Supervisor Micro, Quality Control

Mcneil Ab

United States

Remote

USD 90,000 - 130,000

Full time

2 days ago
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Benefits offered by this job

Competitive compensation and benefits

Job summary

Kenvue is seeking a Supervisor Micro, Quality Control to lead the QC microbiology laboratory on a fixed-term basis. This role reports to the Director of Quality and Compliance and is based onsite in Europe/Middle East/Africa region, Sweden (Helsingborg area).

The incumbent will drive testing quality, investigations, and continuous improvement in a regulated environment. The candidate should have a bachelor’s degree in microbiology or related field, strong GMP knowledge, and prior experience

Qualifications

  • Bachelor's degree in Microbiology, Biology, Life Sciences, or a related field.

Responsibilities

  • Lead and supervise the daily operations of the QC Microbiology laboratory.
  • Ensure microbiological testing follows approved procedures, GMP, and regulatory expectations.
  • Review and approve laboratory data, investigations, and documentation.
  • Manage environmental monitoring, water testing, and microbiological support for manufacturing operations.
  • Support deviation investigations, CAPAs, change controls, and risk assessments.
  • Ensure lab personnel are trained, qualified, and performing activities safely and effectively.
  • Drive continuous improvement to enhance lab efficiency and compliance.
  • Collaborate with Manufacturing, QA, Engineering and Supply Chain to support production goals.
  • Participate in internal and external audits and regulatory inspections.

Job description

Kenvue is currently recruiting for a:

Supervisor Micro, Quality Control
What we do

At Kenvue , we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours. For more information , click here.

Role reports to:

Director Quality and Compliance

Location:

Europe/Middle East/Africa, Sweden, Skane, Helsingborg

Work Location:

Fully Onsite

What you will do

Please note that this is a fixed-term contract position, starting immediately and until June 2027.

As the QC Microbiology Supervisor, you will:
  • Lead and supervise the daily operations of the QC Microbiology laboratory.
  • Ensure microbiological testing is performed in accordance with approved procedures, GMP requirements, and regulatory expectations.
  • Review and approve laboratory data, investigations, and documentation.
  • Manage environmental monitoring, water testing, and microbiological support for manufacturing operations.
  • Support deviation investigations, CAPAs, change controls, and risk assessments.
  • Ensure laboratory personnel are trained, qualified, and performing activities safely and effectively.
  • Drive continuous improvement initiatives to enhance laboratory efficiency and compliance.
  • Collaborate with Manufacturing, Quality Assurance, Engineering, and Supply Chain teams to support production goals.
  • Participate in internal and external audits and regulatory inspections.
Qualifications
Required Qualifications
  • Bachelor's degree in Microbiology, Biology, Life Sciences, or a related field.
  • Experience in Quality Control Microbiology within a pharmaceutical, medical device, consumer health, or regulated manufacturing environment.
  • Strong knowledge of GMP, FDA, EMA, and other applicable regulatory requirements.
  • Experience leading teams and developing laboratory personnel.
  • Strong analytical, problem-solving, and communication skills.
Preferred Qualifications
  • Experience with environmental monitoring programs.
  • Experience with deviation investigations and CAPA management.
  • Knowledge of data integrity requirements and laboratory systems.
  • Experience supporting regulatory inspections and audits.
What's In It For You
  • Opportunity to work with iconic consumer health brands.
  • Collaborative and inclusive culture focused on innovation and quality.
  • Professional development and career growth opportunities.
  • Competitive compensation and benefits package.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

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