Quality Specialist III
at Thermo Fisher Scientific
5048 Tilburg, Noord-Brabant, Netherlands -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 23 Dec, 2024 | Not Specified | 26 Sep, 2024 | 2 year(s) or above | Capital Projects,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
This role reports into the Tilburg site of the Thermo Fisher Scientific Pharmaceutical Services Group. The site produces soft gelatin capsules.
KNOWLEDGE, SKILL, AND REQUIREMENTS:
- Bachelor’s degree and 2 years of related work experience in a pharmaceutical work environment.
- Proven track record to collaborate across the business.
- Strong analytical and problem-solving skills; great attention to detail and excellent decision-making process.
- Expertise in handling small and medium technical and/or capital projects.
- Proven ability to present ideas persuasively and negotiate effectively.
- Excellent written and oral communication skills both internal and external.
Responsibilities:
- Lead and chip in cross-functional meetings to conduct root-cause analysis and determine corrective and preventative actions
- Generate and close CAPAs, Changes, and Deviations including: re-training, SOP revisions, and implementation of new processes within the site
- Identify recurring events and trends within site deviations and propose continuous improvement ideas based on findings
- Assist in the creation, implementation and maintenance of training curriculum, as well as the launch of learning-based training elements for personnel
- Support the site in maintenance of audit readiness
- Perform gap analysis to new and existing regulations and standards
- Partner cross-functionally to implement process improvements; participates and/or may lead cross functional projects.
- Drive continuous improvement and operational excellence culture thru self-detecting and self-correcting processes and systems and instilling strong ownership and accountability.
- Recognize, understand and respond to situations requiring further evaluation and report these events to area management
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Information Technology/IT
IT Software - Other
Software Testing
Graduate
A pharmaceutical work environment
Proficient
1
5048 Tilburg, Netherlands