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embecta

PQS Operator

Posted 4 Days Ago
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Dun Laoghaire, Dublin
Mid level
Dun Laoghaire, Dublin
Mid level
The PQS Operator will monitor and maintain production and quality performance in a manufacturing environment. Responsibilities include routine machine adjustments, adherence to Good Manufacturing Practices (GMP), recording production data, and embracing new technologies. Strong communication and organizational skills are needed to work effectively both independently and as part of a team in a fast-paced, automated production setting.
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embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. For more information, visit embecta.com or follow our social channels on LinkedIn, Facebook, Instagram and X.  

Why join us?  

A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work.  Here our employees can fulfill their life’s purpose through the work that they do every day. 

You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture.  Our Total Rewards program – which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components – is designed to support the varying needs of our diverse and global employees. 

The plant, based in Dun Laoghaire, runs 24/7 and is the Worldwide Centre of Excellence for Pen Needle Manufacturing within the embecta organisation, producing 4.6 billion medical devices annually. Here we employ approximately 450 people across operations, engineering, quality and R&D.

We are now inviting application for our PQS Operator Talent Pool to (11-Month Fixed Term Contract) whose role is to meet operational needs across the site. This includes monitoring and maintaining production and quality performance to meet specified standards in accordance with GMP. This is a busy and varied role.

Main responsibilities will include:

  • The Operator will carry out the full range of responsibilities and duties required to meet current and future operational needs. This includes monitoring and maintaining production and quality performance to meet specified standards.
  • Routine adjustments, repairs and maintenance of machines will be carried out by Operators.
  • Operators will carry out all duties in line with Good Manufacturing Practices (GMP) and will record production and testing data in line with Standard Operating Procedures (SOPs).
  • Operators will use existing technology and will embrace any requirements to acquire additional skills for new tools/equipment etc.
  • Operators will participate in initiatives, projects & teams as required including Continuous Improvement, QIP (Quality Improvement Programme), Lean and 6 Sigma type teams.
  • Must have excellent written and verbal communication skills as well as the ability to accurately document work performed.
  • Ability to work primarily on your own initiative but experience working as part of a team will be required occasionally - You need to have a Strong planning and organizational ability.

About you

  • The successful candidate will have a minimum of 3 years' work experience in a manufacturing environment.
  • You will have knowledge of using IT systems such as manufacturing.
  • Regulated manufacturing/production environment and have a proven ability and willingness to learn.
  • You will be technically qualified with a Leaving Certificate or substantial GMP manufacturing experience and a third level qualification in a technical discipline is desirable.
  • You will need to have an excellent interpersonal and communication skills to execution systems, online self-service portals, training systems and barcode scanners required.
  • Experience of working in a highly automated and high-speed environment and in a controlled clean room environment would be a distinct advantage.
  • You will be hands on and have a sense of urgency.
  • Ability to function as part of a team and work on own initiative.
  • The ideal candidate will have some GMP/GDP experience and high level of safety awareness.

This role will include Shift work, previous experience of Shift patterns is required. You must be willing to work on a 4-shift basis, the company will operate 24 hours/day, 7 days/week.

embecta is an Equal Opportunity/Affirmative Action Employer.  We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

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