Manufacturing Operations Team Member
County Waterford, Munster, Éire / Ireland · Contract
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- Experience
- Any
- Salary
- —
- Openings
- 1
- Posted
- 2 weeks ago
- Work mode
- In office
- Eligibility
- Candidates with experience in cGMP manufacturing environments are suitable, especially those with sterile manufacturing exposure and familiarity with production equipment, compliance procedures, and manufacturing systems.
- Resume
- Required to apply
Where you'll work
Job description
Role overview
This fixed-term full-time position is based in Waterford and runs for 23 months. The role follows a 24/7 rota, covering both day and night shifts. It sits within a large, award-winning biopharmaceutical and medical device campus in County Waterford, where the team supports syringe filling operations and wider site objectives.
About the site
The Waterford location has grown steadily for over two decades and now brings together nearly 800 colleagues. The campus is known for its modern facilities, flexible working culture, career development opportunities, and commitment to employee wellbeing. Onsite amenities include a gym and medical centre.
What the role involves
You will be part of a collaborative manufacturing team responsible for helping deliver safe, high-quality output from syringe filling operations. The position requires close alignment with quality standards, production targets, and site procedures.
Key responsibilities
- Produce products in line with quality standards and safety requirements.
- Run production equipment as part of the manufacturing line to meet output expectations.
- Help maintain schedule adherence and support overall equipment effectiveness (OEE).
- Follow relevant standard operating procedures and complete required training.
- Work in accordance with aseptic practices and procedures.
- Comply with all dress code, cGMP, and personal protective equipment rules.
Requirements
- Previous experience in a cGMP manufacturing environment is essential.
- Experience in sterile manufacturing is preferred but not mandatory.
- Ability to operate, clean, and maintain manufacturing equipment competently.
- Exposure to MES/SCADA and SAP systems is an advantage.
- Strong problem-solving and analytical thinking skills.
- Good understanding of mechanical operations.
- Technical documentation and writing ability.
- Sound knowledge of cGMP requirements.
- Strong interpersonal and teamwork skills.
- Awareness of site KPIs and performance measures.
Additional information
This is a 24/7 shift-based assignment with both days and nights included. The company highlights equal opportunity employment and welcomes people from all backgrounds. The workplace also emphasises progress, inclusion, and continuous improvement.
Company values
The organisation describes its mission as advancing science and improving patient outcomes through the contribution of diverse teams working across multiple locations and functions.