Biocon Biologics is driven by a strong sense of purpose and the unwavering commitment to serve patients and healthcare systems across the globe by unlocking equitable access to high quality biosimilars.

Patent search, literature search, Pre formulation study, Formulation optimization with QBD approach. Scale up at plant level.

Experience into Complex Injectable and Complex Equipment like HPH, Isolator, Wet Mill, ANFD. Experience in injectable and Ophthalmic dosage form like suspension & Gel forming and simple ophthalmic range.

Accuprec Research Labs Pvt Ltd. is FDCA approved, OECD-GLP, NABL accredited and ISO 9001:2015 certified CRO. Head Quarter of the CRO is located at Ahmedabad and branch offices at Canada and USA.

Strong knowledge of GMP, GDP, and regulatory compliance for pharmaceutical warehousing. Exposure of various instruments/ software like empower 3, LIMS and other software.

Candidate should be well versed with operation and maintenance of ointment manufacturing plant and handling PLC, SCADA. Handling of tube filling activity and packing activity of ointment, creams, lotions.

The search for answers to Alzheimers disease and other neurodegenerative disorders remains one of the most pressing goals in brain research. Maciej J. Stawikowski, Ph.D., an assistant professor of chemistry and biochemistry at Florida Atlantic Universitys Charles E. Schmidt College of Science, believes the key may lie in understanding how cholesterol and other lipids move through cells and affect their communication.

BPharm or Post Graduate Degree in Basic, Allied Sciences Biotechnology, Biochemistry, Chemistry, Material Science, Environment Science, Any discipline of Life Sciences OR Graduate, Post Graduate Degree in Professional Course.

Graduate degree in Chemical Sciences Preferably in organic chemistry, Pharmaceutical Sciences. Experience in the area of Phytochemistry, working experience of chromatographic methods Extraction of medicinal and aromatic plants.

Host-Diet-Gut Interaction Post Vegan Diet in Pediatric Autoimmune Hepatitis Project. Graduate in Life Sciences from a recognized university; AND Three years work experience from a recognized institution. OR Masters Degree in Life Sciences.

B.Pharmacy from recognized institute, Approved Diploma in Pharmacy recognized by the pharmacy council of India and registered as pharmacist under the Pharmacy act 1948.

Organize and dispense the drugs, medicines to the employees, pensioners. Maintain digital records of all the dispensary items, drugs. Any other work as assigned by the Competent Authority from time to time. experience as an apprentice trainee from a recognized Institution in Pharmacy trade

Lead optimization and in vivo proof-of-concept studies of novel alpha-ketoamide based protein aggregation modulators for Alzheimers disease. First class M.Pharm / M. S. Pharm. / M.Tech Pharm/ M.Tech in Medicinal Chemistry/Pharmaceutical Chemistry with GATE/ GPAT/ CSIR UGC-NET including lectureship or equivalent examination

Applications are invited from suitable candidates for the post of Research Associate to work on various NDDS level drug delivery systems for clinical applications in the IPCA foundation industrial project sanctioned to undersigned. M. Pharm, M.S. Pharmaceutics , Industrial Pharmacy or any other equivalent discipline.

B.Pharm with degree, diploma in Clinical Research Methodology. The candidate with a minimum 1 year experience in conducting clinical trial will be given preference. The candidate having experience in insurance sector will be preferred. TMC is an autonomous body funded, controlled by the Department of Atomic Energy, Government of India.

Exposure to OSD Manufacturing operations like Granulation, Compression, Pellet coaling, Capsule filling, Primary Packing & Secondary Packing. Expertise in e-BPR and e-log will he added advantage. Experience of HPLC, UV spectrophotometer and Dissolution Tester operation. Experience of Analytical Method Validation/Transfer. Experience of GC, ICPMS and/or LCMS operation.

Redaction of clinical trial documents in accordance with evolving global regulations. Develop training and drive change management for novel processes related to the EU Clinical Trial Regulation and other regulations. Manage and Coordinate redaction of clinical documents in accordance with EMA Policy 0070, Health Canada Public Release of Clinical Information, PRCI, EU Clinical Trial Regulation, and other global regulations. 

B.pharmacy and approved diploma in pharmacy. ECHS invites application to engage featuring medical, paramedical and non-medical staff on contractual bases in ECHS polyclinics ie Amritsar, Tarn Taran and Ajnala for a period of one year