Manufacturing Biotech Associate

1694 MSD Ireland (Dunboyne); Dunboyne; On-site; EUR 42,000 - 64,000; Full time

Benefits offered by this job

Hybrid working model

Job summary

MSD in Dunboyne is seeking a Manufacturing Biotech Associate to join our single-use Biologics Drug Substance facility. You will work in a self-directed team within Downstream Operations, manufacturing Drug Substance while upholding safety, quality, GMP, and compliance standards.

The role requires 24/7 shift operations (days, nights, rotation) and site-based work. You will develop deep downstream knowledge, collaborate across departments, and contribute to continuous improvement and documentation

Qualifications

• A Level 7 or higher qualification in a science, engineering or technical discipline.
• Experience in a GMP or regulated Cleanroom manufacturing environment.
• Excellent communication skills and cross-functional collaboration.
• Willingness to learn, adapt, and train others when proficient.
• Knowledge of Upstream/Downstream processes, especially Downstream.
• Proficiency with manufacturing systems and PC skills.

Responsibilities

• Master complex processes in downstream bioprocessing.
• Aim to be SME across Downstream; deepen micro-level knowledge.
• Be approachable and supportive, fostering team cohesion.
• Display flexibility and problem-solving to meet schedules.
• Participate in inspections, GEMBA and Go-See initiatives.
• Contribute to documentation and production system proficiency.

Skills

GMP Documentation

Good Manufacturing Practices (GMP)

Problem Solving

Lean Manufacturing

Kanban

Multidisciplinary Teamwork

Team Collaboration

Education

Science/Engineering degree (Level 7+)

Tools

MES

DeltaV

SAP

GLIMS

PROCAL

Job description

Job Description An opportunity has arisen for the position of Manufacturing Biotech Associate at our single-use Dunboyne facility. As a Biotech Associate you will be part of a self-directed work team in Downstream Operations, responsible for all procedures and processes associated with the manufacture of Drug Substance. The Manufacturing Biotech Associate leads by example by always upholding the highest standards of Safety, Quality, GMP, Right First Time and Compliance. Ability to work 24/7 shift operations, which include days, nights and in rotation is required. This role is a site-based role.

Responsibilities

• Be strong technically, with an excellent ability to grasp processes and procedures.
• Aspiring to be an SME across the Downstream business unit, be strongly motivated to acquire knowledge and understand all Downstream processes to a micro level
• Be approachable, supportive, inclusive to other team members, while striving to work in a cohesive and proactive team, with a ‘never let a teammate fail’ mindset
• Display flexibility, adaptability, innovation, with an ability to think on your feet, also possess a strong skill set for logical root cause analysis, and problem solving
• Be an excellent communicator, and true team player
• Be able to deliver business unit goals through close collaboration with their team members, but also with colleagues across other departments
• Display high initiative, daily seeks the production schedule, and helps lay plans to achieve it
• Takes part in shift handovers and Tier meetings, raising any concerns or issues promptly and providing options for resolutions
• Be actively involved by participating in inspections, GEMBA’s and Go-See’s, improvement projects and other initiatives
• Perform documentation tasks as authorised, and any other administrative tasks as directed by your manager
• Aspire to become proficient with production systems such as MES, DeltaV, SAP, GLIMS, PROCAL and others
• Deputised if required, to represent the department at meetings and discussions, and performs any other duties as appropriate when assigned by the Manager

What skills you will need

• A Level 7, or higher, qualification in a science, engineering or technical discipline
• Relevant experience in a GMP, or regulated Cleanroom manufacturing environment (experience a definite advantage)
• Excellent communication skills and the ability to work in a cross functional collaborative team
• A willingness to learn, adapt, gain knowledge, and train others when fully proficient
• Be able to demonstrate research or knowledge of the overall Upstream and Downstream processes, and in particular Downstream processes
• Good PC skills, with an ability to work with automated business or manufacturing systems
• Knowledge and understanding of GMP and quality systems
• Troubleshooting and problem-solving competency
• Desire to learn and develop.
• Ability to interact with multiple stakeholders across numerous departments
• Knowledge and experience of Kanban, JIT, 5S and Lean Manufacturing methodologies would be an advantage
• Ability to manage multiple priorities and know when to escal… issues for resolution A proven ability to deliver on tight timelines

Required Skills

• Biotechnology Manufacturing, GMP Documentation, Good Manufacturing Practices (GMP), Kanban, Manufacturing Documentation, Manufacturing Operations, Multidisciplinary Teamwork, Pharmaceutical Manufacturing, Problem Solving

Location and Facility

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 talented and committed people together.

Benefits and Work Arrangements

We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.

Please feel free to speak to us about what flexibility means to you during your application.

Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

Eligibility and Compliance

• Shift: 3rd - Night
• Employee Status: Regular
• Relocation: No relocation
• VISA Sponsorship: Yes
• Travel Requirements: No Travel Required
• Flexible Work Arrangements: Not Applicable
• Valid Driving License: No
• Hazardous Material(s): NA

Professional Policy

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.

Job Posting End Date

Job Posting End Date: 11/11/2026

About the Company

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.