Team Leader, QC Chemical & GMP
at Thermo Fisher Scientific
03013 Ferentino, Lazio, Italy -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 15 Feb, 2025 | Not Specified | 19 Nov, 2024 | 2 year(s) or above | Biology,People Management,Gmp,Minitab,Validation,Ctf,Empower,Chemistry,Statistical Software | 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
When you’re part of Thermo Fisher Scientific, you’ll have the chance to actively performs significant and important work, like helping customers in finding innovative life-saving treatments for severe diseases, protecting the environment or making sure our food is safe. Your work will have real-world implication and impact, and you’ll be supported in achieving your career goals. You will join a team with wide-ranging strengths!
EDUCATION:
- Degree in CTF, Chemistry, Biology or other similar fields.
- Diploma Chemical/Laboratory technician certificate.
EXPERIENCE
- Experience in QC chemical laboratory within pharmaceutical industries (min 2 years)
- Experience in people management (min 1 year)
- Experience in development/validation/transfer of analytical methods (min 2 years)
KNOWLEDGE, SKILLS, ABILITIES
- Knowledge of the principal techniques of chemical-physical and biochemical analysis and validation of analytical methods
- Knowledge of GMP and national/international regulations
- Good problem-solving abilities and Leadership experience.
- Proficiency in Microsoft Office suite and both analytical and statistical software (Empower, MiniTab, Sample Manager)
- Be prepared to work with conflicting priorities, under time constraints and in a dynamic environment
At Thermo Fisher Scientific, each one of our 70,000 outstanding minds has a unique story to tell. Join us and give yourself the opportunity to collaborate with us in our important mission—enabling our customers to make the world healthier, cleaner and safer
Responsibilities:
- Ensures both the coordination, execution and constant supervision of analytical laboratory activities for projects assigned in accordance with GMP requirements, supporting analysts in problems solving.
- Supports scientists in drafting analytical specifications, study protocols/reports and analytical methods. Writes and review SOPs in compliance with current regulations (current EU GMP, US GMP) and company quality standards.
- Coordinates along with the Supervisor and Manager the customer’s management with the aim of maintaining a high level of customer happiness and completing the required activities on schedule
- Participates in calls/meetings with customers to support the discussion on technical topics for their area of expertise
- Collaborates with the Supervisor to identify the requirements for analytical technology transfer from customers, then ensuring the accurate and effective transfer to the laboratories
- Collaborates with the Supervisor in handling laboratory investigations (Out of Specification and Deviation Reports)
- Ensure the execution of Method Development and/or Method Validation for assigned projects
- Ensure effective management of the Team and resources assigned
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Diploma
Diploma chemical/laboratory technician certificate.
Proficient
1
03013 Ferentino, Italy