Identify and develop new business opportunities in global markets. Build and maintain strong relationship with international clients and partners Assist contract negotiation proposals and strategic planning for business growth.
Must know process validation cleaning validation verification and hold time studies. Candidate should also have exposure to EU, MHRA, and USFDA regulatory audits.
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
B.Pharm / M. Sc; Handling the Lab instruments of HPLC, Dissolution, D. T., Apparatus, Weighting Balance, Friability, Hardness Tester, FTIR, UV-Spectrophotometer. Analysis of Raw Material, In-process, Finish Products, Stability Tastings, Process Validation, Participate in Lab incident/OOS/OOT/Analytical Deviation.
Proven track record of leading a large, geographically diverse sales team, including at least 2 years of experience overseeing half of India with a positive P and L outcome. Expertise in developing sales strategies, financial acumen, performance management, strategic project leadership, building and nurturing stakeholder relationships.
The candidate must possess a thorough understanding of relevant disease biology, the clinical landscape, emerging technologies, and the competitive environment.
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.