CHE - 8262 Baxalta Manufacturing Sarl
Quality Systems Specialist - Documentation(m/w/x)
Full-timeOn-siteExperienced
Neuenburg
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BRBristol Myers Squibb
Metrology Intern – Specialist Documentation & Data Management(m/w/x)
Boudry
Full-timeInternshipOn-site
Nejo AI Summary
Updating legacy calibration documents and creating new WIs/SOPs for pharmaceutical operations. Technical discipline formation with quality or metrology domain experience required. Internship at a global biopharmaceutical company.
Requirements
- Technical discipline formation (CFC of polymechanic or equivalent) with experience in quality, document management, or metrology domain
- Basic understanding of metrology concepts
- Reading and interpretation of technical documents
- Interest in pharmaceutical operations, cGMP, and quality systems
- Knowledge of good documentation practices
- Strong attention to detail and accuracy
- Methodical work, structured process adherence, multi-task management
- Good analytical skills for inconsistency/data gap detection
- Strong organization and work rigor
- Effective interaction with various departments and external vendors
- Good written communication skills
- French language proficiency (required), English language knowledge (oral and written, asset)
- Good command of MS Office (Word, Excel)
- Interest in learning Documentation management systems
- Interest in learning CMMS/asset management systems
Tasks
- Update legacy calibration documents
- Align documents with current processes
- Create or revise Risk Class Assessments
- Create or revise equipment lists and instrument data sheets
- Create or revise Work Instructions (WI) and Standard Operating Procedures (SOP)
- Ensure consistent structure, traceability, and applicability of revised documents
- Organize metrology documentation through scanning, archiving, and classification
- Identify inconsistencies or obsolete information
- Propose corrections for documentation
- Verify, correct, and update metrology data in CMMS (BMRAM / Maximo)
- Ensure coherence between CMMS data, calibration documentation, and approved SOP/WI
- Update calibration frequencies, statuses, risk classes, and equipment attributes
- Prepare communication updates for Manufacturing, QA Ops, QC Labs, and MS&T
- Collaborate with internal stakeholders on document reviews
- Collaborate with internal stakeholders on data clarification
- Contribute to prioritization of documentation updates
Education
- Vocational certification
Languages
- French – Business Fluent
- English – Basic
Tools & Technologies
- MS Office
- Word
- Excel
- Documentation management systems
- CMMS
- Asset management systems
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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Metrology Intern – Specialist Documentation & Data Management(m/w/x)
Boudry
Full-timeInternshipOn-site
Nejo AI Summary
Updating legacy calibration documents and creating new WIs/SOPs for pharmaceutical operations. Technical discipline formation with quality or metrology domain experience required. Internship at a global biopharmaceutical company.
Requirements
- Technical discipline formation (CFC of polymechanic or equivalent) with experience in quality, document management, or metrology domain
- Basic understanding of metrology concepts
- Reading and interpretation of technical documents
- Interest in pharmaceutical operations, cGMP, and quality systems
- Knowledge of good documentation practices
- Strong attention to detail and accuracy
- Methodical work, structured process adherence, multi-task management
- Good analytical skills for inconsistency/data gap detection
- Strong organization and work rigor
- Effective interaction with various departments and external vendors
- Good written communication skills
- French language proficiency (required), English language knowledge (oral and written, asset)
- Good command of MS Office (Word, Excel)
- Interest in learning Documentation management systems
- Interest in learning CMMS/asset management systems
Tasks
- Update legacy calibration documents
- Align documents with current processes
- Create or revise Risk Class Assessments
- Create or revise equipment lists and instrument data sheets
- Create or revise Work Instructions (WI) and Standard Operating Procedures (SOP)
- Ensure consistent structure, traceability, and applicability of revised documents
- Organize metrology documentation through scanning, archiving, and classification
- Identify inconsistencies or obsolete information
- Propose corrections for documentation
- Verify, correct, and update metrology data in CMMS (BMRAM / Maximo)
- Ensure coherence between CMMS data, calibration documentation, and approved SOP/WI
- Update calibration frequencies, statuses, risk classes, and equipment attributes
- Prepare communication updates for Manufacturing, QA Ops, QC Labs, and MS&T
- Collaborate with internal stakeholders on document reviews
- Collaborate with internal stakeholders on data clarification
- Contribute to prioritization of documentation updates
Education
- Vocational certification
Languages
- French – Business Fluent
- English – Basic
Tools & Technologies
- MS Office
- Word
- Excel
- Documentation management systems
- CMMS
- Asset management systems
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.
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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