Search Jobs

Connecting expertise with opportunity.

QA Operations Specialist - Boston MA - 15945

Cambridge, MA

Posted: 07/18/2022 Industry: Scientific and Life Sciences Job Number: 14632

Job Description

Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services while treating candidates with the professionalism and respect they deserve.

 

Title: QA Operations Specialist

Hiring Organization: Connexion Systems & Engineering

  • Duration: Temp to
  • Pay rate: $30-35/hr
  • Job Location: Cambridge, MA
  • Job# 14632

 

QA Operations Specialist

The QA Operations Specialist, Cell and Gene Therapy is recognized as an expert internally in the principles and application of quality assurance and compliance. The QA Operations Specialist, Cell and Gene Therapy will be responsible for the day-to-day oversight and release of the incoming raw materials to support manufacturing operations and quality assurance for clinical and commercial drug product manufacturing activities. The Quality Assurance Specialist, Cell and Gene Therapy responsibilities includes, but is not limited to, stablishing inspection, testing and release requirements and participate in the vendor qualification activities.

 

KEY RESPONSIBILITIES:

  • As part of the VCGT GMP Operational Quality group primarily responsible with providing quality oversight and support to Cell and Gene Therapy operations in the following key areas/activities to support of manufacturing operations across all phases of development and commercial such materials management and raw material analytical results
  • Responsible for GMP release of incoming raw material and components per approved specifications.
  • Review incoming materials against specifications and submit samples to QC Labs (internal and external) for testing
  • Review and approval analytical protocols/reports, OOS results, re-test plans, etc., and associated corrective and preventive action plans
  • Responsible for approval of COAs when applicable
  • Experience with vendor qualifications, setting raw material specifications, managing timelines
  • Support of the raw material retains program
  • Support new raw material risk assessments that will consider supplier information, general industry knowledge, and technical evaluations based on process and material knowledge with a focus on suitability of each material for its intended use in the process
  • Generate metrics for routine visibility and trending
  • Support QA in regulatory submissions and inspections
  • Communicate to material managements, QA and manufacturing of any OOS results that may impact release timelines
  • Review documentations generated by QC for accuracy and GDP per procedures
  • Support non-conformance (OOT/OOS) investigations, CAPAs, risk assessments, and change controls associated to in-house testing.
  •  

REQUIRED KNOWLEDGE, SKILLS, AND COMPETENCIES

Key Knowledge/ Skills and Competencies

  • Strong leadership skills with the ability to thrive in a high throughput environment
  • Cross-functional collaborator
  • Results Driven
  • Familiar with Oracle Systems
  • Collaboration / Teamwork
    • Ability to independently lead cross-functional teams and represent the Quality unit
  • Communication
    • Ability to communicate effectively across all organizational levels
  • Critical Thinking / Problem Solving
    • Ability to evaluate quality matters and make decisions utilizing risk-based approach
  • Attention to detail
  • Knowledge in the following areas:
    • Proven experience in raw material release and vendor qualifications program
    • Approving Technical Document Specifications to support the release activities
    • Familiar with Oracle Process manufacturing (OPM) system

 

REQUIRED EDUCATION AND EXPERIENCE:

  • BS degree required, in the biological or chemical sciences preferred.
  • Minimum of 2-3 years of QA or QC, raw material release or inspection experience in a regulated Bio/Pharmaceutical industry with biopharmaceutical products, or biologics required.
  • Demonstrated strong working knowledge of GMP manufacturing.
  • Demonstrated broad working knowledge and experience of regulatory guidance and industry best practice quality control.
  • Experience in leading and supporting investigations and making decisions around issues that arise during data package review.
  • Experience working with oracle systems (OPM)

 

 

.When responding to this job posting you MUST include the Job# and Job Title in your subject line.

If you are active in a job search but this job is not for you, please reach out to . We would be glad to help you find the perfect job!

 

Meet Your Recruiter

Alexandra (Scuncio) Pettit
Team Lead, Sr. Technical Recruiter

Apply Online

Send an email reminder to:

Share This Job:

Related Jobs:

Login to save this search and get notified of similar positions.