Associate Director IT Quality and Compliance - TAPI
at Teva Pharmaceuticals
Rho, Lombardia, Italy -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 23 Dec, 2024 | Not Specified | 27 Sep, 2024 | 10 year(s) or above | Leadership Skills,Operations,Working Experience,Regulations,Computer Science,Supplier Management,Accountability,Manufacturing,Business Strategy,English,Communication Skills,Gamp | 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:
Apply now »
Associate Director IT Quality and Compliance - TAPI
Date: Sep 18, 2024
Location:Rho, Italy, 0000
Company: Teva Pharmaceuticals
Job Id: 58342
WHO WE ARE
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.
YOUR EXPERIENCE, SKILLS AND QUALIFICATIONS
- Bachelor’s degree in Engineering, Computer Science, Science or other related field.
- Minimum of 10 years of experience and strong overall understanding of Computerized System Validation and quality business processes supporting global functions, manufacturing and laboratory operations
- Working experience in API/Pharma companies in a similar role is a must.
- Proven management capabilities managing direct and matrix teams and projects
- Strong understanding of regulations and industry standards such as 21 CFR Part-11, Eudralex Annex-11, GAMP 5, Data Integrity regulatory and industry Guidance and proven ability to pragmatically apply these regulations to operate in an efficient and effective fashion.
- Exposure, working experience and knowledge of GAMP -5 and SCADA systems
- Ability to work with external vendors/suppliers, experience with IT supplier management is desirable.
- Advanced leadership skills, business strategy, accountability, proven experience leading and motivating global, cross-functional teams.
- International experience - a must.
- Advanced experience in working with matrix environment.
- Advanced negotiation skills.
- Advanced knowledge and experience in problem solving.
- Advanced communication skills – written and verbal.
- Advanced agility leadership and teamwork skills.
- Must be able to travel based on business need; up to 30% when critically required (domestic and international).
- Fluent in English – a must
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:10.0Max:15.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Other
Graduate
Engineering computer science science or other related field
Proficient
1
Rho, Lombardia, Italy