Quality Affairs/Management Recruitment

Specialized Quality Affairs/Management Recruitment
At Adaptive Life Science, our Quality Affairs/Management recruitment expertise spans the complete quality ecosystem within Medical Device, IVD, Biotech, and Pharmaceutical organizations. Our consultants don't just understand quality—we live and breathe the intricate processes that define excellence in these highly regulated industries.

Deep Quality Systems Knowledge
Our quality affairs recruitment specialists possess comprehensive understanding of medical device manufacturing across all product types—hardware, software, and diagnostics. We recognize that quality management requirements vary dramatically whether you're implementing ISO 13485 quality management systems, establishing robust CAPA (Corrective and Preventive Action) frameworks, or developing sophisticated post-market surveillance programs.

Our team understands the critical nuances of quality processes: from Design Controls under 21 CFR Part 820 to Risk Management per ISO 14971, from Clinical Evaluation protocols to Unique Device Identification (UDI) implementation. We know that quality professionals must navigate Medical Device Reporting (MDR) requirements, vigilance activities, and the complexities of multi-site manufacturing validation.

Quality Recruitment Across All Company Stages
Whether you're a 10-person startup building your first quality management system or a 15,000+ employee global organization requiring specialized quality expertise, our Quality Affairs/Management recruitment approach adapts to your unique needs. We understand that startup quality professionals wear multiple hats—often serving as quality engineer, regulatory specialist, and compliance officer simultaneously. Conversely, we recognize that established organizations require candidates with deep expertise in specific quality domains like supplier quality management, process validation, or quality auditing.

Proven Quality Professional Network
Our quality affairs recruitment process connects you with seasoned professionals who possess the minimum three years of hands-on experience essential for navigating complex quality challenges. These candidates understand the real-world implications of quality decisions—from production line shutdowns due to non-conformances to successful regulatory inspections that enable market expansion.

By offering free services to quality professionals, we've cultivated relationships with candidates who've managed quality crises, implemented successful quality transformations, and built quality cultures that drive organizational success.

Your Quality Recruitment Authority
When quality failures can result in product recalls, regulatory action, or patient safety issues, you need recruitment partners who understand these stakes. Our specialized Quality Affairs/Management recruitment ensures every placement strengthens your quality infrastructure with proven expertise and deep industry knowledge.

Trust Adaptive Life Science to deliver quality recruitment solutions that protect your brand, ensure compliance, and drive continuous improvement across your organization.
Contact Us
Quality Management/
Quality Assurance
No two roles in quality management are the same, and we know that each company has its own challenges, projects and development plans that the QM function will bring to life.

Our network is built strongly on the foundation of knowing ISO 13485 and the documentation required for compliance, and from there understanding your focus in the device lifecycle.

Whether you are working broadly across the QM/RA topics or responsible for medical safety and CAPA - we have seen it all and want to hear about your challenges and aspirations.
CAPA and Validation
​From building new CAPA systems to be compliant with the MDR or establishing a risk management reporting structure compliant to ISO 14971, we know the challenges and project focusses going through the medical device industry at any one time

​Looking at manufacturing process validation and CSV, our network has technical expertise to comply with the quality standards requirements.
Contact Us
Auditing and Supplier Quality Assurance
Whether you are looking after the devices during production in QA, responsible for MDSAP implementation or visiting suppliers to ensure they are adhering your company quality assurance agreements, our consultants have covered roles all fields.

We understand the importance of strong negotiation, communication and stakeholder management skills to drive the relationship forward a smooth, compliant route to market.
Contact Us
PMS and Vigilance
Medical device safety is always at the top of everyone's mind in this industry. Our consultants are constantly updating their knowledge with regards to post-market surveillance requirements, PMS and PSUR reporting.

We have supported candidates to be successful in roles where safety forms part of a broader role, or for larger medical companies who need a dedicated safety professional responsible for a proactive and comprehensive vigilance system.

Read Our Blogs

July 17, 2025
The Importance of Employee Incentives in Life Sciences: How Do You Compare?

In the fast-evolving world of Medical Devices, IVD, and Biotech, the competition for top-tier talent is fiercer than ever. With innovation cycles accelerating and regulatory landscapes shifting, companies need more than just cutting-edge products, they need the right people behind them. And to attract and retain those people, incentives matter. Why Incentives Are No Longer […]

July 10, 2025
When Is It Okay to Seek External Support for Filling a MedTech Role?

Hiring in the MedTech sector is rarely straightforward. Between regulatory requirements, niche skill sets, and the pressure to innovate quickly, even the most experienced hiring managers can find themselves facing unexpected challenges. If you’ve ever struggled to fill a role, you’re not alone, and it doesn’t mean you’ve failed. It simply means the role is […]

July 4, 2025
Sourcing Leading R&D Medical Device Talent in Germany: A Guide

As a leading recruitment agency specializing in the Medical Device, IVD, Biotech, and Pharmaceutical industry, we understand the importance of finding top talent to drive innovation and growth. Germany is a hub for medical device research and development, with many leading companies and startups driving innovation in the sector. In this guide, we will provide […]

June 17, 2025
Retaining Top Talent in Medical Device Regulatory and Quality Teams

Why Retention Is a Strategic Priority In today’s competitive MedTech landscape, retaining high-performing Regulatory and Quality professionals isn’t just an HR concern, it’s a business-critical strategy. With MDR, IVDR, and evolving FDA expectations continuing to reshape the compliance landscape, the cost of turnover in these functions is more than financial. It’s operational risk, lost knowledge, […]

Submit Vacancy

    linkedin facebook pinterest youtube rss twitter instagram facebook-blank rss-blank linkedin-blank pinterest youtube twitter instagram