Job Title - In-Process Quality Engineer III
Description
Provide on-floor quality oversight across cGMP manufacturing operations, including formulation, filling, sterilization, packaging, and warehouse activities;
Monitor compliance to meet or exceed site SOPs/cGMPs during production and warehouse operations; Support required QA inspections, including sample defect detection;
Provide primary daily support to the production and warehouse area, including tasks such as packaging line clearance verification, material segregation/containment, low product fill response, rework reconciliations/accountabilities, and documentation real time review;
Respond to exceptions within the operations/packaging areas as primary QA event response personnel, performing initial exception impact assessment, product containment, bracketing, initial scope identification, and direction of immediate actions prior to resuming processing;
Assist personnel in the generation of operations/packaging area related exceptions; Support minor exceptions and phase II manufacturing investigations;
Attend daily operations staff communication meetings;
Participate as team member in Facilities meetings regarding operations Preventive Maintenance/Calibration/Work Order status and scheduling;
Assist in punch list generation and verification, as well as area inspections pre/post activity; Perform weekly walkthroughs of the operations/packaging area and communicate any observations to associated area management;
Support batch release functions on an as needed basis; Accurately complete all documentation including but not limited to batch records, logbooks, and deviation reports in compliance with cGMP and data integrity requirements;
Promptly report and assist in investigation of any contamination events or deviations from aseptic practices
Skills
GMP, Quality assurance, CAPA, gowning, SOP
Top Skills Details
GMP,Quality assurance,CAPA
Additional Skills & Qualifications
Bachelor's degree in Life Sciences, Engineering, or a related technical discipline (e.g., Biology, Chemistry, Microbiology, Pharmaceutical Sciences) required;
3-6 years of experience in pharmaceutical manufacturing, quality assurance, or aseptic operations required; Ability to pass visual acuity exam for production and identification of quality product purposes;
Ability to read and understand military time is required;
Excellent reading comprehension and attention to detail for interpreting batch records and SOPs; Strong attention to detail and situational awareness while working in fast paced, regulated environments;
Basic understanding of sterilization processes, material flows, and controlled environment requirements;
Commitment to safety, quality culture, and maintaining high standards of compliance;
Demonstrates initiative and sound decision making while working effectively both independently and as part of a team
Job Type & LocationThis is a Contract position based out of Raleigh, NC.
Pay and BenefitsThe pay range for this position is $40.00 - $45.00/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)
This is a fully onsite position in Raleigh,NC.
Application DeadlineThis position is anticipated to close on Apr 14, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
Actalent is an equal opportunity employer.
About Actalent
Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.