Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. We are looking for a Quality Technician (Clinical Business Unit City North) to join our office in Stamullen, Ireland. General Purpose of Role: To perform the Quality Control function and assist in QA functions required to support PCI Clinical Storage and Distribution Operations. The Incoming Quality Control Inspector is responsible for verifying incoming materials received from suppliers are in compliance with company drawings, specifications, and requirements. The verification process includes, but is not limited to: current revision, total quantity, material type, physical dimensions, aesthetic appearance, etc. and will involve the use of inspection equipment. The position will also be responsible for interacting with internal (other PCI sites and internal departments) and external customers, to determine the cause and disposition of non-conforming material. Main Responsibilities: Conduct QC inspection processes for: Incoming materials Works order checks (IPCs) Master label proofs Label checks Finished product Just in time (JIT) To release PCI manufactured product Co-ordinate and complete temperature reviews To monitor and update the QC status of materials at PCI General; scanning, archiving and filing of quality records Assist in the review of completed batch documents Assist and investigate with the investigation of quality related incidents and events Assist with core QMS activities where required such as SOPs and WIs Assist with general administration duties within the Quality Assurance department Outcomes of Role: Operations satisfaction with service (no delays to Operations due to QC). Fully traceable QC status for all materials at PCI. Specific Qualifications: Leaving Cert and previous experience within cGMP regulated environment. Formal qualification in a scientific discipline an advantage Previous Work Experience: Previous role as a QC inspector or in Operations in a highly regulated manufacturing or warehouse operations process Specific Knowledge / Skills Competence: High level of understanding of the principles and application of GMP (or equivalent). Organizational skills. Show high attention to detail. IT skills (minimum of Excel and Word). Behavioral Competencies: Planning and Organizing Customer service Flexibility Teamwork and collaboration Good communication skills Good written communication skills Judgement and decision making Self confidence Verbal communication Trustworthiness Conscientiousness #LI-VR1 Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don’t say no, we figure out how.