role in identifying, planning and implementing projects focused on wetland restoration and coastal resilience. 
2. Contribute expertise and collaborate on the development, planning and implementation of stewardship, land management and restoration projects on NCF properties.
3. Collaborate on joint projects with local and regional conservation organizations and governmental agencies involved in coastal resilience and coastal and wetland ecology projects, as needed.
4. Coordinate with NCF’s Department of Land Management regarding the need for land management staff and equipment support for Coastal and Wetland Ecology Program projects, as needed. 
Interpretive Education and Community Relations
1. Contribute content related to Coastal and Wetland Ecology Program projects to NCF’s website, social media outlets, newsletters, publications, press releases, video productions and the like, as well as outside requests for content.
2. Develop and participate in NCF’s interpretive education excursion programming aimed at providing experiences that educate participants in coastal resilience and wetland ecology, as well as other outside opportunities as they arise.
Development, Fundraising and Donor Relations
1. Work with the Vice President of Science and Stewardship to identify grant opportunities, write proposals and manage grant awards supporting NCF’s overall research, stewardship and restoration projects.
2. Participate as a senior department representative at fundraising, outreach and donor cultivation events to provide support for the Development Department’s efforts to connect donors with aspects of NCF’s mission that complement their interests.
Dates/Hours:
This is a full-time, year-round exempt position beginning in late-July 2025; exact dates are somewhat flexible. Hours are 40 hours per week, generally during normal business hours from Monday through Friday. Daily hours may be somewhat variable depending on particular projects: early-morning and late-night fieldwork may be required depending on weather, tides, etc. Weekend work will occasionally be required for certain field projects and non-profit events.
Field Work Environment:
A component of this position involves field work involving hiking, standing, bending, kneeling, and hauling field gear. Applicants should be accustomed to occasionally working in inclement weather or at sites with variable terrain, poison ivy, biting insects, etc. such as salt marshes and other wetlands. Nantucket is an area with a high incidence of tick-borne disease so precautions to minimize risk are encouraged. 
TO APPLY:
Applications accepted ONLY through our hiring website: <a href="https://apply.workable.com/nantucket-conservation-foundation/" target="_blank">https://apply.workable.com/nantucket-conservation-foundation/</a>
Application Packet: ONE PDF DOCUMENT including cover letter, resume, contact information for 3 professional references and an unofficial copy of your college transcripts. Incomplete application packets will not be considered. 
Application deadline is June 27, 2025, by 5pm. Applications will be reviewed on a rolling basis so apply early for consideration.
Click APPLY to job and fill out the form. Upload your Application Packet using the “Upload Resume” Link. 
Requirements
1. Master’s degree in Ecology, Botany, Wetland Ecology, Coastal Ecology, Natural Resource Management, Environmental Science, or a related biological/ecological field.
2. At least five years of relevant work experience post-graduate school.
3. Proven organizational skills and ability to independently prioritize, plan, lead and oversee multiple projects.
4. Experience in experimental design, field work (especially freshwater wetland and salt marsh field sampling in New England), data collection, quality control and data analysis (including statistics proficiency).
5. Working knowledge of community and ecosystem ecology; familiarity with plant and wildlife identification. 
6. Proven ability to effectively supervise, mentor, and develop team members, including providing feedback, setting performance goals, supporting professional growth, and fostering a positive, collaborative work environment.
7. Exceptional verbal and written communication skills, with the ability to convey complex information clearly and persuasively to diverse audiences, tailor messaging to different stakeholders, and produce high-quality reporting.
8. Collaboration experience and ability to work well in teams with others from a variety of experience levels to both efficiently execute projects and contribute to departmental strategic planning and oversight.
9. Proficiency with ArcGIS (ArcPro) and experience with interpreting and presenting geospatial research results, database management, map making, and the use of GPS units to collect data in the field.
10. Experience working with environmental monitoring loggers. 
11. Proficiency with Microsoft Office applications and data analysis software. 
12. Valid driver’s license required. 
Benefits
Salary commensurate with experience starting at $80,000, based on a 40-hour work week. Housing is provided in a shared, employee house at an adjusted rate -- salary is negotiable if housing is not needed. Work-related transportation is provided during working hours. Eligible to participate in the Foundation's full-time employee benefit plans and programs (subject to required waiting periods) including group health insurance, group life and accidental death insurance, disability insurance, dental insurance, 401K Plan, paid employee vacation and sick time, and paid holidays.

