CHE - 8262 Baxalta Manufacturing Sarl
Quality Systems Specialist - Documentation(m/w/x)
Vollzeitnur vor OrtBerufserfahren
Neuenburg
Neuer Job?Nejo!
Die KI-Suchmaschine für Jobs
BRBristol Myers Squibb
Metrology Intern – Specialist Documentation & Data Management(m/w/x)
Boudry
VollzeitPraktikumVor Ort
Nejo KI-Zusammenfassung
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.
Anforderungen
- 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
Aufgaben
- 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
Ausbildung
- Abgeschlossene Berufsausbildung
Sprachen
- Französisch – verhandlungssicher
- Englisch – Grundkenntnisse
Tools & Technologien
- MS Office
- Word
- Excel
- Documentation management systems
- CMMS
- Asset management systems
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Bristol Myers Squibb erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Noch nicht perfekt?
- Bristol Myers Squibb
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VollzeitLehrenur vor OrtBoudry - Bristol Myers Squibb
C&Q Engineer(m/w/x)
Vollzeitnur vor OrtJuniorBoudry - Takeda
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Vollzeitnur vor OrtBerufserfahrenNeuenburg - Jabil Switzerland Manufacturing GmbH
Laboratory Technician - Sterility Assurance(m/w/x)
Vollzeitnur vor OrtKeine AngabeLe Locle
BRBristol Myers Squibb
Metrology Intern – Specialist Documentation & Data Management(m/w/x)
Boudry
VollzeitPraktikumVor Ort
Nejo KI-Zusammenfassung
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.
Anforderungen
- 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
Aufgaben
- 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
Ausbildung
- Abgeschlossene Berufsausbildung
Sprachen
- Französisch – verhandlungssicher
- Englisch – Grundkenntnisse
Tools & Technologien
- MS Office
- Word
- Excel
- Documentation management systems
- CMMS
- Asset management systems
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Bristol Myers Squibb erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Über das Unternehmen
Bristol Myers Squibb
Branche
Pharmaceuticals
Beschreibung
The company is dedicated to transforming patients’ lives through science and promotes global participation in clinical trials.
Noch nicht perfekt?
- CHE - 8262 Baxalta Manufacturing Sarl
Quality Systems Specialist - Documentation(m/w/x)
Vollzeitnur vor OrtBerufserfahrenNeuenburg - Bristol Myers Squibb
QC Apprentice(m/w/x)
VollzeitLehrenur vor OrtBoudry - Bristol Myers Squibb
C&Q Engineer(m/w/x)
Vollzeitnur vor OrtJuniorBoudry - Takeda
Product Quality Expert(m/w/x)
Vollzeitnur vor OrtBerufserfahrenNeuenburg - Jabil Switzerland Manufacturing GmbH
Laboratory Technician - Sterility Assurance(m/w/x)
Vollzeitnur vor OrtKeine AngabeLe Locle