Quality Control, Supervisor - Analytical (Night Shift)Location: Portsmouth, NH.
Shift: Night, Monday-Friday: 8:00 pm- 4:30 am
The Quality Control, Nights Supervisor manages team operations to ensure drug products meet high quality and safety standards through disciplined testing and data analysis. They are responsible for organizing stability studies and delivering timely results to support manufacturing demands. Additionally, the supervisor fosters a professional, safe work environment while handling complex technical problems and non-routine assignments
What you will get:- An agile career and dynamic working culture.
- An inclusive and ethical workplace.
- Competitive salary and performance-based bonuses.
- 401(k) matching plan.
- Competitive compensation programs that reward high performance.
- Comprehensive medical, dental, and vision insurance.
- Access to our full list of global benefits: https://www.lonza.com/careers/benefits
What you will do:- Scheduling, planning and assurance of on-time delivery of routine testing in compliance with all cGMP and regulatory requirements. Ensures a safe work environment for employees to perform their duties.
- Creating, reviewing and approving QC documentation. Implementation of robust laboratory management systems, continuous improvement and enhancement of existing systems in a coordinated effort to reduce deviations.
- Schedules and attends department and site related meetings to assure delivery, adherence to quality systems, continuous improvement and customer satisfaction.
- Drives all projects to on-time completion be ensuring task completion and communicating potential issues to stakeholders. Troubleshooting and resolving these issues through team efforts.
- Resolving personnel issues and workplace conflicts. Establishing a cohesive team environment that focuses on achieving corporate goals and right first time initiatives.
- Leading OE initiatives, continuous improvements, implementation of new processes and procedures to support site and corporate growth, hiring and mentoring of staff, supports regulatory and customer audits, creates and executes CAPA plans.
- Perform other duties as assigned.
What we are looking for:- Bachelor's degree in a scientific field, with a preference for Microbiology or Biochemistry; Advanced Graduate degree (M.S./Ph.D.) is preferred.
- 5-10 years of cGMP experience and 2+ years direct supervisory experience; A combination of education and years of experience will be considered.
- Experience in applicable laboratory software and hardware systems.
- Use of GMP Quality Systems such as: TrackWise, LIMS, DMS, Electronic note book.
- Excellent ability to prioritize work load for group and problem solve.
- Proactively shares knowledge with others and encourages analyst development.
- Troubleshoot assay and instrumentation issues involving data mining, trending and analysis to identify problems.
Ready to shape the future of life sciences? Apply now.