Coastal Wetlands Research Ecologist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The Multispecifics Engineering group at AbbVie is seeking a highly skilled and self-motivated scientist to join a dynamic team supporting Discovery Biotherapeutics and lead a team focused on T-cell engagers. This position will impact projects through engineering, production, and characterization of multispecific biopharmaceutical products. The ideal candidate should have extensive experience with biologics and multispecifics production platforms, analytical characterization, and a proven track record implementing multispecific engineering and production strategies to advance early- and late-stage discovery programs. The ideal candidate will also have people and project management experience. The applicant should be an enthusiastic, creative scientist who will make tangible contributions to the pipeline.
Key Responsibilities:
<ul>
<li>Responsible for design, engineering, and production of multispecific biologics, primarily to support Oncology projects</li>
<li>Serve as a Multispecifics Engineering representative in cross-functional teams with Oncology, Discovery Biotherapeutics, and Development Sciences, providing project updates, analysis, and advice; recognized expert in multispecific design and production</li>
<li>Serve as the Biologics Lead on projects to coordinate activities and transitions from hit generation through candidate nomination</li>
<li>Supervise a team of scientists, evaluate team performance, and be accountable for the effective performance of the team</li>
<li>Identify and solve technical problems independently, conceive and implement innovative research ideas</li>
<li>Ensure consistency and quality of technical reports</li>
<li>Present original work internally across departments and at internal and external scientific conferences; may author or co-author peer-reviewed scientific papers or patents</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>BS, MS, or PhD in Biochemistry, Biochemical engineering or related discipline with typically 14+ (BS), 12+ (MS), or 6+ (PhD) years of experience&nbsp;in bi- and trispecific engineering or T-cell engagers</li>
<li>Experience with protein, biologics, fragments, or multispecifics (e.g. bispecifics, trispecifics, bispecific protein fusions) design, expression and purification</li>
<li>Experience managing direct reports and providing performance evaluations and development opportunities</li>
<li>Excellent organizational skills and the ability to manage multiple projects simultaneously</li>
<li>Team player with the ability to operate in a fast-paced multi-disciplinary environment</li>
<li>Candidate must be a goal-oriented team player with excellent verbal and written communication skills and strong can-do attitude</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with sequence analysis tools (Vector NTI, Geneious, Genedata)</li>
<li>Experience with mass spectrometry analysis and software (Protein Metrics)</li>
<li>Experience with CRO coordination for production</li>
<li>Expert understanding of current state of protein expression/separation/analytical technologies</li>
<li>Ability to explore and develop new approaches to further advance innovative purification and screening technologies for multispecifics</li>
<li>Extensive knowledge of biologic pipeline progression from exploratory through candidate nomination with program management experience preferred</li>
<li>Bi- and tri-specific design to support T-cell redirection and Oncology projects</li>
<li>Recognized in the scientific community through a sustained record of peer-reviewed publications and patents preferred</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Principal Research Scientist I, Discovery Biotherapeutics - T-cell Engager Multispecifics Group Lead

<h3>Job Description</h3>
Job Description
Location: Devens MA
Reports to: Director, Separations Sciences
FLSA Status: Exempt
Summary:
The Principal Application Scientist is responsible for conducting chromatography services, developing chromatographic methodology and providing technical insights to YMC America customers. This is a hands-on lab position that will utilize YMC chromatography products to conduct lab services mainly at internal YMC facilities and occasionally externally at customer sites. The developed insights will be used for promoting YMC products and for technical support / troubleshooting of clients who use YMC products.
The Principal Application Scientist will also be responsible for technical support of YMC chromatography media, technology and lab systems. They will be a “face of YMC technology” at customer sites and conferences. This will include support of instrument rentals, feasibility studies, methods development and other activities that enable customers to solve purification dilemmas by leveraging YMC technologies.
