Formulation Development Scientist
အလုပ်အကျဉ်းချုပ်
Formulation Development Scientist Male/Female (3) Post
- ဘွဲ့ အမျိုးအစား: ဘွဲ့ရ
- အတွေ့အကြုံအဆင့်: အကြီးတန်း
- အတွေ့အကြုံကြာချိန်: 2 years
လုပ်ငန်းတာဝန်သတ်မှတ်ချက်
Duties and Responsibilities
- Develop new technologies, processes and product formulations for solid and liquid dosage form of pharmaceuticals. Projects can range from new product development, current product improvement, and ingredient evaluation.
- Write, generate and review protocols, development reports, and master batch records.
- Help and develop the process of the plant and assist in evaluating new equipment.
- Responsible for creating, evaluation, and formatting the product image to commercialization.
- Validate processes, procedures and formulations consistent with GMP requirements
- Source, develop and work with outside laboratories and manufacturing facilities to identify and support innovative products and delivery methods
- Formulate and modify existing formulas to meet regulatory guidelines, cost parameters and claims
- Think creatively in prototype preparation and in problem solving
- Collaborate with colleagues to define project scope, timing, product costs
- Working knowledge of industry trends
- Interact closely with other members of the team, etc.
- Perform other related duties as required
- Ability to interact successfully with peers
- Demonstrated compliance with procedures and policies.
- Strong communication skills both written and verbal.
- Strong attention to detail
- Willingness to work flexible hours.
Requirements and Qualifications
- Masters of Science in a pharmaceutical –related field or PhD, Phar.D., or equivalent qualification with good competence in the relevant technical area.
- At least 2 years relevant experience in solid drug development for ANDA, OTC, Nutraceutical products
- Experience in using design of experiments when developing new formulations.
- Experience in working on ANDA’s and CMC portion of the filing.
- Experience in Scale up and technology transfer of solid dosage and preferably softgels.
- Experience in solid dosage forms, including modified release formulation, sustained release, multi-particulates, pulse, ODT, both tablets and capsules technologies
- Experience in oral solutions development a plus.
- Experience in cGMP related to pharmaceutical manufacturing for the US market
- Working knowledge of core processes: development, and manufacturing
- Excellent team and interpersonal skills

