Senior Manufacturing Biotech Associate

MSD; Dunboyne; On-site; EUR 85,000 - 115,000; Full time

Job summary

MSD is seeking a Senior Manufacturing Biotech Associate for its Dunboyne single-use facility. You will lead a self-directed team in Solution Prep Operations, handling drug substance manufacture. The role requires 24/5 shift work, days, nights, and rotation, and is site-based.

You will mentor teammates, apply Lean Six Sigma, and maintain SME-level knowledge of MES, SAP, DeltaV, and related systems. Strong GMP experience and cross-functional collaboration are essential.

Qualifications

• A Level 7, or higher, qualification in a science or engineering discipline, with a minimum of 3 years' experience in a GMP regulated Manufacturing environment.
• Strong experience in a highly regulated pharmaceutical manufacturing environment.
• Excellent communication skills and the ability to work in a cross functional collaborative team.
• Possess a detailed overview of Upstream and Downstream processes, with expertise in Downstream manufacturing.
• Proven ability to work with automated systems such as MES, SAP, DeltaV.

Responsibilities

• Lead local work teams and achieve or exceed the production schedule.
• Participate in shift handovers, inspections, and continuous improvement projects.
• Perform EBR and documentation reviews, QC investigations, and related tasks.
• Utilise Lean Six Sigma tools to support CI initiatives.
• Mentor and coach less experienced team members to build a cohesive team.

Skills

Biopharmaceutical Manufacturing

Biotechnology

CNC Operations

Computer Literacy

Data Analysis

FDA Regulations

GMP

Manufacturing

Problem Solving

Multidisciplinary Teamwork

Education

Bachelor’s degree or higher in science/engineering

Tools

MES

SAP

DeltaV

Job description

An opportunity has arisen for the position of Senior Manufacturing Biotech Associate at our single-use Dunboyne facility. As Senior Biotech Associate you will be part of a self-directed work team in Solution Prep Operations, responsible for all procedures and processes associated with the manufacture of Drug Substance. Ability to work 24/5 shift operations, which include days, nights and in rotation is required. This role is a site-based role.

Bring energy, knowledge, innovation to carry out the following: As a senior team member, be strong technically, with an excellent grasp of processes and procedures. Already an SME on many processes, be strongly motivated to acquire knowledge and understand all Downstream processes to a micro level Proactively train, coach and mentor less experienced team members, by being approachable, supportive, inclusive and generous with knowledge, while striving to work in a cohesive and proactive team, with a 'never let a teammate fail' mindset Display flexibility, adaptability, innovation, with a reflexive ability to think on your feet, also possess a strong skill set for logical root cause analysis, and problem solving Be able to organise and lead local work teams, also deliver business unit goals through strong and cohesive collaboration with other departments, within a matrix reporting environment Display high initiative and be ready to take responsibility; thinks ahead, seeks the production schedule daily, organises local work teams and lays plans to achieve or exceed the schedule Takes part in shift handovers and Tier meetings, raising concerns or issues promptly and providing options for resolutions. Be actively involved by participating in inspections, GEMBA's and Go-See's, OPPS, improvement projects and other MPS initiatives Perform EBR and documentation reviews, QN investigation and closure, and any other documentation or administrative tasks as directed by your manager Utilise Lean Six Sigma Tools to support the initiative of continuous improvement (CI) Be proficient to SME level with production systems such as MES, DeltaV, SAP, GLIMS, PROCAL and others Deputised when 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 or engineering discipline, with a minimum of 3 years' experience in a GMP regulated Manufacturing environment.
• Strong experience in a highly regulated pharmaceutical manufacturing environment.
• Excellent communication skills and the ability to work in a cross functional collaborative team.
• Possess a detailed overview of the overall Upstream and Downstream processes, with particular expertise and working knowledge of the Downstream manufacturing process.
• Maintain a high level of expertise and working knowledge of the process equipment.
• A proven ability to work with automated systems such as Manufacturing Execution System (MES), Systems Applications and Products (SAP), Delta V etc.
• Strong knowledge and understanding of manufacturing GMP and quality systems.
• Demonstrate 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.
• Ability to manage multiple priorities and know when to elevate issues for resolution.
• Excellent trouble shooting skills as an ability to coach and mentor self-directed teams through complex problem solving.
• High degree of problem-solving ability and adherence to scheduled timelines.
• A proven ability to deliver on tight timelines.

Required Skills:

• Biopharmaceutical Manufacturing
• Biopharmaceutical Manufacturing
• Biotechnology
• CNC Operations
• Computer Literacy
• Data Analysis
• FDA Regulations
• Flexibility Training
• Good Manufacturing Practices (GMP)
• Industrial Manufacturing
• Information Systems
• Kanban
• Laboratory Techniques
• Manufacturing
• Manufacturing Execution Systems (MES)
• Manufacturing Processes
• Manufacturing Quality Control
• Master Batch Records
• Material Selection
• Matrix Management
• Multidisciplinary Teamwork
• Pharmaceutical Manufacturing
• Pharmaceutical Process Development
• Problem Solving
• Process Equipment {+ 9 more}

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.

So, if you are ready to: Invent solutions to meet unmet healthcare needs,

Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Not Applicable Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 11/20/2026

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.