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<h3>Job Description</h3>
Job Description
Duties &amp; Responsibilities:
<ul>
<li>
Assemble plastic and metal components into medical devices in accordance with approved manufacturing procedures.
</li>
<li>
Utilize small hand tools (both manual and electric), manual presses, assembly fixtures, calibrated instruments, measurement equipment, microscopes, and test fixtures.
</li>
<li>
Utilize documentation such as Bill of Materials, product flow charts, work orders, check sheets, visual aids, production reports and assembly drawings to assemble product and record results.
</li>
<li>
May perform soldering, fabricating, crimping, mechanical assembly, sealing, ultra-sonic welding, bonding and gluing with adhesives, Epoxy or RTV.
</li>
<li>
Kitting assemblies using a parts list, scanner and inventory software as required.
</li>
<li>
Participates in any routine start up or end of day equipment inspections or verifications.
</li>
<li>
Inspects work throughout the assembly process and communicates any quality or operational issues to appropriate leader.
</li>
<li>
Maintain neat, orderly and clean work area to ensure efficiency and no safety hazards. Participate in safety programs, meetings, and trainings as required. Bring safety concerns to the attention of management.
</li>
<li>
Participate in continuous improvement activities as part of a cross-functional team.
</li>
<li>
Meet all quality, quantity and good manufacturing practices to satisfy customer and Regulatory Affairs requirements. Read and/or understand operating procedures for specific products where training has been completed.
</li>
<li>
Show constant attention to detail, and immediately inform supervisor of anything out of the ordinary, or anything which does not conform to the approved process sheets.
</li>
<li>
Work with Engineers and line leads to resolve issues and correct procedures to ensure quality and efficiency.
</li>
<li>
Maintain Clean Room integrity by using proper attire and adherence to Clean Room environment practices and procedures as applicable.
</li>
<li>
Maintain accurate records/documentation related to quality, work in progress, test results, labor (e.g. timecards), and special projects.
</li>
<li>
Adhere to general safety rules, manufacturing procedures, company policies and procedures, ISO, QSR, and FDA regulations.
</li>
</ul>
Company DescriptionConnexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve. 
<h3>Company Description</h3>
Connexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve.

Assembler (Cleanroom)

<h3>Job Description</h3>
Job Description
Position: Medical Technologist / Medical Laboratory Scientist – General Supervisor We are a small, independent laboratory within a Rheumatology clinic seeking a full-time Medical Technologist or Medical Laboratory Scientist to serve as General Supervisor under the direction of the Laboratory Director. Position Overview The Laboratory Supervisor will oversee daily laboratory operations, ensuring compliance with CLIA, CMS, and DPH requirements as well as established safety and quality standards. This role requires both technical expertise and leadership skills to guide a small team of technicians while maintaining efficiency, accuracy, and regulatory compliance. This is a generalist position with primary responsibilities in: ● Clinical chemistry ● Hematology ● Synovial fluid analysis ● Manual differentials Additional duties include developing and maintaining standard operating procedures (SOPs), performing venipuncture for sample collection, conducting assays, and ensuring timely and accurate reporting of results. Key Responsibilities ● Supervise and support daily laboratory operations under the Laboratory Director ● Ensure adherence to quality assurance, quality control, and safety standards ● Write, review, and update SOPs in alignment with regulatory requirements ● Perform and oversee testing in chemistry, hematology, and synovial fluid analysis ● Conduct and review manual differentials with accuracy and efficiency ● Perform venipuncture and specimen collection as needed ● Prepare for and maintain readiness for regulatory inspections (CLIA, CMS, DPH) ● Train and mentor laboratory staff, fostering professional growth and development Qualifications ● ASCP or AMT certification preferred, or certification-eligible within 6 months and certified within 1 year ● Associate’s or Bachelor’s degree in Medical Laboratory Technology, Medical Laboratory Science, or equivalent with at least 24 credit hours of academic science (minimum of 8 hours in biological sciences and 8 hours in chemical sciences) ● Minimum of 3 years of laboratory experience (including clinical rotations) ● Proficiency in manual differentials required ● Commitment to ongoing continuing education as required by certifying agency ● Strong organizational, communication, and leadership skills