Responsibilities:
<ul>
<li>Conduct certain YMC America’s lab studies (Insight Services) under the direction of the Director, Separations Sciences. Lab facilities include those in Devens, MA and certain university collaborations. This role includes some instrument maintenance and support for the in-house lab/pilot facility.</li>
<li>Maintain a high-level working knowledge of YMC chromatography products (resins, columns, services and systems) and impart that understanding in the support of sales as a non-sales technical expert.</li>
<li>Assist in internal and external bench chromatography (CUBE) and pilot (TWIN) studies in the America’s. This includes the occasional on-site and remote set-up and training of lab instruments (Contichrom CUBE).</li>
<li>Influence potential customers to recognize the value and benefits of YMC resin and system technologies in a non-sales role.</li>
<li>Attend conferences and technical meetings as a representative of YMC America. </li>
<li>Deliver occasional presentations, papers and / or posters at industry events. Generate reports on competitive techniques and technologies.</li>
<li>Co-author white papers / applications notes that can be used to promote understanding of YMC products.</li>
<li>Assist in the review of results from external users of YMC products and provide feedback on how to better use the product in question.</li>
<li>Troubleshoot existing customer separation problems when their technical experiences / insights are applicable.</li>
<li>Play an active role in the development of new applications for existing analytical and prep products. </li>
</ul>
Required Experience &amp; Knowledge:
<ul>
<li>Bachelor’s degree in chemistry, chemical engineering, or a related field.</li>
<li>A minimum of three years’ experience as a lab scientist with an emphasis on Chromatography. </li>
<li>Must have a solid knowledge of chromatographic theory, techniques and associated instruments.</li>
<li>Hands-on experience with prep chromatography techniques and instrumentation. Particularly, as applied to peptide and/or oligonucleotide pharmaceutical compounds.</li>
<li>Ability to prioritize obligations, make self-directed decisions, multi-task, and function effectively with multiple deadlines. </li>
<li>Must be willing to travel up to 20% of the time.</li>
<li>Must possess strong documentation and technical writing skills and be able to apply relevant scientific principles and practices.</li>
<li>Must communicate clearly and concisely across levels, both orally and in writing, with a strong command of the English language.</li>
<li>Must be able to work under minimal supervision and able to work independently and in a team environment.</li>
</ul>
Preferred Skills and Experience:
<ul>
<li>A post-undergraduate degree in Chemistry, Chemical Engineering, or a related degree.</li>
<li>Experience of 3+ years performing lab services preferably related to the pharmaceutical industry, including some form of lab management responsibilities.</li>
<li>Working knowledge of automation systems for lab and production equipment in the life sciences related field.</li>
<li>Demonstrated experience in writing technical papers. Past publication experience is a plus.</li>
<li>Working knowledge of both large molecule biopharmaceutical processes and small molecule processes.</li>
<li>Language/communication skills with Spanish, German or Japanese is preferred.</li>
</ul>

PRINCIPAL APPLICATION SCIENTIST

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
We are seeking an experienced and highly motivated in vivo biologist to join our Circuit Biology team within Discovery Psychiatry. The successful candidate will play a key role in facilitating insights of circuit dysfunction in psychiatric disorders and treatment. This is an excellent opportunity to work at the forefront of psychiatry drug discovery research, contributing to target validation and compound profiling studies within a dynamic and collaborative team. &nbsp;
Key Responsibilities
<ul>
<li>Independently conceive, execute, and communicate original technical ideas and novel multi-disciplinary research that achieves project and area goals.</li>
<li>Drive internal in vivo rodent electroencephalography (EEG) efforts by developing and optimizing recording strategies</li>
<li>Develop and maintain in vivo behavior and EEG technology, methodology, and utility in psychiatric drug discovery.</li>
<li>Generate, through lab-based activities EEG and behavioral endpoints to support projects</li>
<li>Ensure alignment of efforts with the broader goals of cross-functional teams</li>
<li>Present findings to internal teams and external collaborators or conferences</li>
<li>Contribute to strategic decision-making in psychiatry drug discovery</li>
<li>Provide scientific guidance and training to junior scientists and research associates</li>
</ul>
Qualifications 
Required Qualifications
<ul>
<li>Bachelor’s Degree or equivalent education and typically, 10 years of experience, Master’s Degree or equivalent education and typically 8 years of experience, PhD and no experience necessary.</li>
<li>Extensive experience in rodent EEG surgical techniques, recordings, and analyses.</li>
