Biologics Manufacturing Operator - Upstream / Downstream

Microbial Solutions | Charles River; Keele; On-site; GBP 25,000 - 35,000; Full time

Job summary

An established industry player is seeking an upstream Biologics Manufacturing Operator to join their team. This role involves executing assigned work related to the development and manufacture of processes, ensuring compliance with cGMP standards. You will have the opportunity to work in a collaborative environment, contributing to innovative drug therapies that impact health and well-being globally. If you are self-motivated, possess strong communication skills, and have a background in science, this position offers a chance to build a fulfilling career in a dynamic field.

Qualifications

• Minimum HNC/HND in a science subject or equivalent; Degree preferred.
• Previous practical laboratory experience is desirable.

Responsibilities

• Execute and complete assigned programmes of work in a timely manner.
• Perform manufacturing operations in compliance with cGMP standards.
• Maintain high standards of laboratory documentation.

Skills

Laboratory Skills

Communication Skills

Self-motivation

Teamwork

Flexibility

Education

HNC/HND in Science

Degree in Biochemistry

Degree in Biotechnology

Degree in Biochemical Engineering

Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development, and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales, or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Summary

Our manufacturing site in Keele is offering an opportunity for an upstream Biologics Manufacturing Operator. Responsible for executing assigned work related to in-house and contracted programmes for development, transfer, or cGMP manufacture of processes.

What You’ll Be Doing

• Execute and complete assigned programmes of work in a timely manner.
• Record data and communicate results effectively.
• Perform operations following appropriate training, maintaining and updating training manuals.
• Maintain the 5S system of facility management.
• Complete and maintain laboratory notebooks and documentation to high standards.
• Participate in multidisciplinary teams within the Operations Group.
• Perform manufacturing operations in compliance with cGMP standards.
• Ensure processes meet cGMP requirements during development.

Skills and Experience

• Minimum HNC/HND in a science subject or equivalent; Degree in Biochemistry, Biotechnology, or Biochemical Engineering preferred.
• Previous practical laboratory experience is desirable.
• Strong written and verbal communication skills and practical skills.
• Self-motivated, show initiative, and team-oriented.
• Flexible working abilities.

Additional information about our Biologics Testing Solutions and Charles River’s mission, values, and global presence is included to provide context but should be concise and relevant to the role. The description should focus on the responsibilities, skills, and minimum requirements for the Biologics Manufacturing Operator position.