Lab Supervisor

<h3>Job Description</h3>
Job Description
Boston, MA USA | Full-time | Hybrid | Fixed-term | 3 – 6 months 
About us 
Riverlane’s mission is to master quantum error correction (QEC) and unlock a new age of human progress. From advances in material and climate science, to complex chemistry simulation for new drug design, quantum computers will help humanity solve some of its most important challenges. But without QEC, the industry’s defining technical challenge, such breakthroughs can never be achieved. Riverlane is the world leader in QEC technology. QEC is a complex problem that requires a range of skills, talent and passion. 
We recently raised $75 million to accelerate our cutting-edge R&amp;D. We partner with many of the world’s leading quantum computing companies and governments to accelerate their path to utility-scale quantum computers. We’re making remarkable progress and growing fast. Join us! 
 About the internship 
Our full-time internships are designed to enable current PhD students in a quantitative field to step out of their PhD research for a short time period and translate their skills and expertise into an industrial setting. We welcome and encourage applications from people who do not have a background in quantum computing, including computer scientists, software engineers and developers. There are three areas a PhD intern can work in - you can view more details here. 
As a Riverlane PhD intern in the US, you will join us at our Boston office, where you will work on the core challenges in developing the error correction stack. This work requires a wide range of backgrounds and skills, including those with backgrounds in computer science, software/ embedded software engineering, verification, digital design, electrical and electronic engineering, experimental physics (and related disciplines), who also have a keen interest in working on challenging problems in quantum error correction. 
Projects that an intern could work on in Boston include: 
<ul>
<li>Implementing decoders in software or on dedicated hardware </li>
</ul>
<ul>
<li>Building tools to model noise of different qubit types </li>
</ul>
<ul>
<li>Systems integration </li>
</ul>
Our Quantum Error Correction research team has several exciting themes. Within each key area, there will be multiple projects on which an intern could work. The details of the specific project will be tailored to make the best use of your background and skills. 
Every intern will have a dedicated supervisor who will support you to try and produce a concrete output by the end of the internship e.g. a paper, product, or software tool. 
Previous internship projects have been highly successful, as evidenced by interns leading contributions to various publications, for example: “Error-corrected Hadamard gate simulated at the circuit level”, G.P. Gehér, et al. (2024). 
 What you will do 
<ul>
<li>Develop an understanding of quantum algorithms and industrial applications, control systems for quantum computers, and/or the error correction schemes required for large scale quantum computing. </li>
</ul>
<ul>
<li>Research, devise and develop algorithms and software to enhance Riverlane’s capabilities in the above areas. </li>
</ul>
<ul>
<li>Contribute to one or more projects that are core to Riverlane’s scientific goals </li>
</ul>
<ul>
<li>Discuss ideas with colleagues and communicate research in the form of presentations and reports </li>
</ul>
Requirements
What we need 
<ul>
<li>Currently pursuing (or actively enrolled to imminently start) a PhD degree in a highly numerate subject, such as a Science, Mathematics, Computer Science, Engineering or another related technical field (QEC experience is a bonus, but not required!) </li>
</ul>
<ul>
<li>Evidence of creative, high-quality academic work </li>
</ul>
<ul>
<li>Strong ability in algorithmic and abstract reasoning </li>
</ul>
<ul>
<li>Excellent critical thinking and problem-solving ability </li>
</ul>
<ul>
<li>Experience with at least one general purpose programming language </li>
</ul>
<ul>
<li>Strong communication skills, both written and verbal, with a track record of communicating scientific results to colleagues and other audiences </li>
</ul>
<ul>
<li>Ability to take initiative and to work well as part of a team </li>
</ul>
<ul>
<li>Passion for translating academic expertise into an applied industrial setting </li>
</ul>
 Important notes 
<ul>
<li>We can only accept applications from current PhD students (or those who are enrolled to imminently their start their PhD) who are local to the United States currently. Regrettably, we are unable to provide relocation or sponsorship.</li>
</ul>
<ul>
<li>PhD internships are full-time and between 3 and 6 months in length. Start dates can be flexible in 2026 – please let us know your preferred dates when you apply. </li>
</ul>
<ul>
<li>This internship is based at our Boston, MA office in the US. </li>
</ul>
<ul>
<li>Please note that we require a signed agreement from you assigning the ownership of any IP produced during your internship to Riverlane. </li>
</ul>
 How to apply 
Please upload a cover letter and CV. Your cover letter should explain why you are applying for the internship and what skills and experience you can bring to the role. 
Deadline 
Please submit your application by Sunday 16th November 2025. Interviews will be held in Boston, MA or via video (Teams) in late November/early December 2025. 
Stipend 
Interns receive a competitive stipend. We will also pay for any expenses incurred as part of your role e.g. travel to meetings or conferences etc. We are unable to pay for travel to the office or accommodation in Boston. 
Benefits
What can you expect from us 
Alongside your stipend, you can expect a diverse work environment that brings together experts in many fields (including software and hardware development, quantum information theory, physics and maths) and over 20 different nationalities. We also offer free snacks and refreshments and a regular program of learning events. 
If you have any queries, please contact <a href="mailto:jobs@riverlane.com" target="_blank">jobs@riverlane.com</a>.
Everyone is welcome at Riverlane. We are an equal opportunities employer and encourage applications from eligible and suitably qualified candidates regardless of age, disability, ethnicity, gender, gender reassignment, religion or belief, sexual orientation, marital or civil partnership status, or pregnancy and maternity/paternity. 
Women and other underrepresented groups may be less likely to apply for a role unless they meet all or nearly all of the requirements.  If this applies to you, we still encourage you to apply - you may be a great fit, even if you don’t meet every single qualification. We’d love to hear from you.  
If you need any adjustments made to the application or selection process so you can do your best, please let us know. We will be happy to help.

