Sorry, the offer is not available,
but you can perform a new search or explore similar offers:

Bioprocess Associate

Job Description About PSC Biotech   Who we are?   PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA...


Psc Biotech Ltd - County Meath

Published a month ago

Bioprocess Associate

About PSC Biotech   Who we are?   PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global op...


Psc Biotech Ltd - County Meath

Published a month ago

Technical Director

The Technical Director will lead the technical and operational aspects of our water treatment company Aquachem, overseeing the design, implementation, and op...


Neylons Facility Management - County Meath

Published 24 days ago

Qa Technologist

Job Title: QA TechnologistLocation: County MeathSector: Food ManufacturingAbout the Role:A leading food company in County Meath is seeking a QA Technologist ...


Next Generation - County Meath

Published 10 days ago

Biotech Associate

Details of the offer

PE Global is currently recruiting for a Biotech Associate for a leading multi-national Biotech client based in Meath. This is an initial 11-month contract shift position. ROLE: The production of biologic drug substance on their designated shift team and will be responsible for the preparation, operation and monitoring of equipment, use of business systems and carrying out tasks including but not limited to the cleaning, validation, in-process testing. The progression of an automated recipe using paperless technology in order to generate the drug substance through inoculation and cell culturing activities directing to filtration and purification of the product. Setting up the single use equipment between runs, carrying out the production process according to world class GMP and EHS standards and driving to optimise and improve the processing activities through use of standard work and lean processing techniques. Focusing on delivery to the patient through living the Dunboyne culture including a commitment to safety, focusing on right first time in everything we do and concentrating on the engagement and development of self and peers. Maintain a high standard of safety /GMP compliance at all times. Maintain a high level of personal expertise and working knowledge of all aspects of the manufacturing process and process equipment through continuous training and development. Liaise with other groups and individuals to ensure planning of tasks is effective and linked into the manufacturing process plan. Support approved projects and continuous improvement initiatives that are in alignment with site strategies. Be an advocate for continuous improvement. REQUIREMENTS: Experience in a highly regulated pharmaceutical manufacturing environment. Good understanding in the production of biologic drug substance and experience an advantage. Ability to work as part of a shift team and on own initiative in a constructive manner. Ability to think logically and be proactive under pressure. Flexible and self-motivated. A science qualification in a technical, engineering or science-based discipline or equivalent. Interested candidates should submit an updated CV. ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***

#J-18808-Ljbffr


Nominal Salary: To be agreed

Source: Jobleads

Job Function:

Requirements

Built at: 2024-11-11T04:11:21.481Z