Company Name: PT Selatox Bio Pharma
Location: Kabupaten Bekasi
Posted Date: 11/10/2024 16:29
Salary:
Job Description
- PT. Selatox Bio pharma Corporation is a 100% owned subsidiary of Daewoong Pharmaceutical in Korea, which develops and produces BIOLOGICAL PRODUCT SUCH AS BOTULINUM TOXIN and aims to expand globally. Daewoong Pharmaceutical is one of the leading pharmaceutical companies in Korea with a sales revenue of over 1.3 billion USD. The company is actively focusing on research and development as well as global expansion. Daewoong Pharmaceutical invests more than 15% of its revenue into research and development and has over 100 research and business partners worldwide.
- We plan to establish a production base for botulinum toxin products in Indonesia as a global bio hub strategic base and target the global market with better accessibility and services through the development and production of competitive new products.
- we have a vision of becoming a “2030 leading global biopharmaceutical company.” With the goal of becoming a world-class botulinum toxin company.
- [Basic requirements]
Major:
Pharmacy, chemical, biology, biotechnology, chemical engineering, and microbiological
- Bachelor degree or higher in the related field
- Minimum 1 year or more working experience in the related field
Language:
Fluent in spoken and written English language communication
- Smart, able to work in fast-pace, and good interpersonal skill
- Strict attention to detail and strong problem-solving skills
- Willing to be placed at Jababeka Cikarang
- [Preferred requirements]
- Licensed Pharmacist
Language:
Fluent in spoken and written Korean language
- Person with professional work experience in pharmaceutical company
- Excellent talents in the field of advanced science and technology who have been recommended for employment by the competent government
- Able to communicate effectively; fluent in Korean – both spoken and written
Job Description:
- Analytical test method verification (QA)
- Verification of compendium (USP, EP, JP, etc.) test methods
- Review and study of guidance and regulations on product approval and registration overseas, and management of registration and status for each targeted country
- Support for transfer of analysis technology for test methods and preparation of validation documents in English
- Support for environment monitoring trend report preparation, disinfectant effectiveness evaluation, etc.
- Ensure the implementation and compliance with Good Manufacturing Practices
- Write, review, and approve validation master plans, validation plans, SOP’s and other validation documentation
- Prepare validation plan/protocols for production processes such as process validation, cleaning validation, filtration validation, etc
- Prepared and evaluate SOP, Work Instruction and Forms in the company as well as determine and supervise the implementation of a record keeping system of all activities
- [Only CV in English will be processed]