The International Society for Pharmaceutical Engineering, Inc.
Pharmaceutical Manufacturing Quality Assurance
The International Society for Pharmaceutical Engineering, Inc., Sanford, North Carolina, United States, 27330
Job Title: Manufacturing Quality Specialist
Job Description
We are seeking a Quality Assurance Associate to support a major pharmaceutical client. The QA Associate will be responsible for real-time batch record review on the manufacturing shop floor, among other duties.
Responsibilities Execute real-time review of batch documentation and other manufacturing documentation, analyzing for errors, corrections, and compliance. Perform housekeeping and GMP walkthroughs of the facility. Initiate and participate in triage for on-the-floor events. Collaborate with cross-functional teams to meet and exceed timelines. Execute or review room and line clearances. Make quality decisions in real-time according to regulations ICH Q7 and 21CFR211 and internal procedures.
Essential Skills Batch Record Review experience. GMP experience in a manufacturing facility. At least 6 months of pharmaceutical quality experience.
Additional Skills & Qualifications Experience with quality assurance in the pharmaceutical industry. Knowledge of vaccine manufacturing processes.
Work Environment The role involves working on the shop floor 90-100% of the shift. The work environment includes both pharma manufacturing areas and office space with a desk. The position requires adherence to aseptic gowning procedures and has a dress code of business casual with closed-toed shoes.
Pay and Benefits The pay range for this position is $35.00 - $40.00/hr.
Benefits 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 Sanford, NC.
Application Deadline This position is anticipated to close on Aug 8, 2025.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
#J-18808-Ljbffr
Responsibilities Execute real-time review of batch documentation and other manufacturing documentation, analyzing for errors, corrections, and compliance. Perform housekeeping and GMP walkthroughs of the facility. Initiate and participate in triage for on-the-floor events. Collaborate with cross-functional teams to meet and exceed timelines. Execute or review room and line clearances. Make quality decisions in real-time according to regulations ICH Q7 and 21CFR211 and internal procedures.
Essential Skills Batch Record Review experience. GMP experience in a manufacturing facility. At least 6 months of pharmaceutical quality experience.
Additional Skills & Qualifications Experience with quality assurance in the pharmaceutical industry. Knowledge of vaccine manufacturing processes.
Work Environment The role involves working on the shop floor 90-100% of the shift. The work environment includes both pharma manufacturing areas and office space with a desk. The position requires adherence to aseptic gowning procedures and has a dress code of business casual with closed-toed shoes.
Pay and Benefits The pay range for this position is $35.00 - $40.00/hr.
Benefits 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 Sanford, NC.
Application Deadline This position is anticipated to close on Aug 8, 2025.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
#J-18808-Ljbffr