About the Company
The firm is more than 200 years of experience in producing the quality standards helping major bio-pharmaceutical firms in delivering high-quality medicines to relieve many diseases. This is an organization supplying methods at free of cost for the product development and maintaining the standards. This is distributed across the globe serving mankind.
About the Job:
Experience: 3-6 years of experience in Analytical laboratory
Qualification: Need to have master's degree in MSc and M. Pharma
Demonstrated history of reliably in finishing the tests on time, with top notch for plan and Programming interface's.
Capable in chromatographic examination, especially in HPLC, GC.
Capable in dealing with other related logical instruments, for example, Auto titrator, KF, FTIR, UV spectrometer, Thermal equipment, Elemental analyzer, SOR, TLC and so on.
Capable in wet synthetic examination.
Should have powerful relational abilities, both composed and verbal.
Ought to know about Engage programming.
Should have great specialized and insightful abilities to determine or investigate issues autonomously.
Ought to have major areas of strength for an of GLP guidelines and openness to outer administrative reviews.
Having knowledge of Lab Management System (LMS) and Electronic Laboratory Notebook, ERP, QR coding system is an added advantage.
Hands-on experience in handling instruments like MS is an added advantage.
Understanding monograph procedures and participating in compendial methods for reference materials (USP, FCC, NF, etc.).
Prior experience in a high-volume pharmaceutical manufacturing QC laboratory or Analytical R&D, or a contract pharmaceutical analytical laboratory testing organization is a plus.
Awareness of ISO/IEC 17025 is desirable.