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<h3>Job Description</h3>
Job Description
Discover Veranova
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focuses 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:
We’re seeking a motivated scientist to support the development of next-generation antibody-drug conjugates (ADCs). In this role, you’ll perform hands-on conjugation and purification experiments with antibodies, peptides, and oligonucleotides, optimizing processes that directly impact the success of innovative therapeutics. Working under the guidance of experienced technical leads, you’ll gain valuable experience while contributing to projects that drive real-world impact.
Core Responsibilities: 
<ul>
<li>Develop and implement phase appropriate bioconjugation development strategies for the attachment of cytotoxic payloads, peptides, oligonucleotides, or other small molecules to antibodies, proteins, peptides, or other therapeutic entities.</li>
<li>Delivers experimental output with a high degree of scientific integrity, schedule and target adherence, and quality with guidance. </li>
<li>Exhibits safety awareness by conducting lab and other operations in a safe manner and holding themselves accountable for safe behavior in the work environment. </li>
<li>Act on feedback and shows continuous commitment to learning and development.</li>
<li>Makes efforts towards independently working and consistently meeting deadlines.</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 the project milestones.</li>
<li>Builds an understanding of process chemistry for developing active pharmaceutical ingredients.</li>
<li>May maintain technical equipment.</li>
<li>Accomplishes other duties which are within the employee’s skills and abilities per reasonable request.</li>
</ul>
Qualifications: 
Required
<ul>
<li>Bachelor’s degree (or equivalent experience) in a chemistry related discipline.</li>
<li>Experience with bioconjugation lab and analytical techniques desired.</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>Good written and verbal communication skills.</li>
<li>Ability to work independently and in a team environment.</li>
</ul>
Preferred
<ul>
<li>Master’s degree (or equivalent experience) in a chemistry related discipline.</li>
</ul>
Special Factors 
<ul>
<li>While performing the duties of this job it is required to stand, walk, and use hands to operate objects, tools, or controls; reach with hands or arms; climb, balance, stoop, kneel, or crouch when necessary for the job activity.</li>
<li>Must be able to 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 works 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 misson 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. 
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 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>
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.
#LI-Onsite

Associate Scientist - Bioconjugation

<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 
Purpose
Describe the primary goals, objectives or functions or outputs of this position.
Investigate, identify, develop, and optimize new methods and techniques to generate reliable and reproducible data in a timely manner. Read and adapt scientific literature to accomplish assignments and demonstrate broad and versatile technical expertise within discipline.
Responsibilities
<ul>
<li>Independently design, develop, and optimize robust analytical methods using separations-based techniques (HPLC, icIEF, CE-SDS) to characterize biopharmaceutical products</li>
<li>Implement and innovate new experimental protocols/techniques.</li>
<li>Understand the goal and maintain a high proficiency in his/her projects as well as the overall program.</li>
<li>Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments.</li>
<li>Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner.</li>
<li>Perform routine and complex tasks competently and independently and generate reliable and consistent results.</li>
<li>Troubleshoot complex analytical issues and implement innovative solutions to improve method performance and efficiency.</li>
<li>Impact projects mostly through lab and/or pilot plant based activities.</li>
<li>Responsible for compliance with all applicable Corporate and Divisional policies and procedures.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li>
</ul>
Qualifications 
Qualifications
<ul>
<li>Bachelors degree&nbsp;in Biochemistry, Bioengineering, or Pharmaceutical Sciences with 5 years of relevant experience or Master’s Degree in Biochemistry, Bioengineering, or Pharmaceutical Sciences or equivalent education with typically two years of experience.</li>
<li>Theoretical and practical knowledge to carry out the job functions.</li>
<li>Strong understanding of protein biochemistry and analytical method development principles.</li>
<li>Experience in developing and optimizing methods for charge variant analysis, including both icIEF and CEX techniques, with the ability to transfer these methods to a QC environment.</li>
<li>Proficiency in AKTA purification and fractionation to support comprehensive characterization workflows.</li>
<li>&nbsp;Proficiency in operating and troubleshooting analytical instrumentation (e.g., Agilent, Waters HPLC systems, Maurice, PA800 systems).</li>
<li>Experience with the qualification and validation of analytical methods in accordance with ICH, FDA, and USP guidelines, ensuring methods are suitable for late-phase development and regulatory submissions.</li>
<li>Experience using automation to standardize high-throughput workflows.</li>
<li>Familiarity with statistical tools for data analysis, Empower and regulatory guidelines.</li>
<li>Experience collaborating with the process development, quality control, and regulatory affairs teams to align analytical strategies with project timelines and goals.</li>
<li>Knowledge of AAV separation techniques and awareness of future advancements in the field.</li>
<li>Capable of providing technical guidance and mentorship to junior scientists and laboratory staff.</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>

