About
Find out if this opportunity is a good fit by reading all of the information that follows below.
If you have 2 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you! ABOUT THE PROJECT
- KEY RESPONSIBILITIES: Develop and implement cleaning validation strategies for new equipment and processes.
Execute cleaning validation studies, including sampling, testing, and data analysis.
Conduct risk assessments to identify critical cleaning parameters and acceptance criteria.
Ensure that cleaning validation activities comply with regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., ICH, PDA).
Work cross functionally to lead any cleaning validation studies, process performance qualification and new product introductions in the manufacturing facility.
ABOUT YOU
- ARE YOUR SKILLS A MATCH? The successful candidate must possess a Bachelor/master's in engineering, or Science related discipline.
Previous cleaning validation experience is an advantage.
Strong knowledge of regulatory requirements and industry standards related to cleaning validation (e.g., FDA, EMA, ICH, PDA).
Ability to work independently and as part of a team The ideal candidate would have biopharmaceutical Process / Validation knowledge.
Apply via this advert or contact Kathy Gillen on if you have any more questions about this role! You will need to hold a Stamp 1G/Stamp 4 visa to apply. xyswxtq
LSC do not provide work permit/visa sponsorship.
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Languages
- English
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