Operations Technician

Job Description

About PSC Biotech

 

Who are we?

PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.

 

‘Take your Career to a new Level’

PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.

 

Employee Value Proposition

Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.

 

Overview

• Reporting to the Operations Coach, our Operations Technician, as part of the IPT team, perform various production and operations related tasks as part of an empowered team to aid in the manufacture and reliable supply of product. Ensure that objectives are effectively achieved, consistent with company’s requirements to ensure compliance, safety, and reliable supply to our customers.
  

Requirements

What you will do:

• Bring energy, knowledge, innovation and leadership to carry out the following:
  
• Work as part of the manual inspection team. Inspecting product and incoming materials in a GMP manner.
  
• Using systems such as SAP, MES, and GLIMS.
  
• Good understanding and experience in visual inspection
  
• Maintain clean rooms, perform housekeeping, and manage materials in production areas with a focus on continuous process improvement through Lean Principles.
  
• Contribute to writing/revising operational procedures, training materials, and participate in investigations, change control, and Kaizen events.
  
• Comply with policies, procedures, regulatory requirements, and cGMP.
  
• Promote a safe and compliant culture.
  
• Perform other assigned duties as required.
  

 

Skills Required:

• In order to excel in this role, the successful candidates will have:
  
• Leaving Certificate or equivalent education requirement.
  
• Proven organizational skills.
  
• Excellent attention to detail
  
• Trouble shooting skills.
  
• Goal/results orientated.
  
• Preferred apprenticeship, certificate, or diploma in a related discipline.
  
• Knowledge of regulatory requirements and codes in Irish, European, and international standards.
  
• Proficiency in Microsoft Office and job-related computer applications.
  
• Effective communication and interpersonal skills for collaboration with colleagues and external customers.
  
• Understanding of own department's role in relation to other departments and business processes.
  
• Self-motivated and flexible approach.
  
• Effective time management and multitasking skills.
  
• Training skills.
  
• Focus on customers and patients.
  
• Collaboration.
  
• Act with candour and courage.
  
• Make rapid, disciplined decisions.
  
• Drive results.
  
• Demonstrate ethics and integrity.
  

As well as above the successful candidates will be expected to demonstrate behaviours in line with our Ways of Working and Values outlined below:

• Ways of Working
  
• Win as one team
  
• Focus on what matters
  
• Act with Urgency
  
• Experiment, learn, and adapt
  
• Embrace diversity and inclusion
  
• Speak up and be open-minded
  
• Values
  
• Patient’s First
  
• Ethics and Integrity
  
• Respect for People
  
• Innovation and Scientific Excellence
  
  

Requirements
We encourage applications from candidates with a 3rd level qualification in Engineering, Quality, or a related discipline. Additionally, we seek individuals who possess the following skills and knowledge: Proven experience in documentation control within the Pharm/Bio Pharm industry Extensive understanding of project life cycles and demonstrated experience in project activities Familiarity with engineering project management tools and systems

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