Pharma Manufacturing Engineer - Katalyst Healthcares & Life Sciences

Responsibilities:

• Oversee and optimize pharmaceutical manufacturing processes, ensuring compliance with industry standards and regulatory requirements.

• Ensure adherence to GMP, GDP, and other pharmaceutical regulations, including ISO standards, across all manufacturing activities.

• Support and execute process validation activities, including the development and implementation of IQ, OQ, and PQ protocols.

• Maintain detailed and accurate documentation of manufacturing processes, validations, and quality checks.

• Collaborate with teams across different manufacturing sites, ensuring consistent quality and process adherence.

• Identify opportunities for process improvements and implement strategies to enhance efficiency, quality, and safety in manufacturing.

• Conduct quality checks and audits to ensure products meet all necessary standards and specifications.

• Work closely with cross-functional teams, including R&D, Quality Assurance, and Operations, to support project goals and timelines.

Requirements:

• 2-4 years of experience in pharmaceutical manufacturing or a related field.

• Bachelor's degree in engineering, Pharmaceutical Sciences, or a related discipline.

• Strong knowledge of GMP, GDP, process validation, and regulatory requirements in the pharmaceutical industry.