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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:
R&D/Scientific Quality
Job Category:
Professional
All Job Posting Locations:
Zuchwil, Switzerland
Job Description:
We are searching for the best talent for a Staff Scientist – Microbiology & Sterility Assurance (Supplier / External Manufacturing).
Purpose We are looking for a Staff Scientist to join our team supporting Microbiological Quality & Sterility Assurance (MQSA) across external manufacturing and suppliers within DePuy Synthes (EMEA).
In this role, we support end‑to‑end MQSA activities across the supply network, with a focus on contamination control, sterilization, cleaning processes, and controlled manufacturing environments. We work closely with Quality, Regulatory Affairs, Supply Chain, and Procurement teams to help ensure product quality, audit readiness, and reliable supply.
This position plays an important role in safeguarding microbiological quality and supporting compliant supplier and external manufacturing operations.
You will be responsible for
Supporting end‑to‑end Microbiological Quality & Sterility Assurance (MQSA) activities related to suppliers and external manufacturing processes
Contributing to change requests and projects impacting controlled environments, cleaning, and sterilization processes
Supporting contamination control strategies, including environmental monitoring and investigation activities
Providing technical guidance and training on microbiological quality and sterility assurance
Acting as subject matter expert for investigations, CAPA, non‑conformances, audit observations, and risk assessments
Supporting due diligence activities (e.g., acquisitions, partnerships) by providing MQSA expertise and risk input
Supporting development and updates of supplier quality agreements
Coordinating and participating in supplier audits, including preparation, on‑site support, response review, and follow‑up activities
Partnering with cross‑functional teams to support supplier qualification and lifecycle management
Contributing to remediation activities following audits or regulatory findings
Building strong relationships with external partners, including manufacturers, suppliers, sterilization providers, and testing laboratories
Coaching and supporting colleagues and partners in MQSA practices
Qualifications / Requirements
Bachelor’s degree in Microbiology, Biological Sciences, Engineering, or a related field
At least 6 years of experience in microbiology and sterilization assurance within the medical device or pharmaceutical industry
Strong knowledge of microbiological control, contamination control, and sterilization processes
Familiarity with applicable standards and regulations (e.g., ISO, EN, AAMI)
Experience conducting or supporting investigations, test method development, and validation
Knowledge of regulatory and quality requirements related to suppliers and external manufacturing
Experience supporting audits, inspections, or compliance assessments
Strong communication and collaboration skills, with the ability to work across functions and levels
Ability to work independently while contributing effectively to team objectives
Fluent in English (French and/or German are a plus)
Demonstrates an understanding of AI concepts and frameworks, including awareness of responsible and ethical AI practices, and uses effective prompting techniques to support efficiency and productivity
What we offer We offer a collaborative environment where we work together to ensure high standards in microbiological quality and sterility assurance across a global supply network. This role provides opportunities to develop expertise, work with external partners, and contribute to continuous improvement.
Additional role information This role may involve working in controlled environments (e.g., cleanrooms) and requires appropriate gowning practices where applicable.
The position includes regular interaction with suppliers and external partners, as well as participation in audits and inspections.
Travel within EMEA is expected (approximately 20–30%).
Our commitment to inclusion We are an equal opportunity employer and value diversity in our workforce. We welcome applications from people of all backgrounds, experiences, and perspectives.
If reasonable accommodation is needed during the recruitment process or while performing the role, support is available at every stage—please let us know how we can help.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
Switzerland - Requisition Number: R-083855 Ireland - Requisition Number: R-085047 UK - Requisition Number: R-085054 Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
#J-18808-Ljbffr
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:
R&D/Scientific Quality
Job Category:
Professional
All Job Posting Locations:
Zuchwil, Switzerland
Job Description:
We are searching for the best talent for a Staff Scientist – Microbiology & Sterility Assurance (Supplier / External Manufacturing).
Purpose We are looking for a Staff Scientist to join our team supporting Microbiological Quality & Sterility Assurance (MQSA) across external manufacturing and suppliers within DePuy Synthes (EMEA).
