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APDM Pharmaceuticals Pvt. Ltd

APDM Pharmaceuticals Pvt. Ltd is Hiring Hiring for R&D for Analytical Development

Job Description

Department: Analytical Development

Experience: 02-05 Years    

Location: Ahmedabad (R&D)

 

Responsibilities:

  1. Analytical method development / Validation by HPLC / GC.
  2. Analysis of in Process / Stability Analysis of RS, Assay, Dissolution and Other test.
  3. Co-ordination with F&D, QA and Project Management.
  4. Review of analytical Development.
  5. Calibration of instruments.
  6. Carry out standard analytical research on pharmaceutical items.
  7. Putting in place internal processes and systems to guarantee compliance with regulatory standards and cGLP practices for analytical operations at internal research and development centers.
  8. Troubleshooting concerning test procedures, stability analyses, test outcomes, and, if required, developing new experiments
  9. Managing the execution and coordination of pharmaceutical product analytical method transfer activities.
  10. Observing the master calibration schedule for the calibration of analytical instruments.
  11. Technical evaluation and analysis of pharmaceutical compounds (API) for project implementation.
  12. Technical document review and clearance prior to dossier batch execution and registration.
  13. Drafting and reviewing analytical development reports, methods of analysis procedures, and specifications.
  14. Writing and reviewing analytical protocols and reports, including those pertaining to method feasibility, validation, transfer, and analysis.

 

Apply on: hr@apdmpharma.com

 

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Job Overview

  • Posted Date : 24-Apr-2024
  • Location : Ahmedabad
  • Qualification : M.Sc/M.Pharm/B.Sc/B.Pharm/Life Science
  • Experience : 02-05 Years
  • Company : APDM Pharmaceuticals Pvt. Ltd

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Company Information

We are a worldwide network of CMOs, CDMOs, and CROs that provide pharmaceutical services. Our organization boasts over a century of CDMO experience, half a century of R&D, and decades of regulatory and quality assurance expertise. In the pharmaceutical industries in the USA, UK, EMEA, Canada, and other PICS countries, we have established ourselves as reputable, trustworthy, and value-added service providers. 

Following the successful establishment of a top-tier CDO business, we have expanded into full-service CDMO and technical service providers to quicken product development, launch, or site transfer for pharmaceutical businesses in an effort to obtain a competitive advantage and larger market share. We have a great deal of expertise handling CMOs and CDOs in Asia, Europe, and the UK in order to transfer technology quickly for projects.

We can collaborate honestly and assiduously with a vast network of wonderful people and business partners. We have been in this business since the 1990s, have seen significant changes over many years, and have adjusted to make a difference.
We have competent technical staff members with the necessary training and expertise.