Manufacturing Process Specialist

Manufacturing Process Specialist

Location: Barnahely, Ringaskiddy, Cork

Duration: 12 months initially

Hours: 39

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

Reporting to Operations Manager, this position is responsible for representing operations on capital project teams and supporting first line troubleshooting of the day-to-day activities within Operations - These activities include but are not confined to: This will involve: 

• Represent Operations on cross functional project implementation teams.

• Monitoring and troubleshooting of the manufacturing process and equipment issues and process optimization

• Monitoring and reporting of process performance using statistical process control

• Troubleshooting of DCS (e.g Delta V) and PLC control systems

• Investigating and resolving issues raised within the Manufacturing Department

• Participate in/ Lead Cross Functional teams when required.

• Support of Commissioning and Qualification activities

• Preparation and updating of Batch Records, Procedures and Work Instructions

• Provide process and equipment related training as required within the Manufacturing Department

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

General scope of responsibilities:

• Lead by example and strive to perform to high standards at all times.

• Carry out routine and non-routine tasks delegated by the Operations Manager

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

• Completion of all documentation in compliance with site procedures and GDP.

• Lead and Support investigation and resolution of problems on plant.

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

how to succeed

You will have excellent interpersonal skills and the ability to operate as part of a team. You will have excellent communication skills, written and verbal and will have great problem solving. You will also bring:

• A relevant third level qualification in either Microbiology, Biochemistry, Pharmacy, Biotechnology, Science or Engineering

• Validation or Large Molecule experience

• Manufacturing experience within a GMP regulated environment in upstream fed batch bioreactors

• Experience of the cell culture or purification processes

• Project / New equipment installation experience

• Process engineering experience

• Commissioning and qualification experience

• Postgraduate Qualification.

• Experience of Microsoft Word, Excel and Outlook.

• Experience of DCS (e.g. Delta V), SCADA and PLC systems

• Experience of SAP, LIM’s and/or other business systems

• 6-Sigma/Kepner-Tregoe or similar problem solving/decision making methodology training

benefits

This role offers a very competitive hourly rate. This contract will run for 12 months and has a strong chance of extension. On site min. 3 days a week.

you are welcome here

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.

Janssen UK: https://www.janssen.com/uk/

Janssen Ireland: https://www.janssen.com/ireland/

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”.