About the job

Level 5 - Amgen Dun Laoghaire – Dublin

Overview:

The Manufacturing Manager - Manufacturing Support at Amgen Dun Laoghaire reports to the Senior Manager Manufacturing and provides oversight of New Product Introduction (NPI), Life Cycle Management changes (LCM) and/or major capital Expenditure (CAPEX) Projects for the Formulation and Aseptic Filling areas in compliance with Good Manufacturing Practices.

The Manufacturing Manager manages the daily work of direct reports responsible for Manufacturing Projects. Champions driving process efficiencies as part of the projects that are being introduced to operations. Mentors’ employees by sharing technical expertise and guidance. Establishes priorities and deliverables for team in line with organisational goals and business objectives. Plans and organises all project assignments /resourcing on projects of various complexity. Translates complex data into actionable information. Supports coordination of activities across business units and exercises decision making independently. Has broad manufacturing, tech transfer & compliance knowledge. Identifies process gaps and introduces innovative solutions to improve operating efficiencies. Can clearly articulate, educate and challenge others. Interfaces with management on significant matters.

Responsibilities:

Monitoring resources and training models to ensure that appropriate resource/staff management to meet project targets
Builds and fosters collaborative relationships within his/her team and other departments
Coach and develop team of Operations Leads
Promotes a culture of safety, ensuring the team is engaged and aligned with the site safety initiatives
Deliver project plans in accordance with agreed manufacturing & project requirements
Effectively communicate relevant information to peers, manufacturing operators, cross functional departments, and senior management
Act as a delegate for the Snr Manager Manufacturing as required
Evaluate, plan, and implement solutions for process improvement opportunities
Provide expertise and support for quality system investigations ensuring timely and effective assessment of events and appropriate actions to protect product quality and patient safety
Contribute and assist with corporate, FDA, HPRA and other regulatory bodies during company audits

Qualifications & Relevant Experience preferred:

Bachelor’s degree in Engineering or Science.
Strong GMP and other applicable GxP knowledge.
Demonstrated experience working in cross functional work centre teams with the ability to handle multiple projects simultaneously.
5+ years’ experience in Syringe/Vial aseptic Drug Product manufacturing operations or have a demonstrated leadership skills with the capacity to learn quickly and adapt to new technology.
Excellent written and verbal communication skills including facilitation and presentation skills.
Demonstration of strong leadership, negotiation and influencing skills.
Ability to deal with complexity and ambiguity.
Demonstrated ability to lead, motivate, coach and mentor.
Excellent teamwork skills with the ability to collaborate, communicate and be accountable.
Project management skills including the ability to manage multiple projects and evaluate project resource requirements.

Responsibilities

About the job

Level 5 - Amgen Dun Laoghaire – Dublin

Overview:

Responsibilities:

Monitoring resources and training models to ensure that appropriate resource/staff management to meet project targets
Builds and fosters collaborative relationships within his/her team and other departments
Coach and develop team of Operations Leads
Promotes a culture of safety, ensuring the team is engaged and aligned with the site safety initiatives
Deliver project plans in accordance with agreed manufacturing & project requirements
Effectively communicate relevant information to peers, manufacturing operators, cross functional departments, and senior management
Act as a delegate for the Snr Manager Manufacturing as required
Evaluate, plan, and implement solutions for process improvement opportunities
Provide expertise and support for quality system investigations ensuring timely and effective assessment of events and appropriate actions to protect product quality and patient safety
Contribute and assist with corporate, FDA, HPRA and other regulatory bodies during company audits

Qualifications & Relevant Experience preferred:

Bachelor’s degree in Engineering or Science.
Strong GMP and other applicable GxP knowledge.
Demonstrated experience working in cross functional work centre teams with the ability to handle multiple projects simultaneously.
5+ years’ experience in Syringe/Vial aseptic Drug Product manufacturing operations or have a demonstrated leadership skills with the capacity to learn quickly and adapt to new technology.
Excellent written and verbal communication skills including facilitation and presentation skills.
Demonstration of strong leadership, negotiation and influencing skills.
Ability to deal with complexity and ambiguity.
Demonstrated ability to lead, motivate, coach and mentor.
Excellent teamwork skills with the ability to collaborate, communicate and be accountable.
Project management skills including the ability to manage multiple projects and evaluate project resource requirements.