VerGo Pharma Research Laboratories Hiring in Manufacturing, Analytical Development, QC, and Engineering

Vergo Pharma Research Labs Goa Hiring For Production Executive
  • Full Time
  • goa

GOA Pharma Jobs: VerGo Pharma Research Laboratories Hiring in Multiple Departments

VerGo Pharma Research Laboratories Pvt. Ltd., a leading Contract Development and Manufacturing Organization (CDMO) based in Verna, Goa, is currently seeking qualified candidates for various positions in Manufacturing, Analytical Development, Quality Control, and Engineering. If you have the relevant experience and qualifications, this is an excellent opportunity to advance your career in the pharmaceutical industry.

Job Location: Verna, Goa

About VerGo Pharma Research Laboratories: VerGo Pharma is renowned for its commitment to quality and innovation in pharmaceutical research and development. The company is expanding its team and looking for talented professionals to join their dynamic workforce.

Available Positions and Qualifications

1. Analytical Development

  • Qualification: MSc/B.Pharm/M.Pharm
  • Experience: 2-3 years in Analytical Development and Validation
  • Responsibilities:
    • Conduct analytical method development and validation.
    • Perform stability testing and document results.
    • Ensure compliance with regulatory standards.

2. Engineering

  • Qualification: Diploma or BE in Electrical Engineering
  • Experience: 2-5 years in pharma documentation, validation, and protocol execution
  • Responsibilities:
    • Oversee electrical systems and ensure their proper functioning.
    • Validate and execute engineering protocols.
    • Maintain detailed documentation of engineering processes.

3. Quality Control (QC)

  • Qualification: B.Sc/M.Sc/B.Pharm
  • Experience: 2-3 years in HPLC analysis, RS analysis, and chemical analysis
  • Responsibilities:
    • Conduct routine and non-routine analysis of raw materials and finished products.
    • Utilize HPLC and other analytical techniques.
    • Maintain accurate and detailed documentation.

4. Manufacturing

  • Qualification: B.Pharm/M.Pharm
  • Experience: 2-4 years in Granulation, Compression, Coating
  • Responsibilities:
    • Oversee manufacturing processes such as granulation, compression, and coating.
    • Ensure compliance with GMP standards.
    • Maintain detailed records of production activities.

How to Apply

Interested candidates are invited to send their CVs to Ensure to include details of your current CTC and notice period.

Upload your CV/resume or any other relevant file. Max. file size: 3 GB.

You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

Share with your friends and pharma related groups.Join whatsapp - -