Tech, Operations

MSD; Dunboyne; On-site; EUR 42,000 - 54,000; Full time

Job summary

MSD in Ireland (Dunboyne) is seeking a Manufacturing Bioprocess Associate for an onsite shift role. You will contribute to end-to-end production operations for Fed Batch and Continuous Manufacturing, operating equipment per batch records and SOPs.

Join a cross-functional team focused on safety, quality, and compliance within a cutting-edge biologics facility, working to ensure robust manufacturing processes and successful product releases for patients worldwide.

Qualifications

• 2+ years’ experience in GMP manufacturing or equivalent.

Responsibilities

• End-to-end production operations for both Fed Batch and Continuous Manufacturing.
• Operating equipment according to electronic batch records, sampling plans and SOPs.
• Maintaining safety and compliance culture on site.
• Working in a cross-functional, flexible process team.

Skills

Analytical Laboratory Equipment

Biopharmaceutical Industry

Collaboration

Contamination Control

GMP Compliance

Manufacturing Processes

PAS-X

SAP Workflows

Teamwork

Upstream Operations

Education

Level 6 qualification in science or engineering

Job description

Job Description

A fantastic opportunity has arisen for a Manufacturing Bioprocess Associate.

This is an onsite shift role.

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

The Manufacturing Bioprocess Associate, is responsible for:

• End-to end production operations for both Fed Batch and Continuous Manufacturing.


• Operating equipment according to electronic batch records, sampling plans and standard operating procedures.


• Conducting all work activities with a strict adherence to the safety and compliance culture on site.


• Working as part of a multi-disciplined, dedicated process team where flexibility and teamwork are an essential requirement.

What skills you will need:

In order to excel in this role, you will more than likely have:

• Level 6 qualification in a science or engineering discipline desired.


• 2+ years’ experience in a GMP Manufacturing requirement shall be deemed equivalent.


• Ability to work independently and within a cross-functional team.


• Familiarity with contamination control and batch release requirements.


• Familiarity with Emerson DeltaV, Pas X, and the use of Automation in a manufacturing Process.


• Experience with various Single Use technologies in a manufacturing environment.


• Understanding of Upstream and Downstream Unit Operations for mAb manufacturing.

Our facility in Dunboyne joined our network in September 2020. Our Dunboyne site is our Company’s first Biologics Drug Substance Single Use Commercialisation Facility, playing an important role in helping to commercialise key medicines. The cutting-edge innovation and collaboration between our Company’s research and manufacturing teams will significantly accelerate the time it takes to bring a medicine to market for the benefit of patients around the world.

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.

As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.

Required Skills:

Analytical Laboratory Equipment, Biopharmaceutical Industry, Collaboration, Contamination Control, GMP Compliance, Manufacturing Processes, PAS-X, SAP Workflows, Teamwork, Upstream Operations

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: Yes

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: 10/17/2026*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.