Manufacturing Associate, Randstad

Randstad

Location:
United Kingdom, Didcot

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Not provided

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Job Description:

Randstad is seeking a highly motivated and digitally proficient Manufacturing Associate to join a growing team in Harwell, Oxfordshire. In this role, you'll be at the forefront of our manufacturing processes, using your technical skills and scientific mindset to ensure quality and efficiency.

Job Responsibility:

Operate Cutting-Edge Technology: You'll become an expert in operating our state-of-the-art manufacturing equipment, ensuring smooth production and adherence to cGMP compliance and safety regulations
Be a Problem Solver: You'll be on the front lines, responding rapidly to equipment and process issues, and proactively identifying potential risks to ensure seamless operations
Embrace Continuous Improvement: You'll be a key part of our continuous improvement initiatives, participating in projects, collaborating with cross-functional teams, and contributing your ideas to make our processes even better
Maintain a High Standard of Excellence: You'll adhere to strict safety procedures, gowning protocols, and manufacturing documentation to ensure a clean, safe, and compliant work environment
Team Up for Success: You'll work closely with colleagues in Quality Assurance, participate in incident investigations and CAPA tasks, and collaborate effectively with others to achieve our goals.

Requirements:

A Scientific Mindset: You have a solid understanding of scientific principles and a passion for learning new technologies
GMP Manufacturing Experience: You have at least 3 years of experience in a GMP manufacturing environment, ideally in the pharmaceutical industry
Technical Expertise: You have experience with filtration, chromatography, and cold chain management
Collaborative Spirit: You enjoy working with others, communicating effectively, and contributing to a team-oriented environment
Proactive and Detail-Oriented: You are meticulous in your work, pay attention to detail, and are proactive in identifying and resolving issues
Adaptable and Flexible: You're comfortable with a fast-paced environment, can adapt to changing demands, and are willing to work overtime when needed.

Nice to have:

Experience in the pharmaceutical industry
Knowledge of cGMP compliance and safety regulations.

Additional Information:

Job Posted:
April 23, 2025

Expiration:
June 28, 2025

Employment Type:

Fulltime

Work Type:

On-site work

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Manufacturing Associate