Manufacturing Bioprocess Associate

Job Description

An amazing opportunity has arisen for a Manufacturing Bioprocess Associate, in Dunboyne.

In this shift role (12/7), you will provide operational support for shop floor operations of the Late Stage and Launch Pipeline, at our new state of the art single use biotechnology facility.

At our company, we aspire to be the premier research-intensive biopharmaceutical company. Our Biologics facility in Dunboyne is a state-of-the-art facility that integrates leading-edge technology with a dynamic workspace to support seamless connection and collaboration. BioNX provides Biologics Drug Substance manufacturing for Clinical Supply, Registration & Commercial Launch, operating in a multi-product mode to adapt to changing demands.

What you will do:

• Support end-to-end production operations for both Fed Batch and Continuous Manufacturing.
• Operate equipment according to electronic batch records, sampling plans, and standard operating procedures.
• Support weekend or out-of-hours work on select time frames to support manufacturing activities.
• Conduct all work activities with strict adherence to the safety and compliance culture on site.
• Support the authoring of electronic batch records, sampling plans, work instructions, and standard operating procedures.
• Work as part of a multi-disciplined, diverse, and dedicated process team where flexibility and teamwork are essential requirements.

What skills you will need:

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

Required

• Level 6 qualification in a science or engineering discipline.
• 2+ years of experience in a GMP Manufacturing environment.
• Ability to work independently and within a cross-functional team.
• Familiarity with contamination control and batch release requirements.
• Understanding of Upstream and Downstream Unit Operations for mAb manufacturing.

Preferred

• Familiarity with Emerson DeltaV, Pas X, and the use of Automation in a manufacturing process.
• Experience with various SingleUse technologies in a manufacturing environment.
• Knowledge in cell expansion and or, cell banking operations.

Required Skills:

Adaptability, Adaptability, Analytical Thinking, Applied Engineering, Automation, Cleanroom Gowning, Cognitive Flexibility, Computer Literacy, Contamination Control, Equipment Set Up, Fabrication Processes, GMP Environments, GMP Operations, Good Manufacturing Practices (GMP), In-Process Control (IPC), Manufacturing Environments, Manufacturing Processes, Manufacturing Support, Mechatronics, Problem Resolution, Process Manufacturing, Production Scheduling, Recordkeeping, Standard Operating Procedure (SOP) Management, Sterile Manufacturing {+ 2 more}

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:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

05/13/2026

*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.