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:
QualityJob Sub Function:
R&D/Scientific QualityJob Category:
ProfessionalAll Job Posting Locations:
Blackpool, Lancashire, United KingdomJob Description:
About Orthopaedics
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
We are searching for the best talent to join our DePuy Synthes business as a Scientist – Microbiologist in Blackpool, UK.
Purpose:
You will be responsible for supporting end‑to‑end contamination control and sterility assurance practices across Global Orthopedics. This role supports research and development, manufacturing, sourcing, and delivery activities to ensure compliance with applicable international regulations and standards. You will report to a Sterility Assurance Supervisor or Sterility Assurance Manager and collaborate with internal and external partners to support product cleanliness, sterility assurance, and regulatory compliance.
You will be responsible for:
- Supporting R&D activities, including design for cleanability, decontamination, and sterilizability.
- Supporting selection, validation, and adoption of sterilization modalities and processes.
- Establishing and maintaining contamination control, environmental monitoring, and sterility assurance programs.
- Providing sterility assurance input into new manufacturing operations, equipment, facilities, and suppliers.
- Supporting design and validation of manufacturing processes, packaging systems, and controlled environments from a microbiological perspective.
- Supporting MAKE initiatives through risk assessments, bioburden management, and dose audit programs.
- Leading or supporting non‑conformances, CAPAs, and observations related to sterility assurance and contamination control.
- Working with internal and external laboratories to support microbiological and sterility testing in compliance with cGMP and SOP requirements.
- Supporting inspections, audits, regulatory submissions, and design history file documentation.
- Influencing standards and best practices through participation in internal councils and external industry or standards associations.
Qualifications / Requirements:
- Bachelor’s degree in Microbiology, Biology, Engineering, or a related discipline; advanced degree (MS or PhD) preferred.
- Minimum of 1-2 years’ experience in a medical device or pharmaceutical GMP and/or similarly regulated environment.
- Experience in microbiology, sterilization validation (terminal, aseptic, and/or reprocessing), and environmental controls.
- Proven experience troubleshooting microbiological, aseptic processing, or sterilization non‑conformances and CAPA activities.
- Strong knowledge of regulatory requirements including FDA QSR and ISO 13485; familiarity with ISO/EN/AAMI standards preferred.
- Experience interacting with regulatory or auditing bodies (e.g. FDA, EU authorities) preferred.
- Strong interpersonal, organisational, and written and verbal communication skills.
- Ability to work independently while collaborating effectively in a team environment.
- Strong organisational, time‑management, and flexibility skills.
- Proficiency in Microsoft Office applications (Word, Excel, PowerPoint) and analytical software.
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.
At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.
Here’s what you can expect:
• Application review: We’ll carefully review your CV to see how your skills and experience align with the role.
• Getting to know you: If there’s a good match, you’ll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
• Staying informed: We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
• Final steps: For successful candidates, you will need to complete country‑specific checks before starting your new role. We will help guide you through these.
Finally, at the end of the process, we’ll invite you to share feedback in a short survey — your input helps us continue improving the experience for future candidates.
Thank you for considering a career with Johnson & Johnson. We’re excited to learn more about you and wish you the best of luck in the process!
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Required Skills:
Preferred Skills:
Agility Jumps, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Database Backup, Data Savvy, Disruptive Innovations, Issue Escalation, Problem Solving, Process Oriented, Product Improvements, Quality Control (QC), Quality Control Testing, Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Report Writing