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Cleaning Validation Engineer

Amaris ConsultingSingapore

30+ days ago

Job description

Amaris will be prioritizing applicants who are currently based in Singapore.

Key Responsibilities :

Develop and execute cleaning validation protocols for pharmaceutical manufacturing equipment and processes.
Ensure compliance with regulatory requirements and industry standards for cleaning validation.
Generate, execute, and report on testing for multiple phases of commissioning and qualification.
Troubleshoot and resolve cleaning validation issues to ensure compliance and operational efficiency.
Maintain documentation and records related to cleaning validation processes.
Collaborate with cross-functional teams to define cleaning validation requirements and specifications.

Qualifications and Skills :

Bachelor's degree in engineering, chemistry, or a related field.

Experience in cleaning validation within the pharmaceutical or biotech industry.

Knowledge of regulatory requirements such as FDA, cGMP, and industry guidelines related to cleaning validation.

Strong understanding of validation principles and practices for cleaning processes and equipment.

Excellent communication and collaboration skills.

Detail-oriented with strong analytical and problem-solving abilities.

Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability or other characteristics.