QA Team Manager- Compliance

Posted 2 Days Ago
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Ilfracombe, North Devon, Devon, England
Senior level
Biotech
The Role
The QA Team Manager is responsible for the daily management and performance of functional teams, implementing quality management systems, leading audits, and driving quality improvement initiatives while maintaining regulatory compliance. This role involves managing teams under pressure and collaborating with various stakeholders.
Summary Generated by Built In

Be part of something altogether life-changing!

Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.

Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.

What you’ll do:

  • Responsible for Daily Management of the Functional team and their performance; Leads people using Danaher Values and Core Behaviors with a GEMBA presence.
  • Maintain Quality Management System in accordance with Corporate, BU and regulatory requirements advocating complainant change management.
  • Leads and implement strategic initiatives to reduce the number of internal and external non-conformities, process efficiencies or any other strategic Quality improvement initiatives utilizing Danaher Business System tools.
  • Lead customer, 3rd party and internal audits.
  • Member of the Quality Management Team & deputize for the Senior Quality Manager where required.
  • Managing team(s) working with minimum supervision under pressure to tight deadlines with customer focus.

Who you are:

  • Bsc in applicable field (e.g Science, Engineering) or equivalent experience in Quality in a regulated manufacturing industry (e.g Pharma, Biopharm, Life Science, Biotech)
  • Essential previous experience in Quality Assurance; Problem Solving, Analytical and Continual Improvements.
  • Certified Lead Auditor in ISO 9001:2015 or 13485:2015
  • Proven background leading and managing teams working with minimum supervision under pressure to tight deadlines with customer focus.
  • Demonstrated experience working a high matrix environment, influencing differing stakeholders to achieve common and business objectives.

It would be a plus if you also possess previous experience in:

  • Ideally having a recognized Institute Membership (e.g Chartered Quality Institute, Chartered Management Institute)
  • Msc advantageous
  • Knowledge of Lean Manufacturing and Six Sigma

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Top Skills

Iso 13485
Iso 9001
The Company
Bengaluru, Karnataka
8,399 Employees
On-site Workplace

What We Do

Cytiva, now with the life sciences business from Pall Corporation, is a global life sciences leader dedicated to helping customers discover and commercialize the next generation of therapeutics. Together, we bring dedicated technical expertise and a broad portfolio of tools and technologies that enable the development, manufacture, and delivery of transformative medicines to patients.

Visit cytiva.com to learn more.

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