Process Microbiology Associate – GMP Ops (12-Month)

Johnson & Johnson; Cork; On-site; EUR 34,440,000 - 48,216,000; Full time

Job summary

Johnson & Johnson Innovative Medicine in Ireland is seeking an Operations Process Microbiologist reporting to the Senior Plant Microbiologist. You will actively participate in the microbiological control and assurance program within the operations department, ensuring cGMP and EHS regulatory compliance.

Responsibilities include leading commissioning, qualification, validation activities, maintaining documentation, training new recruits, supporting investigations, and collaborating with

Qualifications

• Bachelor degree in a scientific/technical field.
• Minimum 3 years of experience in pharmaceutical or GMP regulated environment.
• Knowledge of shop floor manufacturing processes.
• Working knowledge of data analytics.

Responsibilities

• Lead by example and strive to perform to high standards at all times.
• Assure safe completion of activities following environmental practices and procedures.
• Carry out routine and non-routine tasks delegated by the Team Lead.
• Comply with cGMP/EHS regulatory requirements and site procedures.
• Complete documentation in compliance with GDP and site procedures.
• Support commissioning, qualification, and validation activities for current and future projects.
• Prioritize and schedule activities to meet Master Production Schedule requirements.
• Lead investigations and resolve problems on the plant.
• Participate in Cross-Functional teams as necessary.

Skills

Data analytics

GMP experience

Shop floor knowledge

Education

BSc in a scientific/technical discipline

Job description

Johnson & Johnson Innovative Medicine in Ireland is seeking an Operations Process Microbiologist reporting to the Senior Plant Microbiologist. You will actively participate in the microbiological control and assurance program within the operations department, ensuring cGMP and EHS regulatory compliance.

Responsibilities include leading commissioning, qualification, validation activities, maintaining documentation, training new recruits, supporting investigations, and collaborating with