Job Description
- Develop new products, conduct research to improve formulations and manufacturing processes of existing products to ensure optimal quality and efficiency
- Research and collect relevant documents and propose specifications for raw materials, finished products, active ingredients, excipients, and packaging materials; prepare material estimates for product development projects
- Propose and conduct pre-formulation studies and report results
- Propose formulations and processes for trial batches, prepare trial batch documentation, produce research samples according to approved batch records, and report results
- Support validation activities for three process validation batches
- Draft manufacturing procedures and submit them to the regulatory affairs department
- Draft and conduct training for Standard Operating Procedures (SOPs)
- Perform other related tasks as assigned by the Head of Department
Job Requirements
- 2–6 years of experience in a similar position
- University degree in Pharmacy
- Good knowledge of GMP regulations
- Proficient in Microsoft Office and good English skills
- Honest, careful, meticulous, and responsible
Benefits
- Competitive salary based on qualifications and experience
- 13th-month salary and annual salary review according to company policy
- Paid annual leave and public holidays as per regulations
- Full participation in Social, Health, and Unemployment Insurance as required by law
- Opportunities to attend professional training courses
- Provided with full work equipment
- Annual health check-up program
- Participation in company teambuilding and travel programs
- Professional, dynamic working environment with career growth opportunities
- Provided free lunch, coffee, tea, and snacks during breaks
- Hazardous allowance according to company policy
Workplace
- Ho Chi Minh City: Lot E9-3a, Street No. 1, Hiep Phuoc Industrial Park, Hiep Phuoc Commune, Nha Be District, Ho Chi Minh City
Working Hours
- Monday to Friday: 07:15 AM – 04:20 PM
- One Saturday per month