Job Vacancy Associate III (Senior) Downstream Manufacturing Thermo Fisher Scientific



Job title: Associate III (Senior) Downstream Manufacturing

Company: Thermo Fisher Scientific

Job description: Job Description

Job Title: Associate III (Senior) Downstream Manufacturing

Requisition ID:

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.

Location/Division Specific Information

Alachua, FL – Viral Vector Services Division

How will you make an impact?

The Associate III (Senior) position will support cGMP manufacturing activities to ensure that Thermo Fisher Scientific Viral Vector Services provides clients with gene therapy products for pre-clinical and clinical use. This position will perform hands on cGMP production of recombinant protein and viral vectors under the supervision of the Downstream Manufacturing Leadership.

What will you do?

The Associate III (Senior) will maintain a culture of safety by identification of near misses, safety walkthroughs and assisting with resolution of safety observations. Ensuring MFG chemicals are properly stored and labeled. This position will adhere to the Quality Management Systems by living the Quality values every day and holds peers across the site accountable as well. Ensuring documentation of all activities meet cGMP requirements. Assist with the on-time closure of Nonconformance’s/ CAPAs, as needed. Additionally, this position will lead Practical Process Improvement (PPI) initiatives and continuous improvements. Able to run daily huddles assign tasks to other technicians. Ensure tasks are executed with a method of prioritization – interpret production schedules and complete tasks accordingly. Actively provide feedback and escalate issue or take action and provide resolution as appropriate. e.g. issuing work notifications or collaborating with other departments to provide closure. Active participant of performance huddles and assisting Supervisors to plan out and populate process schedules. This will apply to the below task breakdown:

Downstream GMP Production (90% of time spent on floor)

  • Fully trained on all unit operations associated with their department (ex. column chromatography, TFF, filtration, ultracentrifugation).
  • Viewed as an SME/expert in at least one unit operation.
  • Provide critical evaluation of processes, including foresight and thinking ahead.
  • Act as a guide to new employees during onboarding process.
  • Responsible for the upkeep of manufacturing equipment and maintaining an up to date skills matrix.
  • Conduct downstream production suite preparation and/or request necessary components and raw materials, labels, etc. to successfully execute production batch records.
  • Able to assist in all Department functions, such as maintaining suite, supplies, equipment, logbooks and data in accordance with site SOPs and policies.
  • Act the lead technician in the independent execution of unit operations.
  • Performs equipment testing and routine trouble-shooting and maintain an up to date skills matrix.
  • Support and conduct other sub-team (Upstream, Fill Finish, Support Operations) tasks and related production processes, when required.

Prepare and Review Documents (5%)

  • Review, revise, and author manufacturing batch records.
  • Complete preventative maintenance and work notifications tasks on time.
  • Collaborate with quality and PD to review and signoff on executed batch records.
  • Own the executed batch record reconciliation and other production related documents.
  • Working with Downstream managers, review, revise, and author Work Instructions (WI)/SOPs/Material Specifications (SPEC)

Process Development and Improvement (5%)

  • Assist Downstream Manufacturing Manager/supervisor in the development or optimization for downstream processes for manufacturing.
  • Assist in the technical transfer of processes from Process Development laboratories to manufacturing.

How will you get here?

Education/Experience

  • High School Diploma / minimum 3+ years of relevant experience or superior demonstration of skill sets or background
  • Bachelor’s Degree in related field / 1+ years of relevant experience

Knowledge, Skills, Abilities

  • Intermediate understanding of downstream processing methods (Chromatography, TFF, Nanofiltration, Ultracentrifugation, detergent treatment, sterilizing grade filtration).
  • Excellent communication skills.

Working Hours/Overtime

  • This position will start as a fulltime, 2-2-3 rotating shift schedule (12hr shifts/ Every other weekend ).
  • Overtime and weekend work will be required as needed.

At Thermo Fisher Scientific, each one of our 75,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission-enabling our customers to make the world healthier, cleaner and safer.

Job Category

Operations

Thermo Fisher Scientific

is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Expected salary:

Location: Alachua, FL

Job date: Sun, 03 Jul 2022 06:19:46 GMT

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