Job Description

An amazing opportunity has arisen for a Bioprocess Associate to join our dynamic Upstream Operations team. In this pivotal role, you will oversee the entire manufacturing process of large-scale drug substances at our cutting-edge facility.

As a Bioprocess Associate, you'll be at the forefront of operations, responsible for preparing, operating, and monitoring state-of-the-art equipment. Your expertise will ensure that all tasks—ranging from but not limited to cleaning and validation to in-process testing and essential maintenance—are executed in strict accordance with current Good Manufacturing Practices (cGMPs).

Join us in making a significant impact in the field of biopharmaceuticals!

What you will do:

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

Foster a safety-focused culture and ensure a compliant cGMP work environment at all times.

Support Operations team to consistently deliver on specific area Key Performance Indicators (KPIs), e.g. Health and Safety metrics, Production Plan, Operational Improvements and Efficiency, compliance and team training.

Execute commercial manufacturing processes according to established work instructions and Standard Operating Procedures.

Generate SOPS/Electronic Batch Records.

Embed Lean tools and principles throughout all areas of work.

Assist maintenance, engineering, quality, and other teams as needed.

Coordinate with various teams to ensure effective task planning aligned with the manufacturing process.

Escalate issues when necessary.

This is a shift-based role (24/7 Operations). 12-hour shift on a 4- cycle schedule.

What skills you will need:

To excel in this role, you will need to have:

Minimum of a Level 7 qualification in a science or engineering discipline.

A level 6 with a minimum of 3 years’ experience in a GMP Manufacturing requirement shall be deemed equivalent.

Euthanistic team player capable of working both independently and collaboratively within an energetic, fast-paced environment that demands flexibility and initiative.

Able to collaboratively across different functions and with diverse stakeholders.

Proficiency in troubleshooting and strong problem-solving skills.

Excellent communication skills.

Capable of handling multiple tasks simultaneously.

Applicants must be legally eligible to work in Ireland.

Desirable but not essential skills:

Experience in the biopharmaceutical sector or related manufacturing industries.

Experience with manufacturing control systems, including Delta V, MES, SAP, LIMs.

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:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills:

Accountability, Accountability, Analytical Problem Solving, Applied Engineering, Biopharmaceutical Industry, Biopharmaceuticals, Computer Literacy, Data Entry, Equipment Maintenance, GMP Compliance, GMP Documentation, Good Manufacturing Practices (GMP), Health Safety, Industrial Sectors, Key Performance Indicators (KPI), Maintenance Processes, Maintenance Troubleshooting, Manufacturing Documentation, Manufacturing Operations, Manufacturing Processes, Manufacturing Quality Control, Media Preparation, Process Improvements, Production Operations, Regulatory Compliance {+ 5 more}

Preferred Skills:

Job Posting End Date:

10/2/2025

*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.

Requisition ID:R365276