PhD Internship 2026 - Quantum Science, US

<h3>Job Description</h3>
Job Description
*US Citizenship Required
*Onsite at a NEFSC Facility
POSITION DESCRIPTION:
Think Tank is a woman-owned small business with more than 27 years of proven success delivering exceptional IT and marine fisheries services to the federal government. We are currently seeking an ideal candidate for the position of Marine Biologist to support an upcoming proposal with the National Oceanic and Atmospheric Administration. Résumé of successful candidate(s) will be included with our proposal. 
The Marine Biologist contributes scientific expertise to support the research, assessment, and conservation of marine species including marine mammals, sea turtles, seabirds, and pinnipeds. This position involves both fieldwork and laboratory/data analysis responsibilities.
RESPONSIBILITIES:
<ul>
<li>Conduct population and ecological studies using visual, acoustic, and satellite data.</li>
<li>Participate in tagging, biological sampling, health assessments, and telemetry deployments.</li>
<li>Analyze behavioral, health, and distributional data using quantitative and spatial models.</li>
<li>Contribute to field planning, equipment maintenance, and data archiving.</li>
<li>Assist with scientific writing, presentations, and outreach.</li>
</ul>
REQUIREMENTS:
<ul>
<li>Bachelor's or Master's degree in marine biology, ecology, or related field. PhD preferred.</li>
<li>Experience with marine species identification, tagging, and field sampling.</li>
<li>Familiarity with acoustic analysis tools (e.g., Raven, Pamguard) and programming (Python, R).</li>
<li>Ability to perform physically demanding fieldwork under variable condition</li>
<li>Experience with animal handling and small boat operations is a plus.</li>
</ul>

Marine Biologist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Canam Bridges designs, manufactures and installs steel bridges for major infrastructure contractors across North America. Canam Bridges is a member of Canam Group, which has over 5,100 employees and operates 22 plants in North America, as well as engineering offices in Canada, Romania, India and the Philippines.
Job Description 
Your life at Canam Bridges As a Metrologist at Canam Bridges, you will be responsible for taking factory measurements using “Station Total” and “Laser Tracker Faro” surveying tools. Your analytical mind will allow you to use your 3D vision superpowers to complete dimensional measurements. To break your routine, you will alternate between taking factory measurements, recording data, and writing reports. Your computer knowledge will make you an expert in AutoCAD and Polyworks. That said, it is your team that will give you the most satisfaction, because at Canam Bridges, we are a solid combination of expertise and pride!
Job Description Assist Plant Manager and production staff in developing production plans, ensure production objectives are met, offer recommendations, and implement production events and programs. The Metrologist is responsible for performing such work consistent with the company’s corporate mission, values, and departmental financial objectives.
Essential Functions
<ul>
<li>Assist in the production-planning process, schedules, assignments, and&nbsp;production sequences to meet production goals.</li>
<li>Read and analyze data, production schedules, and other records and reports to determine production productivity and to evaluate current production estimates and outputs.</li>
<li>Identify direct and indirect labor issues and production problems, make recommendations, and assist management in developing a corrective action plan.</li>
<li>Compile production planning notes, sketches, prints, schedules, contract documents and specifications into a formal build plan.</li>
<li>Aid in the detailing and manipulation of models to accommodate additional views for fabrication per planning session. Assist on designing fixtures and jigs to aid fabrication.</li>
<li>Responsible for conventional and CNC machining, to include managing direct labor to accomplish coverage on equipment in support of production needs.</li>
<li>Train and assist production members in the operation of conventional and CNC machining equipment in line with formal build plans.</li>
<li>Perform other job duties as assigned by the Plant Manager.</li>
</ul>
Qualifications 
<ul>
<li>Associate’s degree (A. A.) or equivalent from two-year college or technical school and/or experience in detailing and fabrication.</li>
<li>Must be able to use logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to production or productivity problems.</li>
<li>Experience with AutoCAD, Tekla, FeatureCam, Polyworks, Station Total, Laser Tracker Faro, and other software preferred.</li>
<li>Ability to communicate information and ideas in speaking, so others will understand.</li>
<li>Analyze information and evaluate results to choose the best solution and solve problems.</li>
<li>Must be able to schedule events, programs, and activities, as well as the work of others.</li>
<li>Job requires a willingness to lead, take charge, and offer opinions and direction.</li>
</ul>
 Additional Information 
Work Environment General office and production environment. Daily exposure to computer display and shop environment.&nbsp;&nbsp;
Remuneration We offer a competitive compensation and benefits package, as well as excellent opportunities for training and advancement.
Canam&nbsp;is an Equal Opportunity/Affirmative Action employer.&nbsp;All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
If you need a reasonable accommodation for any part of the employment process, please contact us by email at <a href="mailto:lorri.boynton@canamgroupinc.com" target="_blank">lorri.boynton@canamgroupinc.com</a> and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this e-mail address.

