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3 Jobs Found 

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Quality Manager

Sigmar

Waterford, Waterford
12 days ago
Waterford, Waterford
12 days ago

My client is looking for a Quality Manager to join their ever-growing team in Waterford.

You will be part of a team that has a passion for innovation and creativity!  

Reporting to the General Manager the Quality Manager aims to ensure the product or service is fit for purpose, consistent, and meets both external and internal requirements.

Job Responsibilities

  • Ensure the company is Audit ready and remains up to date with ISO requirements.
  • Quality system development, implementation, and maintenance.
  • Ensuring product specifications and customer requirements are met.
  • Ensuring all processes meet ISO and AS requirements.
  • Oversee the design and execution of commissioning and validation protocols on manufacturing equipment, software, and process, and approve validation documentation.
  • Measure, control, and improve product and process robustness.
  • Ensure schedule adherence and compliance.
  • Manage quality issues.

Job Requirements

  • Level 8 in Scientific/Technical discipline.
  • 10+ years of experience in Manufacturing.
  • In-depth understanding of ISO 13485.
  • Experience leading and developing teams.
  • Experience in Quality management and system management.

For a confidential discussion on this or any other current job opportunity please contact Meggan on 021 235 9144 / mtully@sigmar.ie

Following your application for this specific role, Sigmar may contact you regarding other positions that we feel you may be suitable for. If you do not wish to be contacted about other opportunities please let us know. For further information please refer to the Privacy Statement on our website.

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QC Manager

Clarity Life Science

Waterford, Co. Waterford
30+ days ago
Waterford, Co. Waterford
30+ days ago
Head of Quality Control (QC) Manager
A highly sought after Pharmaceutical company is looking to hire a high profile QC Manager for their open position on their state of the art manufacturing site in the south east of Ireland. The company is looking to hire an experienced person who can fulfil the needs of this position. The purpose of this job will be to manage and co-ordinate all activities in the laboratory including but not limited to scheduling and people management.
The candidate should have strong abilities to handle the following responsibilities:
1) Assist the Head of Operations in achieving company goals.
2) Ensuring that the existing laboratory tools are used to generate and maintain performance related metrics.
3) Oversee the timely closeout of deviations and/or investigations.
4) And to follow all guidelines and regulations of the companies Health & Safety rules.
Qualifications
Qualified to a minimum of degree level in science discipline with a post-graduate qualification advantageous.
1) At least 5 years experience in pharmaceutical laboratory
2) Supervisory management experience advantageous
3) Previous cross-functional project experience
4) GLP expert
5) Knowledge of GMP guides
Other Valuable Skills
1) People management skills
2) Multi-tasking, ability to manage conflicting deadlines
3) Strong Analytical skills
4) Strong computer skills proficient in MS office, ECDL certification is advantageous
5) Proven time management skills
Behaviours
1) Leadership.
2) Ability to deal with cross-functional groups.
3) Adaptability
4) Attention to detail
5) Problem solving/analysis
Qualified and interested candidates are strongly encouraged to apply with their most update CV for the attention of Mark Tierney from Clarity Recruitment. All applications are treated in the strictest of confidence.
To discuss other suitable vacancies that we have open currently, please contact us directly at +353 1 567 3123
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QA Manager

Clarity Life Science

Waterford, Co. Waterford
30+ days ago
Waterford, Co. Waterford
30+ days ago
Head of Quality Assurance (QA) Manager
Due to ongoing expansion plans this well known Pharmaceutical company is looking to hire an experienced and exceptional QA Manager for their open position on their state of the art manufacturing site in the South East of Ireland.
The purpose of this job will be to manage and coordinate all Commercial Quality Assurance activities for the company.
The candidate should have strong abilities to handle the following responsibilities:
  • CACI Management
  • Manage Vendor Qualification
  • Manage Self Inspection Program
  • To perform additional tasks as agreed to supportive effective running of the business
  • Implement performance evaluations for direct reports
  • Ownership of deviation procedures and approval of investigations: Including Incidents, Deviations & Complaints, Out-of-Specifications, Out-of- Calibrations, Out-of-Trends and Planned Changes
  • Contract manufacturing organization management
  • Manage QA support for all departments: Operations, Engineering, Finance, Regulatory; Clinical Affairs, Business Development, IT and Technical Services
  • Implement Safety requirements as per site documentation including SOPs, Safety Statement and COPs
Qualifications
  • Qualified to a minimum of degree level in science discipline, with a post-graduate qualification advantageous
  • At least 7 years experience in pharmaceutical industry, working within the Quality Assurance function
  • Experience of structuring tasks and objectives of QA team
  • Previous cross-functional project management expertise
  • cGMP guideline expertise
  • Lead auditor experience-API, CMO (Sterile & non-sterile experience)
Other Valuable Skills
1) People management skills
2) Multi-tasking, ability to manage conflicting deadlines
3) Strong Analytical skills
4) Strong computer skills proficient in MS office, ECDL certification is advantageous
5) Proven time management skills

Behaviours
1) Leadership.
2) Ability to deal with cross-functional groups.
3) Adaptability
4) Attention to detail
5) Problem solving/analysis
Qualified and interested candidates are strongly encouraged to apply with their most updated CV for the attention of Mark Tierney from Clarity Recruitment. All applications are treated in the strictest of confidence.
To discuss other suitable vacancies that we have open currently, please contact us directly at +353 1 567 3123
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Job Type

Full Time

Posted

12 days ago

Description

My client is looking for a Quality Manager to join their ever-growing team in Waterford.

You will be part of a team that has a passion for innovation and creativity!  

Reporting to the General Manager the Quality Manager aims to ensure the product or service is fit for purpose, consistent, and meets both external and internal requirements.

Job Responsibilities

  • Ensure the company is Audit ready and remains up to date with ISO requirements.
  • Quality system development, implementation, and maintenance.
  • Ensuring product specifications and customer requirements are met.
  • Ensuring all processes meet ISO and AS requirements.
  • Oversee the design and execution of commissioning and validation protocols on manufacturing equipment, software, and process, and approve validation documentation.
  • Measure, control, and improve product and process robustness.
  • Ensure schedule adherence and compliance.
  • Manage quality issues.

Job Requirements

  • Level 8 in Scientific/Technical discipline.
  • 10+ years of experience in Manufacturing.
  • In-depth understanding of ISO 13485.
  • Experience leading and developing teams.
  • Experience in Quality management and system management.

For a confidential discussion on this or any other current job opportunity please contact Meggan on 021 235 9144 / mtully@sigmar.ie

Following your application for this specific role, Sigmar may contact you regarding other positions that we feel you may be suitable for. If you do not wish to be contacted about other opportunities please let us know. For further information please refer to the Privacy Statement on our website.