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Job Description
Perform bioanalytical processes in a cGMP regulatory environment to support bulk drug substance manufacture.
As a QC Analyst in the Bioassay Lab, your day will include:
- Ensuring all work is in compliance with current GMP, regulatory standards, and company policies
- Reviewing data from other analysts for accuracy and completeness
- Performing bioassays in compliance with cGMP practices
- Sub-culturing mammalian cell lines and performing cell counts
- Maintaining laboratory reagents and supplies
- Preparing reagent aliquots and media for use in cell-based assays
- Maintaining equipment in the laboratory
- Conducting laboratory investigations and generating reports
- Initiating and completing CAPAs
- Writing new and updating current SOPs
- Presenting bioanalytical data reports clearly and concisely
- Identifying and implementing lab process improvements
This role is ideal for individuals with:
- Current or prior experience working with bioassays in a regulated environment
- A proven ability to work independently or as part of a team
- Strong trouble-shooting and problem-solving skills
- Strong attention to detail and excellent written and oral skills
To be considered for this opportunity, you must hold a BS/BA in Life Sciences or related field, or an equivalent combination of education and experience with 2+ years of experience working in a regulated testing environment.
Regeneron is an equal opportunity employer and provides a comprehensive benefits package, including health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees.