Katalyst Healthcares & Life Sciences Jobs Hiring Now
Katalyst Healthcares & Life Sciences is hiring for 406 open roles on Migrate Mate as of July 16, 2026, concentrated in engineering (Non-Software) and business analysis. Migrate Mate updates Katalyst Healthcares & Life Sciences's live openings daily. Katalyst Healthcares & Life Sciences is a life sciences staffing and consulting firm that places professionals across biotech, pharmaceutical, and medical device organizations.
Find Katalyst Healthcares & Life Sciences JobsOverview
Katalyst Healthcares & Life Sciences hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 406
- Top team
- Engineering (Non-Software)
- Seniority
- Across all levels
- Work type
- 27% remote or hybrid
- Top location
- Portsmouth
Open Roles at Katalyst Healthcares & Life Sciences
Showing 25 of 406+ Katalyst Healthcares & Life Sciences jobs
The Design Quality Engineer (DQE) at Philips is responsible for ensuring that products are designed and developed in compliance with regulatory standards, quality requirements, and customer expectations. This role works closely with R&D, regulatory, manufacturing, and suppliers to embed quality into product design.
Responsibilities:
Design Control:
- Ensure compliance with Design Control requirements (21 CFR Part 820 / ISO 13485) throughout product lifecycle.
- Participate in design planning, design reviews, and design verification/validation activities. (cross-functional design reviews, ensuring closure of action items).
- Review and approve design inputs, outputs, and technical documentation.
- Support traceability matrix (DHF, DMR, DHR) creation and maintenance.
- Ensure Design Verification & Validation (V&V) activities meet requirements.
- Review and approve, Engineering Change requests/Orders (ECR/ECOs).
- Ensure design changes follow proper change control processes.
- Builds and nurtures effective relationships with internal and external stakeholders, providing expert guidance and mentorship to cross-functional teams, ensuring alignment with quality standards and successful project milestones.
- Validates critical design inputs such as usability, reliability, performance, manufacturability, and safety, ensuring alignment with both quality standards and regulatory requirements.
- Design transfer to manufacturing, ensuring process readiness.
- Guide comprehensive risk management activities throughout the product lifecycle to ensure risks are identified and mitigated.
- Facilitate FMEA (Design and Process) and hazard analysis.
- Ensure risk controls are implemented, verified, and documented.
- Ensure preparation for quality audits and inspections, maintaining documentation to demonstrate compliance.
- Record, manage, and execute CAPA processes including root cause analysis and implementation of solutions.
- Contributes to the development, implementation, and revision of QMS processes.
- Bachelor's Degree in Medical Sciences, Healthcare Management, Industrial Engineering, Supply Chain Management or equivalent.
- Knowledge of medical device regulations, requirements, and standards, such as 21 CFR Parts 820, ISO 13485, ISO 14971, European Medical Device Directive (93/42/EEC), EU Medical Device Regulation (EU MDR), Canadian Medical Devices Regulation (SOR/98-282), etc
- Change Management (Including design and Manufacturing transfer).
- Minimum of 5+ years' experience in FDA regulated medical device environments, with a focus on Design Assurance/Control, detailed knowledge of Risk.
- You have detailed experience in identifying, promoting, and supporting processes and design quality tools for use in tracking/preventing product defects, design traceability, and Design for Reliability.
The Design Quality Engineer (DQE) at Philips is responsible for ensuring that products are designed and developed in compliance with regulatory standards, quality requirements, and customer expectations. This role works closely with R&D, regulatory, manufacturing, and suppliers to embed quality into product design.
Responsibilities:
Design Control:
- Ensure compliance with Design Control requirements (21 CFR Part 820 / ISO 13485) throughout product lifecycle.
- Participate in design planning, design reviews, and design verification/validation activities. (cross-functional design reviews, ensuring closure of action items).
- Review and approve design inputs, outputs, and technical documentation.
- Support traceability matrix (DHF, DMR, DHR) creation and maintenance.
- Ensure Design Verification & Validation (V&V) activities meet requirements.
- Review and approve, Engineering Change requests/Orders (ECR/ECOs).
- Ensure design changes follow proper change control processes.
- Builds and nurtures effective relationships with internal and external stakeholders, providing expert guidance and mentorship to cross-functional teams, ensuring alignment with quality standards and successful project milestones.