Metrology Technician

<h3>Job Description</h3>
Job Description
Wildlife Technician
Critter Control is a National Wildlife and Pest Management firm, servicing the Massachusetts&nbsp;area. We have been in business locally for over 22&nbsp;years and have over 100 offices nationwide. Our outstanding customer service and the high-quality solutions offered to our clients are what set us apart from other companies.
We are looking to fill a full-time&nbsp;position&nbsp;for a Wildlife Control Service Technician to handle residential and commercial accounts.
The ideal candidate will have a strong work ethic, possess a willingness to learn, and be&nbsp;committed to meeting the same high standards that we have established to satisfy our clients.
Must have excellent communication skills and excel in customer service.
Previous experience in the pest control or nuisance wildlife control industry is preferred.
Applicant Requirements:
- Professional in appearance and communication
- Organized with an emphasis on document management and daily route management
- Must possess a strong ability to operate a tablet and smartphone
- Comfortable handling face-to-face, email, and phone interactions with clients
- Able to implement basic sales and customer service practices
- Able to lift and carry&nbsp;75&nbsp;pounds
- A dedicated problem solver
- Comfortable climbing ladders and performing thorough home inspections
- Applicant must be available to work weekends
- This is a non-smoking position
Benefits :
- 401k with employer contribution match
- Medical, Dental, &amp; Vision Insurance
- Vacation and PTO
- Paid Holidays
-&nbsp;Company Vehicle
- Company Phone
- Fuel Card
- Work Attire
Job Type: Full-time
Compensation (once fully licensed): $23.00/Hour (plus commission)
Required education:
·&nbsp;&nbsp;&nbsp;High school or equivalent
Required experience:
·&nbsp;&nbsp;&nbsp;Comfortable with ladders and attics?: 1 year
Required license or certification:
·&nbsp;&nbsp;&nbsp;Valid Massachusetts&nbsp;Drivers License

Wildlife Technician

<h3>Job Description</h3>
Job DescriptionSalary: 
Description: 
We are seeking an experienced Quality Control Microbiologist to join Marianas Technical Operations organization, advancing personalized medicine and radiopharmaceuticals. This person will be responsible for routine microbiological testing including environmental monitoring, environmental monitoring performance qualifications, growth promotion, bioburden, endotoxin, and sterility testing to support product release. In addition to supporting routine testing, this role will ensure that work is completed with SOPs and adheres to strict quality standards.
 
Illustrative Breadth of Responsibilities:
<ul>
<li>Perform environmental monitoring and environmental monitoring performance qualifications (viable, non-viable, and surface monitoring) of classified areas and maintain database of recovered data and isolates to actively trend EM data.</li>
<li>Perform bioburden, endotoxin, and sterility testing to support product release.</li>
<li>Conduct growth promotion testing and release of media.</li>
<li>Ensures aseptic operator qualification and process simulations are performed aseptically according to GMP compliance.</li>
<li>Microbial enumeration and data analysis from microbiological testing.</li>
<li>Experienced with raw material testing is considered a plus.</li>
<li>Identifying, investigating, and resolving microbial action limits, Out of Specification (OOS) results, and deviations.</li>
<li>Maintain laboratory equipment in accordance with internal procedures.</li>
<li>Adhere to SOPs to ensure high quality standards.</li>
<li>Track progress against project timelines, generate regular status updates, and communicate progress and risks to management.</li>
<li>Adhere to safe laboratory practices.</li>
<li>Multi-task across several projects and manage time effectively to achieve results.</li>
<li>Perform other duties as assigned.</li>
</ul>
Requirements/Skills:
<ul>
<li>Bachelors degree in microbiology or related field with a minimum of two years of experience working in a GMP environment in the pharmaceutical or biotechnology industry. Experience working with radiopharmaceuticals will be considered as a plus.</li>
<li>Experience with cGMP and GMP regulations.</li>
<li>Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements.</li>
<li>Good understanding of the radiation safety regulations and guidelines is preferred.</li>
<li>Comfortable handling radioactivity and follow proper ALARA (As Low As Reasonably Achievable) technique Strong communication skills, with motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships.</li>
</ul>
Mariana Oncologys Principles
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>

Quality Control Analyst II, Microbiology

<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>

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