Summary
Overview
Work History
Education
Skills
Certification
Timeline
Generic
Emmet Murray

Emmet Murray

Dublin

Summary

Knowledgeable [Desired Position] with solid background in leading production teams and optimizing workflows. Proven ability to streamline operations and enhance productivity within manufacturing settings. Demonstrated leadership skills and problem-solving capabilities to ensure efficient and quality output.

Overview

21
21
years of professional experience
1
1
Certification

Work History

Packaging Project/‘Start-up’ - Production Lead

MSD
05.2020 - Current
  • Capital project $320M released on- time to supply to APAC market.
  • Commercial operations start-up to supply 33M packs to APAC market
  • Packaging Dept -Qualification activities FAT/IQ/OQ & PPQ delivered to aggressive timelines.
  • Supervised production line to ensure quality control and adherence to safety protocols.
  • Enhanced communication between team members, fostering a collaborative work environment.
  • Improved production efficiency by overseeing daily operations and coordinating team efforts.
  • Trained new hires on production procedures, ensuring a quick ramp-up time and consistent performance levels across the team.

International Relocation – Production Lead Janumet

MSD
08.2016 - 04.2020
  • Bulk Manufacture Janumet - Lead & manage production team of 25+ Technicians
  • Facilitate daily Tier process -make problems visible, assign countermeasures
  • Ensure that Shift(s) objectives are achieved while reliably supplying quality product at a competitive cost, consistent with our Company, Regulatory Agency, Local code requirements for quality, Good Manufacturing Practices (GMP)
  • Promote the behaviours and principles that drive continuous improvement and be willing to challenge the norm
  • Maintain cross functional engagement between PTO, E&M, QA & Operations
  • Coach and mentor direct reports to assess their performance continually
  • Promote compliance with SHE/EHS, cGMP / Quality requirements
  • Lead and implement continuous improvement opportunities
  • Janumet model area -Core team member lead by example and set expectations
  • IPT Rep QSIP Deviation Management
  • Preparation of Quality Notification Investigation Report’s, SOP’s and Change Control
  • Motivation and development of staff promote inclusion maintain engaged workforce
  • Utilise MPS tools to identify the root cause of problems, implement effective CAPA’s to ensure non recurrence
  • On-going sponsorship of direct reports to further enhance their ‘skillset’
  • Assist in the management of regulatory on-site audits
  • Core team member Emergency Response Team – Site Incident Controller
  • Vaccines Packaging Project – provide operations input during design and layout reviews

Operations Coach

MSD
10.2012 - 08.2016
  • Lead & manage production team within the Specialty Packing department
  • Facilitate daily Tier process -make problems visible, assign Countermeasures
  • Deliver output to planning schedule
  • Coach and mentor direct reports to assess their performance continually
  • Promote compliance with SHE/EHS, cGMP / Quality requirements
  • Lead and implement continuous improvement opportunities
  • Key member of the IPT Leadership Team
  • Core team member for the decommission of Sachet/Cartoning line, stock build and transfer of product to an alternative site within the Network
  • IPT Lead on Site Deviations Reduction Team-achieved 90% reduction in 2014 & 2015
  • Deputise Site Lead Deviation Reduction Team- achieved 86% reduction 2015
  • Preparation of Quest Deviation Investigation Report’s, SOP’s and Change Control
  • Motivation and development of staff, promote inclusion maintain engaged workforce
  • Utilise MPS tools to identify the root cause of problems, implement effective CAPA’s to ensure non recurrence
  • Sponsor direct reports to achieve LSS accreditation
  • Assist in the management of regulatory on-site audits

Packaging Manager

Niche Generics
05.2010 - 10.2012
  • Lead and Manage the Packaging department reporting directly to the Head of Operations
  • Day to day supervision of a team of Production operators and Shift Leaders on Blister thermoforming tabletting packaging lines 25 direct reports
  • Draft/Oversee Validation protocols in conjunction with machinery upgrades
  • Drive efficiencies / yields / RFT
  • Implement new systems and initiatives
  • Daily production meetings
  • Monitor performance; manage resources and prioritise to achieve targets
  • Ensure compliance with SHE, cGMP and other business regulations
  • Schedule adherence and daily target output
  • Drafting of Deviation Investigation Report’s, SOP’s and Change Control
  • Assistance with customer complaints
  • Responsible for training of new and existing operators
  • Ensure SOP’s adherence for specific tasks
  • Employee recruitment / retention