<li>Demonstrated expertise in the design and execution of hypothesis-driven studies related to synaptic and circuit function</li>
<li>Ability to process and interpret large datasets using appropriate software tools</li>
<li>Strong ability to work in cross-functional teams and effectively communicate scientific finding</li>
</ul>
<ul>
<li>Desired Qualifications</li>
<li>Previous industry experience within early discovery, preferably within psychiatry research</li>
<li>Expertise in rodent behavioral models and preclinical models for anxiety and depressive disorders, and/or schizophrenia</li>
<li>Track record of impactful publications&nbsp;</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist, In Vivo Electrophysiology

<h3>Job Description</h3>
Job DescriptionThe Role: Title: Senior/Principal Scientist, Immunology and Pharmacology Job summary: The PharmaEssentia Innovation Research Center is building a world-class new drug discovery team in Boston area. We are seeking a highly motivated and independent Senior/ Principal Scientist in immunology/cancer pharmacology with a track record of scientific excellence in immunology or oncology, to join our team in Greater Boston, MA USA. As a key project team member, you will be focused on delivering all aspects of in vitro, in vivo, and ex-vivo pharmacology support. You will bring your theoretical and practical expertise to establish assay systems and deliver datasets that will have direct impact on the drug discovery process and pipeline. The Company: It’s not often that you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together. PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology, oncology and immunology, with one approved product and a diversifying pipeline. We believe in the potential to improve both the health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung. Our new research center, PharmaEssentia Innovation Research Center (PIRC), aims to leverage our current expertise in oncology and immunology therapeutic areas to identify and develop novel therapeutic opportunities. Therefore, we are recruiting talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs through disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. PIRC offers a competitive benefit package, including a competitive 401k match, medical/dental/eye care benefits, and other benefits. Summary of Key Responsibilities:
<ul>
<li>Work with in-house data scientists and or CRO to identify new targets for new project initiation. </li>
<li>Design and conduct POC study for target validation. </li>
<li>Assist discovery project leaders to set up goals and objectives for the achievement of project milestones. </li>
<li>Support cross-functional teams and work collaboratively with project leaders to ensure the timely generation and dissemination of critical program data.</li>
<li>Stay up to date with relevant technical and intellectual scientific expertise in Immune-oncology and Pharmacology and have a genuine passion for this field of research.</li>
<li>Prepare and deliver clear and accurate scientific presentations for internal and external use.</li>
</ul>
 Essential Qualifications: &nbsp;
<ul>
<li>Ph.D. in oncology, immunology, immuno-oncology, pharmacology, pharmaceutical sciences, or a related discipline.</li>
<li>9+ years of relevant post-PhD experience in industry.</li>
<li>Demonstrated scientific capability as evidenced by high-quality independent research and high impact peer-reviewed scientific publications, presentations, projects as a leading contributor. </li>
<li>Comprehensive knowledge of immunology, autoimmunity and cancer biology.</li>
<li>Extensive hand-on experiences in the initiation and leading drug discovery projects in the industry setting.</li>
<li>Strong track record of success in leading projects achieving discovery/development milestones.</li>
<li>Work independently, assess and report data in a clear and concise manner, with a clear understanding of its implications within the overall context of drug discovery.</li>
<li>Strong interpersonal and collaboration skills together with evidence of delivery in a team-oriented, collaborative environment.</li>
<li>Excellent communication and presentation skills: impactful oral and written communication.</li>
</ul>
 EEO Statement: At PharmaEssentia Innovation Research Center (PIRC), we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants without regard to race, color, religion, sex, pregnancy (including childbirth and related medical conditions), national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information (including characteristics and testing), military and veteran status, and any other characteristic protected by applicable law. PIRC believes that diversity and inclusion among our team are critical to our success as a global company, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool.&nbsp; PIRC does not accept unsolicited agency resumes. Staffing agencies should not send resumes to our HR team or to any PIRC employees. PIRC is not responsible for any fees related to unsolicited resumes from staffing agencies. &nbsp;
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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