Process & Cleaning Validation Specialist II
at Thermo Fisher Scientific
03013 Ferentino, Lazio, Italy -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 20 Jan, 2025 | Not Specified | 20 Oct, 2024 | 2 year(s) or above | English,Communication Skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
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