Lab Quality Control Technician

Johnson & Johnson; Blackpool; On-site; GBP 25,000 - 35,000; Full time

Job summary

Join a leading pharmaceutical company as a Quality Control Technician, where you'll engage in cutting-edge technology and ensure compliance with quality standards. This full-time, on-site position involves performing critical testing on raw materials and finished products, supporting laboratory investigations, and collaborating with various departments. You'll thrive in an inclusive environment that values diverse perspectives and experiences, contributing to innovations that make a real difference in healthcare. If you are passionate about quality and compliance, this role offers a fantastic opportunity to advance your career in a dynamic setting.

Qualifications

• Minimum 1 year experience in a laboratory setting.
• A Level in Science or Mathematics or equivalent required.
• Experience in a quality environment preferred.

Responsibilities

• Perform physical and analytical testing of materials.
• Ensure compliance with cGMP and ISO standards.
• Support documentation and training within the lab.

Skills

Laboratory Experience

Analytical Testing

Communication Skills

Microsoft Office

cGMP Compliance

Time Management

Team Collaboration

Education

A Level in Science or Mathematics

BSc in Scientific Subject

Job description

Quality Control Technician

Location: Blackpool

Duration: 12 months

Hours: 37 hours per week

Imagine your next project as a Quality Control Technician, working at the forefront of cutting edge work and technology with one of the leading Pharmaceutical companies in the world!

roles and responsibilities

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

• Ensure that testing is performed in a timely manner
• Day to day performance
• Physical testing of raw material, in process and finished product
• Analytical testing of raw material, in process and finished goods
• Chemical testing of raw material, in process and finished goods
• Management of consumables and materials used in testing
• Cleaning of items for testing within the laboratory
• Execution of the laboratory cleaning program
• Review of internal and external testing data
• Interface with other departments to ensure timely testing of products and material
• Support with laboratory investigations and non-conformance investigations
• Ensure the principles of cGMP are applied and that all documentation is followed to comply with ISO9000, ISO13485, FDA QSRs and the Medical device directive
• Support documentation revisions

Quality and Compliance Related Responsibilities

• Ensures that all activities are carried out in compliance with all regulations and laws governing business and quality operations
• Staff: Responsible for ensuring compliance with all local, national, international and company regulations, policies and procedures for Health, Safety and Environmental compliance.

GMP documentation and Quality Systems

• Support investigations to assist in the completion of Non-conformance reports and OOS excursions

Training

• Ensure that own training records are up to date and complete
• Assist in the training of other staff

Validation

• Support validation of test methods and equipment for the project team

External communications

• Liaise with approved manufactures to ensure data is retrieved and available
• Ensure that consumables are ordered in a timely manner to avoid testing delays

how to succeed

• Minimum of A level in Science or mathematics discipline (international equivalents acceptable)
• Desired BSc degree in Scientific subject (Chemistry, Pharmacy, Forensics etc…)
• Minimum 1 years experience in a laboratory setting (Practical laboratory experience gained through a degree is acceptable)
• Experience with Microsoft office applications (Word, Excel, PowerPoint, Office)
• Desired previous experience working within a quality environment in the Food, Consumer, Pharmaceutical or Medical device industry
• Able to follow procedures to ensure the principles of cGMP are upheld
• Able to communicate and present information and ideas effectively
• Able to work to deadlines
• Able to react to a changing environment and under time pressures
• Able to work as part of a team to work towards a common goal
• Able to manage own time and prioritize own workload to ensure timely completion of assigned work
• Credo values: Integrity and Credo based actions
• Customer focus: Results and Performance driven with a sense of Urgency
• Talent development: Collaboration, Self-awareness, Adaptability

details

This role offers a very competitive hourly rate.

This contract will run for a 12 month duration and has a chance of extension.

Full time on-site position.

you are welcome here

DePuy 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-US/companies/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.

questions

If you would like some additional information about the role please contact: [e-mail]

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”.