Supervisor, Quality Control Analytical Chemistry Laboratory
Afton Scientific, LLC
Job Description
At Afton Scientific , we're more than a contract manufacturing organization—we're a trusted partner helping bring injectable therapies from clinical development to commercial production. Our work supports pharmaceutical innovators around the world, and every member of our team plays a role in improving patients' lives.
\n \nWe're seeking an experienced Supervisor, Quality Control Analytical Chemistry Laboratory to lead our analytical chemistry team and help ensure the quality, safety, and compliance of the products we manufacture. This is a hands-on leadership role for someone who enjoys developing people, solving technical challenges, and driving continuous improvement in a regulated laboratory environment.
\n \nWhat You'll Do
\n \nAs the QC Analytical Chemistry Laboratory Supervisor, you will:
\n- \n
- Lead and develop a team of analytical chemists supporting pharmaceutical manufacturing. \n
- Oversee daily laboratory operations to ensure quality, efficiency, and regulatory compliance. \n
- Review analytical data and laboratory documentation for accuracy, completeness, and compliance. \n
- Support method development, method validation, and laboratory investigations. \n
- Ensure laboratory activities comply with cGMP, GDP, GLP, FDA, USP, ICH, and other applicable regulatory requirements. \n
- Coordinate instrument qualification, calibration, maintenance, and troubleshooting. \n
- Participate in client interactions, audits, and regulatory inspections. \n
- Drive operational excellence and continuous improvement initiatives within the laboratory. \n
What We're Looking For
\n \nThe ideal candidate will possess:
\n \n- \n
- Bachelor's degree in Chemistry or a related scientific discipline. \n
- 5–7 years of pharmaceutical Quality Control laboratory experience (pharmaceutical manufacturing environment strongly preferred). \n
- Extensive hands-on experience with HPLC and other analytical instrumentation. \n
- Experience with analytical method development and validation . \n
- Strong understanding of cGMP , GDP , and pharmaceutical laboratory compliance. \n
- Experience reviewing analytical data and laboratory quality documentation. \n
- Experience with LIMS (Laboratory Information Management Systems) . \n
- Experience performing routine Quality Control analytical testing. \n
- Experience with ELISA and biologics testing is highly desirable. \n
- Previous supervisory or team leadership experience preferred. \n
- Excellent communication, coaching, and problem-solving skills. \n
Why Join Afton Scientific?
\n \nAt Afton Scientific, you'll join a collaborative team committed to scientific excellence, innovation, and continuous improvement. We invest in our employees through ongoing development opportunities while providing the chance to work with advanced analytical technologies in a growing pharmaceutical manufacturing environment.
\n \nWhat We Offer
\n \n- \n
- Competitive salary \n
- Annual bonus opportunity \n
- Comprehensive medical, dental, and vision coverage \n
- 401(k) with company match \n
- Paid time off and paid holidays \n
- Professional development and career growth opportunities \n
- Collaborative, team-oriented culture \n
- The opportunity to help manufacture therapies that improve patients' lives \n
If you're an analytical laboratory leader who enjoys developing people while maintaining the highest standards of quality and compliance, we'd love to hear from you.
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