What are the responsibilities and job description for the Quality Control Supervisor 3286898 position at Metro Assoc.?
Job Title: Quality Control Supervisor
Employment Type: Full-Time
Relocation Assistance: Available for Qualified Candidates
Job ID: 3286898
Company Overview
Our client, an award-winning leader in the pharmaceutical and biotech industries, is recognized for its commitment to product quality, innovation, and regulatory excellence. They are seeking a skilled Quality Control Supervisor to join their team in Danbury, Connecticut. This role is vital to maintaining high-quality standards and supporting manufacturing operations in a cGMP-regulated environment.
Position Summary
The Quality Control Supervisor will lead the development, implementation, and oversight of quality control systems. You will manage inspection and testing operations, troubleshoot analytical methods, and ensure compliance with stringent regulatory standards and internal protocols.
Key Responsibilities
- Supervise exempt and non-exempt staff to ensure adherence to SOPs, USP, cGMP, and data integrity standards.
- Act as a subject-matter expert, supporting sub-teams with issue resolution and timely completion of tasks.
- Perform real-time reviews of records, chromatograms, sequences, and logbooks to verify compliance.
- Provide expertise in troubleshooting analytical methods and instrumentation, guiding team members as needed.
- Schedule and oversee testing of raw materials, in-process materials, finished products, and stability samples.
- Analyze test data to identify anomalies or trends, approve results, and lead investigations into out-of-specification findings.
- Implement and monitor Corrective and Preventive Actions (CAPAs) resulting from investigations.
- Perform or approve bench analyses as required.
- Collaborate with cross-functional teams on high-impact projects.
- Ensure compliance with FDA, ISO 13485/9001, and European regulatory standards.
Minimum Qualifications
- Bachelor’s degree in a scientific discipline with 5 years of relevant experience, or a Master’s degree with 3 years of experience.
- Proven supervisory experience in a pharmaceutical or biotech environment.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Strong interpersonal, organizational, and problem-solving skills.
- Experience with HPLC, Empower software, and testing of raw materials and finished products.
Preferred Qualifications
- In-depth knowledge of quality systems management and CAPA implementation.
- Familiarity with cGMP regulations and data integrity standards.
Benefits
- 15 days of paid time off plus 18 paid holidays, including company-wide shutdowns in July and December.
- Comprehensive medical, dental, and vision insurance plans.
- Employer contributions to a 401(k) retirement plan.
- Health Savings Account (HSA) options.
- Annual performance-based bonus opportunities.
Ideal Candidate
The ideal candidate will bring a robust background in pharmaceutical quality control, with expertise in quality systems management and analytical testing. Familiarity with Empower software and experience in raw material and finished product testing are highly desirable. Candidates local to Danbury, CT, or open to relocation, are encouraged to apply.
Application Note
All applications will remain confidential. If your qualifications closely match this exciting opportunity, we will contact you promptly to discuss next steps.
Take the next step in your career with an industry leader. Apply today!
Job Type: Full-time
Pay: Up to $100,000.00 per year
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Application Question(s):
- What locations in the USA or states are you interested in?
- 3286898 What type of compensation is desired for a new position?
Education:
- Bachelor's (Required)
Experience:
- Recent Scientific discipline: 5 years (Required)
- Recent Supervisory: 1 year (Required)
- Recent HPLC, raw materials: 1 year (Required)
- Recent Finished products testing, & Empower software: 1 year (Required)
- Recent Knowledge of cGMP, FDA, and ISO regulations: 1 year (Required)
- Recent pharmaceutical quality control: 1 year (Preferred)
- Recent Quality Control Supervisor: 1 year (Required)
Ability to Commute:
- Danbury, CT 06813 (Preferred)
Ability to Relocate:
- Danbury, CT 06813: Relocate before starting work (Required)
Work Location: In person
Salary : $100,000
