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Sr. Quality Engineer - Manufacturing(m/w/x)
Quality engineering for continuous blood pressure monitor manufacturing with contract partners. ISO and FDA QSR knowledge required. Flexible work location, hybrid schedule, occasional international travel.
Requirements
- Bachelor's degree in technical or scientific field
- 5-8 years experience in quality or manufacturing
- Team leadership skills
- Independent project prioritization, execution, and reporting
- Knowledge of ISO and FDA/Quality System Requirements
- Strong project management skills
- Strong time management skills
- Familiarity with Risk Management per ISO 14971
- Creative problem solving for complex issues
- Effective problem solving for complex issues
- Ability to work on multiple tasks concurrently
- Ability to manage changing priorities
- Proficiency with MS Teams
- Proficiency with MS Word
- Proficiency with MS Excel
- Proficiency with MS PowerPoint
- Proficiency with AI tools
- Proficiency with eQMS systems
- Bachelor's Degree
- Mid-Senior level experience
Tasks
- Lead quality engineering activities with contract manufacturers
- Support IQ, OQ, PQ processes and non-conformance resolution
- Conduct process and test method validations
- Resolve manufacturing non-conformances with contract manufacturers
- Approve DHRs, DHF deliverables, product releases, and change orders
- Coach manufacturing personnel and contract manufacturers on GMP and QMS
- Lead cross-functional teams to resolve quality issues
- Navigate the CAPA process
- Drive product improvement and operational efficiency projects
- Support internal labeling reviews for required markings and symbols
- Lead supplier management activities for contract manufacturers
- Conduct supplier audits, qualifications, and assessments
- Support QMS audits with internal and external auditors
Work Experience
- 5 - 8 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- MS Teams
- MS Word
- MS Excel
- MS PowerPoint
- AI tools
- eQMS systems
- ISO 13485
- ISO 14971
- FDA 21 CFR Part 820
- MDR
- FMEA
Benefits
Flexible Working
- Flexible work location
- Hybrid work schedule
Other Benefits
- Occasional international travel
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Sr. Quality Engineer - Manufacturing(m/w/x)
Quality engineering for continuous blood pressure monitor manufacturing with contract partners. ISO and FDA QSR knowledge required. Flexible work location, hybrid schedule, occasional international travel.
Requirements
- Bachelor's degree in technical or scientific field
- 5-8 years experience in quality or manufacturing
- Team leadership skills
- Independent project prioritization, execution, and reporting
- Knowledge of ISO and FDA/Quality System Requirements
- Strong project management skills
- Strong time management skills
- Familiarity with Risk Management per ISO 14971
- Creative problem solving for complex issues
- Effective problem solving for complex issues
- Ability to work on multiple tasks concurrently
- Ability to manage changing priorities
- Proficiency with MS Teams
- Proficiency with MS Word
- Proficiency with MS Excel
- Proficiency with MS PowerPoint
- Proficiency with AI tools
- Proficiency with eQMS systems
- Bachelor's Degree
- Mid-Senior level experience
Tasks
- Lead quality engineering activities with contract manufacturers
- Support IQ, OQ, PQ processes and non-conformance resolution
- Conduct process and test method validations
- Resolve manufacturing non-conformances with contract manufacturers
- Approve DHRs, DHF deliverables, product releases, and change orders
- Coach manufacturing personnel and contract manufacturers on GMP and QMS
- Lead cross-functional teams to resolve quality issues
- Navigate the CAPA process
- Drive product improvement and operational efficiency projects
- Support internal labeling reviews for required markings and symbols
- Lead supplier management activities for contract manufacturers
- Conduct supplier audits, qualifications, and assessments
- Support QMS audits with internal and external auditors
Work Experience
- 5 - 8 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- MS Teams
- MS Word
- MS Excel
- MS PowerPoint
- AI tools
- eQMS systems
- ISO 13485
- ISO 14971
- FDA 21 CFR Part 820
- MDR
- FMEA
Benefits
Flexible Working
- Flexible work location
- Hybrid work schedule
Other Benefits
- Occasional international travel
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Hilo by Aktiia
Industry
Healthcare
Description
Hilo by Aktiia develops technology to help people control their blood pressure, aiming for a world where no lives are lost or damaged from its effects. Their cuffless blood pressure monitor is medically accurate and CE Marked.
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