Executive R&D – Analytical Laboratory

Department

Quality Management & Regulatory Affairs

Job Description

  • Perform Stability Studies analysis of finished products at development and commercial stage
  • Development of stability protocols and reporting
  • Execute and maintain equipment calibration

Education

M.Sc Chemistry or Pharm D from a reputable University

Experience

1 to 3 years of relevant experience

Skills

  • Understands HPLC, Spectrophotometer and other equipment’s used in QC Laboratory
  • Awareness of ICH guidelines, USP, BP and other international standards
  • knowledge of analytical techniques
  • GMP awareness
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Executive Quality Assurance

Department

Quality Management & Regulatory Affairs

Job Description

  • To coordinate with production, QC, Supply Chain & export distribution department for timely release of products Conduct audit of batch records that is BMR AR
  • Conduct audit of batch records and make relevant entries in SAP
  • Annual Product Quality Review
  • On time reporting of quality issues found during auditing of batch records with root cause analysis and rectification.

Education

Pharm- D or MSc (Chemistry) from an accredited University

Experience

One to two years of experience in Quality Assurance

Skills

  • Sound knowledge of quality assurance operational process in Pharmaceutical Industry
  • Must have concept & knowledge of cGMP, line clearance & in process checks
  • Must have the ability to review & write technical documents related to batch records
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Sr. Executive New Products Development

Department

Quality Management & Regulatory Affairs

Job Description

  • Formulation and process development of new generic products (tablets, capsules, dry powder suspension)
  • Supervision of lab scale and scale-up batches of new products
  • Preparation of product assessment reports, development protocol and BMRs
  • Initial Risk assessment and preparation of analysis reports

Education

Pharm D from a reputable University

Experience

1 to 2 years of relevant experience

Skills

  • Basic Pharmaceutical and product development knowledge
  • Good communication skills (Written & verbal)
  • Awareness of ICH guidelines, USP, BP and other international standards
  • Knowledge of analytical techniques
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Executive Quality Control

Department

Quality Management & Regulatory Affairs

Job Description

  • Prepare specifications of MDIs
  • Arrange in-process samples during batch manufacturing
  • Prepare online reports for bulk and in-process stage testing
  • Prepare detailed reports at finish product stage testing

Education

M. Sc Chemistry or Pharm D from a reputable University

Experience

1 to 2 years of relevant experience

Skills

  • Understands HPLC, Spectrophotometer and other equipment’s used in QC Laboratory
  • Awareness of ICH guidelines, USP, BP and other international standards
  • knowledge of analytical techniques
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