Site Quality Manager (Head of Quality)
at Sanofi US
Miskolc, Borsod-Abaúj-Zemplén megye, Hungary -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 06 Nov, 2024 | Not Specified | 07 Aug, 2024 | N/A | Completion,Analytical Skills,Citizenship,Soft Skills,Color | 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:
EXPERIENCE:
- Proven pharmaceutical quality assurance experience
SOFT SKILLS:
- Excellent communication negotiation and problem-solving skills
- You will be a highly motivated and self-driven leader of people
- Initiative – able to work in a self-directed manner to see issues through to completion
- Lean/SMS tools & culture knowledge
- GMP and health-related regulations knowledge
- Legal authority regulations knowledge
- Analytical skills
EDUCATION:
- Pharmacist or chemical engineer degree
IF THE DESCRIPTION FITS YOUR EXPERIENCE AND SPARKS YOUR INTEREST, WE ENCOURAGE YOU TO APPLY SO WE CAN GET IN CONTACT WITH YOU!
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Pursue Progress. Discover Extraordinary.
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At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
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Responsibilities:
- Keeping quality systems up-to-date and ensuring audit readiness: Continuously maintaining, developing, and updating the company’s quality systems to always meet audit requirements.
- Overseeing quality control processes: Inspecting the quality of raw materials, semi-finished, and finished products, continuously reviewing and optimizing quality control procedures.
- Coordinating defect management and corrective actions: Identifying, analyzing, and determining root causes of quality issues, and developing and implementing necessary corrective actions.
- Conducting quality transformation and establishing new operational principles: Transforming the quality mindset, introducing new operational principles, and enhancing the corporate culture to improve quality.
- Leading continuous improvement projects: Managing initiatives and projects aimed at improving the quality of products and processes.
- Adapting to new quality paradigms and organizing quality training: Training employees on quality standards, procedures, and best practices to ensure quality-focused work and enhancing the company’s adaptability to new quality paradigms.
- Preparing and analyzing quality reports: Regularly preparing reports on quality metrics, analyzing data, and making recommendations for process improvements based on these reports
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Clinical Pharmacy
Graduate
Chemical
Proficient
1
Miskolc, Hungary