Visit the customers as per the generated database and understand the current infrastructure, specified and potential needs. Analysing customer feedback data to determine whether customers are satisfied with company products and services.

Review and approve development protocols, reports, and technical documents for formulation, analytical, and process development.

Full time Bachelors Degree in Pharmacy. Candidate belonging to General/ EWS category and candidates belonging to SC/ST/OBC(NCL)/PWD category applying against unreserved posts should have first class degree/minimum 60% marks in the Minimum Educational Qualification for consideration against unreserved posts.

M.Sc. In Biochemistry / Microbiology / Biotechnology OR M.S. (Pharm.) / M. Pharm / M.Tech. in Biotechnology. Project sponsored by Department of Biotechnology Ministry of Science and Technology, Govt. of India, New Delhi

Masters Degree in Biotechnology / Microbiology from a recognized University or Equivalent. OR PhD in Biotechnology / Microbiology with 3 years of experience in Research and Development in Industry, Academic institutions or Science and Technology Organizations and Scientific activities and services. 

B.S. 4 years programme / BPharm / MBBS / Integrated BS- MS / MSc / BE / BTech or equivalent degree, with 55% marks and passing of NET / GATE test.

M.Pharm in Pharmaceutics with first division. Experience in working on drug delivery optimization and formulation techniques.

Graduation in Science (Eg. B.Pharm, Life Sciences, B.Sc Biotech, Zoology, Botany, tec.) with PG Diploma in Clinical Research is mandatory.

Dean, Professor, Associate Professor, Assistant Professor, Research Faculty. Pharmaceutical Sciences (Pharmacology/Pharmacognosy/Pharmaceutical Sciences or Analysis)

Applicants must be Indian citizens currently in the final year of their undergraduate studies or enrolled in a postgraduate program in any academic discipline. Candidates who have completed their undergraduate or postgraduate degrees within the last two years from the internship’s start date are also eligible.

Responsible for quality oversight of personnel, process and practice to meet the cGMP and compliance requirement.

Master degree in Pharmacy, Clinical Pharmacology, Pharmacy Practice, and Clinical Research. OR Pharm.D / MBBS / BDS from a recognised university / institute.

Monitoring production processes, ensuring adherence to Good Manufacturing Practices, and conducting real-time quality checks and inspections on the manufacturing floor. 

M.Pharm, B.Pharm, M.Sc, B.Sc Openings at Stallion Laboratories Pvt. Ltd. For following Positions at OSD Formulation facility - Unit-ll

Senior Manager QC Microbiology is responsible for leading and managing the Micro and Environmental Monitoring teams. This role involves setting goals, managing performance, and providing clear direction in line with company goals, with safety as the foundation of all activities.

Person should know IPQA related activities of OSD Manufacturing activity. B.Pharm, MSc in Production, QA, QC

EHS Monitoring PTW Compliance. Safety Audit Inspection lmpart training. Safety engagement, GMP. Experience of Store activities. SAP knowledge must.

Cancer-fighting antibody drugs are designed to penetrate tumor cells and release a lethal payload deep within, but too often they don’t make it that far. A new study shows how this Trojan Horse strategy works better by exploiting calcium differences outside and inside cells.

Patients with diabetes have an increased risk of complications after stent implantation, according to a study from Karolinska Institutet in Sweden published in Diabetes Care. The study, which includes over 160,000 patients, emphasises the importance of tailoring treatment strategies for this specific patient group.