Job ID R-507577 Date posted January 12, 2025

Be part of something bigger at BD. Here, you’ll help us continually improve how we do things every day; to be more efficient, more effective and better serve our customers. You’ll do this within an exceptional team all striving to make sure that everything we do complies with regulations and standards, not just because it’s the right thing to do, but because our products impact people’s quality of life. Here, you’ll put your compliance experience, high expectations and attention to detail to the very best use: advancing the world of health™. At BD, you can make a true difference of one.

  • Job Type:
    Full-Time
  • Job Level:
    Entry to Senior
  • Travel:
    Varies
  • Salary:
    Competitive
  • Glassdoor Reviews and Company Rating

Responsibilities

Job Description Summary

The additive role involves the solution preparation of all additives used in the Company’s leading diagnostic products. The additives are to be made, in a strict GMP environment, encompassing all aspects of good laboratory practice (GLP).

This role demands a very organised and safe working methodology. You will report to the Additive and Chemistry Coordinator and ultimately the Laboratories Leader.

Job Description

We are the makers of possible

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Why join us?

A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.

Become a maker of possible with us!

If you are looking to be part of a team that manufactures millions of lifesaving medical devices throughout the world each year and if you thrive in a highly technical fast paced manufacturing environment, then Push Button at BD is the ultimate place to work. With state-of-the-art technology, which includes packaging robots, quality assurance vision inspection systems, ultraviolet curing, precision liquid dispensing, Allen Bradley PLC and HMI technology, all within a highly integrated automated assembly unit, Push Button is one of the Southwest’s most technically advanced manufacturing lines and we are looking for talented individuals to ensure that our world class product continues to advance the world of health.

This is a day shift onsite role (11am - 11pm, 3 days on and 3 days off) offers a competitive salary plus a 32% shift premium.

Our generous benefits including:

  • Matched contribution Pension scheme up to 10% of salary

  • Life assurance and critical illness cover

  • Private Medical Insurance

  • Share save scheme – matched up to £150/month

  • Reward & recognition scheme linked to Health and Safety and Continuous Improvement

  • Employee Assistance Program, supporting physical, mental and financial wellbeing

  • Flexible benefits including cycle to work scheme

  • Subsidised canteen

  • Free car parking

  • 24 days holiday (25 after 5 years)

Main responsibilities will include:

  • Review the manufacturing plan daily to plan and prepare liquid and powder additives in a timely manner.

  • Generate production orders for additives within SAP and complete all associated transactions.

  • Be conversant with the Quality system and able to retrieve the necessary documents, such as DMS, additive dispensing records etc. from the networked system.

  • Maintain a high standard of tidiness and cleanliness within the area and adhere strictly to GMP.

  • Understand the need to work aseptically and follows aseptic handling procedures to maintain the integrity of sterile additives and components.

  • Clean and prepare of carboys, dispense equipment and other utensils in readiness for autoclaving. Understand and trained in the use of the autoclave and maintain the card index system to track autoclaved parts.

  • Clean and sanitise SST reservoirs and other equipment used in the transfer of silica based additives, training production operators in performing this task.

  • Competent in the use of all mixing and cleaning equipment within the additive preparation area.

  • Liaise with chemistry and microbiology laboratories and manufacturing representatives to ensure that all manufacturing, microbiological and chemical requirements are in place before additive preparation begins.

  • Understand and implement the Health and Safety requirements involved when handling toxic and corrosive chemicals (COSHH), using correct PPE and following Manual Handling Regulations.

  • Carry out any reasonable request of the Additive and Chemistry Coordinator, Laboratories Leader or the Quality Control Manager.

About you:

  • Completed GCSE or equivalent education is essential.

  • Proven experience working in a production environment in a related industry is a distinct advantage.

  • Demonstrated experience following aseptic handling procedures is a distinct advantage.

  • Experience working and maintaining additive products and following correct GMP.

  • Autoclave experience is a distinct advantage.

  • Ability to work effectively in interdisciplinary teams with good people skills.

  • Must be computer literate and possess a good ability to communicate at all levels.

  • May be required to lift heavy items when working in the lab, however where necessary, lifting equipment will be provided.

Click on apply if this sounds like you!

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

To learn more about BD visit: https://bd.com/careers

Required Skills

Optional Skills

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Primary Work Location

GBR Plymouth - Belliver Industrial Estate

Additional Locations

Work Shift

GB-Con-PLY Yellow 11-23-Shift A type (United Kingdom)
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Success Profile

What makes a successful Quality Professional at BD? Check out the top traits we’re looking for and see if you have the right mix.

  • Ambitious
  • Collaborative
  • Goal-oriented
  • Persuasive
  • Results-driven
  • Self-starter

Advancing the world of health™

BD is one of the largest global medical technology companies in the world and is advancing the world of health™ by improving medical discovery, diagnostics and the delivery of care. BD helps customers enhance outcomes, lower costs, increase efficiencies, improve safety and expand access to health care.

BD is unique in how fully dedicated it is to a specific disease state. It makes it clear how the work we do directly impacts the daily lives of the patients we serve.


Eric Rainis
Senior Director Quality Management

To know that our products touch 30 million people with diabetes around the globe is powerful and fuels our teams to deliver best in class products to them each and every day.


Bridget Bagnato
VPGM Injection

It is inspiring to see BD products to be used globally to advance human healthcare.


Yang Zeng
Manager Medical Laboratory

BENEFITS

Healthcare

401(k)/
Retirement Plans

Professional Development

Paid Time Off

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