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Formulation Development Scientist

Job Summary

Formulation Development Scientist Male/Female (3) Post

  • Minimum Qualification: Bachelor
  • Experience Level: Senior level
  • Experience Length: 2 years

Job Description/Requirements

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

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Yangon
| Full Time |
MMK 800,000 - 1,000,000
1w