Role OverviewThe Biochemist I – GMP position will be responsible for the different stages of manufacturing various BioLegend’s regulated product produced in our US FDA registered cGMP manufacturing facility.
What You Will Do
Prepare various buffers for manufacturing activities, perform incoming inspection of raw materials, perform formulation and vialing of regulated products, and maintain batch records and other documentations in compliance with ISO13485:2016 and cGMP.
Why It Might Be a Fit
The ideal candidate will be organized and detail oriented, have strong communication skills, and is able to work in a very fast paced environment.
Requirements
- Bachelor’s degree with 1-year biotechnology industry experience
- 1 year of working experience with Good Documentation Practices (GDP)
- Advanced pipetting skill is highly preferred
- Familiarity with raw material supply receiving and inspection processes
- Excellent verbal and written communication skills
- Demonstrated knowledge of aseptic techniques in biosafety cabinet
- Demonstrated ability to work well in small groups and adhere to timelines
- Excellent attention to detail and organizational skills
Benefits
- Medical, Dental, and Vision Insurance Options
- Life and Disability Insurance
- Paid Time-Off
- Parental Benefits
- Compassionate Care Leave
- 401k with Company Match
- Employee Stock Purchase Plan
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