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Company

Thermo Fisher Scientific

Address , , Pr
Employment type FULL_TIME
Salary
Expires 2023-06-27
Posted at 1 year ago
Job Description

When you’re part of the team at Thermo Fisher Scientific, you’ll do meaningful work that makes a positive impact on a global scale. You can achieve it verifying that established government and customer procedures are being adhered to, in all production areas and stages. Your work will have real-world impact, and you’ll be supported in achieving your career goals.

Essential Job Functions:

The position will be responsible to ensure the custody and management of the site official documentation such as: SOPs, Forms, Specifications, master documents and completed batch records. It will provide support to help maintain cGMP compliance in all operating units with a focus on document management (scanning, filing, archival, tracking, and reconciliation). Will support the site operations as may be requested by internal and external clients. 70%

What will you do in this role?

  • Support administration roles within electronic management system and Learning Management System. 15%
  • Other duties as assigned by the Quality Assurance Supervisor and GMP and Compliance Manager. 10%
  • Support audits by locating appropriate documentation and personnel needed to support the audit. 5%

Education and Experience

A minimum of associate degree education or equivalent with 3 years quality assurance or production experience in a Pharmaceutical or related industry.

Knowledge, Skills, Abilities

  • Is regularly required to talk and hear. The employee frequently will be sat and stand for long time. Occasionally needed to lift, stand; walk; use hands to finger, handle, or feel; reach with hands and arms; and stoop, kneel, or crouch. The employee must frequently lift and/or move up to 50 pounds.
  • Strong verbal and written communication skills, successful in partnering with colleagues of differing cultural, language and educational backgrounds.
  • While performing the duties of this job, it is required to write, read/review written documentation for extended periods of time.
  • Must have strong digital literacy, including Microsoft Word, Excel and Access.
  • Very high attention to detail and concern for standards are required.
  • Critical thinking with ability to prioritize multiple projects simultaneously in a dynamic environment
  • Strong communication and influencing skills, which command the respect of the peer group, broad employee groups, and executives throughout the company. Ability to effectively market ideas to a diverse leadership team.
  • Able to flex work schedule to match site needs
  • Must be capable to recognize, understand and respond to situations requiring further evaluation and report these events (process, safety, personnel, etc.) to senior specialists or area management.
  • Ability to make decisions and work with minimal to moderate supervision.

Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 90,000 colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

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.