Gene Therapy Scientist II

Gene Therapy Scientist II

20 Nov 2024
Ohio, Dublin, 43016 Dublin USA

Gene Therapy Scientist II

Gene Therapy Scientist Scientist IIJob DescriptionThe Scientist II is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing (CMF). Working in collaboration with the Manager of Plasmids Operations and staff, the Scientist II will provide hands-on assistance for all day-to-day Plasmid Core production operations, including execution of production processes, documentation, as well as facility and equipment maintenance. A Scientist II will support production efforts to deliver all products in a timely, compliant, and fiscally responsible fashion by following appropriate practices, batch records, and Standard Operating Procedures (SOPs) for manufacturing biological products.Responsibilities

Support Plasmids resources and supply chain by ordering and maintaining materials inventory to meet production goals.

Support daily operational activities related to the GMP manufacturing of biological products by ensuring the availability of materials with the proper documentation surrounding GMP activities.

Work closely with Plasmids management to ensure continuous improvement objectives are identified and met using metrics and other statistical means.

Operate and perform the calibration, validation, and cleaning of all facility equipment and systems as specified in SOPs.

Assist in process documentation review, revision, remediation, and process change controls.

Skills & Qualifications

Bachelor's or Master's degree in Life Science field.

3+ years of experience working in Aseptic Processing, Cell Culture, or GMP.

Experience in Drug Compounding, Drug Manufacturing, or Food Manufacturing/FDA preferred.

Prior cell-based experience (either mammalian cell or eukaryotic cell) preferred.

Knowledge and understanding of aseptic technique, cell culture, and liquid separation techniques.

Experience leading projects and developing others preferred.

Must be comfortable occasionally lifting/pushing/pulling 30 lbs.

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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Job Details

  • ID
    JC52922994
  • State
  • City
  • Full-time
  • Salary
    N/A
  • Hiring Company
    Actalent
  • Date
    2024-11-20
  • Deadline
    2025-01-19
  • Category

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