Bioprocess Technician

Russell Tobin; Dublin; On-site; EUR 42,000 - 45,000; Full time

Job summary

Russell Tobin is hiring for an 11-month contract in Dublin 15, Ireland, to support biopharmaceutical manufacturing. You will execute manufacturing processes, operate equipment per GMP, and help maintain quality documents.

The role requires a Level 6 qualification, 3+ years in a cGMP manufacturing facility, and experience with Delta V or MES. The team emphasizes continuous improvement and collaboration across cross-functional groups.

Qualifications

• Level 6 qualification in Engineering or Science or equivalent experience.
• 3+ years in a large-scale biopharma manufacturing facility.
• Experience with Delta V, MES or similar control systems.

Responsibilities

• Execute commercial manufacturing processes according to established work instructions.
• Operate production equipment within the assigned functional area while adhering to GMP standards.
• Create and update operating procedures and other manufacturing documentation.
• Review batch and exception reports and support related investigations and QA audit activities.
• Support continuous improvement initiatives and operational excellence across manufacturing processes and equipment.

Skills

Problem-solving

Communication

Teamwork

Education

Level 6 qualification in Engineering/Science

Tools

Delta V

MES

Job description

Join a globally recognized biopharmaceutical organization dedicated to discovering, developing, and delivering innovative medicines that improve the lives of patients worldwide. Offering a state-of-the-art biologics manufacturing environment, this opportunity provides exposure to advanced technologies, large-scale commercial manufacturing, and a strong culture of continuous improvement. You'll work alongside talented cross-functional teams, contribute to life-changing therapies, and be part of a company that values innovation, collaboration, diversity, professional development, and operational excellence.

• 11-month contract
• Dublin 15, Ireland
• €20.71/hour on PAYE

Responsibilities include:

• Execute commercial manufacturing processes according to established work instructions.
• Operate production equipment within the assigned functional area while adhering to GMP standards.
• Create and update operating procedures and other manufacturing documentation.
• Review batch and exception reports and support related investigations and QA audit activities.
• Support continuous improvement initiatives and operational excellence across manufacturing processes and equipment.

Qualifications:

• Level 6 qualification in an Engineering/Science related discipline or relevant experience in a regulated industry (cGMP, ISO, or similar cleanroom environment).
• 3+ years of experience in a large-scale biopharmaceutical manufacturing facility.
• Experience with Delta V, MES, or similar control and data acquisition systems.
• Strong problem-solving, communication, and teamwork skills with the ability to work in a fast-paced environment.

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Russell Tobin is an equal opportunity employer. We do not discriminate on the basis of the race, religious creed, color, national origin, ancestry, physical disability, mental disability, reproductive health decision making, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, age, sexual orientation, veteran or military status, or any other characteristic protected by applicable federal, state, or local law.

Russell Tobin is a Fair Chance employer. We consider all qualified applicants, including those with criminal histories, in a manner consistent with applicable state and local Fair Chance laws and ordinances, including, the California Fair Chance Act and all applicable local Fair Chance ordinances.

We are committed to providing reasonable accommodations to applicants and employees with disabilities. If you require a reasonable accommodation to participate in the application or interview process, or to perform the essential functions of this role, please contact us.