QC Micro Analyst — Quality & Compliance Specialist

Johnson Johnson; Cork; Sur place; EUR 34 000 - 55 000; Plein temps

Résumé du poste

Johnson & Johnson Innovative Medicine is seeking a QC professional to support equipment, lab utilities, and testing procedures in GMP-compliant operations. The role emphasizes QC testing, documentation review, and cross-functional collaboration to meet site goals.

This is an onsite 12-month contract in Ireland, with a competitive hourly rate. Applicants should hold a third-level degree in science or pharma and have at least 3 years in a quality/compliance role within pharma, ideally with

Qualifications

• Third level degree in a science or pharmaceutical discipline.
• Minimum of 3 years' experience in a quality or compliance role within the pharmaceutical industry (ideally previous experience as a Micro Analyst)

Responsabilités

• Is an active member of the QC group and participates in key activities.
• QC Material Release & Scheduling Activities.
• QC Key Performance Indicators.
• QC Documentation Review & Approval.
• Site Cross Functional Teams.
• Comply with EHS rules and procedures.
• Delivers on the department Goals & Objectives & Continuous Improvement initiatives.
• Support relevant internal and external site audits as required.
• Maintains and develops knowledge of analytical methods, technology and compliance demands.
• Foster a culture of quality, safety and compliance across the Site in line with the J&J Credo.

Connaissances

Quality Assurance

Compliance

Documentation Review

GMP Knowledge

Formation

Bachelor's degree in science or pharmaceutical discipline

Description du poste

Johnson & Johnson Innovative Medicine is seeking a QC professional to support equipment, lab utilities, and testing procedures in GMP-compliant operations. The role emphasizes QC testing, documentation review, and cross-functional collaboration to meet site goals.

This is an onsite 12-month contract in Ireland, with a competitive hourly rate. Applicants should hold a third-level degree in science or pharma and have at least 3 years in a quality/compliance role within pharma, ideally with