PRIMARY RESPONSIBILITIES
- Participate in transfer and qualification activities in support of our pre-clinical and clinical programs
- Execute QC testing to support release and stability analysis for drug substance and drug product
- Manage method qualification and release testing conducted at contract testing organizations
- Conduct testing investigations and deviations to support root cause analysis and corrective and preventative actions, as required
- Implement QC systems and procedures compliant with cGMP
- Manage programs for critical laboratory reagents, assay controls/reference standard, and equipment
- Independently analyze and summarize data in technical reports and presentations
- Author, review, and/or approve data, logbooks, SOPs, CoAs, analytical methods, protocols, reports, deviations, and other quality records
- Maintain the QC Unit in a state of compliance and inspection readiness
BASIC QUALIFICATIONS
- BS/MS in biology, immunology, biochemistry or a related scientific discipline with at least 2-5 years industry experience
- Experience working in a regulated GMP QC laboratory
- Proficient in a range of analytical methods (mammalian cell culture, flow cytometry, ELISA, qPCR etc.) and aseptic technique
- Strong knowledge of US cGMP regulations/guidelines
- Detail oriented and organized with the ability to work in a fast-paced environment
- Effective communication skills, both verbal and written, across various functions including manufacturing, quality assurance, and analytical development.
PREFERRED QUALIFICATIONS
- Familiarity with the validation process