Job Title: Pharmaceutical Manufacturing Specialist
This exciting opportunity at an award-winning pharmaceutical organization is seeking a skilled professional to oversee the production of materials at various stages of the product lifecycle. The successful candidate will have experience in pharmaceutical or biopharmaceutical manufacturing, specifically in sterile production environments.
The ideal background includes a strong understanding of GMP regulatory guidelines and quality systems. Aseptic practices are essential, with certifications related to cleanroom operations and environmental monitoring highly desirable.
Responsibilities include:
1. Overseeing the production of materials at various stages of the product lifecycle (clinical, non-clinical, and pre-clinical stages)
2. Handling batch preparation activities such as vial washing, load sterilization, and area preparation for production
3. Performing activities in accordance with the required cleanliness classification of the production area (e.g., sterile, Grade A, or other)
4. Carrying out sterile operations such as compounding, sterile filtration, and sterile filling
5. Working with external vendors to develop or improve single-use technologies
Qualifications and Experience Required:
* 3rd Level Qualification in a relevant discipline (e.g., Life Sciences, Engineering, Pharmaceutical Sciences, etc.)
* Minimum 12-18 months of experience in the pharmaceutical or medical device industry
* Experience working in cleanroom environments is essential
Benefits:
* Shift allowance bonus
* Pension scheme
If you are a detail-oriented individual with excellent collaboration skills and a passion for delivering high-quality results, we encourage you to apply for this challenging role.