Deskripsi Pekerjaan
Are you a passionate and skilled Formulation Officer looking to make a significant impact in the pharmaceutical industry? Mensa Group, proudly ranked among the Big 10 local pharmaceutical companies in Indonesia, invites you to join our dynamic Research & Development team in Cibitung, Jawa Barat. We are at the forefront of developing innovative and high-quality pharmaceutical products that enhance the well-being of communities across Indonesia and beyond. This is an exceptional opportunity to contribute to the entire product lifecycle, from initial concept to commercialization, working with state-of-the-art facilities and a collaborative team dedicated to scientific excellence.
As a Formulation Officer, you will be instrumental in researching, developing, and optimizing various pharmaceutical dosage forms, including solids, liquids, and semi-solids. Your expertise will be crucial in designing formulations that not only meet stringent quality, efficacy, and safety standards but also address market needs and regulatory requirements. You will collaborate closely with analytical development, production, and quality assurance teams, ensuring seamless transitions from laboratory scale to pilot and commercial production. Mensa Group fosters an environment of continuous learning and innovation, encouraging our team members to explore new technologies and methodologies in pharmaceutical development. If you are driven by scientific curiosity, possess a keen eye for detail, and are eager to grow your career within a reputable and expanding organization committed to making a difference, Mensa Group is the place for you. Join us in shaping the future of healthcare through groundbreaking pharmaceutical solutions!
Tanggung Jawab
- Conduct research and development activities for new pharmaceutical formulations, including pre-formulation studies and excipient selection.
- Design and execute experiments for developing various dosage forms (e.g., tablets, capsules, syrups, creams).
- Optimize existing formulations to improve stability, bioavailability, and manufacturing efficiency.
- Prepare detailed formulation reports, protocols, and standard operating procedures (SOPs) in compliance with Good Manufacturing Practices (GMP).
- Collaborate with analytical, process development, and production teams to ensure successful scale-up and technology transfer.
- Perform stability studies and interpret results to determine product shelf-life and storage conditions.
- Stay updated with the latest advancements in pharmaceutical science, regulatory guidelines, and industry best practices.
- Troubleshoot formulation-related issues during development and production.
Kualifikasi
- Bachelor's degree in Pharmacy, Pharmaceutical Science, Chemical Engineering, Chemistry, or a related field.
- Minimum of 2-4 years of experience in pharmaceutical formulation development, preferably in a manufacturing setting.
- Strong understanding of pharmaceutical dosage forms, excipients, and manufacturing processes.
- Proficiency in laboratory techniques and equipment used in formulation R&D.
- Familiarity with GMP (Good Manufacturing Practices) and pharmaceutical regulatory requirements (e.g., BPOM, ICH guidelines).
- Excellent analytical, problem-solving, and critical thinking skills.
- Ability to work independently and collaboratively in a fast-paced R&D environment.
- Good written and verbal communication skills in English and Bahasa Indonesia.