Zydus Cadila is one of India's leading healthcare companies and a global healthcare provider with strengths all along the pharmaceutical value chain. The group’s 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).
We invite candidates for the following positions based at Ahmedabad for our Pharmaceutical Technology Centre (PTC), Zydus Research Centre (ZRC) and Zydus Biologics.
Post: Supervisor / Officer / Executive / Sr. Executive, Manager, Scientific Officer / Research Associate, Senior Research Associate
Supervisor / Officer / Executive / Sr. Executive
Quality Control (Protein analytics): M.Sc. Biotechnology/ Biochemistry with 2-8 years of hands-on experience of handling equipments such as HPLC/UPIC, CZE, UV Spectrophotometer. SDS- PAGE, IEF, RT-PCR, ELISA etc. Should also have knowledge of handling stability studtes and GMP documentation and must be famiar with cGMP requirements.
Quality Control (Bio-assay): M.Sc. Biotechnology/Bochemistry/ Microbiology with 2-8 years of hands-on experience of conducting Bioassay. Must be familiar with cGMP requirements.
Quality Control (Microbiology): M.Sc. Microbiology with 2-6 years of hands-on experience of microbial identification, microbiological testing of material/products, sterility testing, BET, Environmental monitoring of clean room, water system monitoring and microbioiogical validations / studies. Must be fanilar with cGMP requirements.
Quality Control (Physico chemical): M.Sc. Chemistry with 2-8 years of hand&on experience of handling equipment such as HPLC, GC, IR, KF auto titrator, Coulometer, melting points. Should also have experienoe in chemical analysis of raw materials, water and packaging material.Must be familiar with cGMP requirements.
Quality Assurance: B.Pharm / MPharm-M.Sc. (Biotechnology / Biochemistry / Microbiology) with 2-8 years of handeon experience of IPQA activities, reviewing of batch manufacturing records, handling of qualification/Validation activity, change control, deviation, investigation, CAPA, vendor qualification activities Must be familiar with cGMP requirements.
Quality Reviewer: M Sc. Biotechnology/ Biochemistry/ Aerobiology with 2-8 years of experience in review of analytical data, change controls, deviations, validation and qualification reports, having exposure in investigation of out of specification, out of trend and laboratory incidents. Must be familiar with cGMP requirements.
Manufacturing (Downstream Process): M.Sc. 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, filtration techniques etc. Should also have knowledge of GMP documentation and must be familiar with cGMP requirements.
Manufacturing (Upstream Process): M.Sc. Biotechnology/ Biochemistry, M.Tech / B.Tech with Biotechnology / Biochemistry / Biochemical Engineering with 2-8 years of hand-on experience of handing equipments such as Bioreactor, Oise Stack Centrifugation, Filtration Techniques etc. Should also have knowledge of GMP documentation and must be familiar with cGMP requirements.
Manager
Quality Control: M.Sc. Biotechnology/ Biochemistry /Microbiology with 10-15 years of hands-on experience & knowledge of handing various
QC equipments such as HPLC/UPLC, CZE, UV Spectrophotometer, SDS-PAGE, IEF, RT-PCR, ELISA, Bio-assays etc. Should also have knowledge of handling stability studies, analytical method validations, equipment qualifications and GMP documentation. Must be famiar with cGM Prequirements and have good leadership quality.
Scientific Officer / Research Associate
Analytical Development (Stability): B.Sc / M.Sc. / B.Pharm/ M.Pharm with 2-8 years experience in analyzing stability samples or experienoe in quality control; hands-on experience on HPIC, UV and dissdution testing. The incumbent should have knowledge of ICH stability guideines and should be familiar with cGMP requirements.
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Research Associate
Analytical Method Development: M.Pharm/M.Sc. with 2-6 years' experience in analytical method development of solid oral and injectable dosage forms. The incumbent should have knowledge of regulatory guidelines and hands-on experience on HPLC, UV and dissolution testing.
Research Associate
Formulation Development: M.Pharm with 2-6 years experience in formulation development of solid oral and injectable dosage forms for regulated and emerging markets.
Research Associate/ Sr. Research Associate
Regulaltory Affairs: M.Pharm with 2-8 years of working experience for filling ANDA, pod approval amendments, labelling and exposure to eCTD tool and also working experience for dossier compilation and submission for emerging markets, with exposure to ACTD format.
Research Associate/ Senior Research Associate/ Associate Research Scientist
Process Development (Peptide based API): M.Sc / Ph.D. Chemistry/Biochemistry with 4-10 years of hands-on experienced well- versed in process development for peptide based API's using solid phase techniques. Should have been involved in at least 2-3 tech transfers to the commercial site for above described function, know how of peptide based API requirements (quality) is desirable, process development for peptide based APIs.
Research Associate/ Senior Research Associate/ Associate Research Scientist
Purification: M.Sc/ Ph.D. Chemistry/ Analytical Chemistry with 4-10 years of experience and knowledge of development of purification techniques such as ion-exchange and prep-HPLC. Should have been involved in at least 2-3 tech transfers to the commercial siteslor above described function. Know how of peptide based API requirement (quality and economics) is desirable, development of purification methods for the crude peptide (manufactured by solution/solid phase synthesis).
|
Date |
City |
Venue |
Timing |
|
22nd August 2015 |
Ankleshwar |
Shalimar Hotel, Valia Road, Near G.I.D.C. Reservoir, Ankleshwar, Gujarat-393002 |
9 am to 5 pm |
|
23rd August 2015 |
Ahmedabad |
Hotel President, Off. C.G. Road, Opposite Municipal Market, Navrangpura, Ahmedabad, Gujarat |
9 am to 5 pm |
| 23rd August 2015 |
Baroda |
Hotel Pride Biznotel Alankar Towers, Sayaji Gunj, Vadodara 390020, Gujarat, India |
9 am to 5 pm |
Ref: Times Ascent, dated Aug 20, 2015
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