QC Packaging Analyst at Eurofins

, , Ireland -

Full Time

Start Date

Immediate

Expiry Date

27 Apr, 26

Salary

0.0

Posted On

27 Jan, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Attention To Detail, Documentation Skills, Quality Control, cGMP Knowledge, Team Player, Organizational Skills, Flexibility, Communication Skills

Industry

Medical and Diagnostic Laboratories

Description

Company Description ****We have an opportunity for a full time permanent QC Packaging Analyst to join our PSS Site in Shanbally Cross**** Consider joining Eurofins PSS® where people are the most important element in our business. Eurofins PSS® is the global leader of scientific insourcing services. PSS® is not only a leader in the industry, but also one of the first insourcing service providers, now celebrating over 15 years of service in Ireland and over 22 years of service globally. For more information about Eurofins PSS® please visit our website and watch a message from our Global Head, Beth Di Paolo. We currently have exciting opportunities to join our innovative and multi award-winning Professional Scientific Services (PSS) teams. The excellent service provided via our PSS model is delivered while maintaining the same commitment to excellence, expertise and cGMP compliance available at our Eurofins facilities. What can Eurofins offer you as an employee of ours? Developmental opportunities and career progression The opportunity to work with our client - a world -leading pharmaceutical and biotechnology company Location is easily accessible Private Medical Insurance Income protection and life assurance Annual discretionary bonus Free parking onsite Full use of the canteen facilities on the client site Additional annual leave days with continued service The opportunity to work on products helping to save lives across the world. Job Description The purpose of this job is to support QC packaging operations in a GMP-regulated environment. The QC Packaging Analyst is responsible for performing testing of packaging components on the client site. The ideal candidate has a keen eye for detail, strong documentation skills, and thrives in a fast-paced, team-oriented setting. Job Responsibilities: Work independently to carry out quality control checks on packaging components (primary and secondary components). Support relevant tasks in QC Packaging area such as logging in components, batch release and archiving activities where appropriate. Ensure all storage areas where packaging components are housed are kept in good condition. Practice good housekeeping in the area. Maintain 5S standards in the lab area. Maintain detailed record keeping, which is accurate, complete, legible & in accordance with cGMP requirements. Identify issues with packaging components and alert the relevant personnel in QCIP of all issues as appropriate. Support the investigation and resolution of packaging component investigations. Assist leadership in QC area to bring visibility on progress with QC Packaging analysis, maintain testing metrics, any backlogs and/or components in the pipeline. Provide support to the QCIP team to help with raw materials testing as required. Carry out transactions on Oracle/LIMS as required. Ensure the QC Packaging analysis area is inspection ready at all times. Participate in regulatory inspections. Assist with writing, review and revision of QC/Packaging documentation as necessary. (e.g., batch records, standard operating procedures, etc.) Demonstrate commitment to a high level of safety awareness within the laboratory. Proactively support continuous improvement and Lean initiatives within the packaging analysis remit. Maintain an exemplary personal training record. Execute all operations activities in a safe manner and in strict accordance with SOPs, cGMP regulations and site Quality standards. Participate in cross site teams as required. Provide assistance to other members of staff where required. Other duties as assigned. Qualifications BSc in science or a related subject. Knowledge of cGMPs. Good team player, organised, detail-orientated, strong documentation skills. Flexible, adaptable to changing priorities. Passionate about quality and customer service. Excellent communication skills both written and verbal. Additional Information *This is an opportunity to join Eurofins on a full time, 12 Month Fixed Term Contract. Working a 39 hour week, 08:30 – 17:00. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. In 2024, Eurofins generated total revenues of EUR €6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.

Responsibilities

The QC Packaging Analyst is responsible for performing quality control checks on packaging components and supporting relevant tasks in the QC Packaging area. They must maintain detailed records and ensure compliance with cGMP requirements.