Department
Health & Biotech
Category
Health & Biotech
Job type
Part-Time
Experience
1 Year
Description
- Transfer, Support Development and optimize pharmaceutical products, including preparation of technical documentation and manufacturing instructions.
- Support the production of experimental, registration, and validation batches, ensuring accurate documentation and data integrity.
- Prepare and review pharmaceutical development reports, validation protocols, reports, and CTD Module 3 documentation.
- Participate in process validation, technology transfer, scale-up activities, and maintenance of validated manufacturing processes.
- Investigate manufacturing deviations, out-of-specification results, and technical issues, implementing corrective and preventive actions where required.
- Perform statistical analysis of experimental and production data to support process improvements and quality enhancement initiatives.
- Ensure compliance with GMP, quality systems, environmental, health and safety requirements, and applicable company procedures.
Qualifications
Highest qualification: University
- University degree in Pharmacy, Chemistry, Biology, Pharmaceutical Technology, or a related scientific discipline.
- Minimum 1 year of experience in pharmaceutical manufacturing, pharmaceutical development, or a related GMP-regulated environment.
- Knowledge of pharmaceutical manufacturing processes, technology transfer, process validation, and quality systems.
- Proficiency in MS Office and experience working with computerized systems such as SAP, Change Control, CAPA, or Deviation Management is an advantage.
- Good command of English, both written and spoken.
- Ability to perform data analysis and apply statistical methods to support scientific and manufacturing activities.
- Strong problem-solving, collaboration, communication, change management, and continuous learning mindset.