Quality Control Supervisor, IPC- Swing Shift
About The Position
The Quality Control Supervisor for the In-Process Control (IPC) team supervises Laboratory Analysts to meet testing requirements in support of the manufacturing schedule. The role works closely with QC Managers to ensure policies and procedures are followed as written and revised when necessary. It also coordinates with Operations and Supply Chain Management to support timely release of raw material, in-process, intermediate, and equipment-cleaning verification test data. The supervisor is responsible for laboratory organization and cleanliness. The position follows a Monday–Thursday, four-day, 10-hour schedule starting at 2 p.m. The supervisor directly manages Laboratory Analysts and oversees assigned projects and team workflow.
Requirements
- Bachelor’s degree in chemistry, physics, engineering, or a related scientific discipline.
- Experience with GC, HPLC, TOC, and FT-IR analysis.
- Experience with compendial raw material testing.
- At least 3 years of experience leading and developing successful teams.
- 5 years of GMP experience.
- Excellent verbal and written communication skills.
- Excellent interpersonal and leadership skills.
- Excellent organizational skills and attention to detail.
- Excellent time-management skills, with a proven ability to meet deadlines and motivate teams.
- Ability to collaborate and work in cross-functional teams.
- Strong math, analytical, and problem-solving skills.
- Ability to prioritize tasks and delegate when appropriate.
- Ability to function well in a fast-paced and sometimes stressful environment.
- Proficiency with Microsoft Office Suite or related software.
- Must be authorized to work for an employer in the U.S.; visa sponsorship or takeover of sponsorship is not available.
- Must be able to meet in-office attendance requirements.
Responsibilities
- Directly supervise Laboratory Analysts.
- Recruit, interview, hire, and train new staff.
- Oversee the daily workflow of assigned projects and the team.
- Provide constructive and timely performance evaluations.
- Perform other supervisory duties as assigned.
- Adhere to GMP laboratory standards.
- Maintain laboratory organization, supplies, and cleanliness.
- Write, revise, and approve SOPs.
- Conduct training activities.
- Participate in audits and inspections.
- Execute validations, qualifications, and batch records.
- Conduct scientific and technical reviews.
- Interface with vendors and, as needed, clients.
- Develop work plans.
- Manage cleaning verification assessments.
- Perform other duties as assigned.
Benefits
- More than four weeks of paid time off accrued annually.
- Employer contributions to a retirement account begin after 90 days and require no employee match or vesting period.
- Multiple health plan options with minimal employee contributions.
- Basic life and long-term disability coverage, with the option to increase or add coverage.
- Employee Assistance Program supporting employee wellbeing.
- Access to pet insurance.
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What This Job Offers
Job Type
Full-time
Career Level
Manager
