What are the responsibilities and job description for the Quality Control Supervisor position at Ragan and Massey LLC.?
Quality Control Supervisor – Pharmaceutical Start-Up
We are seeking a highly motivated Quality Control (QC) Supervisor to join our growing pharmaceutical start-up. This role is critical in ensuring that all products meet regulatory, safety, and quality standards. The ideal candidate will oversee QC operations, maintain compliance with Good Manufacturing Practices (GMP), and support continuous improvement in our production processes.
Key Responsibilities:
- Supervise daily QC activities, including incoming and production inspections, testing, documentation, and batch release.
- Develop, implement, and maintain quality control procedures to ensure product integrity and consistency.
- Ensure compliance with FDA, cGMP, and other regulatory requirements.
- Oversee laboratory testing of raw materials, in-process samples, finished products, and stability programs.
- Ensure currency and consistency of product labeling and label inventory.S
- upport maintenance and calibration of QC instruments and equipment.
- Investigate and resolve quality-related issues, including deviations and non-conformances.
- Train and mentor QC team members to uphold high-quality standards, and support training and development of Production personnel in cGMPs, Quality, and procedures.
- Collaborate with production, development, and regulatory teams to drive continuous improvement.
- Prepare reports and maintain accurate QC documentation for audits and inspections, and reporting to Senior Management. Support Regulatory reporting requirements.
Qualifications & Skills:
- Bachelor's degree in Chemistry, Microbiology, Pharmaceutical Sciences, or a related field.
- 3 years of experience in a QC role within a pharmaceutical or biotech environment, with at least 1 year in a supervisory capacity.
- Strong knowledge of analytical techniques, including HPLC, GC, UV-Vis, and microbiological testing.
- Familiarity and experience with regulatory requirements (FDA, cGMP, USP, ICH).
- Excellent problem-solving, communication, and leadership skills.
- Detail-oriented with strong organizational and writing/ documentation abilities.
This is an exciting opportunity to contribute to a fast-paced, innovative start-up and play a key role in ensuring the quality and safety of our pharmaceutical products. If you thrive in a dynamic environment and are passionate about quality assurance, we'd love to hear from you!
Job Type: Full-time
Pay: $25.00 - $30.00 per hour
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Schedule:
- Monday to Friday
- Weekends as needed
Application Question(s):
- Do you have experience with analytical techniques, including HPLC, GC, UV-Vis, and experience with regulatory requirements?
- Are you familiar with regulatory requirements with FDA, cGMP, USP, or ICH?
Education:
- Bachelor's (Required)
Experience:
- Quality control: 3 years (Required)
- Supervising: 1 year (Required)
Ability to Commute:
- Ponchatoula, LA 70454 (Required)
Ability to Relocate:
- Ponchatoula, LA 70454: Relocate before starting work (Preferred)
Work Location: In person
Salary : $25 - $30