The waiting list for the said post will be approved for the next 12 months, also after the completion of the recruitment process, if the post becomes vacant due to resignation of an employee at any place in the future, appointment orders will be given to the candidates on the waiting list without conducting a fresh recruitment process.

Overcoming Mycobacterium Tuberculosis through Novel Therapeutic Strategies by Targeting its Replisome. Candidates with strong interest and working experience in Organic Synthesis and Nanotechnology may apply.

Degree in Pharmacy ;  Registered as a Pharmacist under the Pharmacy Act, 1948;  3 years experience in a Hospital Pharmacy, Government Medical Store in planning the requirements of drugs/medicines, monitoring the distribution/consumption of drugs manufacturing stock solutions and galenical preparations.

The candidate should have experience in rDNA technology. Have knowledge on Bacterial genome engineering and its analysis. Master degree in Life Sciences, Pharmacology, Chemical Sciences from a recognised university.

Ph.D. in Human Genetics, Genomics, Biotechnology, Biochemistry, Zoology from Indian University, Institute with NIRF ranking or those who have done PhD from abroad. The candidate must have at least two original research publications in Q1 or Q2 journals or SCOPUS, Web of Science listed journals. 

Operate production equipment such as injectable machines, sterile machines, parenteral machines, formulation machines, filling machines, capping machines, compounding machines, washing machines, sealing machines, Visual inspection & packing machines.

After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.

Collecting and submitting in-process samples, finished product samples, stability samples, control samples, cleaning samples, and other samples as per the respective procedures, batch manufacturing records and packing records, protocols. Conducting AQL inspections and periodic inspections of control samples

Responsible for implementation of quality systems within the site. Review of Change controls, Deviations, Investigations, CAPA, OOS and OOT reports. Responsible for review of validation protocols and reports.

Master, Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences, Animal Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University

The posts in the advertisement are not regular posts of the State Government but purely contractual posts. There will be no right of permanence on the said posts and the Government service rules are not applicable for these posts, nor will the applicant be entitled to inclusion in the Government regular service or service protection through the Government or to claim in this regard.

A Diploma in Pharmacy. Must have registered with Tamil Nadu Pharmacy council and must keep the Registration alive by renewing it regularly every year.

D.Pharma in aggregate and registered with State Pharmacy Council or Pharmacy Council of India. Individuals qualified in B.Pharma. Applications invited from Domiciles of Districts Of Tamil Nadu, Andhra Pradesh, Telangana, Union Territory Puducherry (Karaikal, Yanam & Puducherry) And Andaman & Nicobar Island (Nicobar, North & Middle Andaman And South Andaman)

Junior Research Fellow to work under the research project entitled Wastewater to biofuel and bio products : Cyanobacterial bio refinery through a green circular bio-economy.

D.Pharma with minimum 55% in aggregate and registered with State Pharmacy Council, Pharmacy Council of India. Individuals qualified in B.Pharma with minimum 50% marks and registered with State Pharmacy Council, Pharmacy Council of India will also be eligible.

Synthesis of polymer conjugates via different chemistry, preparation of microbeads with X-ray imaging moieties, physicochemical characterization, study the drug loading and release kinetics, biocompatibility evaluation, data collection and interpretation, preparation of reports.

Review of environment monitoring records. Sterility testing of the finished products and sterile API. Should have good knowledge in QMS activities.

AstraZeneca and Alteogen Inc. have entered into an exclusive license agreement for ALT-B4, a novel hyaluronidase utilising Hybrozyme platform technology. Under the terms of the agreement, AstraZeneca will acquire worldwide rights to use ALT-B4 to develop and commercialise subcutaneous formulations of several oncology assets. Alteogen will be responsible for clinical and commercial supply of ALT-B4 to AstraZeneca.

Zydus Life sciences Limited has received final approval from the United States Food and Drug Administration USFDA to manufacture Apalutamide Tablets, 60 mg.