We are currently recruiting for a challenging opportunity with a Pharmaceutical organization based in Carlow. This is an excellent position for anyone looking to join a leading multinational that excels in its field.
Duties include:
* Developing and validating cleaning cycles and equipment, ensuring compliance with regulatory requirements.
* Creating and implementing validation strategies, coordinating with external vendors, writing protocols, submitting samples, analyzing test results, and preparing technical reports.
* Executing routine business activities such as equipment periodic reviews, cleaning periodic reviews, CAPAs, deviations, change control, risk assessments, and providing support during commissioning phases.
* Providing technical input and support, presenting as a subject matter expert on relevant topics during regulatory inspections, and representing the IPT on cross-functional project teams.
* Ensuring adherence to the highest standards of Compliance (Quality and Safety), site EHS policy, cGMP, and other business regulations.
This role requires:
* Experience as a validation specialist in a pharmaceutical or highly regulated environment, preferably with a B.Sc. Degree or equivalent qualification in Chemical Engineering, Biochemistry, Microbiology, Chemistry, or a related field.
* Proficiency in at least three of the following areas: C&Q validation, Cleaning Validation, Equipment validation, Process operations or manufacturing, Process Engineering.
* Familiarity with GxP systems associated with this role, including GLIMS and eVAL, electronic batch records.
This is an excellent opportunity for someone with the right skills and experience to contribute to a leading multinational in the pharmaceutical industry.
Estimated Salary: €60,000 - €80,000 per annum.