Senior Quality Control Analyst
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.
Requirements
- BS in Chemistry, or equivalent, with 5+ years related experience -OR- MS in Chemistry or equivalent with 2+ years related experience
- Routine use of common analytical techniques such as HPLC/UPLC, GC, NMR, UV-Vis, pH meter, KF, FTIR, or Refractive index.
- Maintain and troubleshoot laboratory equipment.
- Experience with more advanced analytical techniques as required
- Previous GMP experience
- Applicants for this role must be authorized to work in the United States without further employer sponsorship.
Responsibilities
- Independently deliver experimental output with a high degree of scientific integrity, both on time and on target, with a focus on quality.
- Independently create, maintain, analyze and/or update QC data following established methods and relevant specifications.
- Contribute to Continuous Improvement in the optimization of test methods and Quality Control (QC) processes.
- Train other staff on test methods and QC operations.
- Provide guidance to QC team members and other departments regarding technical or compliance topics.
- Prepares high-quality written documents including generation and revision of Standard Operating Procedures (SOPs), test methods, and other GMP documents.
- Own Quality Management Systems (QMS) records (i.e., deviations, CAPA, root cause analysis etc.) and drive toward completion.
- Manages data by following established procedures, standards and processes. Uses the concepts of ALCOA+ to maintain Data Integrity.
- Perform chemical testing of raw materials, intermediates, and Active Pharmaceutical Ingredients (APIs) in support of GMP in-process, production, and stability testing.
- Responsible for utilizing common analytical techniques such as: HPLC, GC, LC-MS, KF, FTIR, NMR, and wet chemistry methods.
- Execute advanced analysis, and project management with minimal supervision.
- Troubleshoot technical problems with equipment and methods.
- Own Deviations and Corrective and Preventive Actions (CAPA) and perform root cause analysis.
- Share knowledge and information with other members of staff.
Benefits
- Comprehensive health & wellness benefits.
- Access to mental health resources and wellness programs.
- Generous PTO and holiday pay policies.
- Eligibility for performance-based bonuses.
- Attractive 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
Senior
