CHE - 8262 Baxalta Manufacturing Sarl
Quality Systems Specialist - Documentation(m/w/x)
Full-timeOn-siteExperienced
Neuenburg
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BRBristol Myers Squibb
Associate Specialist Manufacturing Process Excellence(m/w/x)
Boudry
Full-timeOn-siteEntry Level
Nejo AI Summary
Supporting GMP documentation and equipment qualification for pharmaceutical operations. Bachelor's degree and French proficiency required. 4-day work week, company car for private use.
Requirements
- Bachelor's degree or equivalent in technical discipline
- 0-2 years of pharmaceutical operations experience
- Understanding of GMP and technical processes
- Proficiency in French (mandatory)
- Proficiency in English
- Encouraged to apply if role intrigues despite resume mismatch
Tasks
- Support manufacturing process documentation
- Commission and troubleshoot equipment
- Write technical documentation
- Participate in equipment qualification activities
- Ensure timely closure of quality records
- Provide expertise in manufacturing processes
- Write system requirement definitions
- Support equipment enhancement post-commercialization
- Support data integrity risk assessment
- Prepare and assist with new equipment setup
- Participate in equipment qualification tasks
- Deploy and maintain level 1 maintenance
- Act as primary point of contact for equipment troubleshooting
- Write LO/TO documentation
- Participate in A3 problem-solving initiatives
- Lead local continuous improvement initiatives
- Provide technical expertise for investigations and CAPAs
- Support process improvement and other technical topics
- Ensure on-time closure of quality records
- Lead change control as directed by the production team
Education
- Bachelor's degree
Languages
- French – Native
- English – Business Fluent
Benefits
Other Benefits
- Competitive benefits
- Employee resource groups
- Reasonable workplace accommodations
Flexible Working
- Work-life balance programs
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Bristol Myers Squibb 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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BRBristol Myers Squibb
Associate Specialist Manufacturing Process Excellence(m/w/x)
Boudry
Full-timeOn-siteEntry Level
Nejo AI Summary
Supporting GMP documentation and equipment qualification for pharmaceutical operations. Bachelor's degree and French proficiency required. 4-day work week, company car for private use.
Requirements
- Bachelor's degree or equivalent in technical discipline
- 0-2 years of pharmaceutical operations experience
- Understanding of GMP and technical processes
- Proficiency in French (mandatory)
- Proficiency in English
- Encouraged to apply if role intrigues despite resume mismatch
Tasks
- Support manufacturing process documentation
- Commission and troubleshoot equipment
- Write technical documentation
- Participate in equipment qualification activities
- Ensure timely closure of quality records
- Provide expertise in manufacturing processes
- Write system requirement definitions
- Support equipment enhancement post-commercialization
- Support data integrity risk assessment
- Prepare and assist with new equipment setup
- Participate in equipment qualification tasks
- Deploy and maintain level 1 maintenance
- Act as primary point of contact for equipment troubleshooting
- Write LO/TO documentation
- Participate in A3 problem-solving initiatives
- Lead local continuous improvement initiatives
- Provide technical expertise for investigations and CAPAs
- Support process improvement and other technical topics
- Ensure on-time closure of quality records
- Lead change control as directed by the production team
Education
- Bachelor's degree
Languages
- French – Native
- English – Business Fluent
Benefits
Other Benefits
- Competitive benefits
- Employee resource groups
- Reasonable workplace accommodations
Flexible Working
- Work-life balance programs
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Bristol Myers Squibb 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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Bristol Myers Squibb
Industry
Pharmaceuticals
Description
The company is dedicated to transforming patients’ lives through science and promotes global participation in clinical trials.
Not a perfect match?
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