Scientist I

<h3>Job Description</h3>
Job DescriptionThe Company We are Alloy Therapeutics—a biotechnology ecosystem company empowering the global scientific community to make better medicines together. Through a community of partners, we democratize access to pre-competitive tools, technologies, services, and company creation capabilities that are foundational for discovering and developing therapeutic biologics. The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. At Alloy, we believe our industry should compete on getting the best drugs to patients as quickly as possible, not exclusive access to the best platforms. As a reflection of our relentless commitment to the scientific community, we reinvest 100% of our revenue in innovation and access to innovation. MAY THE BEST DRUG WIN. Alloy is headquartered in Waltham, MA with additional labs in Cambridge, UK; Basel, Switzerland, and Athens, GA. Successful members thrive in our shared culture of accountability, deliberate trust, and open communication. As a team we aspire to work together to exceed expectations and collectively contribute across the global organization to always maintain our nimble, startup culture. This is an on-site and full-time position in Waltham, MA. At Alloy, we have an ethos of “Mentorship-By-Apprenticeship” in all of our positions.&nbsp;&nbsp;We strive to have workers in the office when needed to interact organically and face-to-face.&nbsp;&nbsp;Of course, as a lab-based operation, our cells and animals grow 7 days a week, 365 days per year.&nbsp;&nbsp;We respect and value our colleagues for their hard work that requires them to be in the lab every day.&nbsp;&nbsp;We ask our people who have more flexible accommodations, like this position, to appreciate their colleagues who have less flexibility.&nbsp;&nbsp;We are all one team! The Team Alloy’s In Vitro Pharmacology team collaborates with drug discovery partners to conduct in vitro studies on therapeutic candidates across diverse modalities. Our team delivers comprehensive functional screening and characterization of biologics to support discovery and selection of lead candidates. Primary modalities are monoclonal, multispecific, and TCR-mimic antibodies, but also include cell therapies and genetic medicines. As Alloy Tx enters its next phase of growth, we are expanding our capabilities to include mechanistic studies that enhance preclinical development and further advance our translational research efforts. The Role&nbsp; We are seeking a highly motivated Scientist for in vitro screening and pre-clinical development to join our dynamic and fast-paced team. In this role, you will support the execution of in vitro functional cell-based assays to evaluate the potency, mechanism of action, and pharmacological properties of biologic therapeutics. This role requires exceptional organizational skills, a commitment to scientific excellence, and the ability to adapt to a dynamic environment. You will report to the Head of In Vitro Pharmacology and will work collaboratively in a matrixed environment to drive biologics discovery while supporting rapid decision-making in a fast-moving biotech setting. How You’ll Drive Impact&nbsp;
<ul>
<li>Execute: Support in vitro functional characterization of drug candidate molecules.</li>
<li>Develop: Bring a proactive mindset to optimize workflows for more efficient and effective data generation.</li>
<li>Deliver: Support screening campaigns to meet experimental timelines for monoclonal and multispecific antibodies, as well as TCR-mimic antibodies.</li>
<li>Collaborate: Work closely across multi-disciplinary teams in biologics discovery programs spanning all Alloy sites. Engage with an inclusive and collaborative work environment.</li>
<li>Communicate: Clearly convey scientific concepts, experimental results, and interpretations to internal and external stakeholders.&nbsp;</li>
</ul>
 Principal Responsibilities&nbsp;
<ul>
<li>Expand, bio-bank and characterize primary and immortalized cell lines to validate target expression and enable downstream assays.</li>
<li>Generate engineered cell lines using lentiviral, CRISPR or other techniques.&nbsp;</li>
<li>Support day-to-day lab and experimental workflows, including cell line inventory maintenance.</li>
