Massachusetts Staffing
Quality Control Incoming Inspector Second Shift
We are seeking a detail-oriented QC Incoming Inspector to join our team on the second shift. This role is critical to ensuring the quality and compliance of raw materials and in-process products used in manufacturing. Ideal candidates will have a strong attention to detail and a passion for quality assurance in a regulated environment. Key Responsibilities
Perform quality line clears and in-process inspections during inspection and packing, following SOPs. Inspect incoming raw materials, issue lot numbers and control labels, and release approved materials for manufacturing. Review inspection documentation (MPS) for approval and release. Monitor annual retain inspections and coordinate retesting with QC. Participate in investigations for out-of-specification (OOS) materials and support MRB activities. Serve as a subject matter expert (SME) and provide training to new team members and QA personnel. Author and maintain documentation, including DCRs and biennial reviews of procedures. Ensure all work is documented according to Good Documentation Practices (GDP). Stay current on training for all assigned procedures and participate in additional projects as needed. Qualifications
Associate's degree in life sciences or equivalent relevant experience. 01 year of experience in a cGMP facility or QA/QC role (internship experience considered). Proficiency with Microsoft Office and ERP systems. Preferred Experience & Skills
Bachelor's degree preferred. Experience working in a clean room environment. Strong communication and documentation skills. Pay and Benefits: The pay range for this position is $22.00 - $23.00/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 Bedford, MA. Application Deadline: This position is anticipated to close on Sep 26, 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, please email actalentaccommodation@actalentservices.com for other accommodation options.
We are seeking a detail-oriented QC Incoming Inspector to join our team on the second shift. This role is critical to ensuring the quality and compliance of raw materials and in-process products used in manufacturing. Ideal candidates will have a strong attention to detail and a passion for quality assurance in a regulated environment. Key Responsibilities
Perform quality line clears and in-process inspections during inspection and packing, following SOPs. Inspect incoming raw materials, issue lot numbers and control labels, and release approved materials for manufacturing. Review inspection documentation (MPS) for approval and release. Monitor annual retain inspections and coordinate retesting with QC. Participate in investigations for out-of-specification (OOS) materials and support MRB activities. Serve as a subject matter expert (SME) and provide training to new team members and QA personnel. Author and maintain documentation, including DCRs and biennial reviews of procedures. Ensure all work is documented according to Good Documentation Practices (GDP). Stay current on training for all assigned procedures and participate in additional projects as needed. Qualifications
Associate's degree in life sciences or equivalent relevant experience. 01 year of experience in a cGMP facility or QA/QC role (internship experience considered). Proficiency with Microsoft Office and ERP systems. Preferred Experience & Skills
Bachelor's degree preferred. Experience working in a clean room environment. Strong communication and documentation skills. Pay and Benefits: The pay range for this position is $22.00 - $23.00/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 Bedford, MA. Application Deadline: This position is anticipated to close on Sep 26, 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, please email actalentaccommodation@actalentservices.com for other accommodation options.