Troikaa Pharmaceuticals - Walk In on - 13th April 2023 for - B. Pharm, M. Pharm, MS/M.Sc

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Troikaa is a young and fast growing system oriented pharmaceutical company. Troikaa is recognized as a discovery company, manufacturing innovative products based on varied Novel Drug Delivery Systems. The company has developed through in-house R&D, unique patented technology platforms for intra-oral, parenteral, sustained release and topical drug delivery. All these innovations are backed by requisite clinical trials. The company has two state of the art manufacturing facilities in India. The plants are designed for approvals in regulated markets. The company has a near zero product failure record. Plants are equipped to manufacture tablets, capsules, liquicaps, parenterals (including parenteral emulsions), topical and inhalation anesthetic products. We have marketing networks in India, South East Asia, Latin America & Africa. Company intends to enter the highly regulated markets by year 2009.

Job Vacancy Details: 

  • Department: R&D Analytical
  • Qualification: B. Pharm, M. Pharm, MS/M.Sc
  • Experience: With 1-6 years of experience
  • Job Location: Virochannagar, Sanand
  • Salary: 2-6 Lacs P.A.
Time and Venue
13th April , 09:30 AM – 05:00 PM
Troikaa Pharmaceuticals Ltd. ‘Troikaa House-1’, Satya Marg, Bodakdev, Ahmedabad -380054, Gujarat
Contact – Pankaj Gupta ( 9099901634 )

Job description

  1. Method developments and validation of analytical method on said sophisticated instruments like HPLC , Gas chromatograph UV Spectrophotometry , autititratour , dissolution etc. as per ICH / Pharmacopeia guideline.
  2. Preparation of protocol and report there off.
  3. Very well versed with the sample preparation on Microwave digestion system
  4. Creating and executing method development and method validation test protocols for finished products and generating the appropriate analytical methods.
  5. Stability testing of products for new formulations and ongoing stability trials, using physical (pH, viscosity) and instrumental (HPLC, UV, Dissolution) techniques, as appropriate.
  6. Writing analytical specifications using current pharmacopoeias and reviewing existing analytical specifications.
  7. Writing/reviewing Standard Operating Procedures (SOPs),
  8. Ensuring that procedures are carried out carefully and accurately to eliminate errors.
  9. Ensuring good relations and communications with all members of the team and responding politely and in a timely fashion to internal and external customers.
  10. Observing and complying with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP).

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