QUALITY ASSURANCE AND REGULATORY AFFAIRS MANAGER IN GENETICS

at  Unilabs

Bern, BE, Switzerland -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate31 Jan, 2025Not Specified02 Nov, 20243 year(s) or aboveFrench,Business Correspondence,Communication Skills,German,Procedure ManualsNoNo
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Description:

Introduction
Unilabs is the largest provider of medical laboratory diagnostics for prescribers and hospitals in Switzerland and employs around 800 people.

Your Tasks

  • Promote and embody the company vision and policies while maintaining the genetic laboratory’s licensure and accreditations. Manage and enhance the Quality Management System (QMS) in compliance with ISO 15189, ISO 17025, IVDR, and company standards, assisting with quality-related issues and fostering a culture of quality through education.
  • Communicate significant changes affecting laboratory capabilities to accreditation bodies, and prepare accreditation dossiers while accompanying auditors and coordinating responses to findings. Identify and document non-conformances, assess risks, and conduct root cause analyses, reporting trends at quality meetings.
  • Oversee post-market incident activities, drive continuous improvement through monitoring indicators and corrective actions, and organize annual Quality Management Review meetings with relevant teams. Ensure compliance of in-house devices with IVDR requirements, collaborate with procurement on supplier compliance, and implement risk management procedures.
  • Represent the Quality and Regulatory functions during M&A due diligence and integration processes, and participate in crisis management to ensure business continuity while performing other assigned duties as needed.

Your Profile

Education and Experience

  • Bachelor’s degree or master’s degree in a technical/ process engineering/QA discipline, with significant related professional experience within the laboratory environment.
  • Prior in-depth experience working in an ISO 15189 accredited diagnostic laboratory with a focus on Quality Management Systems.
  • Ideally experience with medical device regulation and/or in-vitro diagnostic directive regulation.
  • 3 years of People Leadership Operations experience, preferred.
  • Fluent in French and English, German is a plus
  • Minimum Years Recommended and/or Preferred: 8-10 years

Required skills

  • Excellent interpersonal, organizational & communication skills with excellent attention to detail.
  • Self-motivated and driven critical thinker able to work in high pace and rapidly changing environment.
  • Responsive problem solver and action oriented.
  • Ability to affect change.
  • Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions.

We Offer

  • An exciting and dynamic work environment with a lot of internationality
  • Taking responsibility and unfolding your potential
  • A positive working atmosphere with a partnership and appreciative corporate culture
  • Attractive fringe benefits as well as a 40-hour week and 5-weeks vacation
  • Annual fee for your personal analyses and special prices for radiological advice from the Unilabs Group

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Responsibilities:

  • Promote and embody the company vision and policies while maintaining the genetic laboratory’s licensure and accreditations. Manage and enhance the Quality Management System (QMS) in compliance with ISO 15189, ISO 17025, IVDR, and company standards, assisting with quality-related issues and fostering a culture of quality through education.
  • Communicate significant changes affecting laboratory capabilities to accreditation bodies, and prepare accreditation dossiers while accompanying auditors and coordinating responses to findings. Identify and document non-conformances, assess risks, and conduct root cause analyses, reporting trends at quality meetings.
  • Oversee post-market incident activities, drive continuous improvement through monitoring indicators and corrective actions, and organize annual Quality Management Review meetings with relevant teams. Ensure compliance of in-house devices with IVDR requirements, collaborate with procurement on supplier compliance, and implement risk management procedures.
  • Represent the Quality and Regulatory functions during M&A due diligence and integration processes, and participate in crisis management to ensure business continuity while performing other assigned duties as needed


REQUIREMENT SUMMARY

Min:3.0Max:10.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

The laboratory environment

Proficient

1

Bern, BE, Switzerland