Role OverviewThe Associate QC Chemist will work closely with the QC Chemistry Manager and Quality Control Method Transfer Scientists to support development, readiness, and routine testing activities for the Quality Control Chemistry laboratory. This role is crucial in generating ALCOA+ data and upholding our Quality Mindset through attention to detail, on-time delivery, and commitment to Quality excellence.
What You Will Do
The QC Chemist will perform routine and batch-related testing on incoming components, raw materials, in-process samples, finished product, and stability samples according to validated methods. They will also create/revise SOPs and other relevant documents, participate in laboratory investigations/deviations, and provide SME support where needed.
Why It Might Be a Fit
The ideal candidate will have a passion for working within a team, a desire to drive Quality processes in a regulated setting, and a commitment to upholding the integrity of data generated for clients. They will have excellent written and oral communication skills, and be able to clearly and concisely articulate complex issues to a range of target audiences.
Requirements
- Bachelor's Degree in Science (Chemistry or Biochemistry)
- Minimum of 3+ years of biopharma industry experience, with at least 2 years of hands-on experience in a GMP environment/Quality Control testing in a regulated environment or other related experience
- High proficiency level in operating UHPLC/HPLC, GC, SoloVPE, UV-VIS, TOC, particulate matter analyses, method validation/transfer, and relevant laboratory computer systems with associated data integrity requirements
Benefits
- Smoke-free campus
- Equal Opportunity Employer
- Prohibits discrimination and harassment of any kind
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