QA Specialist

Actalent

Philadelphia, PA

Apply

JOB DETAILS

SALARY

$36.05–$40.87 Per Hour

SKILLS

Artificial Intelligence (AI), Asset Management, Biology, Biotech and Pharmaceutical, Calibration, Candidate Screening, Change Control, Change Management, Cleanroom, Code Reviews, Continuous Improvement, Corrective Action, Cross-Functional, Design Services, Documentation, Equipment Maintenance/Repair, Facilities Engineering, Facilities Management, GMP (Good Manufacturing Practices), Genetics, HVAC, Hospital, Internal Audit, Maintain Compliance, Maintenance Services, Manufacturing, Medical Equipment, Metrology, Preventative Maintenance, Process Improvement, Product Testing, Quality Assurance, Quality Control, Record Keeping, Regulations, Regulatory Compliance, Standard Operating Procedures (SOP), Systems Maintenance, Technical/Engineering Design, Time Management, Writing Skills

LOCATION

Philadelphia, PA

POSTED

1 day ago

Job Title: QA Specialist
Job Description
The Facilities Quality Assurance Specialist is responsible for providing quality oversight and support for facility, utility, and equipment-related activities within a GMP-regulated manufacturing environment. This role ensures that facility systems, maintenance activities, calibration programs, and quality system records comply with internal procedures, GMP requirements, and applicable regulatory standards. The ideal candidate will have hands-on experience authoring and reviewing Change Controls, CAPAs, and Deviations/Investigations, along with experience supporting facility and equipment quality systems.
Responsibilities

Author, review, and approve Change Controls related to facilities, utilities, equipment, preventive maintenance, calibration, and infrastructure upgrades.
Lead or support deviations, non-conformances, and investigations related to facilities, utilities, environmental systems, and equipment performance.
Initiate, track, and support closure of Corrective and Preventive Actions (CAPAs) to ensure timely and effective resolution of quality events.
Assess the impact of facility/equipment-related issues on product quality, validation status, and GMP compliance.
Ensure all quality records are accurate, complete, and inspection-ready.
Provide QA oversight for GMP facility operations, including HVAC, purified water systems, compressed gases, cleanrooms, and other critical utilities.
Review and approve maintenance, calibration, and qualification documentation for GMP equipment and facility systems.
Partner with Facilities, Engineering, Validation, Manufacturing, and Quality Control to ensure changes to equipment and utilities are properly evaluated and documented.
Support quality oversight of contractors, vendors, and service providers performing work on GMP systems.
Utilize Blue Mountain software to review, track, and maintain calibration, preventive maintenance, and asset lifecycle records.
Ensure assets within Blue Mountain are maintained in a compliant state with accurate statuses, due dates, and historical documentation.
Support periodic reviews and audits of calibration/maintenance records within Blue Mountain.
Coordinate with Facilities and Metrology teams to ensure timely execution of calibration and PM activities.
Maintain knowledge of current GMP regulations, internal SOPs, and applicable regulatory expectations related to facilities and utilities.
Participate in internal audits, regulatory inspections, and client audits as a subject matter resource for facilities quality systems.
Identify compliance gaps and drive continuous improvement initiatives within the facilities quality function.
Support development, revision, and review of SOPs, work instructions, and quality documentation related to facilities and engineering processes.

Essential Skills

3-7+ years of Quality Assurance experience in a GMP-regulated pharmaceutical, biotech, medical device, or related manufacturing environment.
Experience supporting facility, utility, equipment, engineering, or maintenance quality systems strongly preferred.
Demonstrated experience writing and managing Change Controls, CAPAs, and Investigations/Deviations.
Experience with Blue Mountain software required or strongly preferred.
Experience with equipment calibration, preventive maintenance programs, and asset management systems is highly desirable.
Prior experience working cross-functionally with Facilities, Engineering, Validation, and Manufacturing teams.

Additional Skills & Qualifications

Bachelor's degree in Life Sciences, Engineering, Quality, or related technical discipline preferred.
Equivalent combination of education and relevant GMP experience may be considered.

Work Environment
The work environment involves a GMP-regulated manufacturing setting. The role requires collaboration with various teams, including Facilities, Engineering, Validation, Manufacturing, and Quality Control. Utilization of technologies such as Blue Mountain Regulatory Asset Manager is essential. Ensuring compliance with GMP regulations and maintaining inspection readiness are vital components of the role.
Job Type & Location
This is a Contract position based out of Philadelphia, PA.
Pay and Benefits
The pay range for this position is $36.05 - $40.87/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 Philadelphia,PA.
Application Deadline
This position is anticipated to close on Jun 30, 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 actalentaccommodation@actalentservices.com 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.

About the Company

Actalent

Resume Resources

Free Resume Templates Free Resume Builder