Manufacturing Process Specialist

Manufacturing Process Specialist

Location: Ringaskiddy, Cork

Duration: 12 months

Hours: 39 hours per week, days

Imagine your next project as a Manufacturing Process Specialist working at the forefront of cutting edge work and technology with one of the leading Pharmaceutical companies in the world!

roles and responsibilities

The Manufacturing Process Specialist will be responsible for day-to-day Downstream activities for a large scale (15,000L) Feed Batch Suite. 

• Monitoring and troubleshooting of the manufacturing process to support process optimization

• Execution of Continuous Improvement projects focused on reliability, cycle time reduction and yield

• Lead change controls to improve aspects of the downstream process

• Preparation and updating of Electronic Batch Records (PasX) and Work Instructions

• Support and lead Non-Conformance investigations utilizing A3 RCPS methodology

• Completion of assigned tasks to support manufacture of quality biomedicines in accordance with cGMP and EHS requirements.

General Scope of Responsibilities: 

• Responsible and accountable for assuring the safe accomplishment of job activities, following good environmental practices and procedures. Commit to and demonstrate safe behaviour in every activity.

• Carry out routine and non-routine tasks delegated by the Operations Manager according to appropriate procedures, values, and standards.

• Carry out all activities in compliance with corporate and cGMP/EHS regulatory requirements.

• Compliance with Manufacturing and general site procedures at all times and completion of all documentation in compliance with site procedures and GDP.

• Lead and Support investigation and resolution of problems on plant and participate in and lead Cross-Functional teams as necessary.

• Generate and assist with generation, review, and revision of Manufacturing documentation as necessary. 

• Ensure that personal training requirements are completed in compliance with site procedures. 

Leadership Responsibilities / Individual Contribution 

• Report to (Senior) Operations Manager

• Represent Operations on cross functional project teams.

• Be familiar with daily activities in Manufacturing.

•  Facilitate an environment of continuous improvement.

• Facilitate an environment of open communication.

• Lead investigations in work area as necessary.

• Lead Cross-Functional teams as necessary to support site goals.

• Support training of other Manufacturing colleagues.

• Collaboration and teamwork.

• Initiative and motivation.

• Share ideas and suggestions for improvement and encourage others to do the same.

• Demonstrate Credo value of integrity.

how to succeed

• Minimum bachelor’s degree in either Process Engineering, Biochemistry, Biotechnology, Science or Engineering. 

• Manufacturing experience within a GMP regulated environment. 

• Experience of the Purification processes 

• Project / New equipment installation experience

• Process Engineering experience

Desirable:

• Working experience with Emerson DeltaV 

• Instrumentation and Automation troubleshooting

• Experience in implementation of process improvements

• Data gathering and analysis; utilizing tools like OSI Pi, SIMCA MVA, Excel, Claude etc..

• Ability to operate as part of a team with attention to detail. 

details

This role offers a very competitive hourly rate. This contract will run for a 12 month duration. It’s an on-site position, full time, regular day hours. 

you are welcome here

Johnson & Johnson Innovative Medicine is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about Johnson & Johnson Innovative Medicine

Patients inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science and compassion, we confidently address some of the most complex diseases of our time and unlock the potential medicines of tomorrow.

Our diverse portfolio spans multiple therapeutic areas — Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina.

We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.

application process

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email. The pay rate for this role will depend on how you are paid. PAYE, LTD & Umbrella options are available. 

questions

If you would like some additional information about the role please contact: simone.strong@randstadsourceright.co.uk

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.