Analytical Scientist (m/w/d) temporary for 2 years
at Sandoz
Rudolstadt, Thüringen, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 25 Aug, 2024 | Not Specified | 26 May, 2024 | 5 year(s) or above | Pharmaceutical Industry,Ethics,Gmp,Regulatory Guidelines | 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:
WHY SANDOZ?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!
The future is ours to shape!
Essential Requirements:
- Academic degree in a technical or scientific subject, ideally chemistry, pharmacy or minimal 5 years experience in Respiratory Analytical Laboratory testing
- Good understanding of analytical methods and technologies for respiratory product development
- Experience in development functions preferably in the pharmaceutical industry
- Strong knowledge of GMP and regulatory guidelines
- Independent way of working and excellent team player
- Compliance with Sandoz standards for quality, ethics and behavior
- Fluent in German and English (oral and written
Responsibilities:
YOUR KEY RESPONSIBILITIES:
Your responsibilities include, but not limited to:
- Design, plan, perform and document scientific experiments as well as analysis and interpretation of the results to drive analytical method development and validation/verification for excipient, API and respiratory finished product in a GMP environment.
- Define, supervise and report (ICH) stability studies for API and respiratory finished products.
- Act as key contact for all analytical related issues within the assigned projects, to ensure proper communication with all involved partners.
- Define and present (justification of) specification for packaging material, excipient, API and finished product.
WHAT YOU’LL BRING TO THE ROLE:
Essential Requirements:
- Academic degree in a technical or scientific subject, ideally chemistry, pharmacy or minimal 5 years experience in Respiratory Analytical Laboratory testing
- Good understanding of analytical methods and technologies for respiratory product development
- Experience in development functions preferably in the pharmaceutical industry
- Strong knowledge of GMP and regulatory guidelines
- Independent way of working and excellent team player
- Compliance with Sandoz standards for quality, ethics and behavior
- Fluent in German and English (oral and written)
REQUIREMENT SUMMARY
Min:5.0Max:10.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Respiratory analytical laboratory testing
Proficient
1
Rudolstadt, Germany