Walk in: Multiple vacancies in Surya Pharma | R&D - Process development lab, ARD-API / Bulk drug / Formulation, Production-Sterile API, CRD - Chemical Research Development, Phytochemical, QC

 

Surya Healthcare is a subsidiary of Surya Pharmaceuticals Limited with widespread domestic and international operations. The force behind Surya Healthcare is its parent company Surya Pharmaceuticals Limited. It is uniquely positioned in the Pharmaceutical trade known for its competencies in API, formulation and contract manufacturing across different therapeutic segments serving both domestic and international clients.
The medicines market in India is highly fragmented with over 500,000 family-owned small sized chemists & drugists operating across the country.The company cited gaps in the way medicines and FMCG items are sold and managed across India, formulated an entry strategy and has entered the organized retailing space in the healthcare domain through a chain of chemist stores under the brand name VIVA-Your family Chemist. Its time to change customers deserve the experience and assurance of genuine medicines.

Post: R&D - Process development lab, ARD-API / Bulk drug / Formulation, Production-Sterile API, CRD - Chemical Research Development, Phytochemical, QC

Job Description:
R&D - PROCESS DEVELOPMENT LAB
Requirement    : The candidate should have experience in Process
Development any of the following Product Categories : Penicillin/ Cephalosporins/ Sterile Bulk.

ARD- ANALYTICAL RESEARCH AND DEVELOPMENT - API / BULK DRUG /FORMULATION
Requirement   : The candidate should have experience in underneath job description : Method development and validation of API or Formulation for related substances and assay by HPLC. Method validation of intermediates for API or formulation by HPLC/GC. Method transfer from development to routine for API & Formulation. Calibration of HPLC instrument. Analysis of samples received from RA for solving the queries of Regulatory Agencies. Responsible for maintaining GLP in the laboratory. Routine Analysis of Samples. Analytical method development and validation by LCMS and characterization of impurities.

PRODUCTION - STERILE API    
Requirement    : The candidate should have exposure in: Monitoring the area includes Washing. Solution, and Aseptic processing area. Monitoring shift wise activities, Man power planning for optimum utilization. Document verifications ( BPCR. ECR. EUR. Environment monitoring record, entry and exit record) Planning and Execution of daily Production Activity Monitoring of Moist and Dry heat sterilization's like Autoclave and DHS for routine monitoring. Carried out the training for the operators and supervisors. Carried out the execution of media fill validation. Involved in preparation and maintenance of cGMP records. Coordinate with QA and QC Dept. Monitoring the Blending activity.

CRD- CHEMICAL RESEARCH DEVELOPMENT - API / BULK DRUG INDUSTRY.
Requirement   : The candidate should have experience in underneath job description : Process Development for API's & Intermediates. Literature Search, Preparation of Laboratory Development report and Technology transfer document Exposure of Kilo lab / Pilot plant/plant. Process commercialization. Validation Knowledge for GMP, GLP, cost analysis. Patent & Regulatory Product 1) Antibiotics : Cephalosporins, Penicillin and Carbapenems. 2) Non-Antiblotlcs: Cardiovascular, CNS. ami diabetic,  NSAIDs , Analgesic ctcARD - Analytical.

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