Manufacturing Manager (Manufacturing Support)

Career Category Manufacturing Job Description Manufacturing Manager (Manufacturing Support) 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.

Responsibilities

• 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.
• 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

Requirements

• Bachelor’s degree in Engineering or Science.
• 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. .

Pay

Salary Range EUR - EUR