Quality Systems Specialist

Job Title: Quality Systems Specialist Job Description
The Quality Systems Specialist manages and optimizes change control processes across manufacturing products, processes, equipment, facilities, and computerized systems to support strategic, tactical, and operational quality goals. This role ensures robust oversight of GxP operations, maintains compliance with current Good Manufacturing Practices (cGMP), and contributes to the continuous improvement of the quality management system.
Responsibilities
- Manage change controls related to manufacturing products, processes, equipment, facilities, and computerized systems to support key strategic, tactical, and operational objectives.
- Independently review, initiate, complete, and thoroughly document critical, major, and minor change controls in both local and global systems for GxP operations.
- Facilitate cross-functional meetings with stakeholders and leadership to align on proposed changes and ensure compliance with quality management system expectations.
- Lead complex change review discussions, guide teams to a common decision on approach and follow-up actions, and accurately document decisions, evaluations, and rationales.
- Support management and monitoring of change records to ensure adherence to organizational and departmental metric targets, maintaining associated tracking tools and databases.
- Develop and generate quality system metrics and trending reports to support the management review process and escalate quality or compliance issues as required.
- Support the maintenance and continuous improvement of quality systems processes, identifying opportunities to strengthen controls and efficiency.
- Work directly with operating entities and internal stakeholders to ensure timely completion and effective follow-up of change-related tasks.
- Participate in compliance audits as required, providing documentation, explanations, and support related to change control and quality systems.
- Maintain programs and processes that ensure high-quality products and compliance with current Good Manufacturing Practices (cGMP).
- Write and implement changes to controlled documents such as standard operating procedures (SOPs), specifications, and methods as needed.
- Provide guidance and technical knowledge to junior staff, monitor the performance of daily tasks, and support their development in quality systems and change control.
Essential Skills
- Minimum of six years of experience in change control within a GxP environment.
- 6+ years of relevant experience in a GMP environment for biologics manufacturing with demonstrated change control experience.
- Strong background in quality assurance and document control in regulated manufacturing settings.
- Hands-on experience managing change control processes for manufacturing products, processes, equipment, facilities, and computerized systems.
- Proficiency in generating, analyzing, and trending quality system metrics to support management reviews.
- Ability to facilitate cross-functional meetings and navigate complex change review discussions to reach aligned decisions.
- Experience writing, revising, and implementing controlled documents such as SOPs, specifications, and methods.
- Technical sciences degree (BS or BA) from a scientific or technical discipline.
- Demonstrated understanding of cGMP requirements and GxP operations in biologics manufacturing.
Additional Skills & Qualifications
- Experience with both small molecule and large molecule products, with a strong preference for biologics.
- Proven ability to work collaboratively with cross-functional teams and internal stakeholders.
- Strong attention to detail and commitment to thorough documentation and record-keeping.
- Ability to interpret and apply quality management system expectations and regulatory requirements to practical operations.
- Effective communication skills for leading discussions, presenting metrics, and supporting audits.
- Capability to provide mentorship and technical guidance to junior staff in quality systems and change control.
Work Environment
This role operates in a regulated GMP biologics manufacturing environment that emphasizes quality, compliance, and continuous improvement. The Quality Systems Specialist works closely with manufacturing, quality, and other functional teams, frequently engaging in cross-functional meetings and audit activities. The position involves extensive use of computerized quality systems, change control tools, and document management platforms, as well as interaction with tracking databases for metrics and trending. Work is typically performed during standard business hours, with flexibility as needed to support audits, critical change activities, and management reviews. The environment is professional and structured, with clear procedures, controlled documentation, and established quality management system processes guiding daily work.
Job Type & Location
This is a Contract position based out of Foster City, CA.
Pay and Benefits
The pay range for this position is $45.00 - $65.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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 hybrid position in Foster City,CA.
Application Deadline
This position is anticipated to close on Oct 9, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 [email protected] 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.