Job Title: Research Associate, Analytical Development
About the Job
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Who You Are:
You are an energetic, and highly motivated research associate who works well in a team-setting to support the different GMP QC testing activities in Analytical Development. You perform self-guided, hands-on laboratory activities to maintain the integrity of analytical samples through coordination, tracking, proper handling, maintenance, and monitoring.
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The Team:
This position resides within the Analytical Development group, part of the Global Biologics CMC Development organization at Sanofi, Framingham, and Waltham, MA. The Analytical Development group has the overall responsibility to develop, qualify and validate robust analytical methods to support release and characterization testing of candidates in early-stage development (Phase I/II). The Analytical Development group also performs cGMP compliant drug substance and drug product release and stability testing in addition to compendial and raw material QC testing.
Job Highlights:
- Perform GMP and non-GMP sample coordination, handling and maintenance (receive, label, store, pull, transport, distribute, pack, ship, and dispose) according to procedures (SOPs) and stability protocols and maintain tracking and inventory records in electronic systems or worksheets.
- Maintain equipment used to store samples, including water and LN2 refill, defrost and cleaning. Monitor, track, and coordinate routine calibration, validation, and PM.
- Monitor and analyze environmental information (temperature and humidity) generated by the transport and storage equipment monitoring devices and escalate alarms or trends as appropriate, transferring samples to alternate equipment when necessary.
- Draft procedures (SOPs) and ensure that the documents adhere to GMP requirements as appropriate.
- Maintain a GMP compliant laboratory environment.
About you
Basic Qualifications:
- Bachelor's degree in Biochemistry, Analytical Chemistry, Biology, or related discipline with 1-2 years of relevant experiences.
- Minimum 1 year working in GXP laboratory
- Minimum 1 year working with LIMS and performing sample maintenance related activities
Preferred Qualifications:
- Good oral and written communication skills.
Why Choose Us?
- Bring the miracles of science to life alongside a supportive, future-focused team.
- Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
- Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
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