Senior Scientist - HPLC, GC, KF

This job is with Thermo Fisher Scientific, an inclusive employer and a member of my Gwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

Work Schedule
First Shift (Days)  Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Senior Scientist – HPLC, GC, Analytical Chemistry

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

ONSITE:
This is a fully onsite role based at our customer’s site in  (Waltham, 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:

Provide routine analytical testing to support early phase and late phase small molecule drug development using HPLC, GC, particle size, KF, dissolution
Perform lab equipment/instrument maintenance.
Follow experimental or qualified analytical procedures and responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol, and product specifications.
Evaluate and implement new analytical approaches, automation, and software to improve the quality and efficiency of analytical development work and to solve problems encountered during drug development.
Author technical protocols and reports.
Maintain excellent written documentation (e.g., lab notebook and test forms).
Ensure execution of work assignments by laboratory staff to meet cycle times

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’)
OR  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:

Proven experience with HPLC and GC based methods

Experience with at least one of the following methods: HPLC, GC, MS, Dissolution Testing, Karl Fischer
Experience in writing technical documents, such as SOPs and study reports, in a non-GxP…