Fresher

M. Pharm Pharmaceutical Quality Assurance, Pharmaceutics, Industrial Pharmacy and Ph.D. in relevant discipline, preferably in Pharmaceutical Quality Assurance. fresh and experienced; good track record of publications, patents, grants

This is a non-supervisory position to support development of Reference materials. The successful applicant in this role will work on projects including Analytical Method Development for in process samples for synthetic lab.

Promote pharma product portfolio to healthcare professionals and institutions. Develop and maintain strong relationships with doctors, pharmacists, and key opinion leaders. Achieve sales targets and ensure market growth in the assigned territory.

Keep a daily log to document all activities completed each day. Perform duties in compliance with Company’s policies and procedures, including but not limited to those related to HIPAA and compliance.

Hands-on experience in a professional pharmaceutical environment. Exposure to innovative practices, research methodologies, and industry standards. Opportunity to collaborate with skilled professionals and enhance your career prospects.

Handling HPLC. Compilation of Raw Data for Review. Sampling and Release of Raw material and Packaging Mate. Analysis & preparation of water Trends.

0-2 years Knowledge of GMP, FFS, Semi solid manufacturing process, BMR -BPR preparation, knowledge of ALCOA, Audit readiness, EHS adherence in manufacturing

Must have excellent skills and knowledge of bioanalytical sample processing techniques. Very good understanding of current bioanalytical guidelines of various regulatory agencies such as USFDA, ANVISA, ICH etc.

Operational Excellence - Build on technical expertise, expanding it in complementary directions. Use technical expertise and creativity to proactively identify potential problems and address them using appropriate resources in discussion with team leads.