US
0 suggestions are available, use up and down arrow to navigate them
What job do you want?

Apply to this job.

Think you're the perfect candidate?

Senior Specialist Quality Assurance III

Careers Integrated Resources Inc Durham, NC (Onsite) Contractor
Job Title: Quality Assurance Specialist – Equipment Qualification 


Role Overview:

We are seeking an experienced Quality Assurance professional to provide end-to-end QA support for equipment qualification in a sterile pharmaceutical manufacturing environment. The role focuses on ensuring compliance during the qualification phase of a new facility producing existing vaccines. The candidate will support document review and approval, collaborate with cross-functional teams, and maintain alignment with cGMP and regulatory standards.




Key Responsibilities:

  • Provide QA oversight for the qualification of manufacturing equipment (e.g., isolators, incubators, washers, lyophilizers, fillers, formulation vessels, cappers, and inspection systems).

  • Review and approve commissioning and qualification documents: URS, FAT, IQ, OQ, PQ.

  • Perform pre- and post-reviews of equipment documents; ensure compliance at every qualification stage.

  • Support pre-approval inspection readiness activities for new product launches.

  • Review/approve GMP documentation: batch records, change controls, SOPs, risk assessments, validation protocols, and technical reports.

  • Collaborate with cross-functional teams (Operations, Engineering, Validation) to ensure timely project execution.

  • Ensure alignment with company Quality Management System (QMS) and current cGMP regulations.

  • Independently manage QA assignments and escalate complex issues to management as needed.




Qualifications & Skills:

  • Bachelor’s degree in Biology, Microbiology, Chemistry, Pharmacy, Chemical Engineering, or equivalent required.

  • Minimum 5 years of experience in the pharmaceutical industry, preferably in sterile manufacturing environments.

  • At least 3 years of experience with equipment qualification: URS, FAT, IQ, OQ, PQ for sterile manufacturing systems, facilities, and utilities.

  • Strong knowledge of regulatory expectations (FDA, EU, etc.) related to sterile product manufacturing and validation.

  • Proven ability to manage multiple equipment documents and support qualification milestones.

  • Exceptional attention to detail, collaborative mindset, and strong communication and interpersonal skills.




Top 3 Key Attributes:

  1. Strong attention to detail

  2. Proven experience in equipment qualification

  3. Effective collaboration and communication skills across teams

Get job alerts by email. Join Our Talent Network!

Job Snapshot

Employee Type

Contractor

Location

Durham, NC (Onsite)

Job Type

QA - Quality Control

Experience

Not Specified

Date Posted

04/21/2025

Job ID

25-44384

Apply to this job.

Think you're the perfect candidate?