Quality Control Technician

5 days ago

Westerville, United States Actalent Full time
Job DescriptionJob Description

Actalent is currently hiring for a Quality Control Technician in a gene therapy manufacturing lab in Columbus, Ohio An ideal candidate will have a Bachelor's of Science degree and long term interest in the Cell and Gene Therapy laboratory. This is a long term opportunity and has a ton of room for growth

These openings are on a 2nd Shift 3PM- 11:30PM and will run Monday to Friday

Job Description

  • Will work primarily in the Quality Control Laboratory to support the testing and analysis of cGMP produced viral vectors and cells.
  • Works in close collaboration with the QC manager and QC staff to cultivate and enact strategic direction to the GMP area.
  • Sample assays that need to be run, and running same assays 5 nights a week most of the time.
  • Perform the proper operation, calibration, validation, cleaning, and maintenance, of QC lab equipment.
  • Under the guidance of staff, duties will include: performance of QC methods, development of methods, analysis of microbiological environmental monitoring samples, writing/revising SOP’s, equipment maintenance and monitoring, and materials management of QC and Production supplies.
  • Additional tasks include periodic cleaning of clean room facility and periodic assistance with manufacturing of viral vector products.
  • Ensure all product samples are adequately labelled and all aspects of sample allocation and transition are appropriately documented in the respective format and systems.
  • Ensure full accountability for product as it is allocated across sample requirements and storage conditions.
  • Evaluate processes associated with sample management to identify gaps and implement improvements.
  • Ensure documentation is completed, reviewed, filed and archived according to Standard Operating Procedures (SOPs).
  • Maintain compliance with applicable regulatory requirements for cellular and gene therapy products.
  • Performs in accordance with established policies, procedures, and techniques and requires training common experience or working knowledge related to the tasks performed.
  • Documentation of all activities performed according to SOPs.

Additional Skills and Qualifications

  • BS degree in Biology or other science field
  • Preferred experience includes: aseptic technique, mammalian cell culture, PCR, and ELISA procedures
  • Highly Prefer experience from GMP manufacturing
  • Looking for people that understand the regulatory and documentation constraints in a GMP environment.

INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO: JGASSER @ ACTALENTSERVICES.COM

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.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

  • Hiring diverse talent
  • Maintaining an inclusive environment through persistent self-reflection
  • Building a culture of care, engagement, and recognition with clear outcomes
  • Ensuring growth opportunities for our people

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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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