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Quality Control Supervisor / QC Supervisor

Fountain Valley, CA · On-site

$75K/yr

Yakult USA, the world's leading probiotic drink manufacturer, is hiring the Quality Control Supervisor. Must have 10+ years of experience in a Food/Beverage related manufacturing environment with 5+ ...

CookUnity

Quality Control Supervisor

New York, NY

The Role The Quality Control Supervisor is responsible for overseeing the performance of the QC area, ensuring compliance with operational procedures, and driving continuous improvement across all ...

Aampower

Quality Control Supervisor

Gallatin, TN

Job Posting Title Quality Control Supervisor Summary Dauch is searching for a Quality Control Supervisor to join our team. This position will be based out of our Gallatin, TN location. The Quality ...

Nuclein

Quality Control Supervisor

Austin, TX · On-site

The Quality Control Supervisor will be responsible for training personnel and planning, facilitating, and executing QC activities to inspect and test Nuclein's diagnostic medical devices ...

nathr

Quality Control Supervisor

Monroe, WA · On-site

$32.08 - $38.81/hr

Quality Control (QC) Supervisor Pay: $32.08 - $38.81/hour Schedule: Monday to Friday 8:00am-4:30pm Location: Monroe, WA ** This position requires on-site work at the company's Monroe, WA location.

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Quality Control Supervisor Pharma information

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$30.5K

$81.3K

$129.5K

How much do quality control supervisor pharma jobs pay per year?

As of Sep 13, 2026, the average yearly pay for quality control supervisor pharma in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

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For Quality Control Supervisor Pharma jobs, the most frequently searched job titles are:

Quality Control Supervisor

Sellersville, PA • On-site

Piramal Pharma Limited
See more jobs at Piramal Pharma Limitedexternal

Full-time

Re-posted 10 days ago

Job description

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Division
Piramal Pharma Solutions
Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.
This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.
Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.
For more details, please visit : www.piramalpharmasolutions.com
Job Title
Quality Control Supervisor
Job Description
Piramal Pharma Solutions is seeking an experienced and motivated QC Supervisor to lead a team of Quality Control analysts in the Sellersville, PA facility. This role is responsible for supervising laboratory operations, ensuring compliance with GMP requirements, supporting laboratory investigations, and driving operational excellence within the Quality Control department. The QC Supervisor oversees a team of approximately 4-5 analysts performing analytical chemistry and microbiological testing on raw materials, finished products, environmental monitoring samples, cleaning validation samples, and stability studies.Key Responsibilities
  • Supervise daily activities of approximately 4-5 QC analysts.
  • Plan, coordinate, and prioritize laboratory testing activities to support manufacturing and supply chain schedules.
  • Review analytical data generated from HPLC, UPLC, GC, and ICP-MS testing.
  • Ensure testing is performed in accordance with approved SOPs, USP, EP and regulatory requirements.
  • Coordinate sampling, testing, and laboratory support activities for production operations.
  • Manage cleaning validation and cleaning verification testing programs.
  • Facilitate communication and testing activities with external laboratories.
  • Perform data review and auditing to support lot disposition decisions.
  • Lead and document OOS, OOT, deviation investigations, CAPAs, and change controls.
  • Support laboratory inspection readiness and regulatory compliance initiatives.
  • Support Empower, LIMS, and TrackWise systems administration activities.
  • Prepare, review, and approve validation and verification protocols and reports.
  • Maintain and periodically review departmental SOPs.
  • Provide training, coaching, performance management, and development for QC analysts.
  • Participate in site quality initiatives and represent QC on cross-functional project teams.
  • Other duties as deemed necessary
Education & Experience
  • Bachelor's degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, or related scientific discipline.
  • Minimum 7 years of technical laboratory experience in a GMP-regulated environment.
  • Minimum 5 years of leadership or supervisory experience.
  • Experience with analytical chemistry and/or microbiological testing.
  • Hands-on experience with HPLC, UPLC, and GC instrumentation.
  • Knowledge of GMP, FDA, ICH, and USP requirements.
  • Experience with Empower, LIMS, and TrackWise preferred.
Knowledge, Skills & Abilities
  • Strong leadership and team development skills.
  • Excellent written, verbal, and interpersonal communication skills.
  • Strong analytical and problem-solving capabilities.
  • Proficiency in Microsoft Office applications.
  • Knowledge of data integrity principles and laboratory compliance requirements.
  • Ability to manage multiple priorities in a fast-paced environment.

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