Process Operator

Posted 6 Days Ago
Be an Early Applicant
Newquay, Cornwall, England
1-3 Years Experience
Biotech
The Role
The Production Operator is responsible for producing medical devices and membrane products, ensuring they meet quality standards, performing quality checks, and complying with safety standards and procedures. Duties include operating equipment safely, completing necessary documentation, and maintaining production efficiency in a factory environment.
Summary Generated by Built In

Be part of something altogether life-changing!

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.

Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.

The Production Operator for Cytiva is responsible for producing medical device / Membrane products using approved quality standards to procedures specified by the company.

This position is part of the Medical Device / Membrane departments located in Newquay and will be on site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

What you will do:

  • Be responsible for operating in a safe and compliant manner, i.e. wearing safety equipment or using relevant guards, etc.
  • Ensure the product is produced according to the relevant company procedures and work instructions.
  • To perform and record quality checks as required.
  • To stop the process when components are away from standards defined in the relevant control plans and work instructions.
  • To complete the necessary paperwork correctly as required by the company and/ or the requirements of the quality system.

Who you are:

  • Have experience of assembling high quality components in a medium/high volume factory environment.
  • Flexibility to be able to work shifts when required.
  • Self Motivated and able maintain good timekeeping.
  • Competent in the completion of documents and able to follow relevant standard operating procedures

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The Company
Marlborough, MA
8,399 Employees
On-site Workplace

What We Do

Cytiva, now with the life sciences business from Pall Corporation, is a global life sciences leader dedicated to helping customers discover and commercialize the next generation of therapeutics. Together, we bring dedicated technical expertise and a broad portfolio of tools and technologies that enable the development, manufacture, and delivery of transformative medicines to patients.

Visit cytiva.com to learn more.

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