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Assembly & Packaging Production Manager

Employer
Thornshaw Recruitment
Location
Ireland (IE)
Salary
Negotiable
Start date
25 Jan 2023
Closing date
24 Feb 2023

View more

Discipline
Manufacturing, Production
Hours
Full Time
Contract Type
Permanent
Experience Level
Management

Job Details

On behalf of my client, a global medical device company we are working with them on a new opportunity for an Assembly & Packing Production Manager. This is a full-time permanent position based in Dublin.

Reporting to the Director of Operations, the Assembly and Packing Production Manager is responsible for directing the activities and priorities for their department. They provide technical, operational, compliance and efficiency leadership to the team.

The Assembly and Packing Production Manager is responsibilities:

  • Leadership and management of the department to deliver site goals and objectives.
  • Effective and efficient use of resources to manufacture products to meet sales demand.
  • Output is expected to increase significantly through growth of existing product and introduction of new products.
  • Scheduling production capacity in line with business needs.
  • Shift operations are required to meet demand.
  • Utilise business and software software tools to analyse reports on production capacity and requirements and identify methods for improving productivity and reducing overall manufacturing costs via lean manufacturing and problem solving.
  • Identification and resolution of production and yield issues through the use of systematic problem-solving techniques and data analysis.
  • Motivate and support the team to ensure department can reliably and consistently deliver.
  • Identify improvement projects and introduce Lean Principles to improve service, scrap and costs.
  • Management of Out of Specification results, Non-Conformances, Deviation and other relevant Quality Systems issues which relate to the department
  • Owner of department related Change Controls, Design Changes, PA’s (Preventive Actions), CAPA’s (Corrective Action, Preventive Action) and Audit Actions. 
  • Work with Technical Services, QA, New Product Introduction (NPI) and other key functional groups to take ownership of manufacturing aspects of new products as they are transferred from R&D to commercial manufacture.
  • Participation in cross functional site management activities.
  • Demonstrate the leadership and commitment to the quality management system.
  • Ensure Compliance to Environmental, Health and Safety regulations. 

Skills and Behaviours: 

  • A logical and planned approach to all tasks.
  • Excellent communication skills (both written and verbal), excellent interpersonal and presentation skills and be team focused.
  • Ability to manage complex projects involving multiple functions.
  • Ability to gain consensus on key quality/operational decisions.
  • Ability to make decisions based upon a ‘bigger picture’ outlook.
  • Strong analysis/problem solving skills. Strong attention to detail/quality focus.
  • Balanced cost/quality/customer focus.
  • Willingness and ability to collaborate with and influence other groups in a positive, team-based environment.
  • Be an active learner and developer of self and others with excellent organisational skills.

Education and Experience: 

  • Primary degree/diploma qualification in a Management, Technical, Engineering or equivalent subject.
  • At least 5 years industrial experience in a similar role in manufacturing industry.
  • Experience of process automation.
  • Experience working in cGMP environment.
  • Ideally will have experience of managing shift operations.
  • First-hand experience of audits by regulatory authorities. 
  • Ideally will have participated in FDA, HPRA and/or other regulatory authority audits.
  • Experience Lean and 6 sigma manufacturing principles. 
  • Data Recording and Analysis, Problem Solving Techniques, etc.
  • Experience managing a team and should have a demonstrated track record and success in team building skills.

For a full Job Spec and to apply for this role please call Katie on +353 1 895 5770 or e-mail kgarry@thornshaw.com

Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. www.thornshaw.com Tel: +353 1 2784671

 

 

 

 

 

 

 

Company

thornshaw-title

Thornshaw Scientific Recruitment was first established in 1999 and since then has become a leader in Scientific recruitment.  In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.

Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.

Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.

Our Industries

We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years. 

Our Specialities

Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.

Our Mission

thornshaw-ourmission

For further details on our services contact Tina at +353 1 2784701 or email tdunne@thornshaw.com

 

Company info
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