Senior Team Lead

20 hours ago


Sligo, Sligo, Ireland beBeeTeam Full time
Senior Team Lead Position Overview

Phibro Animal Health is seeking a skilled and experienced Senior Team Lead to join our Research and Development team in Ireland. This key role will provide technical leadership and expertise in investigation and resolution of process deviations, root cause analysis, and CAPAs.

The successful candidate will have a strong understanding of pharmaceutical manufacturing processes and regulations, including GMP, ICH, and compendia guidelines. They will be responsible for leading cross-functional teams, developing and implementing process improvements, and ensuring compliance with safety, health, and welfare legislation.

This is an excellent opportunity for a motivated and innovative individual to take on a senior leadership role and contribute to the company's continued growth and success.

Key Responsibilities:
  • Lead, motivate, and develop the TSA team, providing technical expertise and leadership for investigation and resolution of process deviations, root cause analysis, and CAPAs.
  • Provide team leadership, setting work goals, controlling and meeting goals, professional and personal development of team members.
  • Conduct process monitoring/trending, support QA with generation and closure of annual product reviews.
  • Use Continuous Improvement tools for incremental change, implementation of new production methods, technology transfer, examination of production methods prior to their transfer to production, including validation (when needed).
  • Actively engage with TSA Peers in other business units and TSA Leadership to share knowledge, challenges, and solutions.
Requirements:
  • Minimum of a Honors Bachelors degree in a technical discipline (e.g., biochemistry, chemistry, biotechnology, biopharmaceuticals). Advanced degrees such as MSc. and PhD. are desirable.
  • At least 5 years' experience in the biotechnology and/or pharmaceutical industry, with experience of new product introductions and product support.
  • Knowledge of the processes and equipment necessary for the manufacture of pharmaceuticals (oral solid dose), parenterals, and/or biologicals.
  • Experience in authoring, review, and execution of validation studies and reports is a must.
  • Ability to prioritize workload for self and reports, flexible and agile in support of the sites overall goal.
Benefits:
  • Competitive salary and benefits package.
  • Opportunities for career advancement and professional development.
  • Collaborative and dynamic work environment.
How to Apply:

Interested candidates should submit their resume and cover letter to [insert contact information].

Responsibilities
  • Mid-Senior levelInformation Technology
  • IndustriesPharmaceutical Manufacturing

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