Job Description

A fantastic opportunity has arisen for a Biotech Technician Associate (BTA) on the Cell Banking/Cell expansion team at our site in Dunboyne, Co. Meath.

Our facility in Dunboyne is a premier, state-of-the-art facility that enables and advances our best work. By integrating leading-edge technology with a dynamic, activity-based workspace, the facility supports seamless connection and collaboration within and across teams and functions. Our Dunboyne facility provides Biologics Drug Substance manufacturing for Clinical Supply, Registration, and Commercial Launch.

Job Purpose

As a Biotech Technician Associate (BTA), you will play a crucial role in our manufacturing division by executing key production processes, ensuring compliance with safety and quality standards, and contributing to the continuous improvement of our operations. Your efforts will directly impact on the production of biologic drug substances that advance the prevention and treatment of diseases.

Bring energy, knowledge, and innovation to carry out the following:

• Execute automated recipes using paperless technology for drug substance production, including inoculation, cell culturing, filtration, and purification.
• Set up single-use equipment between runs and carry out production processes according to GMP and EHS principles.
• Optimize and improve processing activities using standard work and lean processing techniques.
• Support operations team to consistently deliver on KPIs such as EHS metrics, Production Plan, OEE, compliance, and team training.
• Complete Enablon Good Catches to support our safety culture.
• Provide immediate feedback to reinforce good safety and improvement behaviours.
• Execute commercial manufacturing processes according to established work instructions and SOPs.
• Ensure all manufacturing documentation support tasks comply with good manufacturing practices.
• Address any safety concerns promptly.
• Work as part of a dedicated process team, emphasizing flexibility and teamwork.
• Adhere to Right First-Time principles.
• Assist and support maintenance, engineering, quality, or other colleagues as needed.
• Demonstrate understanding of key manufacturing operations principles and practices in a regulated environment.
• Communicate effectively across various departments within the facility.
• Generate and support continuous improvement ideas within the area of interest.
• Maintain a good understanding of upstream/downstream processes and the manufacturing process.
• Celebrate and recognize team and individual achievements.
• Act as an Emergency Response Team (ERT) member during emergencies if trained.
• Maintain and support high standards of safety and GMP compliance.
• Participate in problem-solving activities by referencing relevant past experiences.
• Engage in inspections, GEMBA’s, and Go-See’s.
• Participate in process deviation reviews and Gemba walkdowns.
• Mentor new staff members in specific plant activities.
• Be prepared to answer auditor questions during site walkdowns.
• Implement innovative solutions to drive a high-performance organizational culture.

What skills you need

• Min. Level 5 Post Leaving Certificate Diploma in Science/Engineering/Computing/Culinary or equivalent.
• Min. of 3-4 years' experience in a Manufacturing/Construction/Culinary/FMCG/Lab environment.
• OR Min. Level 6 in Science/Engineering/Culinary or equivalent.
• Min. 1-2 years' experience in a Manufacturing/Construction/Culinary/FMCG/Lab /Project environment.
• Experience in pharmaceutical processing or in a highly regulated facility.
• Understanding of Lean Six Sigma and its methodologies.

This role is site-based and involves working a 12/7 shift pattern (4 days on, 4 days off).

We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world’s most challenging healthcare needs. So, if you are ready to: Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world’s leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today.

Additional location(s) Compensation Information:

Required Skills:

Biopharmaceutical Manufacturing, Equipment Maintenance, Good Manufacturing Practices (GMP), Manufacturing Documentation, Manufacturing Operations, Manufacturing Processes, Manufacturing Quality Control, Media Preparation, Process Improvements, Standard Operating Procedure (SOP)

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

na

Job Posting End Date:

11/25/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.