Quality Manager Specialist NPI - Global Operations
at AstraZeneca
Gärtuna, Stockholms län, Sweden -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 12 Aug, 2024 | Not Specified | 13 May, 2024 | N/A | Good 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:
Join the team where everyone feels a personal connection to the people that we impact. From our science labs to manufacturing at scale, we are committed to delivering at the highest quality. It’s inspiring and rewarding work, influencing every part of the product lifecycle to deliver life-changing medicines!
At AstraZeneca, we strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.
Welcome to External Quality (EQ), a global Quality organization within AZ Operations where the community is vibrant, and we never stop developing. We are now looking for a Quality Manager Specialist for the NPI release team to help us manage release and launch of NPIs from external suppliers. This is a place where you will feel included in the conversation, where every voice is heard and makes a difference.
What you’ll do
As a Quality Manager Specialist, you will support the setup of new product release flows of new products from ‘Contract Manufacturing Organisations’ (CMO’s) and establish release for the product into BAU within EQ. This is a diverse and interesting role working with contractors and a broad range of AstraZeneca internal sites and functions. You will collaborate with colleagues and customers across many countries and interact cross-functionally with supply chain, technical, regulatory and project teams in AZ.
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Gärtuna, Sweden