Quality Control Supervisor

Kelly; Irvine (CA); On-site; USD 120,000 - 160,000; Full time

Job summary

Kelly Science & Clinical in Irvine, CA is seeking a Quality Control Supervisor to lead day-to-day operations in its analytical laboratory within a GMP environment. This direct-hire role offers the chance to guide a skilled team and ensure the quality and integrity of pharmaceutical materials and products.

The ideal candidate combines strong analytical chemistry expertise with hands-on leadership and a proven ability to drive compliance, training, and audits.

Qualifications

• Bachelor’s degree in Chemistry or related discipline (or equivalent).
• At least 8 years of experience in a GMP analytical chemistry lab with instrumentation such as HPLC, GC, CE, ICP, FTIR, TOC, and dissolution apparatus.
• Demonstrated ability to lead laboratory staff and drive day-to-day execution.
• Strong communication and active-listening skills for cross-functional collaboration.
• Excellent organization and ability to manage concurrent responsibilities with minimal supervision.

Responsibilities

• Lead daily laboratory operations in a GMP setting.
• Set testing priorities, schedules, and staff assignments to ensure timely, reliable output.
• Protect data quality and ensure regulatory compliance; support audits and inspections.

Skills

Leadership

Communication

Active listening

Organization

Education

Bachelor’s degree in Chemistry or related discipline

8+ years GMP analytical chemistry laboratory experience

Tools

HPLC

GC

CE

ICP

FTIR

TOC

Dissolution apparatus

Job description

Kelly® Science & Clinical is seeking a Quality Control Laboratory Supervisor or direct-hire opportunity with one of our clients, a leading small molecule CDMO at their Irvine, CA facility. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Workplace: Onsite in Irvine, CA.

Position Title: Quality Control Supervisor

Position Type: Direct hire

A leading small-molecule contract development and manufacturing organization (CDMO) is seeking a Quality Control Supervisor to lead day-to-day operations in its analytical laboratory. This is an opportunity for an experienced GMP laboratory professional to guide a skilled team, strengthen laboratory execution, and help ensure the quality and integrity of pharmaceutical materials and products.

You will set the laboratory’s daily direction, balancing priorities, people, and compliance—while serving as a trusted partner to other departments. The ideal candidate combines strong analytical chemistry expertise with a hands‑on, people‑first leadership style and sound judgment in a regulated environment.

What you’ll do

• Lead daily laboratory operations
• Set testing priorities, schedules, and staff assignments to support timely, reliable laboratory output. Provide day-to-day direction, coaching, and feedback, and serve as a communication link between the QC laboratory and other facility departments.
• Protect data quality and compliance
• Ensure analytical results are reviewed in accordance with company policy and that laboratory practices meet applicable regulatory requirements. Supervise and perform laboratory investigations, and help prepare for internal and external audits and inspections.
• Develop and support the team
• Participate in recruiting and onboarding, conduct performance and compensation reviews, and deliver or support procedural, cGMP, and safety training. Build collaborative working relationships across the organization.
• Oversee equipment calibration schedules and ensure required calibrations and maintenance are completed on time. Author standard operating procedures and support the review and revision of existing procedures.
• Contribute hands‑on expertise
• As needed, perform analytical testing of raw materials, in‑process samples, and finished products using laboratory instrumentation such as HPLC, GC, CE, ICP, FTIR, TOC, and dissolution apparatus. Serve as backup for laboratory management and take on related responsibilities as needed.

What you’ll bring

• A bachelor’s degree or higher in Chemistry or a related discipline, or an equivalent combination of education and experience.
• At least 8 years of experience in a GMP analytical chemistry laboratory, including hands‑on experience with instrumentation such as HPLC, GC, CE, ICP, FTIR, TOC, and dissolution apparatus.
• Demonstrated ability to lead laboratory staff, set direction, and support effective day‑to‑day execution.
• Strong communication and active‑listening skills, with the ability to build productive relationships at all levels of an organization.
• Excellent organization, attention to detail, and prioritization skills; able to manage concurrent responsibilities with minimal supervision.