vacancies

Candidate having experience in network pharmacology, cell culture protocols, molecular biology protocols, animal handling, surgery in experimental animals, will be given preference. Experience or basic knowledge in in vitro cell culture and fundamental knowledge of molecular pharmacology will be preferred.

PhD with 3 years experience in Biological Science, Biotechnology, Biochemistry, Bioengineering, Pharmaceutical Technology or any branch of Life Sciences Relevant to essential criteria. 

Post Graduate degree in Biotechnology Life Science subject with two year experience from recognized university. Post Graduate degree in Bio informatics subjects with two year experience from recognized university.

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.

Have good exposure in Plant Maintenance & Instrumentation related work in sterile facility. Have good exposure in Sterile IPQA & Sterile Qualification Related activity.

Must be from Parenteral background & exposure to Aseptic vial, Bottle filling process is desirable. To be aware and responsible for achieving quality objective and fulfilling the requirements of applicable quality procedures. Sound technical knowledge of Aseptic area & Controlled area related activities.

As per the batch manufacturing procedures and packing protocols, samples such as in-process samples, finished product samples, stability samples, control samples, cleaning samples, and other samples should be collected and submitted

Having Injectable Experience of Analysis of raw material. In-process, Finish products, Stability testing, Process validation. Hands on Experience of HPLC, GC, LBPC, Osmometer, KF Auto titrator and UV - Visible spectrometer, LIMS,QMS,Participate in Lab incident , OOS, OOT, Analysis of deviation.

Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. Conducting signal detection and risk assessment activities to identify potential safety issues.