Manufacturing Operations Team Member

Sanofi; Waterford; On-site; EUR 28,000 - 45,000; Full time

Job summary

Sanofi Waterford is recruiting for a Manufacturing Team Member on a fixed-term, full-time basis. The role supports syringe filling operations within a cGMP manufacturing environment at the Waterford site, operating on 12‑hour day/night shifts (24/7) with a 4 on/4 off cycle.

Location: Waterford. The position emphasizes adherence to quality, safety, aseptic practices, and compliance with SOPs and training as part of a highly engaged operational team.

Qualifications

• Experience of working in a cGMP manufacturing environment.
• Good problem solving and analytical skills.
• Excellent interpersonal skills.

Responsibilities

• To ensure our products are manufactured with quality and safety guidelines
• Operate equipment as part of the production lines to achieve the required level of output
• Maintain and support scheduled adherence to production and OEE
• Complete as relevant SOP’s and training
• Adherence to aseptic practices and procedures
• Adhere to all relevant dress requirements with respect to cGMP’s and PPE rules

Job description

23 month FTC

We have multiple openings consisting of 24/7 shifts, (days and nights) and 4 on and 4 off (12hr days).

About The Job

The manufacturing team member is critical to the delivery and success of syringe filling operations within Sanofi Waterford. In this role you will be an integral part of a highly engaged and functional operational team who are aligned with site business objectives.

Location: Waterford

Job type: Fixed term, Full time

About Sanofi

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Key Responsibilities

• To ensure our products are manufactured with quality and safety guidelines
• Operate equipment as part of the production lines to achieve the required level of output
• Maintain and support scheduled adherence to production and OEE
• Complete as relevant SOP’s and training
• Adherence to aseptic practices and procedures
• Adhere to all relevant dress requirements with respect to cGMP’s and PPE rules

About You

To excel in this role you will need to have:

Essential Requirements

• Experience of working in a cGMP manufacturing environment

It Would Be Advantageous To Have (not Essential)

• Previous steriles experience is desirable
• Competent in the operation, cleaning, maintenance of all manufacturing equipment
• MES/SCADA and SAP experience
• Good problem solving and analytical skills
• Demonstrated good understanding of mechanical operations
• Technical writing skills
• Good knowledge of cGMP
• Excellent interpersonal skills
• Understands site KPI’s

Pursue Progress, discover Extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!