350 Lilly Deutschland GmbH
Senior Manager Chemical Testing(m/w/x)
Full-timeOn-siteSenior
Alzey
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35350 Lilly Deutschland GmbH
Senior Manager Device and Incoming Testing(m/w/x)
Alzey
Full-timeOn-siteSenior
Nejo AI Summary
Supervising laboratory personnel for device and incoming goods testing of commercial pharmaceutical products at a global pharmaceutical company. 5-10 years regulated QC experience, Head of Quality Control qualification, and LIMS/LES systems experience required. Excellent company pension plan, access to Corporate University for continuous learning.
Requirements
- Master's degree or Bachelor's with extensive practical experience in GMP, management science related field
- Sufficient qualification for Head of Quality Control
- Minimum of 5-10 years of regulated industry experience in QC
- Experience with Devices and Incoming goods testing
- Previous experience with Laboratory IT systems such as LIMS and LES
- People management
- Fluent written and oral skills in German and English
- Participation in Regulatory inspections such as EMA, FDA
- Management experience of third-party laboratories
- Demonstrated knowledge and application of regulations applicable to the pharmaceutical industry and related quality systems
- Ability to mentor / train others, share learning
- Ability to travel (approximately 10-20 %)
Tasks
- Manage device testing and incoming goods testing activities
- Maintain a safe work environment and lead safety initiatives
- Ensure compliance with cGMP procedures and Quality Systems
- Supervise laboratory personnel and set performance standards
- Perform laboratory device testing for commercial products
- Manage incoming goods testing for commercial products
- Conduct method transfer, verification, and validation
- Participate in flow and process teams for collaboration
- Handle change management and deviation management
- Conduct laboratory investigations
- Organize the lab according to the 5S principle
- Ensure proper training for all analysts and technicians
- Build and maintain relationships with testing labs across the network
- Oversee QC laboratory equipment setup and qualification
- Support regulatory submissions and inspections
Work Experience
- 5 - 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- LIMS
- LES
Benefits
Retirement Plans
- Excellent company pension plan
Other Benefits
- Individual benefits
Career Advancement
- Career development opportunities
Learning & Development
- Access to Corporate Lilly University
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of 350 Lilly Deutschland GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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35350 Lilly Deutschland GmbH
Senior Manager Device and Incoming Testing(m/w/x)
Alzey
Full-timeOn-siteSenior
Nejo AI Summary
Supervising laboratory personnel for device and incoming goods testing of commercial pharmaceutical products at a global pharmaceutical company. 5-10 years regulated QC experience, Head of Quality Control qualification, and LIMS/LES systems experience required. Excellent company pension plan, access to Corporate University for continuous learning.
Requirements
- Master's degree or Bachelor's with extensive practical experience in GMP, management science related field
- Sufficient qualification for Head of Quality Control
- Minimum of 5-10 years of regulated industry experience in QC
- Experience with Devices and Incoming goods testing
- Previous experience with Laboratory IT systems such as LIMS and LES
- People management
- Fluent written and oral skills in German and English
- Participation in Regulatory inspections such as EMA, FDA
- Management experience of third-party laboratories
- Demonstrated knowledge and application of regulations applicable to the pharmaceutical industry and related quality systems
- Ability to mentor / train others, share learning
- Ability to travel (approximately 10-20 %)
Tasks
- Manage device testing and incoming goods testing activities
- Maintain a safe work environment and lead safety initiatives
- Ensure compliance with cGMP procedures and Quality Systems
- Supervise laboratory personnel and set performance standards
- Perform laboratory device testing for commercial products
- Manage incoming goods testing for commercial products
- Conduct method transfer, verification, and validation
- Participate in flow and process teams for collaboration
- Handle change management and deviation management
- Conduct laboratory investigations
- Organize the lab according to the 5S principle
- Ensure proper training for all analysts and technicians
- Build and maintain relationships with testing labs across the network
- Oversee QC laboratory equipment setup and qualification
- Support regulatory submissions and inspections
Work Experience
- 5 - 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- LIMS
- LES
Benefits
Retirement Plans
- Excellent company pension plan
Other Benefits
- Individual benefits
Career Advancement
- Career development opportunities
Learning & Development
- Access to Corporate Lilly University
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of 350 Lilly Deutschland GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
350 Lilly Deutschland GmbH
Industry
Healthcare
Description
The company is a global healthcare leader dedicated to discovering and bringing life-changing medicines to those in need.
Not a perfect match?
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