- Validates critical design inputs such as usability, reliability, performance, manufacturability, and safety, ensuring alignment with both quality standards and regulatory requirements.
- Design transfer to manufacturing, ensuring process readiness.
- Guide comprehensive risk management activities throughout the product lifecycle to ensure risks are identified and mitigated.
- Facilitate FMEA (Design and Process) and hazard analysis.
- Ensure risk controls are implemented, verified, and documented.
- Ensure preparation for quality audits and inspections, maintaining documentation to demonstrate compliance.
- Record, manage, and execute CAPA processes including root cause analysis and implementation of solutions.
- Contributes to the development, implementation, and revision of QMS processes.
- Bachelor's Degree in Medical Sciences, Healthcare Management, Industrial Engineering, Supply Chain Management or equivalent.
- Knowledge of medical device regulations, requirements, and standards, such as 21 CFR Parts 820, ISO 13485, ISO 14971, European Medical Device Directive (93/42/EEC), EU Medical Device Regulation (EU MDR), Canadian Medical Devices Regulation (SOR/98-282), etc
- Change Management (Including design and Manufacturing transfer).
- Minimum of 5+ years' experience in FDA regulated medical device environments, with a focus on Design Assurance/Control, detailed knowledge of Risk.
- You have detailed experience in identifying, promoting, and supporting processes and design quality tools for use in tracking/preventing product defects, design traceability, and Design for Reliability.
Job Roles at Katalyst Healthcares & Life Sciences
Working at Katalyst Healthcares & Life Sciences
Katalyst Healthcares & Life Sciences's 406 open roles are across all levels, and about 27% are remote or hybrid. The most active teams are engineering (Non-Software), business analysis, and manufacturing operations. Katalyst Healthcares & Life Sciences is a life sciences staffing and consulting firm that connects skilled professionals with roles in bioprocess manufacturing, quality engineering, regulatory affairs, and laboratory operations across the biotech, pharmaceutical, and medical device sectors. Most Katalyst Healthcares & Life Sciences roles are based in Portsmouth, with some in Boston and Irvine.
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Browse jobs by roleKatalyst Healthcares & Life Sciences Jobs: Frequently Asked Questions
How many jobs is Katalyst Healthcares & Life Sciences hiring for right now?
Katalyst Healthcares & Life Sciences is hiring for 406 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in engineering (Non-Software) and business analysis. Openings span cleanroom manufacturing, quality engineering, bioprocess operations, microbiology, computer system validation, and people operations, reflecting active hiring across both technical and support functions within the life sciences sector.
What kinds of roles does Katalyst Healthcares & Life Sciences hire for?
The most active teams are engineering (Non-Software), business analysis, and manufacturing operations. Katalyst Healthcares & Life Sciences regularly posts openings in bioprocess and cleanroom manufacturing, quality engineering and quality systems, laboratory operations, microbiology, computer system validation, and medical device assembly, along with occasional people operations roles. Most postings are across all levels, spanning hands-on technician positions through senior specialist and principal-level engineering roles.
Are Katalyst Healthcares & Life Sciences jobs remote or in-person?
A mix of remote and on-site. About 27% of Katalyst Healthcares & Life Sciences's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Portsmouth. Each Katalyst Healthcares & Life Sciences listing shows its work location so you can filter before applying.
How do I apply to a job at Katalyst Healthcares & Life Sciences?
Find a Katalyst Healthcares & Life Sciences role on Migrate Mate, then follow the listing through to Katalyst Healthcares & Life Sciences's own application process. Katalyst Healthcares & Life Sciences manages its own recruiting and hiring decisions directly. Reviewing the job description carefully before applying is recommended, as requirements vary across technical, scientific, and operational roles within the life sciences industry.
Does Katalyst Healthcares & Life Sciences hire entry-level?
Most of Katalyst Healthcares & Life Sciences's open roles on Migrate Mate are across all levels as of July 16, 2026. Check individual Katalyst Healthcares & Life Sciences listings for stated experience requirements.
Where is Katalyst Healthcares & Life Sciences hiring?
Most Katalyst Healthcares & Life Sciences roles are based in Portsmouth, with some in Boston and Irvine, and about 27% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.