Process & Cleaning Validation Specialist II

at  Thermo Fisher Scientific

03013 Ferentino, Lazio, Italy -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate22 Dec, 2024Not Specified27 Sep, 20242 year(s) or aboveCommunication Skills,EnglishNoNo
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Description:

JOB DESCRIPTION

About Thermo Fisher Scientific Inc.
Thermo Fisher Scientific Inc. is a global leader in serving science, with a mission to enable our customers to make the world healthier, cleaner, and safer. As one team of 100,000+ colleagues, we are committed to accelerating research, solving complex scientific challenges, driving technological innovation, and supporting patients in need. We value diverse experiences, backgrounds, and perspectives, and foster a collaborative and inclusive work environment.

REQUIREMENTS:

  • Bachelor’s Degree or equivalent in a scientific/pharmaceutical area
  • 2 years of previous related experience in the pharmaceutical sector
  • Knowledge of pharmaceutical techniques, production, and aseptic filling processes
  • Experience in risk management and client service/project management
  • Proficiency in Microsoft Office software
  • Fluent in English with advanced written and oral communication skills

Responsibilities:

  • Evaluate manufacturing process documents and equipment cleaning procedures for validation purposes
  • Develop protocols and conduct process validation for product manufacturing and aseptic filling (Media fill)
  • Perform cleaning validation of cleaning procedures and ensure periodic cleaning verification
  • Manage validation protocols for cleaning, process, and Media Fill
  • Collaborate with other departments to define protocol contents and actions to be carried out
  • Validate manufacturing processes, cleaning procedures, and APS/Media Fill
  • Support the drafting and approval of documents for new product transfer and validation
  • Handle deviations related to validation activities
  • Ensure accurate execution of validation activities and detailed analysis of results
  • Draft validation reports and ensure proper archiving of all documentation
  • Provide quality support for new product transfer and process qualification
  • Actively participate in the design, construction, and implementation of new processes or manufacturing departments


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

A scientific/pharmaceutical area

Proficient

1

03013 Ferentino, Italy