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Recruitment for M.Pharm, B.Pharm, M.Sc in Multiple Departments at Zydus Cadila | walk in

 

Clinical courses

 

Clinical courses

Zydus Cadila is one of Indias leading healthcare companies and a global healthcare provider with strengths all along the pharmaceutical value chain. The groups state-of-the-art manufacturing infrastructure is spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim and the R &D Centers are spread across Ahmedabad, Baroda and Mumbai (Thane).

Executive/Sr. Executive/Asst. Manager/Dy. Manager - Biologics
Quality Control (Protein analytics) / (Bio assay) / (Microbiology) / (Physico chemical): M.Sc./B.sc (Biotechnology / Biochemistry / Microbiology / Chemistry) with 2-8 years of hands on experience of handling equipment & tests such as HPLC / UPLC, CZE, UV Spectrophoto-meter, SDS-PAGE, IEF, RT-PCR, ELISA, Bioassay, microbial identification, microbiological testing of material/products, sterility testing, BET, environmental monitoring of cleanroom, water system monitoring and microbiological validations/studies etc. GC, IR, KF auto titrator, coulometer, melting points, should also have experience on chemical analysis of raw materials, water and packaging material, handling stability studies and GMP documentation. Must be familiar with cGMP requirements.

Quality Assurance: B. Pharm/M. Pharm- M.Sc. (Biotechnology) with 2-8 years of hands on experience of IPQA activities, reviewing of batch manufacturing records, handling of qualification / validation activity, change control, deviation, investigation, CAPA, QMS, vendor qualification activities. Must be familiar with cGMP requirements.

Manufacturing (Downstream Process) / (Upstream Process): MSc. Biotechnology / Biochemistry, M. Tech/B.Tech with Biotechnology / Biochemistry / Biochemical engineering with 2-8 years of hands on experience of handling equipment such as Chromatography systems, Ultrafiltration systems, Bioreactor, Disc Stack Centrifugation, Filtration Techniques, knowledge of GMP documentation. Must be familiar with cGMP requirements.

 

Scientific Officer/ Sr. Scientific Officer/ Research Associate / Sr. Research Associate - ZRC
Mammalian cell culture (Clone Development): MSc.(Any Life sciences area)/M.Pharm with Biotechnology with 3-4 years of experience in mammalian cell culture such as handling of cell lines, optimization and execution of stable/ transient transfections, clone screening, media/process optimization at shake flasks & small scale bioreactors to improve yields & quality, cell bank preparations., Should have sound scientific know-how of clone generation processes in CHO cell line.

PK/PD/ Immunogenicity (Clone Development and Immunoassays) : MSc. (Any life sciences area) / M.Pharm (Biotechnology/Pharmacology) with 2-5 years of experience in activities like development, validation & execution of PK/PD/Immunogenicity/Nab assays (ELISA/CLIA/MSD) to support pre-clinical & clinical studies for Biosimilars/Biologics in a GLP set up, experience in animal handling, preparation of MOAs, validation plans & reports, study reports. Should have scientific understanding of PK/PD/ADA of biologics in animals &humans; basic knowledge of biostatistics.

Molecular Biology (Clone Development): PhD in field of life sciences(Preferred Molecular Biology)/M. Tech(Biochemistry/Biotechnology) with 3-5 years of experience in recombinant DNA technology,hands of experience in various Cloning techniques, DNA sequencing, Hybridization, Real time PCR & SDS PAGE, western blot, IEF etc. for protein characterization. Should be able to independently design strategies for molecular cloning & molecular biology based assays, should be well versed with routinely used Bioinformatics software. Should have a good scientific understanding about biologics

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SENIOR/MIDDLE LEVEL POSITION:
Process Development (Upstream and Downstream Processes): Ph.D (Microbiology / Biotechnology / Biochemistry / Cell Biology / Biochemical Engineering with more than 10 years of hands-on experience in upstream and downstream operations like handling mammalian cell culture process, column chromatography, process development and scale-up. Should have sound knowledge on upstream / downstream manufacturing processes of recombinant biological products. Should have good communication and scientific report writing skills and proven track record to lead a sizeable team.

Characterization of recombinant protein products: Ph.D (Protein Biochemistry / Cell Biology) with more than 10 years of hands-on experience in biophysical and functional characterization of protein products. Should have sound knowledge in analytical method development and validation with good communication and scientific report writing skills and proven track record to lead a sizeable team. Must be familiar with state-of-the-art analytical techniques related to structural analysis, physicochemical characteristics and cell-based bioassays of protein products.

Downstream Purification Process: MSc. (Biochemistry / Biotechnology / M. Tech) with 3 5 years hands-on experience in purification of recombinant proteins, process characterization and protein analysis. Should also have adequate knowledge of downstream chromatography and filtration processes and ability to write scientific documents related to the work. Must be familiar with industry scale purification process of recombinant proteins.

Protein Analytics : MSc. (Biochemistry / Biotechnology / M. Tech) with 3 5 years hands-on experience in HPLC / UHPLC and biochemical analysis of recombinant proteins including various types of protein estimation methods. purification of recombinant proteins, process characterization and protein analysis. Should have sound knowledge in analytical method development and validation with good communication and scientific report writing skills.

Additional Information:
Experience: 2 - 7 Years
Industry Type:Pharma / Biotech / Clinical Research
Role:Other
Functional Area: Other
Location : Ahmedabad

Interview Details:-
Date :-  11.02.2017
Venue Address :- Keys Hotels
#7/1, Hosur main road,Singasandra
Bengaluru-560 068
Timings :- 09.00am to 05.00pm

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