Technologist

Pfizer; Ireland; On-site; EUR 60,000 - 85,000; Full time

Job summary

Pfizer is seeking a Technologist for the Ringaskiddy Clinical Manufacturing Facility (RCMF) to support continuous processing and new product introductions. The role works in cross-functional process teams and travels to observe and transfer processes.

You will develop and execute manufacturing techniques for clinical API products, aiming for safety, quality, cost efficiency, and continuous improvement. The position reports to the Operations Lead.

Qualifications

• Experience in API/biopharma manufacturing or food processing is required.
• NFQ Level 7+ qualification in pharma, biopharma, chemical/process or mechanical engineering or equivalent.
• Experience with API continuous manufacturing is advantageous.
• Strong technical, problem-solving and communication skills.
• Ability to perform in a dynamic, performance-driven environment.

Responsibilities

• Independently prioritizing and scheduling activities to support business needs and to meet requirements of the RCMF manufacturing schedule.
• Working shift patterns to meet business needs and the manufacturing schedule as required.
• Flawless RCMF manufacturing execution against safety, quality and customer service metrics for clinical campaigns conducted within the facility.
• Understanding and use of manufacturing control systems to execute processing steps.
• Assembling and disassembling of process equipment, as required in support of equipment changeover.
• Ensuring that housekeeping standards in the manufacturing facility are maintained to an audit-ready standard at all times.
• Adherence to all relevant quality and safety procedures.
• Monitoring and optimizing the quality and yield of the products including optimization of the process with regard to efficiency, quality and safety.
• Leading and supporting investigations and resolution of process problems that may occur on plant.
• Collection of data, trending and generation of technical reports.
• Leading post-campaign reviews with Pharm Sci colleagues.
• Participating in cross-functional teams leading to accomplishment of RCMF goals.
• Assisting with writing, review and revision of manufacturing documentation as necessary e.g. standard operating procedures, batch books etc.
• Completion of personal training requirements in compliance with site procedures and using facility equipment commissioning and qualification activities as part of a comprehensive learning and development program.
• Providing training and support to new staff members of the RCMF team to ensure that learning objectives are met.
• Co-lead technical transfer of processes from RCMF to Ringaskiddy commercial production facilities
• Develop strong relationships with PGS New Products Value Stream (SEG, NPTL) to support tech transfer activities
• Operational alignment with the small-scale manufacturing facilities in PGS, in particular the New Products Technology Laboratory (NPTL)
• Readiness for and participation in routine safety and quality inspections
• Support the technology and knowledge transfer of new products to the Ringaskiddy New Products Value Stream
• Continuous improvement of the workflows associated with the RCMF operation
• Permitting activities within the RCMF
• Additional areas of responsibility as the business requires
• Participate and excel in the RCMF technologist rotations programme.

Skills

API/biopharma manufacturing experience

NFQ Level 7+ qualification

Continuous manufacturing

Problem solving

Communication skills

Education

NFQ Level 7+ in Pharma/Biopharma/Chemical/Process/Mechanical Engineering

Job description

Technologist Ringaskiddy Clinical Manufacturing Facility (RCMF)

Position Summary

The RCMF facility is a multi-product clinical API manufacturing facility enabled for continuous processing using our FAST platforms. The design is focused on combining existing capabilities from our clinical workflows with the very best advances in technology and architecture to build a truly contemporary API clinical facility which will support the needs of our new products small molecule portfolio into the future. The RCMF will scale up new clinical products developed in our CRD laboratories at our research sites in the U.S. (Groton, Connecticut) and will tech transfer successful new products from the RCMF to our commercial manufacturing site in Ringaskiddy. Reporting to the Operations Lead, the Technologist works in Process Teams that are aligned with new product introduction workflows utilising cutting edge continuous manufacturing technologies. Technologists are members of a dynamic, highly competent, engaged team of colleagues responsible for delivering a fully operational facility with excellent performance across the fundamentals of safety, quality, supply and cost. Technologists will develop and execute manufacturing techniques consistent with the requirements of Pfizer's newest products, and will be committed to continuous improvement, technical up-skilling and personal development in a performance-driven environment. Technologists will be required to travel periodically to observe new processes in transferring facilities; attend, contribute to and present at on and off-site meetings as required.

The accountabilities of the Technologist position include:

• Independently prioritizing and scheduling activities to support business needs and to meet requirements of the RCMF manufacturing schedule
• Working shift patterns to meet business needs and the manufacturing schedule as required
• Flawless RCMF manufacturing execution against safety, quality and customer service metrics for clinical campaigns conducted within the facility
• Understanding and use of manufacturing control systems to execute processing steps
• Assembling and disassembling of process equipment, as required in support of equipment changeover
• Ensuring that housekeeping standards in the manufacturing facility are maintained to an audit-ready standard at all times
• Adherence to all relevant quality and safety procedures
• Monitoring and optimizing the quality and yield of the products including optimization of the process with regard to efficiency, quality and safety.
• Observation of processes & technologies in Pharm Sci Kilo lab facility
• Preparation of RCMF for new product activity from a safety, quality and operational perspective through adherence to the start-up Standard Work Plan
• Real-time analysis of data (e.g. Process Analytical Technology data) and real-time decision-making in partnership with Pharm Sci colleagues
• Leading and supporting investigations and resolution of process problems that may occur on plant
• Collection of data, trending and generation of technical reports
• Leading post-campaign reviews with Pharm Sci colleagues
• Participating in cross-functional teams leading to accomplishment of RCMF goals.
• Assisting with writing, review and revision of manufacturing documentation as necessary e.g. standard operating procedures, batch books etc.
• Completion of personal training requirements in compliance with site procedures and using facility equipment commissioning and qualification activities as part of a comprehensive learning and development program
• Providing training and support to new staff members of the RCMF team to ensure that learning objectives are met.
• Co-lead technical transfer of processes from RCMF to Ringaskiddy commercial production facilities
• Develop strong relationships with PGS New Products Value Stream (SEG, NPTL) to support tech transfer activities
• Operational alignment with the small-scale manufacturing facilities in PGS, in particular the New Products Technology Laboratory (NPTL)
• Readiness for and participation in routine safety and quality inspections
• Support the technology and knowledge transfer of new products to the Ringaskiddy New Products Value Stream
• Continuous improvement of the workflows associated with the RCMF operation
• Permitting activities within the RCMF
• Additional areas of responsibility as the business requires
• Participate and excel in the RCMF technologist rotations programme.

SELECTION CRITERIA

Qualifications/Skills, Knowledge & Experience:

• Relevant experience in either API/ Biopharma manufacturing or food processing
• Have at least a level 7 or higher (NFQ framework) qualification in pharma, biopharma, chemical/process/ mechanical engineering or equivalent
• API continuous manufacturing experience while not essential would be advantageous
• Excellent technical, problem-solving and communication skills
• Performance at a consistent level of excellence in a consistently dynamic operating environment, where the focus will