Company Overview
Pharmagend is a Singapore-based pharmaceutical manufacturer focused on developing and producing high-quality drug products, including oral dosage forms, injectables, creams, inhalations, and eye drops. We prioritize safety, quality, innovation, and sustainability.
Job Summary
Develop and optimize analytical methods for pharmaceutical materials and products, conduct validation studies, perform sample analyses, and collaborate with cross-functional teams to support product development and regulatory compliance.
Responsibilities
- Develop and optimize analytical methods to characterize pharmaceutical raw materials, intermediates, and finished products.
- Conduct method validation studies following regulatory guidelines and internal procedures to ensure accuracy and compliance.
- Perform routine and non-routine sample analyses using various analytical techniques to generate reliable data.
- Prepare and review technical documentation, including method development reports, validation protocols, SOPs, and regulatory submission documents.
- Ensure laboratory activities comply with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and relevant regulatory requirements.
- Identify and resolve technical issues related to analytical methods and instrumentation to maintain method robustness.
- Analyze and interpret analytical data accurately, preparing detailed reports and presentations of findings.
- Collaborate effectively with Formulation Development, Quality Assurance, Quality Control, Regulatory Affairs, Manufacturing, Engineering, and Supply Chain teams to support product development and commercialization.
- Maintain laboratory equipment and instrumentation in good working order, following safety protocols and ensuring a clean, organized environment.
- Stay updated on industry trends, scientific advancements, and technological innovations to continuously improve analytical methods and laboratory practices.
- Perform other duties as assigned by the supervisor.
Preferred competencies and qualifications
- Master's, Ph.D., or Bachelor's degree in Chemistry, Pharmaceutical Sciences, Analytical Chemistry, or related field.
- For Associate Scientist: 2+ years of experience in analytical method development in the pharmaceutical industry or related field fresh graduates will be considered.
- For Scientist: 2 to 5 years of experience in analytical method development in the pharmaceutical industry or related field.
- Hands-on experience with various analytical techniques.
- Proficiency in method development and validation according to ICH guidelines.
- Familiarity with regulatory requirements and quality systems.
- Experience with advanced analytical techniques.
- Knowledge of statistical tools and software for data analysis.
