Planet Pharma
From Planet Pharma's careers page
Status: listed on the employer's own careers page when we last checked (daily). Confirm on their site before applying.
Product Development & Engineering
Lead end-to-end product development activities including design, prototyping, testing, and validation
Drive technical decisions and provide engineering expertise throughout the product lifecycle
Develop and review engineering specifications, design documents, and technical reports
Identify and resolve complex engineering challenges using systematic problem-solving approaches
Cross-Functional Collaboration
Partner with R&D, Quality, Manufacturing, Marketing, and Regulatory teams to ensure alignment
Serve as a technical resource and mentor for junior engineers
Communicate technical concepts clearly to both technical and non-technical stakeholders
Project Leadership
Lead or contribute to multiple concurrent engineering projects
Define project scope, timelines, and deliverables
Track milestones and proactively manage risks and dependencies Quality & Compliance
Ensure products meet regulatory requirements (e.g., ISO, FDA, MDR) and internal quality standards
Support design verification and validation (V&V) activities
Participate in design reviews, FMEAs, risk assessments, and change control processes
Continuous Improvement
Identify opportunities to improve products, processes, and engineering practices
Apply data-driven methods to analyze performance and drive decisions
Stay current with industry trends, emerging technologies, and best practices
B.S. in Mechanical, Electrical, Biomedical, or related Engineering field
Bachelor’s degree or higher in Life Sciences or related discipline
Minimum 5-7 years of experience in Quality Assurance and/or Quality Systems within the medical device industry.
Experience implementing or improving ISO 13485-based QMS.
Strong experience working with Singapore medical device regulatory requirements.
Demonstrated experience supporting or leading GDPMDS/GDP certification projects.
Proven track record of successfully helping organizations obtain and maintain GDP certification
Experience interacting with certification bodies, accreditation bodies, and regulatory authorities.
5-8+ years of product engineering experience
Validation experience, design analysis, V&V testing, PLM, Design Controls, ISO 13485, FDA 21 CFR Part 820
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