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Analytical Research & Development

Asst. Manager/Sr. Executive: M.Sc. Chemistry, 5-7 Years hands on experience of XRPD, DSC, TGA, SEM and Particle size analysis etc.

Engineering

Sr.Manager: BE/B.Tech/ M.Tech [Mech]: 10-12 years experience in Engineering Maintenance of cGMP Compliant API / Chemical Plant. Independently responsible for all maintenance activities, documentation as per cGMP, OSHA, ISO in the respective areas.  

Production

1) Executive / Sr. Executive : B.Sc/M.Sc MSc (Org. Chemistry) : 8 - 12 Years experience.

Job Description :

  • Execute the production plant as per shift operations to achieve consistent product quality, quantity and yield.
  • Trouble shooting of process and operational issues on shop floor.
  • Supervise batch charging and verification of RM Quantities and responsible for maintaining Batch Production records.
  • Check equipments and connected accessories and operate them as per the process norms.
  • Monitor and maintain all parameters as per SOPs and ensure strict compliance with GMP and safety norms
  • Experienced candidates from Pharmaceutical / Chemical Industry only may apply.
  • Knowledge of SOP's and manufacturing processes will be an added advantage.
  • Exposure to regulatory audits and eagerness to work on the shop floor is desired

2) Chemist / Sr.Chemist : B.Sc/M.Sc: 2-8 Years experience.

Job Description :

  • Supervise batch charging and verification of RM Quantities and maintain Batch Production records.
  • Check equipments and connected accessories for cleanliness and operate them as per the process norms.
  • Monitor and maintain all parameters as per SOPs and ensure strict compliance with GMP and safety norms.
  • Seek assistance for or escalate all process deviations/maintenance jobs. Experienced candidates from Pharmaceutical / Chemical Industry only may apply.
  • Knowledge of SOP's and manufacturing processes will be an added advantage.
  • Experience in manufacturing processes such as compression, granulation, coating, capsule filling will be an added advantage.
  • Exposure to regulatory audits and eagerness to work on the shop floor is desired.

3)Shift In-charge: M.Sc./B.Sc./B.Pharma: 8-10 Years experience in API bulk drug production activities as per cGMP guidelines.

4)Chemist: M.Sc./B.Sc./B.Pharma: 1-4 Years experience in API bulk drug production activities as per cGMP guidelines.

Quality Control

Chemist / Executive / Sr. Executive : B.Sc/M.Sc (Chemistry) : 5-8 Years experience.

Job Description :

  • Responsible for allocation and review of analysts work against standards.
  • Maintaining RM control samples, performing routine analysis and reporting test results, conducting internal audits and preparing trend reports.
  • Taking necessary investigative measures for out-of-specification laboratory results and facilitating achievement of production schedules.
  • Responsible for staff development through proper induction and training.
  • Analytical experience in the pharma industry will be preferred.
  • Should be well versed with QC activities of API in process labs.
  • Exposure to regulatory audits and eagerness to work on the shop floor is desired

Quality Assurance

1) Manager QA : B.Sc/M.Sc (Chemistry) : 10 - 15 Years experience.

Job Description :

  • Follow up with Regulatory Audits and Customer Audits.
  • Reviewing all Regulatory documents prior to submission to Regulatory Affairs Department.
  • Implementation of Quality Management System across the site.
  • Data review and submission to RA for DMF deficiencies.
  • Investigations are carried out during Batch deviations, OOS results and customer complaints.
  • Validation Master Plan, Validation Protocols Validation Reports and qualification documents
  • Approving changes to the existing systems, documents, processes, specifications and test methods of Raw materials, Intermediates and Finished Products.
  • Exposure to regulatory audits and eagerness to work on the shop floor is desired

2) Executive / Sr. Executive : B.Sc/M.Sc (Chemistry) : 5 - 8 Years experience.

Job Description :

  • Review process documents stage-wise and facilitate timely release of batches.
  • Perform IPQA checks during production.
  • Review and compile deviations and change controls.  Ensure quality compliance of the product through internal audits.
  • Knowledge of SOP's and IPQA processes and exposure to external audits.
  • Experienced candidates from Pharmaceutical / Chemical Industry preferred.
  • Exposure to regulatory audits and eagerness to work on the shop floor is desired

Microbiology

Manager / Executive : B.Sc/M.Sc : 2 - 8 Years experience.

Job Description :

  • Responsible for maintaining of SOP’S,STP’S,Validation Protocols and reports.
  • Implementation and ensuring the Quality Management system in Microbiology department.
  • Maintaining of inspection & Test Methods.
  • Responsible for overall Microbiology Department functions.
  • Exposure to regulatory audits and eagerness to work on the shop floor is desired
 

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