Sterility Assurance Student Placement 2027
Not disclosed
Salary
Not disclosed by employer
£41,700
Going rate
Skilled Worker going rate
This role may qualify for a Skilled Worker visa
SOC 3115 is an eligible occupation, but we are only 35% sure that is the right code. JANSSEN-CILAG LIMITED is a licensed sponsor, so if the code fits, the role should qualify. Check the occupation eligibility rules against what the job actually involves.
This could also be SOC 3111 (Laboratory technicians) or SOC 2482 (Quality assurance and regulatory professionals). We read the code off the advert, so it is our best guess, not the employer's.
About the role
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:
Career ProgramsJob Sub Function:
Non-LDP Intern/Co-OpJob Category:
Career ProgramAll Job Posting Locations:
Leeds, West Yorkshire, United KingdomJob Description:
Duration: 12 months
Location: Leeds, Yorkshire
Sector: Medical Devices
Department: Quality/Sterility Assurance
DePuy Synthes create products that reconstruct diseased or damaged joints. These products change the lives of our patients and present unique and rewarding challenges for our engineering teams.
In this role, you'll support our Sterility Assurance team in helping ensure the safety and quality of medical implants and surgical instruments. Working alongside scientists, engineers, manufacturing teams, and external partners, you'll gain hands-on experience across the full product lifecycle, from design through to terminal sterilization.
You'll work on a variety of real-world projects, receive training and mentoring throughout the year, and have the opportunity to visit our Blackpool facility to broaden your experience and network.
How You'll Make an Impact:
- Supporting design engineers to develop instrumentation that meets cleaning and sterilization requirements.
- Supporting Sterility Assurance Sterilization/Contamination Control Programme.
- Performing tests to ensure product manufactured on site is clean and sterile (this includes water testing and environmental monitoring of the ISO Class 8 cleanrooms).
- Working with vendors and external laboratories.
- Collaborating with global teams across the USA and Ireland to implement innovative ideas, protocols, and processes.
What We're Looking For:
- Currently studying for a degree (predicted or achieved 2:1 or above) in Medical Engineering, Biomedical Sciences, Microbiology, Bioengineering, or a related field.
- A curious and proactive mindset, with a genuine interest in healthcare, science, and medical technology.
- Strong analytical and problem-solving skills, with the ability to think critically and approach challenges confidently.
- Excellent communication skills and the ability to work effectively with a range of stakeholders.
- A keen eye for detail, strong organizational skills, and an eagerness to learn and develop.
Why join us?
- Build real-world experience at one of the world’s leading healthcare companies.
- Work on projects that have a real impact on business decisions
- Build your professional network across multiple business functions.
- Learn from experienced professionals in a supportive and collaborative environment.
- Take a meaningful step toward your future career while making a difference in patients' lives around the world.
Please note the assessment process will include an Assessment Centre, currently planned for January 2027.
Join us and help shape the future of healthcare.
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.
Required Skills:
Preferred Skills:
This description is the source posting as it read when we added it. We are not affiliated with JANSSEN-CILAG LIMITED, so check their own site for the current details.
Where this offer sits in the market
Quality assurance technicians (SOC 3115) · UK · ONS ASHE 2025 · basic pay · ~43k in sample- Middle half £28,444–41,340
- Median £32,968
- Going rate £41,700
- Threshold £41,700
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Browse more sponsored jobs at JANSSEN-CILAG LIMITEDAbout sponsorship for this role
Does this job guarantee visa sponsorship?
Not necessarily. JANSSEN-CILAG LIMITED holds a sponsor licence, but sponsorship for a specific hire is always the employer's decision. Be upfront in your application that you'll require it.
What salary is needed for this role to be eligible?
The offer must clear both the general threshold and the SOC 3115 going rate of £41,700. New-entrant and shortage discounts can lower it.