Key Responsibilities:
- Supporting biopharmaceutical manufacturing activities (Downstream/Upstream/Central Services)
- Execute manufacturing activities according to production schedules and in compliance with Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) standard operating procedures, and safety regulations.
- Collaborate with cross-functional teams to troubleshoot and resolve process-related issues
- Document all manufacturing activities and maintain accurate records in accordance with regulatory requirements.
Qualifications and Skills:
- Bachelor's in chemical engineering, pharmaceutical engineering/sciences or related field.
- Understanding of cGMP regulations
- Analytical, problem-solving, and communication skills.
- Ability to work effectively in a fast-paced, team-oriented environment
- Able to work in 12 hour shift
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