<li>Execute cell-based functional assays using high-throughput approaches in primary cells, immortalized reporter cell lines, and other disease-relevant cellular systems.</li>
<li>Process human leukopaks, isolate and characterize human PBMCs.</li>
<li>Present experimental data and findings during team meetings.</li>
<li>Ensure timely and successful execution of project activities according to plan.</li>
<li>Maintain detailed and accurate laboratory records in compliance with industry standards.</li>
<li>Maintain laboratory organization and ensure compliance with safety protocols.</li>
</ul>
 Qualifications
<ul>
<li>PhD in Cell or Molecular Biology, or a related field, with 0-2 years (Scientist I) or 3-5 years (Scientist II) of relevant industry experience.&nbsp;</li>
<li>Direct experience with cell line engineering (CRISPR, lentiviral, etc) required.</li>
<li>Flow cytometry and fundamental cell and molecular biology techniques required.</li>
<li>Significant cell culture experience with primary and immortalized cell lines.</li>
<li>Experience handling human blood, leukopak processing, and PBMC isolations.</li>
<li>Hands on experience isolating and/or expanding primary immune cell subsets preferred.</li>
<li>Direct experience with high-throughput cell-based assays a plus.</li>
<li>Experience with live cell imaging (i.e. Incucyte) a plus.</li>
<li>Excellent organization, clear communication and teamwork abilities in a multidisciplinary setting.&nbsp;</li>
<li>Thrives working on a team and collaborating with others to achieve project goals.</li>
<li>Enjoys a dynamic and exciting work environment.&nbsp;</li>
<li>Detail oriented, with rigorous scientific thinking and a passion for drug discovery to improve patients’ lives.</li>
</ul>
Taking Care of Our People We support the individuality of what people need to do outside of work to empower them to do their best at work. While you focus on making better medicine together, we focus on programs and benefits that support a diverse and growing team. Whether you’re single, in a growing family, or nearing retirement, Alloy offers a variety of comprehensive and competitive benefits starting from day one. Compensation
<ul>
<li>Competitive base and equity compensation commensurate with level of experience and independence</li>
<li>401(k) company match</li>
</ul>
Health &amp; Family
<ul>
<li>Generous personal and family medical, dental and vision benefits with 100% of premiums and deductibles covered</li>
<li>Company-paid disability (STD, LTD) and life insurance</li>
<li>Paid parental leave</li>
<li>Family planning support up to $45,000 (e.g., IVF/PGT, adoption, surrogacy, egg retrieval)</li>
</ul>
Unique Perks
<ul>
<li>Unlimited PTO (paid time off) and flexible schedules</li>
<li>Annual stipend for continuing education with commitment to your career through individualized professional development plan</li>
<li>Wellness and Extensive Employee Assistance Program (EAP) including resources for mental wellness</li>
</ul>
Pay Transparency At Alloy Therapeutics, we believe in fostering trust and open communication. For this role, the estimated annual base salary range is $130,000 - $145,000, with the final offer based on factors like your experience, skills, and alignment with our needs.
Additionally, this role is eligible for equity compensation, reflecting our commitment to shared success as we work together to make better medicines.
We are proud to offer competitive compensation and benefits, aiming to support our team’s professional and personal well-being. If you have any questions about pay or benefits, we’re here to help.
Alloy Therapeutics is an equal opportunity employer.&nbsp; All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status, disability, or other legally protected status.&nbsp; If you are unable to submit an application because of incompatible assistive technology or a disability, please contact us at <a href="mailto:recruiting@alloytx.com" target="_blank">recruiting@alloytx.com</a>.&nbsp; We will make every effort to respond to your request for disability assistance as soon as possible. &nbsp;
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bKG7rjSEFO

