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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
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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