Video for this job

Collins McNicholas

Role Responsibilities

  • Support a variety of Validation projects across the Pharma and /or Biologics sites, interact with other departments to ensure that validation projects are appropriately planned, executed and delivered in a timely manner.
  • Some travel may be required intermittently to support the execution of Factory Acceptance Tests.
  • Generation of SDLC documentation in line with current regulatory and corporate requirements.
  • Maintaining an up to date knowledge of relevant regulatory requirements.
  • Support any Departmental initiatives in relation to safety, quality and cost.

Qualifications:

  • Minimum 3rd level Science / Engineering Qualification. Minimum 2 years’ experience working in a Validations environment.
  • Comprehensive understanding of Validation principles and practices. 
  • Good working knowledge of Validations practices, ASTM and relevant EU/FDA regulations. A proven track record that demonstrates the ability to work without direct supervision whilst maintaining adherence to project delivery is fundamental to the role.
  • Good interpersonal and communication skills essential for working across multi-functional teams. 

For a confidential discussion and more information on the role, please contact Stephen Kelly on 091706714.

For more information on our Recruitment and HR Services and to see a full list of our available jobs across Ireland, please visit our website www.collinsmcnicholas.ie

Follow us on LinkedIn and connect with our Recruitment Consultants to discuss the latest jobs as well as our job searching tips and videos!

Firstname (required)

Surname (required)

Your Email (required)

Your mobile (required)

Upload CV (required)

Comment

In order to provide you with our services, we need to process certain personal information about you. We will only use your personal information to deliver the job-seeking or related services you have requested.

We seek your consent to store your data and provide you with the best possible service. If you have any questions regarding our legal obligations to you or your rights under the GDPR please refer to our privacy statement which clearly outlines all of your rights.

Related Articles

Biopharma Report

biopharma industry report biopharmaceuticals
Ensuring that the supply of qualified professionals is sufficient to meet demand will be the crucial step in successfully expanding the biopharma industry in Ireland. The EGFSN (Expert Group on Future Skills Needs) estimates that 5,000 additional staff will be employed in biologics manufacturing by 2020. The number of professionals employed in the production of traditional […]
Read More