Scientist I/II, In Vitro Pharmacology

<h3>Job Description</h3>
Job Description
*US Citizenship Required
*Onsite Position in Woods Hole, MA or Narragansett, RI
*Proposal Effort, Position is Subject to Contract Award
POSITION DESCRIPTION:
Think Tank is seeking a highly motivated Fisheries Stock Assessment Model Developer Level I to support NOAA with the development, evaluation, and implementation of stock assessment methods and models. This role will advance NOAA Fisheries' mission of maintaining sustainable fisheries and healthy marine ecosystems by producing reliable scientific information for fishery management councils and partners.
The ideal candidate will have a strong background in fisheries science, quantitative ecology, or related fields, with demonstrated experience in data analysis, model development, and scientific communication. The position offers the opportunity to collaborate with national and regional stock assessment scientists, contribute to the NOAA Fisheries Toolbox (NFT), and participate in high-impact research and management efforts.
RESPONSIBILITIES:
<ul>
<li>
Prepare proposals and plans for stock assessment methods and model development.
</li>
<li>
Conduct data and statistical analyses to develop and evaluate new models and methods.
</li>
<li>
Perform sensitivity analyses and robustness testing to validate model performance.
</li>
<li>
Collaborate with software developers to ensure assessment tools meet end-user needs.
</li>
<li>
Prepare technical documentation, reports, and user guides for modeling tools.
</li>
<li>
Deliver scientific presentations at internal meetings and international research forums.
</li>
<li>
Provide training for internal and external stakeholders on new methods and model advancements.
</li>
<li>
Draft manuscripts for publication in peer-reviewed journals.
</li>
<li>
Facilitate and lead public and panel reviews of fisheries population assessments.
</li>
</ul>
REQUIREMENTS:
<ul>
<li>Graduate degree (M.S. or Ph.D.) in fisheries science, quantitative ecology, statistics, or related discipline.</li>
<li>
Familiarity with NOAA Fisheries' stock assessments, including analytical techniques and terminology.
</li>
<li>
Proven ability to develop and implement standards in data management and documentation.
</li>
<li>
Demonstrated expertise in:
<ul>
<li>
Project management of complex scientific programs.
</li>
<li>
Coordinating and leading diverse scientific teams.
</li>
<li>
Communicating technical concepts effectively to scientific, management, and public audiences.
</li>
</ul>
</li>
<li>
Strong time management skills and ability to work independently.
</li>
<li>
Adaptability to shifting priorities and fast-paced environments.
</li>
<li>
High attention to detail and commitment to scientific rigor.
</li>
</ul>

Fisheries Stock Assessment Model Developer Level I

<h3>Job Description</h3>
Job DescriptionDescriptionUnder general supervision, responsible for the synthesis of chemicals through various routine manufacturing procedures including the operation of high-pressure reactors. Responsible to work safely with process equipment and hazardous chemicals. Key Responsibilities·&nbsp; &nbsp; &nbsp; &nbsp;Responsible to execute tasks on the manufacturing floor through various routine manufacturing procedures including the operation of high-pressure reactors.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible to operate safely process equipment and work with hazardous chemicals.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible for assembling, configuring and leak testing high-pressure reactors.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible for maintaining in good operational condition production equipment, including high-pressure reactors, process piping and process valves.·&nbsp; Responsibleformaintainingacleanandorderlyworkareawhileobservingstringentsafety requirements.&nbsp;·&nbsp; &nbsp; &nbsp; &nbsp;Responsible for recording and maintaining accurate production, quality and safety records.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible to follow and sustain company`s policies, internal procedures, systems and programs.·&nbsp; &nbsp; &nbsp; &nbsp;May perform computer-based tasks as necessary such as working with Excel and Word software. May perform other facilities duties of a similar complexity as requested, including support of building maintenance, support issues troubleshooting, housekeeping activities, assist Lab activities, and assisting with company`s environmental and safety programs. Minimum Qualifications·&nbsp; &nbsp; &nbsp; &nbsp;Mechanical aptitude and the ability to work with hand tools.·&nbsp; &nbsp; &nbsp; &nbsp;Passing&nbsp; medical evaluation for, and the wearing of a respirator while working is required.&nbsp;&nbsp;Educational Requirements: ·&nbsp; &nbsp; &nbsp; &nbsp;High school diploma or equivalent required ·&nbsp; &nbsp; &nbsp; &nbsp;Previous experience on checmical manufacturing floor or handling chemicals is a plus.&nbsp; Benefits
<ul>
<li>Medical, Dental, Vision - effective day one of employment.</li>
<li>401(k) with company match with immediate vesting - effective first of the month, following date of hire.
<ul>
<li>First 3% is matched dollar-for-dollar.&nbsp;</li>
<li>Second 3% is matched at 70 cents on the dollar.&nbsp;</li>
</ul>
</li>
<li>3 Weeks' Vacation.</li>
<li>12 Paid Holidays.</li>
<li>Basic Life, AD&amp;D, STD, and LTD provided at no cost to employee.</li>
</ul>

