Associate QC Specialist

R.T. Lane Recruitment are currently recruiting for an Associate QC Specialist to work with a Pharmaceutical Company in Carlow.

This is an Initial 12-month contract with strong potential for extension.

**Please note that candidates must hold the correct working visa for Ireland as my client cannot offer visa assistance and must be already residing in Ireland**

** Please note due to a high volume of applicants you will only be contacted if suitable for the position. **

Brief outline of Role:

The successful candidate will need to understand the quality requirements for the introduction of materials to site, will have the capability to communicate the requirements to suppliers and will use good documentation practices and be capable of implementing these at a local level. Position will receive direction and support.

Role Functions

• Work as directed by the Quality Control Manager according to Company safety policies, cGMP and cGLP
• Facilitate and drive effective communication to ensure success through representation of QC team on tier meetings
• Support all aspects of New Material Introduction process ensuring effective interaction with other departments/global teams/ external contract testing labs on matters related to new material introduction, supplier changes and associated qualification
• Participate and support Internal/External Investigations
• Coordinate the creation/ update to Quality standards for raw materials and components at Carlow. Complete impact assessments for change controls related to Carlow processes
• Coordinate any efficiency/ increased Lab capability projects as detailed by Quality Control Manager
• Provide support with audit/inspection requirements to ensure department compliance/readiness. Participate in internal and external audits and inspections, taking the role of auditee for assigned areas of responsibility
• Coordination, ownership, and author as required for Annual Product Review
• Participate in Quality Risk Management

Essential Requirements:

• 2-4 years of experience in a cGMP laboratory environment
• Knowledge of or previous experience in New Material Introduction process
• Proficiency in Microsoft Office and job-related computer applications required
• Good communication, interpersonal skills and ability to work across teams
• Demonstrated ability to drive the completion of tasks
• Demonstrated ability to solve problems/perform investigations
• Method validation and method transfer experience would be advantage

For more information or a full Job Description please contact – Michelle Power, R.T. Lane Recruitment on 022 46969, 087 032 8195 or email michelle@rtlanerecruitment.ie