Thermo Fisher Scientific Job - 30693900 | CareerArc
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Company: Thermo Fisher Scientific
Location: Greenville, NC
Career Level: Mid-Senior Level
Industries: Healthcare, Pharmaceutical, Biotech

Description

Job Description

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:
Pharma Service Group / PDS

How will you make an impact?
This position will be responsible for ensuring quality execution of sterile operations with respect to manufacturing, filling, packaging and inspection, and associated non batch specific activities in the Steriles facility for both commercial and product development services products. Additionally, this position will provide quality guidance and expertise for implementation of practical process improvements and continuous improvement initiatives. Primary responsibilities require consistent production floor presence which necessitate physical fitness for prolonged standing, walking, and repetitive bending, proficiency in both aseptic and non-aseptic gowning, and knowledge of aseptic technique.


What will you do?

  • Perform daily quality assessments of facility, personnel, and documentation both classified and non-classified areas to uncover errors or deficiencies and ensure compliance to site procedures and cGMPs.
  • Daily interaction with personnel to assist with troubleshooting, documentation corrections/notes, and guidance with aseptic technique
  • Fosters quality culture by aiding personnel in understanding application of policies and controls
  • Participates in rapid response and provides quality guidance for deviation events
  • Ensures escalation of deviation events to the appropriate area and quality management
  • Aids in identification of continuous improvement opportunities
  • Performs quality batch record review as designated by supervision
  • Performs quality review and approval of procedures, training documents, and forms as designated by supervision
  • Performs quality review and approval of deviation and change control as designated by supervision
  • Participates in Root Cause Analysis to support deviation investigations
  • Participates in practical process improvement initiatives

How will you get there?
Education:

  • Bachelor's degree, preferably in engineering or microbiology related field
Experience:
  • Previous experience in Quality Assurance or Quality control
  • Previous experience in pharmaceutical industry
  • Ability to troubleshoot process and equipment issues
  • Self-driven, demonstrated ownership & responsibility; Ability to lead, support & motivate a team
  • Technical Writing experience
  • Professional certifications (ex: CQA) and training (Six Sigma) is a PLUS
  • Equivalent combinations of education, training, and relevant work experience may be considered
  • Position requires 12 hour night shift schedule
At Thermo Fisher Scientific, each one of our 70,000 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.

Apply today! http://jobs.thermofisher.com

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.


If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, click here for further assistance.

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.


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