Chemical Facilities Technician I

<h3>Job Description</h3>
Job Description
At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care). 
Position Summary: 
This role is primarily responsible for calibrating and coordinating the calibration of a diverse range of electrical and mechanical equipment while adhering to good manufacturing practices. The role may also perform and/or assist with the installation, maintenance, testing and repair and of the equipment.
Schedule: This position is in-office Monday-Friday.
Position Scope:
<ul>
<li>Manage vendors and calibrates instruments such as, RO systems, clean steam generators, autoclaves, parts washer systems, lab equipment, and manufacturing equipment. </li>
<li>Develop and maintain the Blue Mountain Regulatory Asset Manager (BMRAM) system.</li>
<li>Maintain all calibration records and instrument tagging. </li>
<li>Write/develop Standard Operating Procedures (SOPs), and/or protocols.</li>
<li>Write initial deviations using the QMS system.</li>
<li>Assist in change control documentation and deviation notifications.</li>
<li>Serve as information resource for validation technicians, contractors and vendors.</li>
<li>Perform scheduled, new and emergency calibrations activities with vendors on all critical process equipment and lab instrumentation ensuring compliance with SOPs and cGMPs.</li>
<li>Troubleshoot instrument control loops like temperatures, pressure, flow controllers, etc.</li>
<li>Follow all environmental, health, and safety requirements and protocols.</li>
<li>Understand schematics, logic ladder diagrams, and P&amp;IDs.</li>
<li>Identify/coordinate inventory for spare parts used on critical instruments.</li>
<li>Support operations during 1st shift and be available after hours as needed to support the business.</li>
<li>Assist in equipment selection, specification and commissioning.</li>
<li>Other duties as assigned.</li>
</ul>
Qualifications: 
<ul>
<li>Bachelors degree in STEM or High School degree with equivalent years of experience.</li>
<li>Minimum 6+ years related experience in the areas such as temperature, pressure, flow (liquid &amp; gas), pH, conductivity, humidity, lab instrumentation controllers, depyrogenation oven, steam generators, steam boilers, air compressor, vacuum pumps, and lab instrumentation.</li>
<li>Knowledge of pharmaceutical manufacturing process equipment and lab instrumentation.</li>
<li>Basic knowledge on cleanroom classifications.</li>
<li>Familiarity with FDA, cGMP, SOPs, ASNI/NCSL, EU and ISO standards.</li>
<li>Good organizational skills.</li>
<li>Experience utilizing quality manage systems like Trackwise and BMRAM preferred.</li>
<li>Excellent verbal, writing and interpersonal communication skills.</li>
<li>Ability to gown and gain entry to manufacturing areas wearing personal protection equipment - safety glasses, gloves, gowns, etc. </li>
<li> Ability to be available after hours as needed to support the business.</li>
<li>Ability to lift up to 25 lbs.</li>
</ul>
Why Vericel?
<ul>
<li>Cutting-Edge Science: Work with a leading regenerative medicine product that is transforming patient care.</li>
<li>Career Growth: Be a part of a growing organization with opportunities to expand your impact.</li>
<li>Collaborative Culture: Work alongside a team of dedicated professionals who are passionate about improving lives.</li>
</ul>
EEO Statement
All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. Vericel Corporation is an Equal Opportunity/Affirmative Action Employer.
Vericel Corporation is VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state.

