Biotechnologist (Pharmaceutical)
2 months ago
Amaris will be prioritizing applicants who are currently based in Singapore.
Key Responsibilities:
- Supporting biopharmaceutical manufacturing activities (Downstream/Upstream/Central Services)
- Execute manufacturing activities according to production schedules and in compliance with current Good Manufacturing Practices (cGMP), 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 biotechnology, chemical engineering, pharmaceutical engineering 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 rotating shift.
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.
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