Job Description
About the company.
Meyer Organics is a part of the worlds No. 1 & fastest growing Nutraceutical Company, Vitabiotics Ltd, headquartered at London and operating in 110 countries across the globe. Vitabiotics is committed for the scientific research in nutrient medicine & has been awarded consequently for three years with UK’s prestigious Queen’s Award for excellence and innovation in vitamin research. Meyer has been manufacturing innovative health care products for over three decades & is committed to excel in human health care and research.
Meyer has created a unique portfolio of products in the key segments like Anti-infective, Nutrition Supplements for all age groups, Infertility Supplement, Pain Management, etc.
Position Offers:
- Designation : Asst Manager - R&D
- Reports to : HOD:
- Location : Thane (Head Office)
- Gender : Male
- Qual. & Exp. : Min 5+ years, and M. Pharm.- Pharmaceutics (No other Qual. Will be considered, and PhD will be an added advantage)
- CTC : Upto 13L
- Age : Up to 35 years
- Contact email : rdalvi@meyer.co.in (Candidates to apply who meet ONLY below Mandatory Requirements)
Mandatory Requirements: (You can write critical requirements 2 or 4 points that candidate must have before applying)
1. Education criteria.
2. Excellent Communication skill (Verbal and Written),
3. Nutraceutical background,
4. Team handling experience.
Job Description:
1. Lead and Responsible for formulation development of stable and robust formulations across various dosage forms including Oral Solids, Liquids, Semi-Solids, etc.
2. Conducting the trouble-shooting of formulations/products in terms of Quality improvement and cost improvement.
3. Knowledge of both Drug and Nutraceutical formulation development.
4. Supervising the daily work of assigned associates and also monitoring and resolving technical issues.
5. Visiting various Domestic and International production site for scale up-technology transfer and also to extend technical expertise.
6. Responsible for raw material screening, evaluation and regulatory compliance
7. Responsible for the documentation of formulation development (PDRs) and the generation of technical reports.
8. Preparation of formulation development protocols, and technology transfer dossier (TTD).
9. in depth. knowledge of product development and current regulatory guidelines.
Note: Candidates willing to relocate can also apply.