Metrology Lead

<h3>Job Description</h3>
Job DescriptionFisheries Biological ScientistCooperative Research Branch (CRB) Support ServicesFalmouth, MA (WHOI); Pocasset, MA; and Narragansett, RI
This role participates in all phases of CRB research projects by serving as a team member on cooperative studies and emphasizes collaboration with fishing partners, development of outreach materials, and participation in meetings and conferences for the Northeast Fisheries Science Center (NEFSC) 
Join @Orchard in bridging science and industry to support sustainable fisheries. This role supports the Cooperative Research Branch (CRB) of NOAA’s Northeast Fisheries Science Center (NEFSC), which partners with commercial fishers to generate critical data on fishing effort, catch composition, and marine ecosystems.
As part of this collaborative mission, @Orchard is seeking a Fisheries Biological Scientist team membertocontribute to field-based research projects spanning trawl, gillnet, scallop dredge, lobster trap, longline, and hook-and-line fisheries across the Northeast. From Atlantic wolffish to environmental monitoring, your work will help fill key data gaps and drive science-based management decisions.
In this role, you’ll work side-by-side with NOAA scientists and fishing partners to collect, analyze, and communicate biological and environmental data. You’ll participate in cooperative surveys, support community engagement, and help translate field results into actionable scientific outputs for assessments and outreach.
If you're passionate about marine research, enjoy engaging with the fishing community, and bring strong skills in field science and data interpretation, this opportunity puts you at the heart of impactful ecosystem science.
Key Responsibilities
As a Fisheries Biological Scientist, your primary duties will include:
<ul>
<li>Participating in all phases of research investigation, including problem definition, planning, execution, analysis, interpretation, and reporting of findings, and analyzing and preparing data for use in stock and ecosystem assessments and fisheries management.</li>
<li>Serving as a team member on cooperative research projects that bring the science and fishing communities together to address research questions and data needs. </li>
<li>Coordinating with research and industry partners in defining and refining research approaches and providing regular updates to project teams. </li>
<li>Developing and maintaining project documentation to ensure reproducibility of research, including metadata to support data processing. </li>
<li>Assisting in the documentation and development of research-related permit applications. </li>
<li>Communicating with and collaborating with fishing industry members about project goals, approaches, implementation, and results. </li>
<li>Providing logistical and at-sea support for industry participants in cooperative research programs, including recruitment with community leaders, program introductions, port visits to identify setup requirements and constraints, equipment deployment and training, troubleshooting support, and data collection, and participating in research cruises, as necessary.</li>
<li>Participating in the observation, collection, sorting, and processing of fish catch, biological samples, oceanographic dynamics, and other fisheries information for use in scientific research.</li>
<li>Extracting relevant data sets, creating data summaries, graphs, tables, charts, or data visualizations for technical publications, outreach documents, and leadership briefings. </li>
<li>Conducting statistical analysis and modeling exercises to understand fisheries, population, and ecosystem dynamics </li>
<li>Fulfilling internal and external data requests, as needed.</li>
<li>Producing technical documentation of research goals, methods, results, and applications for dissemination to the public, scientific community, and fishing industry. </li>
<li>Developing and maintaining collaborations with other scientists to progress the utility, application, and impact of cooperative research data in stock assessments, ecosystem-based fisheries science, fisheries oceanography, and other disciplines and management </li>
<li>Participating in industry meetings, scientific symposia, workshops, and conferences to support and present NOAA projects</li>
<li>Providing operational support for cooperative research field work.</li>
<li>Assisting in developing outreach materials, including user manuals, troubleshooting guides, newsletters, and articles on Cooperative Research accomplishments, challenges, and objectives.</li>
<li>Providing logistical and at-sea support for cooperative research field research programs. (possibly)</li>
</ul>
Required Qualifications &amp; Experience
To be successful in the role, candidates must possess the following qualifications:
<ul>
<li>B.S. degree in a field directly related to the task requirements. </li>
<li>Minimum of 2-3 years of experience in the field or in a related area, or of progressively higher-level graduate education leading to a master’s degree or equivalent graduate degree. </li>
<li>Served as a researcher or member of a research team performing research on fisheries or related marine science. </li>
<li>Ability to work collaboratively with members of the commercial fishing industry, including working at sea and at the dock. </li>
<li>Experience with identifying and applying technical solutions within fisheries research settings. </li>
<li>Experience manipulating complex (i.e., fisheries) data sets. </li>
<li>Experience writing scientific documentation. </li>
<li>Experience in the identification, collection, sorting, and processing of fish samples, biological samples, and oceanographic data. </li>
<li>Familiarity with data analysis tools, such as R.</li>
<li>Proficient in current MS Office software programs.</li>
<li>Proficient in the primary G Suite tools, including Gmail, Drive, Docs, Sheets, Slides, Forms, Calendar, Sites, and Meet.</li>
</ul>
Essential Conditions of Employment
<ul>
<li>Driver's License: Must hold a valid state driver’s license with the ability to operate a federal motor vehicle.</li>
</ul>
This position includes authorized overtime, travel, and training as required by the project scope. If you are ready to contribute to a vital environmental mission, we encourage you to apply.
Established in 2010, @Orchard LLC has an exceptional reputation, providing staffing solutions to time-sensitive, talent scarcity issues to deliver better talent management ROI. Our specialty lies in the critical area of program talent acquisition and resource management, not in one narrow skillset, but across many areas of technical and functional delivery. To learn more about our other exciting opportunities, visit our Jobs Page at <a href="http://www.atOrchard.com" target="_blank">www.atOrchard.com</a>.

