# Mgr Quality Control at Johnson & Johnson

Johnson & Johnson is hiring a Mgr Quality Control. Level rates it Little AI ●○○○; you can [apply on Level](https://jobsbylevel.com/go/fedf3656-2c69-4f1f-a1f0-5e54c1193c8f?utm_medium=ai-agent).

AI Level 1, AI centrality 36 out of 100. Uppsala, Uppsala County, Sweden.

## Details

- Company: [Johnson & Johnson](https://jobsbylevel.com/companies/johnson-johnson)
- AI level: AI Level 1 (score 36 out of 100)
- Location: Uppsala, Uppsala County, Sweden
- Posted: October 13, 2026
- Apply: https://jobsbylevel.com/go/fedf3656-2c69-4f1f-a1f0-5e54c1193c8f?utm_medium=ai-agent

## Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Quality Job Sub Function: Quality Control Job Category: People Leader All Job Posting Locations: Uppsala, Uppsala County, Sweden Job Description: JOB POSITION SUMMARY Quality assurance of chemical and microbiological testing and controls performed on products, raw materials/input materials, media, and manufacturing processes (including environmental hygiene), as well as quality assurance of validation and maintenance activities within the chemical and microbiological laboratory. Process Owner for the UQC/UQM laboratory process. Equipment Owner for laboratory systems within UQC/UQM. Review and approve documentation, test methods, and processes for the Quality Control laboratory. Review and approve laboratory investigations and non-conformity investigations. Replace Head of UQ during short-term absences, in accordance with a specific delegation of authority. DUTIES & RESPONSIBILITIES Lead and develop the laboratory to ensure that AMO Uppsala AB and UQ achieve their objectives regarding quality & compliance, delivery reliability, and cost efficiency. Plan and allocate resources and budget for QC Chemistry, Incoming Goods Inspection, and Microbiology. Responsible for cost centers 1213203550 and 1213203650 in accordance with the company's current approval authority policy. Line management responsibility for QC Chemistry, Incoming Goods Inspection, and Microbiology, as delegated. Member of the Quality Leadership Team. Ensure that all required chemical, physical, and microbiological tests and controls are performed on products, raw materials/input materials, media, and manufacturing processes in accordance with pharmacopoeial requirements and other applicable regulations. Ensure that processes are validated and qualified within the chemical and microbiological laboratories, as well as maintenance and calibration activities are in compliance with applicable requirements. Review and approve documents related to chemical, physical, and microbiological testing, test methods, and annual summaries/reports. Review and approve assessments and rationales related to chemical and microbiological testing and results. Review and approve investigations related to laboratory investigations and non-conformities. Ensure support and maintenance of quality specifications for products. EXPERIENCE & EDUCATION Five-year university degree in microbiology, chemistry, pharmacy, natural sciences, engineering, or a related field, or equivalent professional experience within the pharmaceutical industry or another process industry. Relevant leadership training for the position. Basic knowledge of financial accounting and budgeting. At least three to five years of professional experience in quality-related work within a quality-certified laboratory or manufacturing environment. Experience in project management. Experience in people management and leadership. Strong knowledge of GMP (Good Manufacturing Practice) and/or ISO standards, as well as applicable regulations and guidance documents (e.g., CFR, pharmacopoeias). Good IT skills. Demonstrates an understanding of AI concepts and frameworks, including awareness of responsible and ethical

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/mgr-quality-control-at-johnson-johnson-1f19d8

Source: https://jobsbylevel.com/jobs/mgr-quality-control-at-johnson-johnson-1f19d8

## Cite this page

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