Production Manager

Sona Nutritional
01.2008 - 01.2009
  • Managing the overall operations production shift
  • Team building, team performance, team recruitment and team retention
  • Achievement of hourly and daily targets
  • Implement weekly production schedule, including meeting operational deadlines
  • Manage the maintenance schedule of all equipment in the Production department
  • Production and quality conformance, Inspect / review product
  • Motivation and development of staff
  • On the job training of all operations staff
  • Housekeeping and hygiene levels to agreed standards
  • Shift waste control and management
  • Flexible and adaptive approach to operations/ Lead continuous improvement activities
  • Managing the shift under agreed Health & Safety guidelines
  • Take responsibility for all bottling/packaging operations in Sona
  • Ensure that all products received and shipped from Sona Nutrition meets all required quality standards
  • Ensure GMP standards are maintained
  • Manage all quality systems such as deviations, complaints and change control within the packaging/bottling area of the company in collaboration with QP
  • Liaise with the IMB / FSAI in any regulatory issues via Sona QP
  • Carry out periodic Quality reviews in conjunction with QP
  • Assist in the management of any regulatory on site audits

Senior Production Technologist

Takeda Pharma
01.2007 - 12.2007
  • Ensure GMP, Health & Safety and Housekeeping standards are maintained to the highest standards as set out by the company policies
  • Perform documentation reviews i.e
  • Production batch records, SOP’s review and assistance with Deviations and Change control
  • Schedule adherence and closely monitor Line cleans and set-ups
  • Training of new and existing staff
  • Generally to assist in the day to day running of the business and provide assistance

Packaging Operations Supervisor

Wyeth/Pfizer
06.2004 - 12.2006
  • Responsible for the day to day supervision of a team of Production operators (20+) on Blister thermoforming tablet packaging lines
  • This role ensured KPI’s, GMP, Health & Safety and Housekeeping standards were maintained to the highest standards as set out by the company policies
  • Liaising between operator and supervisory group to drive team relations and efficiency
  • Keep in close contact with other departments that have an effect on the line efficiency, (Quality and Maintenance.)
  • Challenge inadequacies
  • Ensure we are producing a product to the highest possible standards and most cost efficient
  • Factory acceptance tests FAT’s, Installation Qualification -IQ, Operational Qualification- OQ, Production Qualification PQs
  • Promote documentation Right First Time (RFT)
  • Drafting of Manufacturing Investigation Report’s
  • Assistance with customer complaints
  • Responsible for training of new and existing operators
  • Responsible for drafting up of new and existing Standard Operating Procedures (SOP) (machine and process related)
  • Area Safety Team Leader – to promote a safe working environment and awareness

Education

Bachelor of Science - Pharmaceutical Sciences

TU Dublin
Dublin
12-2009

Skills

  • Strategic Production Scheduling
  • Quality Assurance
  • Operational Process Enhancement
  • Team Management
  • Process Optimization Expertise
  • Project Management
  • Regulatory Safety Compliance
  • Sustained Performance Improvement
  • 5S Methodology Application

Certification

cGMP, Coaching, Quality Compliance, EHS / SHE, L&D, Lean Six Sigma, FAT IQ, OQ & PQ, Packaging Operations, Solid Dose Manufacture, Cleanroom, Deviation Management, CAPA, GDP and Change Control

Timeline

Packaging Project/‘Start-up’ - Production Lead

MSD
05.2020 - Current

International Relocation – Production Lead Janumet

MSD
08.2016 - 04.2020

Operations Coach

MSD
10.2012 - 08.2016

Packaging Manager

Niche Generics
05.2010 - 10.2012

Production Manager

Sona Nutritional
01.2008 - 01.2009

Senior Production Technologist

Takeda Pharma
01.2007 - 12.2007

Packaging Operations Supervisor

Wyeth/Pfizer
06.2004 - 12.2006

Bachelor of Science - Pharmaceutical Sciences

TU Dublin
Emmet Murray