Operations Manufacturing Team Leader

Sanofi Group

Waterford

On-site

EUR 55,000 - 73,000

Full time

4 days ago
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Benefits offered by this job

Healthcare benefits
14 weeks parental leave
Career progression opportunities

Job summary

Sanofi Waterford is seeking a Manufacturing Operations Team Leader to manage production activities, drive batch release performance, and coordinate cross-functional teams in Rare Disease and General Medicines.

In this role you will ensure cGMP compliance, training, document control, and continuous improvement, leading a production team on site in Waterford, Ireland, with a focus on safety, quality, and efficiency.

Qualifications

  • Degree in Life Sciences, Engineering, Pharmacy, or related discipline.
  • Significant experience in biopharma/pharma manufacturing with batch release exposure.
  • 3–5 years in a team leader or supervisory role.
  • 1–2 years' experience of sterile manufacturing/aseptic processing.
  • Strong knowledge of cGMP and health & safety requirements.

Responsibilities

  • Manage manufacturing areas to meet production objectives.
  • Ensure production complies with cGMP and safety standards through reviews.
  • Train staff against SOPs and GMP requirements relevant to their roles.
  • Define procedures and ensure adherence.
  • Monitor ongoing GMP compliance in their area.
  • Assess training effectiveness at regular intervals.
  • Promote good housekeeping and hygiene practices.
  • Resolve problem-solving reports promptly.
  • Maintain current quality documentation and records.
  • Train/assess team member competence as required.
  • Manage performance of team and ongoing performance.
  • Coordinate manufacturing activities in compliance with cGMP documentation.
  • Contribute to manufacturing documentation reviews and approvals.
  • Assist in changes, validation/revalidation programmes.
  • Provide support and backup to team members.
  • Set team targets and support safety, productivity, and quality goals.
  • Contribute to continuous improvement initiatives.

Skills

Biopharma manufacturing
Team leadership
Lean improvement
Problem solving
Cross-functional
Sterile processing

Education

Degree in Life Sciences / Engineering / Pharmacy

Job description

Waterford

Full time

R

Job title : Operations Manufacturing Team Leader

Location: Waterford, Ireland

About the job

As a Manufacturing Operations Team Leader , you play a critical operational leadership role within Lyo Operations, driving end-to-end batch release performance, deviation management, and cross-functional collaboration across internal teams and external stakeholders supporting Rare Disease, Rare Blood Disorder, and General Medicines.

To provide leadership to their Production Team in the manufacture of products, in compliance with Quality & Safety guidelines.

You act as the central coordination point across all functions involved in the operational support process. While you are not directly accountable for the performance of other departments, you are responsible for establishing and maintaining the governance framework that enables each function to meet its commitments. This includes identifying performance gaps, escalating risks, and driving corrective actions where required.

Main responsibilities
  • Manage the manufacturing areas to ensure that production objectives are met
  • Ensure production of products are undertaken in compliance with cGMP and Safety standards through regular walk through and review of deviations and GMP documentations
  • Ensure staff for which they are responsible are trained against SOPs and GMP requirements relevant to their job
  • Ensure procedures are correctly defined and followed
  • Monitor the level of GMP compliance in their area on an on-going basis
  • Assess the effectiveness of training on a regular basis
  • Actively promote good housekeeping and hygiene practices
  • Ensure problem solving reports are resolved in a timely manner
  • Ensure all quality documentation and records are complete and current
  • Train/assess competence for Team Member as required
  • Manage performance of Team Member and overall team on an on-going basis
  • Ensure that all production activities are organized and executed in compliance with cGMP and in compliance with the associated documentation
  • Involved in the preparation, review and approval of Manufacturing documentation and records.
  • Approval and implementation of changes to relevant systems and assist in validation / revalidation programmes.
  • Provide support and backup to team members
  • Define team targets / goals and support team in achieving them especially in the areas of safety, productivity and quality.
  • Actively contribute to continuous improvement initiatives.
About you
  • Degree in Life Sciences, Engineering, Pharmacy, or a related discipline
  • Significant experience in a biopharmaceutical or pharmaceutical manufacturing environment, with direct exposure to batch release and/or quality operations
  • 3 - 5 years' experience as a team leader / supervisory role
  • 1 - 2 years' experience of sterile manufacturing / aseptic processing
  • Technical knowledge of manufacturing
  • Proven track record in delivering Continuous improvement / Lean initiative programmes
  • Leader who Delivers through collaboration
  • Detailed knowledge of cGMP
  • Excellent interpersonal skills - active listener
  • Good problem solving and analytical skills
  • Effective facilitator
  • Understands site KPI's
  • Full understanding of Health & Safety and legal requirements for the safe operation of his team
Why choose us?
  • Bring the miracles of science to life alongside a supportive, future-focused team
  • Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally
  • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact
  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave

#LI-EUR

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 ( !

The salary range for this position is :54 800,00 - 73 067

Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefit programs.

We are an R&D driven, AI-powered biopharma company committed to improving people's lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people's lives.

We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.

Discover more about us visiting or via our movie We are Sanofi ( a career that makes a difference.

Reinvention is in our DNA. It's what drove our evolution from a small French enterprise to one of the world's leading biopharma companies. Whether it's using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.

This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people driven by a shared purpose: we chase the miracles of science to improve people's lives.

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