M.Pharm

2-8 years of experience in BMR, QMS, PQR, Qualification, AQA, ERP, Control Sample, Process Validation.

The candidates should possess M.Sc. Life sciences, Toxicology, M.S. Pharm. or M. Pharm. in Pharmacology or Pharmacology and Toxicology, Biotechnology PG degree in other relevant branches of life sciences.

Having surrounding knowledge of HPLC, GC, IR, UV, Dissolution and other QC equipment. Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater.

Must know process validation cleaning validation verification and hold time studies. Candidate should also have exposure to EU, MHRA, and USFDA regulatory audits.

To Perform IPQA, To Perform Line Clearance, To withdrawn FG Sample, To support in Validation Activities

Taking the responsibility for bacterial upstream, lysis & Solubilization process. Performing sampling activity during batch processing and updating sampling annexures. Performing pH and conductivity meter calibration, filter integrity test, filtration activity.

To participate in sample processing for PK, ADME assays and handling of LCMS/MS. Ability to adapt to the dynamic team environment. Processing of different matrices samples of PK studies. Optimization of test compounds manually as well as automated on LCMS/MS. M.Pharm in Pharmaceutical sciences, Pharmaceutical Analysis who has interest and passion for LC/MS related bioanalysis

PharmD, M. Pharm, MD Pharmacology candidates with at least one-year experience in Handling pharmacometrics, PKPD analysis. Experience in handling Pharmacometrics software is desirable.

Within this program you will thrive within a fast-paced, dynamic study design. As we are fully embedded with this global pharmaceutical client, you will experience a true one team approach that provides limitless opportunity to develop through training, mentorship, and support from leadership.