Pharma Manufacturing Operations Leader — Quality & CI

Hyper Recruitment Solutions Ltd

Waterford

On-site

EUR 90,000 - 110,000

Full time

4 days ago
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Job summary

Hyper Recruitment Solutions Ltd in Ireland is seeking a Manufacturing Operations Manager to oversee all on-site manufacturing and inspection activities within a regulated pharmaceutical environment, ensuring cGMP compliance and safety while driving operational excellence.

You will lead a high-performing team, develop continuous improvement programs, implement cost-saving process improvements, and ensure robust documentation and training.

Qualifications

  • Degree or higher in a relevant field (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management).
  • Minimum of 5 years’ proven experience in an operations management or equivalent leadership role within a regulated manufacturing environment.
  • Technical knowledge of manufacturing technology, extensive understanding of cGMP, and strong problem-solving skills.
  • Influential leader with excellent interpersonal skills and the ability to inspire and develop teams.

Responsibilities

  • Lead all manufacturing and inspection activities on site, ensuring operational objectives are met efficiently and compliantly.
  • Develop and implement continuous improvement programs that deliver cost savings and process enhancements.
  • Ensure all activities adhere to cGMP, health and safety guidelines, and are supported by properly maintained documentation.
  • Train, develop, and coach team leaders to ensure high levels of competence and performance.
  • Manage the performance of your team, promote GMP and safety practices, and ensure timely resolution of GMP incident reports.

Skills

Leadership
Problem solving
Interpersonal skills
Team development

Education

Bachelor's or higher in Pharmaceutical Chemistry / QA / QM

Job description

Hyper Recruitment Solutions Ltd in Ireland is seeking a Manufacturing Operations Manager to oversee all on-site manufacturing and inspection activities within a regulated pharmaceutical environment, ensuring cGMP compliance and safety while driving operational excellence.

You will lead a high-performing team, develop continuous improvement programs, implement cost-saving process improvements, and ensure robust documentation and training.

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