Quality Control, Supervisor
QualityControl,Supervisor-Analytical(NightShift)
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“Quality Control, Supervisor - Analytical (Night Shift) at Quality Control, Supervisor. Skills: Quality Control, Supervision, Analytical, cGMP. Manage team operations to ensure drug products meet quality and safety standards. Organize stability studies and deliver timely results”
What You'll Achieve.
Ensure drug products meet high quality and safety standards; Deliver timely results to support manufacturing demands; Reduce deviations; Achieve corporate goals; Right first time initiatives
Industry & Context.
Problem solve; Troubleshoot assay and instrumentation issues; data mining; trending; analysis; Troubleshoot and resolve these issues through team efforts
Night Shift: Monday-Friday: 8:00 pm- 4:30 am, Relocation assistance is available
What They're Looking For.
Must Have
2+ years direct supervisory experience, 5-10 years of cGMP experience, 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
Nice to Have
Advanced Graduate degree (M. S. /Ph. D. ), Microbiology degree
What You'll Do.
Manage team operations to ensure drug products meet quality and safety standards
Organize stability studies and deliver timely results
Foster a professional
safe work environment
Handle complex technical problems and non-routine assignments
plan and assure on-time delivery of routine testing
Ensure a safe work environment for employees
review and approve QC documentation
Implement robust laboratory management systems
Enhance existing systems to reduce deviations
Attend department and site related meetings
adherence to quality systems
Drive all projects to on-time completion
Ensure task completion
Communicate potential issues to stakeholders
Troubleshoot and resolve issues through team efforts
Resolve personnel issues and workplace conflicts
Establish a cohesive team environment
Focus on achieving corporate goals
Focus on right first time initiatives
Implement new processes and procedures
Support site and corporate growth
Hire and mentor staff
Support regulatory and customer audits
Create and execute CAPA plans
Perform other duties as assigned
How You'll Work.
Team & Collaboration
Cross-functional coordination; Work with stakeholders; Troubleshoot and resolve issues through team efforts; Establish a cohesive team environment; Collaborate with teams
Communication Scope
Communicate potential issues to stakeholders
Process & Methodology
Drive all projects to on-time completion, Ensure task completion, Communicate potential issues to stakeholders, Troubleshoot and resolve these issues through team efforts, Create and execute CAPA plans
Full Job Description
**_Quality Control, Supervisor - Analytical (Night Shift)_** **Location:** Portsmouth, NH. Relocation assistance is available for eligible candidates and their families. **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: **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, continu
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