Sr. Scientist – FLOW / ELISA / MSD Full-time

Sr. Scientist – FLOW / ELISA / MSD

Shift: Full-Time; Thursday – Monday; 8am-5pm EST

This is a fully onsite role based at our customer's site in (Boston, MA). We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.

Our Laboratories Functional Service Partnership (FSP) team plays a direct role in advancing drug development by creating sustained groups of talent within our customers' organizations to provide long-term support. Through this collaborative approach, our professionals bring their commitment to excellence, industry knowledge, and operational strength directly into customer environments, helping to enhance capabilities and advance the delivery of life-changing therapies.

Key responsibilities:

• Perform and Optimize Assays:
• Execute, optimize, and troubleshoot manual cellular and molecular assays, including ELISA, MSD, Flow Cytometry, and PCR.
• Ensure high-quality and reproducible results through rigorous attention to detail and adherence to protocols.
• Analytical Testing Support:
• Independently perform routine analytical testing to support Cell and Gene Process Development activities.
• Maintain control charts and perform data trending for various assays to ensure consistency and reliability.
• Documentation and Reporting:
• Maintain accurate and detailed records of experimental workflows, protocols, and results.
• Assist in generating comprehensive documentation to support experiments.
• Compile experimental data into clear and concise presentations and reports.
• Perform data visualization and effectively communicate findings to stakeholders.
• Assay Development and Design:
• Develop assay design criteria using Design of Experiments (DOE) and other contemporary development tools.
• Collaborate with cross-functional teams to ensure the successful transfer of developed assays and resolve technical issues during the transfer process

Education and Experience:

• Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar
• Sr. Scientist: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 4+ years')
• OR Masters degree and previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years')
• PhD

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

• Technical Expertise:
• Hands-on experience with a variety of molecular and cell-based assays, including MSD, ELISA, Flow Cytometry, and PCR.
• Proficiency in assay development, validation, and troubleshooting.
• Familiarity with additional molecular-based assays such as NGS and potency assays is a plus.
• Documentation and Reporting:
• Experienced in writing technical documents, including development reports, qualification protocols, and qualification reports, within a CMC-regulated environment.
• Collaboration and Communication:
• Proven ability to work collaboratively across multidisciplinary teams to ensure successful assay development and implementation.
• Strong communication and presentation skills, with the ability to effectively convey complex information to diverse stakeholders.
• Problem-Solving and Critical Thinking:
• Demonstrated ability to solve complex problems, think critically, and design proof-of-concept studies using scientific literature.
• Detail-oriented, highly organized, and capable of managing multiple tasks while meeting deadlines.

Working Environment:

Below is listed the working environment/requirements for this role:

Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.

Able to work upright and stationary and/or standing for typical working hours.

Able to lift and move objects up to 25 pounds

Able to work in non-traditional work environments.

Able to use and learn standard office equipment and technology with proficiency.

May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.

Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Compensation and Benefits

The salary range estimated for this position based in Massachusetts is $95,000.00–$105,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

• A choice of national medical and dental plans, and a national vision plan, including health incentive programs
• Employee assistance and family support programs, including commuter benefits and tuition reimbursement
• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
• Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount