QC Supervisor (2nd Shift)
About The Position
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference. Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. Every role at Veranova plays a part in delivering an exceptional customer experience through ownership and integrity.
Requirements
- BS in Chemistry, or equivalent, with 5+ years related experience OR MS in Organic Chemistry or equivalent with 3+ years related experience.
- Experience with common analytical techniques such as HPLC/UPLC, GC, NMR, UV-Vis, pH meter, KF, FTIR, and Refractive index
- 3+ years’ experience using chromatography (GC, HPLC/UPLC)
- 2+ years' experience with Quality records (e.g. deviations, CAPA, OOS)
- 3+ years’ previous GMP experience
- Experience training other chemists on test methods and QC operations
Nice To Haves
- Previous experience leading other chemists in a GMP environment preferred
- Experience with Empower chromatographic software preferred
Responsibilities
- Oversee and direct the work of Quality Control Chemists who perform GMP testing of raw materials, intermediates, and APIs in support of pharmaceutical manufacturing.
- Interact with Production teams to assess Quality Control support needs and coordinates coverage for all shifts on assigned team.
- Supervise QC personnel (including hiring decisions, evaluations of performance, and identification of training and development needs).
- May be required to perform analysis and report results in accordance with cGMP & GLP requirements.
- Owns and participates in Deviation and OOS investigations, and pushes them toward closure
- Develops, improves, and revises SOPs, test methods, and other GMP documentation.
- Leads the transfer of analytical procedures from the Analytical Development group as well as directly from the client sites.
- Identifies and leads continuous improvement initiatives.
- Communicate with internal and external clients.
- Actively participates in quality and safety audits and walkthroughs.
- Performs work following all state and federal regulations, including but not limited to GMP, DEA, FDA, etc.
- Other responsibilities as assigned
Benefits
- Comprehensive health & wellness benefits
- Access to mental health resources and wellness programs
- Generous PTO and holiday pay policies
- Competitive base salary
- Eligibility for performance-based bonuses
- 401(k) Plan with company match
- Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship
- Tuition Assistance for Undergraduate and Graduate degree programs
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
