Bristol Myers Squibb
Director Strategy and Operations European Markets(m/w/x)
Full-timeWith HomeofficeManagement
Boudry
New Job?Nejo!
Your personal AI career agent
BRBristol Myers Squibb
Associate Director Process Excellence, Launch Operations(m/w/x)
Boudry
Full-timeWith Home OfficeSenior
AI/ML
Nejo AI Summary
Ensuring robust manufacturing processes and technical readiness for new pharmaceutical product launches. Advanced degree in Pharmaceutical Sciences or Engineering, 8+ years pharma manufacturing experience, and French/English fluency required. International environment with global clinical trial participation.
Requirements
- Advanced degree in Pharmaceutical Sciences, Engineering, or related field
- Minimum 8 years of relevant experience in pharmaceutical manufacturing
- 5+ years of team leadership experience in pharmaceutical industry
- Fluency in French and English
- Proven leadership in technical readiness and continuous improvement projects
- Knowledge of regulatory requirements and risk management tools
- Strong working knowledge of GMP and FDA, Eudralex, PICS, and GAMP regulatory requirements
- Excellent communication, presentation, and collaboration skills
- Occasional business-related travel required
- Demonstrated ability to communicate effectively at all levels of the organization
- Excellent skills to influence stakeholders across functions and hierarchical levels
- Experience in Lean Manufacturing/Six Sigma
- Exceptional problem-solving ability
- Ability to effectively utilize Microsoft Office Suite
- Knowledge of regulatory requirements and risk management tools
- Experienced at presenting during regulatory audits (FDA and SwissMedic)
- CAPEX investment project experience
Tasks
- Lead the Process Excellence team
- Ensure robust manufacturing processes and compliance
- Drive technical readiness for new product introductions
- Manage lifecycle and process optimization
- Maintain GMP standards and support regulatory requirements
- Oversee late-stage development priorities and technical transfers
- Develop and implement the Process Excellence roadmap
- Foster a coaching and feedback culture within the team
- Create an environment for accountability and innovation
- Build technical and compliance capabilities per PU requirements
- Ensure technical process ownership within the PU
- Support technical gap assessments and transfer plans
- Contribute to process technology transfer activities
- Oversee batch record authoring and MES creation
- Ensure execution of protocols and reports for new processes
- Drive lifecycle management initiatives and KPI monitoring
- Support data analysis for process trends and shifts
- Provide updates on process performance to management
- Support regulatory filings and maintain inspection readiness
- Manage GMP documentation and related KPIs
- Act as a point of contact for audits and inspections
- Collaborate with Scheduling, Manufacturing, MS&T, and QA
- Align with P1 leadership for decision making and best practices
- Develop training for new products and processes
- Provide training and support to new Process Excellence associates
- Promote adherence to Environmental, Health, and Safety standards
- Manage EHS CAPA and drive safety improvements
- Lead digital, AI, and innovation projects for the PU
- Identify opportunities for process and quality improvements
Work Experience
- 8 years
Education
- Master's degree
Languages
- French – Business Fluent
- English – Business Fluent
Tools & Technologies
- GMP
- FDA
- Lean Manufacturing
- Six Sigma
- Microsoft Office Suite
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.
Not a perfect match?
- 1112 Celgene International SaRL
Technicien de maintenance process(m/w/x)
Full-timeWith HomeofficeSeniorBoudry - Bristol Myers Squibb
Intern - Manufacturing Science and Technology(m/w/x)
Full-timeInternshipWith HomeofficeBoudry - Bristol Myers Squibb
Sr Manager Procurement - Indirect products and services(m/w/x)
Full-timeWith HomeofficeSeniorBoudry - Breitling
Learning & Development Manager(m/w/x)
Full-timeWith HomeofficeSeniorLa Chaux-de-Fonds
BRBristol Myers Squibb
Associate Director Process Excellence, Launch Operations(m/w/x)
Boudry
Full-timeWith Home OfficeSenior
AI/ML
Nejo AI Summary
Ensuring robust manufacturing processes and technical readiness for new pharmaceutical product launches. Advanced degree in Pharmaceutical Sciences or Engineering, 8+ years pharma manufacturing experience, and French/English fluency required. International environment with global clinical trial participation.
Requirements
- Advanced degree in Pharmaceutical Sciences, Engineering, or related field
- Minimum 8 years of relevant experience in pharmaceutical manufacturing
- 5+ years of team leadership experience in pharmaceutical industry
- Fluency in French and English
- Proven leadership in technical readiness and continuous improvement projects
- Knowledge of regulatory requirements and risk management tools
- Strong working knowledge of GMP and FDA, Eudralex, PICS, and GAMP regulatory requirements
- Excellent communication, presentation, and collaboration skills
- Occasional business-related travel required
- Demonstrated ability to communicate effectively at all levels of the organization
- Excellent skills to influence stakeholders across functions and hierarchical levels
- Experience in Lean Manufacturing/Six Sigma
- Exceptional problem-solving ability
- Ability to effectively utilize Microsoft Office Suite
- Knowledge of regulatory requirements and risk management tools
- Experienced at presenting during regulatory audits (FDA and SwissMedic)
- CAPEX investment project experience
Tasks
- Lead the Process Excellence team
- Ensure robust manufacturing processes and compliance
- Drive technical readiness for new product introductions
- Manage lifecycle and process optimization
- Maintain GMP standards and support regulatory requirements
- Oversee late-stage development priorities and technical transfers
- Develop and implement the Process Excellence roadmap
- Foster a coaching and feedback culture within the team
- Create an environment for accountability and innovation
- Build technical and compliance capabilities per PU requirements
- Ensure technical process ownership within the PU
- Support technical gap assessments and transfer plans
- Contribute to process technology transfer activities
- Oversee batch record authoring and MES creation
- Ensure execution of protocols and reports for new processes
- Drive lifecycle management initiatives and KPI monitoring
- Support data analysis for process trends and shifts
- Provide updates on process performance to management
- Support regulatory filings and maintain inspection readiness
- Manage GMP documentation and related KPIs
- Act as a point of contact for audits and inspections
- Collaborate with Scheduling, Manufacturing, MS&T, and QA
- Align with P1 leadership for decision making and best practices
- Develop training for new products and processes
- Provide training and support to new Process Excellence associates
- Promote adherence to Environmental, Health, and Safety standards
- Manage EHS CAPA and drive safety improvements
- Lead digital, AI, and innovation projects for the PU
- Identify opportunities for process and quality improvements
Work Experience
- 8 years
Education
- Master's degree
Languages
- French – Business Fluent
- English – Business Fluent
Tools & Technologies
- GMP
- FDA
- Lean Manufacturing
- Six Sigma
- Microsoft Office Suite
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?
- Bristol Myers Squibb
Director Strategy and Operations European Markets(m/w/x)
Full-timeWith HomeofficeManagementBoudry - 1112 Celgene International SaRL
Technicien de maintenance process(m/w/x)
Full-timeWith HomeofficeSeniorBoudry - Bristol Myers Squibb
Intern - Manufacturing Science and Technology(m/w/x)
Full-timeInternshipWith HomeofficeBoudry - Bristol Myers Squibb
Sr Manager Procurement - Indirect products and services(m/w/x)
Full-timeWith HomeofficeSeniorBoudry - Breitling
Learning & Development Manager(m/w/x)
Full-timeWith HomeofficeSeniorLa Chaux-de-Fonds