In this role, we support end‑to‑end MQSA activities across the supply network, with a focus on contamination control, sterilization, cleaning processes, and controlled manufacturing environments. We work closely with Quality, Regulatory Affairs, Supply Chain, and Procurement teams to help ensure product quality, audit readiness, and reliable supply.
This position plays an important role in safeguarding microbiological quality and supporting compliant supplier and external manufacturing operations.
You will be responsible for
Supporting end‑to‑end Microbiological Quality & Sterility Assurance (MQSA) activities related to suppliers and external manufacturing processes
Contributing to change requests and projects impacting controlled environments, cleaning, and sterilization processes
Supporting contamination control strategies, including environmental monitoring and investigation activities
Providing technical guidance and training on microbiological quality and sterility assurance
Acting as subject matter expert for investigations, CAPA, non‑conformances, audit observations, and risk assessments
Supporting due diligence activities (e.g., acquisitions, partnerships) by providing MQSA expertise and risk input
Supporting development and updates of supplier quality agreements
Coordinating and participating in supplier audits, including preparation, on‑site support, response review, and follow‑up activities
Partnering with cross‑functional teams to support supplier qualification and lifecycle management
Contributing to remediation activities following audits or regulatory findings
Building strong relationships with external partners, including manufacturers, suppliers, sterilization providers, and testing laboratories
Coaching and supporting colleagues and partners in MQSA practices
Qualifications / Requirements
Bachelor’s degree in Microbiology, Biological Sciences, Engineering, or a related field
At least 6 years of experience in microbiology and sterilization assurance within the medical device or pharmaceutical industry
Strong knowledge of microbiological control, contamination control, and sterilization processes
Familiarity with applicable standards and regulations (e.g., ISO, EN, AAMI)
Experience conducting or supporting investigations, test method development, and validation
Knowledge of regulatory and quality requirements related to suppliers and external manufacturing
Experience supporting audits, inspections, or compliance assessments
Strong communication and collaboration skills, with the ability to work across functions and levels
Ability to work independently while contributing effectively to team objectives
Fluent in English (French and/or German are a plus)
Demonstrates an understanding of AI concepts and frameworks, including awareness of responsible and ethical AI practices, and uses effective prompting techniques to support efficiency and productivity
What we offer We offer a collaborative environment where we work together to ensure high standards in microbiological quality and sterility assurance across a global supply network. This role provides opportunities to develop expertise, work with external partners, and contribute to continuous improvement.
Additional role information This role may involve working in controlled environments (e.g., cleanrooms) and requires appropriate gowning practices where applicable.
The position includes regular interaction with suppliers and external partners, as well as participation in audits and inspections.
Travel within EMEA is expected (approximately 20–30%).
Our commitment to inclusion We are an equal opportunity employer and value diversity in our workforce. We welcome applications from people of all backgrounds, experiences, and perspectives.
If reasonable accommodation is needed during the recruitment process or while performing the role, support is available at every stage—please let us know how we can help.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
Switzerland - Requisition Number: R-083855 Ireland - Requisition Number: R-085047 UK - Requisition Number: R-085054 Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
#J-18808-Ljbffr
Staff Scientist - Microbiology & Sterility Assurance (Supplier / External Manufacturing) Arbeitgeber: JOHNSON & JOHNSON
Johnson & Johnson bietet eine herausragende Arbeitsumgebung, die von einer starken Unternehmenskultur geprägt ist, die Innovation und Zusammenarbeit fördert. Als Global Head, IDAR Strategy & Business Operations haben Sie die Möglichkeit, in einem dynamischen Team zu arbeiten, das sich der Entwicklung lebensrettender Medikamente widmet, während Sie gleichzeitig von umfangreichen Weiterbildungs- und Entwicklungsmöglichkeiten profitieren. Die Standorte in Allschwil, Basel und anderen internationalen Büros bieten nicht nur eine attraktive Lebensqualität, sondern auch ein inspirierendes Umfeld, das Vielfalt und Inklusion schätzt.
