EPM Scientific is currently supporting a client based in Denmark, who is searching for a CIP Specialist, on a 6 month contract basis.
Responsibilities:
- Lead the validation and verification of Cleaning-in-Place (CIP) processes to ensure compliance with industry standards.
- Conduct design reviews to evaluate the suitability and efficiency of CIP systems.
- Coordinate and participate in testing activities, ensuring thorough documentation of results and adherence to regulatory requirements.
- Perform supplier inspections to assess quality standards and validate equipment used in CIP processes.
Qualifications:
- Bachelor's degree in Chemistry, Pharmaceutical Process Engineering, or a related field.
- Solid experience with Good Manufacturing Practice (GMP), preferably within Active Pharmaceutical Ingredient (API) manufacturing.
- Expertise in CIP process validation and a deep understanding of CIP-related protocols and requirements.
- Proficiency in English, with strong communication skills for reporting and collaboration.
Desired Skills:
- Attention to detail and thoroughness in documentation.
- Strong problem-solving abilities and a proactive approach to continuous improvement.
- Ability to work effectively in a cross-functional team environment.
