We are seeking a skilled Bioprocessing Specialist to join our team at our Westport facility on a permanent contract.
Job Description:
The successful candidate will be responsible for the manufacturing of pharmaceutical products at different stages of the lifecycle, including clinical, non-clinical, and pre-clinical material. This will involve batch preparation activities such as vial washing, load sterilization, and area preparation.
The ideal candidate will have excellent knowledge of aseptic practices in clean room environments and strong understanding of GMP regulatory guidelines, quality systems, drug product manufacturing, and validation. Experience with single-use technologies is highly desirable.
Required Skills and Qualifications:
* 3rd level qualification in a relevant discipline or 6 months minimum experience in the pharmaceutical or medical device industry
* Prior knowledge of aseptic practices in clean room environments is essential
* Strong knowledge of GMP regulatory guidelines, quality systems, drug product manufacturing, and validation is desirable
Benefits:
This role offers a unique opportunity to work in a dynamic team environment and contribute to the development of new and existing systems regarding single-use technologies. The successful candidate will also have the opportunity to participate in cross-functional teams with other functions, including R&D, Engineering, Quality, Supply Chain, Operations, and Validation.
Why Apply?
This role offers a challenging and rewarding career opportunity for an experienced professional looking to take their skills to the next level. If you have a passion for bioprocessing and a desire to work in a dynamic team environment, then this could be the ideal role for you.