Validation Engineer - Quality Department

10 Mar 2023
31 Mar 2023
Louise Catherine Kelly
Job Type


Validation Engineer - Quality Department

Servier is a global bio-pharmaceutical group with a strong international presence in 150 countries. Servier is an independent group that invests over 20% of its brand-name revenue in Research and Development every year.

To accelerate therapeutic innovation for the benefit of patients, the Group is committed to open and collaborative innovation with academic partners, pharmaceutical groups, and biotech companies.

It also integrates the patient's voice at the heart of its activities. A leader in cardiology, the ambition of the Servier Group is to become a renowned and innovative player in oncology. Its growth is based on a sustained commitment to cardiovascular and metabolic diseases, oncology, neuroscience, and immuno-inflammatory diseases.

They are recruiting for a Validation Engineer to join their growing team in Co. Wicklow.

What's on offer?

  • Strong remuneration package.
  • Benefits including a hybrid work environment, healthcare, pension, and flexible working times.
  • A family-like environment, personality is huge for our client & they are renowned for being both collaborative & supportive.
  • Excellent career progression opportunities.

The Ideal Candidate:

  • Validation experience within the Pharmaceutical/Medical Devices Industry is desirable.
  • A degree level qualification in a scientific or relevant discipline is desirable.
  • The successful candidate will be expected to work co-operatively and flexibly both within the Quality and Production department and with other departments across the site.
  • Excellent communication skills with a collaborative approach to work are also required. Strong attention to detail, refined planning and organisation skills along with an ability to achieve objectives without close supervision in a team-based environment are essential for this role.
  • You thrive in a fast-paced environment and are adaptable.

Duties & Responsibilities:

  • Responsibility for the co-ordination of Process Validation, Cleaning Validation activity and Equipment Validation and maintaining validation/qualification status in the Production Department.
  • Preparation and execution of validation and re-validation protocols and reports, (IQ / OQ / PQ), for the validation of equipment, systems, products and projects.
  • Responsible for Investigating and resolving deviations associated with validation studies.
  • Acting as the primary point of contact for all Production related Validation matters as well as internal and external compliance audits or regulatory inspections.
  • Process Validation regulatory requests relating to the VMP.
  • Contribute to achievement of VMP and site targets.

Call Louise on +353 1 6455216 or email [email protected]

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