Fisheries Biological Scientist

<h3>Job Description</h3>
Job Description:
The Role
We are looking to hire a Director, Quant Strategist to strengthen our US team. By combining hands-on quantitative research with team leadership, the successful candidate will be accountable for developing and monitoring strategies, ensuring model robustness, troubleshooting issues, and driving workflow enhancements.
This role will play a central part in driving our DeFi research efforts and requires a strong technical background, excellent problem-solving skills, and the ability to manage and mentor a small team whilst coordinating our team efforts across multiple stakeholders, and cross-regional teams.
Key Responsibilities
Strategy Research &amp; Implementation
<ul>
<li>Conduct research into yield-oriented strategies across of a range of market structures and venues, with an emphasis on identifying risk-adjusted return opportunities</li>
<li>Design and run backtests to evaluate strategy performance, stress-test assumptions, and establish statistical robustness</li>
<li>Help deeply analyze protocols to understand mechanics, risks, and potential drivers of yield. Translate insights into research hypotheses and strategy ideas</li>
</ul>
Monitoring &amp; Troubleshooting
<ul>
<li>Act as a first line of response for alerts, coordinating with global colleagues to escalate and resolve issues quickly</li>
<li>Translate lessons learned from monitoring into research and operational playbook improvements</li>
</ul>
Team Leadership
<ul>
<li>Manage and mentor a team of quants/analysts: run sprints, allocate tasks, and oversee objectives and results</li>
<li>Conduct code and strategy reviews, enforce testing standards, and support professional development</li>
<li>Foster a culture of collaboration, technical excellence, and delivery focus</li>
</ul>
Risk &amp; Stakeholder Interaction
<ul>
<li>Present weekly PnL, risk metrics, and performance attribution to senior management</li>
<li>Ensure transparent communication and reporting to internal stakeholders</li>
</ul>
The Expertise and Skills You Bring
Technical Expertise
<ul>
<li>Proficiency in Python (e.g., Pandas, NumPy, PyTorch, etc.) and SQL with the ability to write production-quality, maintainable code</li>
<li>Strong grounding in portfolio mathematics, risk modelling and statistical methods</li>
<li>Experience building and maintaining research infrastructure, including data pipelines, backtesting frameworks, and related tools</li>
</ul>
Communication &amp; Engagement
<ul>
<li>Able to distill complex models into actionable insights for technical and non-technical stakeholders</li>
<li>Collaborate style and effective at working across teams and time zones, fostering strong engagement with colleagues</li>
</ul>
Analytical &amp; Research Skills
<ul>
<li>Skilled at working with large, complex, and imperfect datasets, extracting signal from noise, and applying methods ranging from classical statistics to machine learning where appropriate</li>
</ul>
Professional Experience
<ul>
<li>Typically, 10+ years of relevant experience in digital assets, and/or quantitative research</li>
<li>Advanced degree (Master’s or PhD) in a quantitative field (e.g. Mathematics, Statistics, Computer Science, Physics, or a related discipline)</li>
<li>Previous experience managing or mentoring a small team of quants, developers, or researchers</li>
</ul>
Preferred Qualifications
<ul>
<li>Prior exposure to DeFi yield strategies (staking, LP, lending, re-staking)</li>
<li>Experience with systematic trading across traditional asset classes (equities, FX, commodities, fixed income etc.)</li>
<li>Demonstrated initiative in generating ideas and improving processes</li>
<li>Comfort working across time zones and collaborating with distributed teams</li>
</ul>
The Team
Fidelity Digital Assets (FDA) is dedicated to building products and services that help institutions adopt digital assets and innovate within the increasingly digital world of finance. Fidelity Investments began researching blockchain technology and digital assets solutions in 2014, and years of research and development have provided us with the deep expertise necessary to build the future of finance.
Come join the Quantitative Strategies team within Fidelity Digital Assets to help grow our business initiatives within DeFi and contribute to our research and product capabilities using your insights.
Certifications:Category:Data Analytics and Insights
Most roles at Fidelity are Hybrid, requiring associates to work onsite every other week (all business days, M-F) in a Fidelity office. This does not apply to Remote or fully Onsite roles.
Please be advised that Fidelity’s business is governed by the provisions of the Securities Exchange Act of 1934, the Investment Advisers Act of 1940, the Investment Company Act of 1940, ERISA, numerous state laws governing securities, investment and retirement-related financial activities and the rules and regulations of numerous self-regulatory organizations, including FINRA, among others. Those laws and regulations may restrict Fidelity from hiring and/or associating with individuals with certain Criminal Histories.

