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Pfizer Gene Therapy Specialist Vacancy – Biochemistry & Microbiology

Pfizer Gene Therapy Specialist Vacancy – Biochemistry & Microbiology

Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.

Job Title: Gene Therapy Operations Specialist 1

Location: United States – North Carolina – Sanford

Qualifications

  • BS degree in any of the following disciplines: Chemistry, Biochemistry, Biotechnology, Chemical Engineering, Microbiology or equivalent science-related or engineering discipline and 0–2 years experience in manufacturing in the pharmaceutical industry
  • 2 year Associate’s degree in a science-related discipline and 2–4 years experience in manufacturing in the pharmaceutical industry

What You Will Achieve

  • You will be responsible for planning and coordinating various manufacturing activities with process engineers, supervisors, and managers involving multiple site manufacturing departments. You will be managing the manufacturing cGMP documentation system, planning and scheduling batch/buffer activities to support multiple clinical/commercial manufacturing operations.
  • You will be proficient in maintaining manufacturing inventory for consumable items and management duties in multiple vaccine programs/departments in a manner consistent with site and corporate cGMP, safety, environmental and human resources policies, procedures and compliance initiatives. As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
  • It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

  • The Gene Therapy Operations Specialist works as part of a team to execute batch activities in a new state-of-the-art gene therapy manufacturing facility in Sanford, NC. The incumbent is will be responsible for performing GMP activities in an assigned area, but is expected to begin learning operations across multiple areas (cell culture, purification, solution prep, formulation/fill, pack/label) and products. In addition to operating equipment, the operations specialist will be responsible for:
  • Completing GMP documentation
  • Performing operator care activities
  • Identifying ways to improve work and implementing solutions
  • Participating in investigations
  • In addition, the operations specialist may be assigned as a team member on cross-functional teams and be given project assignments to develop problem-solving, technical expertise, and leadership capability.
  • The incumbent must also comply with applicable safety, occupational health, loss prevention, and environmental requirements.
  • Execute batch activities on time and without injury or defect.
  • Monitor the status of training and complete all required training prior to performing associated tasks.
  • Update and maintain information in manufacturing support systems used for planning, variance tracking, and continuous improvement.
  • Proactively implement improvements to business and manufacturing processes that improve flexibility, eliminate waste, and reduce variability.
  • Maintain the accuracy of all documentation needed for operations including SOPs, batch records, and compounding records.
  • Execute and sustain the components of the lean management system such as 5S, standard work, and visual management.
  • Role model OWNIT! behaviors.
  • Perform pre-task safety checks and demonstrate commitment to developing and maintaining a safe workplace.
  • Execute assigned activities associated with the operator care program.

Pfizer Gene Therapy Specialist

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