Senior Biotech R&D Scientist - Bukit Merah

Job Description:

This role requires a strong foundation in biotechnology, molecular biology, or biomedical engineering and hands-on experience in a regulated laboratory environment.

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Key Responsibilities:

• Design and execute experiments related to product innovation, improvement, and process optimization.
• Develop and validate new assays, bioprocesses, or biomedical materials for manufacturing applications.
• Conduct literature reviews and competitive analysis to identify trends and opportunities in biotechnology.
• Collaborate with cross-functional teams (engineering, manufacturing, quality assurance) to support product development and scale-up.
• Provide scientific input during feasibility studies, prototyping, and pilot production stages.
• Analyze data using statistical tools and document findings in detailed technical reports.
• Ensure adherence to Good Laboratory Practices (GLP) and relevant regulatory requirements (FDA, ISO, GMP).
• Maintain accurate lab notebooks and prepare protocols, SOPs, and documentation for product dossiers.
• Assist in the preparation of patents, grant proposals, or scientific publications.
• Evaluate and implement new technologies, equipment, and methodologies that enhance R&D efficiency.
• Stay up to date with scientific advancements and emerging technologies relevant to biomedical manufacturing.
• Participate in scientific conferences, workshops, and industry forums as required.

Requirements:

• Master’s or PhD in Biotechnology, Biomedical Engineering, Molecular Biology, or a related life sciences discipline.
• At least 8 years of hands-on experience in a biotech, medical device, or biomedical manufacturing R&D environment.
• Proficient in molecular biology techniques, assay development, bioprocessing, or material science (depending on focus area).
• Strong analytical and critical thinking skills with a passion for innovation and problem-solving.
• Excellent communication and documentation abilities.
• Familiarity with quality and regulatory standards (e.g., ISO 13485, FDA 21 CFR Part 820) is a strong advantage.

EA Licence No: 23S1615