Quality Systems Supervisor

Quality Systems Supervisor Actalent - 3.5 Carlsbad, CA Job Details Contract $39 - $52 an hour 7 hours ago Benefits Commuter assistance Health savings account AD&D insurance Disability insurance Health insurance Dental insurance 401(k) Paid time off Employee assistance program Vision insurance Life insurance Qualifications Regulatory inspections Document control within pharmaceutical industry Preventive action implementation Compliance audits & assessments Quality control preventive actions Corrective and preventive actions (CAPA) GMP Manufacturing facility Bachelor's degree Team training Data-driven problem-solving Regulatory compliance analysis FDA regulations Audit support Pharmaceutical manufacturing facility experience

Full Job Description Job Title:

Quality Systems Supervisor Position Summary The Quality Systems Supervisor is responsible for overseeing the day-to-day operations of the Quality Management System (QMS) to ensure compliance with ISO, cGMP, ICH, and other regulatory standards. This role leads QMS processes including document control, training, CAPA, deviations, audits, and supplier quality, while driving continuous improvement initiatives. The position also owns the administration and optimization of the MasterControl eQMS platform. Key Responsibilities Lead and manage core QMS functions, including document control, training, CAPA, deviations, change control, audits, and supplier quality Serve as the primary point of contact for internal and external audits, regulatory inspections, and audit readiness activities Oversee the implementation, administration, and continuous improvement of the MasterControl eQMS system, including transition from paper-based processes Drive investigations, root cause analysis, and corrective/preventive actions to ensure timely resolution of quality issues Track, analyze, and report quality metrics to identify trends and support continuous improvement initiatives Partner cross-functionally with Manufacturing, Quality, and Engineering teams to enhance processes and ensure compliance Develop, review, and maintain SOPs, batch records, and quality documentation in accordance with regulatory requirements Supervise, mentor, and develop Quality Systems staff, including onboarding, training, performance management, and coaching Required Qualifications Bachelor's degree in a scientific or technical discipline 5+ years of experience in a GxP and/or ISO-regulated manufacturing environment Strong working knowledge of ISO 9001 and 21 CFR Parts 210/211 Hands-on experience managing audits, CAPA, deviations, and regulatory inspections Experience administering QMS processes and systems, including document control and training Preferred Qualifications Experience with MasterControl or similar electronic QMS (eQMS) platforms Prior leadership or supervisory experience Professional certifications (e.g., ASQ, CQE, CQA) Strong analytical, organizational, and problem-solving skills Excellent communication and cross-functional collaboration abilities Work Environment Fast-paced, highly regulated manufacturing environment Frequent collaboration with QA, Manufacturing, Engineering, and Leadership teams Occasional travel may be required for audits, inspections, or supplier visits Flexibility to support extended hours based on business needs Job Type & Location This is a Contract position based out of Carlsbad, CA. Pay and Benefits The pay range for this position is $39.00 - $52.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Carlsbad,CA. Application Deadline This position is anticipated to close on Jun 3, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.