Director, Quant Strategist

<h3>Job Description</h3>
Job Description
About General Fluidics General Fluidics is a clinical diagnostics startup developing the Axess™ platform, a breakthrough point-of-care system that delivers laboratory-grade performance across clinical chemistry, hematology, and immunoassays from a single blood sample. By integrating three “gold standard” analytical technologies into one compact instrument, we are transforming how clinicians access and act on diagnostic data. Learn more at generalfluidics.com.
The Role We are seeking a highly motivated Senior Research Associate to join our R&amp;D team and help expand our menu of diagnostic assays for veterinary and human health applications. This is an R&amp;D-focused laboratory role—ideal for a scientist who thrives on experimental design, assay development, and hands-on instrumentation work. You will design, troubleshoot, and interpret experiments where answers are unknown, not simply execute QC protocols.
Reporting to the VP of Assay Development, you will work closely with engineers and scientists to optimize assay and instrument performance, generate data for analytical validation, and accelerate our path to regulatory clearance and product launch. This role is best suited for a junior scientist with prior industry experience and&nbsp;self-starter who can work independently under mentorship, with the drive to solve problems in a fast-paced, startup environment.
Key Responsibilities
<ul>
<li>
Design, develop, and validate clinical chemistry, hematology, and immunoassays on the Axess™ point-of-care instrument.
</li>
<li>
Independently plan and execute experiments to optimize assay and instrument performance, collaborating closely with engineers on system integration.
</li>
<li>
Perform data analysis and statistical evaluation to guide assay development and regulatory submissions.
</li>
<li>
Author experimental protocols, R&amp;D reports, and supporting documentation.
</li>
<li>
Support quality assurance through calibration, control protocols, and proficiency testing.
</li>
<li>
Work safely with human and animal blood specimens in compliance with biosafety regulations.
</li>
</ul>
Qualifications
<ul>
<li>
Bachelor’s, Master’s, or PhD in biotechnology, biomedical engineering, chemistry, physics, or related field.
</li>
<li>
3-6 years of prior industry R&amp;D experience (not academic lab or QC/manufacturing)&nbsp;
</li>
<li>
Experience designing and interpreting experiments, analyzing data, and troubleshooting unexpected results.
</li>
<li>
Hands-on laboratory skills: pipetting, assay development, reagent preparation, use of biosafety cabinets.
</li>
<li>
Familiarity with clinical instrumentation (e.g., flow cytometry, hematology analyzers, clinical chemistry, immunoassays) strongly preferred.
</li>
<li>
Exposure to diagnostic assay development, validation, or instrumentation is a plus.
</li>
<li>
Comfortable in a dynamic startup environment: onsite presence, ownership mentality, willingness to push projects forward outside a strict 9–5.
</li>
<li>
Excellent communication skills, with the ability to clearly present scientific concepts and data.
</li>
</ul>
Who You Are
<ul>
<li>
Curious, creative, and excited to tackle open-ended scientific questions.
</li>
<li>
Thrives on independence but values mentorship and collaboration.
</li>
<li>
Driven by the opportunity to help build a transformative diagnostic platform from the ground up.
</li>
</ul>
Company DescriptionGeneral Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus. 
<h3>Company Description</h3>
General Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus.

Senior Research Associate

<h3>Job Description</h3>
Job DescriptionJob Title: Clean Room Assembler Job Description
As a Clean Room Assembler, you will be responsible for assembling product parts on the assembly line in accordance with production guidelines. You will also perform spot checks of products to ensure adherence to approved quality standards.
Responsibilities
<ul>
<li>Assemble assigned product parts on the assembly line following production guidelines.</li>
<li>Perform spot checks of products to ensure adherence to approved quality standards.</li>
<li>Notify management of product discrepancies or equipment malfunctions.</li>
<li>Adhere to established company policies and procedures, paying special attention to safety regulations.</li>
<li>Wear personal protective equipment in accordance with training guidelines.</li>
<li>Perform other related duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>Experience in assembly, preferably in a cleanroom environment.</li>
<li>Ability to work with microscopes, hand tools, and perform medical assembly.</li>
<li>Comfortable using tweezers, cutters, wire strippers, and adhesives.</li>
<li>Strong attention to detail and mechanical assembly skills.</li>
<li>Proficiency in work instruction and hand dexterity.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Strong written communication skills.</li>
<li>Physical dexterity.</li>
<li>Reading skills.</li>
<li>Effective time management.</li>
<li>Mechanical skills.</li>
</ul>
Why Work Here?
Join a dynamic team that values safety and quality in a clean and flexible work environment. Enjoy a supportive company culture that emphasizes personal growth and development.
Work Environment
Work in a clean room environment with flexible hours, typically from 7:00 AM to 3:00 PM.
Job Type &amp; Location
This is a Contract to Hire position based out of NASHUA, New Hampshire.
Pay and Benefits
The pay range for this position is $22.00 - $24.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in NASHUA,NH.
Application Deadline
This position is anticipated to close on Sep 30, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

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