Validation Engineer

Validation Engineer

Location: Blackpool

Working mode: On-site (opportunity to work occasionally from home)

Duration: 6 months

Hours: Full-time, 37 hours per week

Pay rate range: Competitive hourly rate (PAYE & Umbrella options available)

Validation Engineer for the ongoing relocation project to transfer mature medical device manufacturing process from an overseas location to Blackpool. The current process utilises a range of technologies focused around, hot pressing, injection molding, CNC milling, and Dip Coating. To support this transformational project, we require a range of engineering expertise as each process requires validation.

The requirements of this role within the wider project are to cover the validation activities and deliverables for the relocation of the equipment and process. With a high dependency on working with relocating legacy processes with flexibility and speed of delivery. The technical challenge has been deemed to be low as it is a proven product currently on market, but the time constraints and delivery environment (exiting a current site) add challenge to the execution of the project.

roles and responsibilities

In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Process and Equipment Validation support for the transformational relocation project
• Documentation creation for process validation activities working with injection molding, CNC milling, hot pressing, dip coating.
• Performing and overseeing validation activities for multiple manufacturing lines within the project.
• Process readiness and implementation for the process relocation project
• Responsible for communicating business related issues or opportunities to next management level.
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
• For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
• Performs other duties assigned as needed.

how to succeed

• Experience in the Medical Device industry or medical field.
• Demonstrated knowledge of manufacturing principles and practices, and procedures.
• Knowledge of specific business practices and software and software applications.
• Experience using medical device manufacturing processing equipment.
• Experience in validation activities including documentation generation, performing and overseeing for process and equipment validation.
• Verbal and written communication skills.
• Able to enter data on spread sheet and database applications.
• Ability to prioritise own work and work to deadlines
• Ability to communicate effectively with a diverse clientele base.
• Ability to work cooperatively with co-workers and the public.
• Ability to perform duties in accordance with policies and procedures and in to comply civil rights requirements.

benefits

This role offers a very competitive hourly rate. This contract will initially run for 6 months.

you are welcome here

DePuy Synthes is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about DePuy Synthes

DePuy Synthes is the orthopaedic and neurological businesses of Johnson & Johnson - the world's most comprehensive and broadly-based healthcare company. At DePuy Synthes we specialise in our innovations in healthcare products, services and programs that make a real difference to millions of people across the world. We specialise in joint reconstruction, trauma, extremities, craniomaxillofacial, spinal surgery and sports medicine, and also the VELYS™ Digital Surgery portfolio. Contribute to the next healthcare breakthrough with your next project at DePuy Synthes.

https://www.jnjmedtech.com/en-GB/companies/depuy-synthes

application process

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email. The pay rate for this role will depend on how you are paid. PAYE & Umbrella options are available.

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.