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Quality Control, Pharma Industry, R and D, CSIR, Food Industry, Pathology, Medical Writing, coding

Required Drug Substance (Viral Vaccine Experience)- Upstream /Downstream Processing of viral vaccines

Job Opportunity - Drug Substance (Viral Vaccine Experience) Bharat Biotech is looking for skilled professionals with hands-on experience in Drug Substance manufacturing for Viral Vaccines. Details are provided below  1. Location: Hyderabad 2. Experience: 2-6 Years 3. Key Skills & Experience Required a. Experience in Upstream /Downstream Processing of viral vaccines b. Operation and handling of bioreactors, fermenters, centrifuges, chromatography systems, filtration units c.  Knowledge of cell culture techniques (mammalian/avian cell lines)  d. Familiarity with aseptic techniques, GMP documentation, batch records e. Understanding of process optimization, scale-up, and technology transfer f. Exposure to in-process testing, troubleshooting, and equipment cleaning/sterilization g. Ability to work in a regulated, fast-paced manufacturing environment 4. How to Apply Interested candidates can share their updated CV to kiran4978@bharatbiotech.com Mention subject line as: Appl...
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Vacancy In Analytical Development Laboratory (ADL) and Bio-Pharma- M. Pharm/ M. Sc.

WALK-IN INTERVIEW AT TORRENT PHARMA 

Details are Provided below 

1. Job Location-  R and D Centre  Gandhinagar (Gujarat)
2. Department- Analytical Development Laboratory (ADL) and Bio-Pharma
3. Grade - Executive 
4. Experience- 3 to 8 Years 
5. Qualification- M.Pharm/M.Sc
6. Job/Skill Set
a. HPLC/GC/IC method development, Validation and Transfer for API, complex OSD, complex generics products like long acting injectables, nasal sprays, peptide injections, peptide OSDs. Oncology and Topical products etc using various analytical technique.
b. Expertly in peptide characterization
c.  Expertly in clinically relevant dissolution method development and establishing IVIVC/IVIVR.
d. Clesely werking with CRO/CDMO/CTL to develop and validate analytical method using various technique
e. Having exposure to regulated, Semi Regulated & India markets
f. Hands on experience of analytical instruments like HPLC, GC, Ion Chromatography, Particle size analyzer etc.
g. Hands on experience on NG/G Tube, IVRT/IVPT, Solid State characterization, Impurity characterization, API Sameness study
h. Well versed with USP/EP/BP/IP and various current regulatory guidelines (ICH/EMEA/FDA)
i. Hands on experience on Nitrosamine and Genotoxic impurities method development,
j. Validation and Transfers by LCMS/GCMS
k. Expertise in routine analysis and FnD Suppert, Comparative evaluation of methods with alternative vendor methods versus existing primary vendor and regulatory impact analysis
l. Experience in Dissolution method development, Comparative dissolution, Multimedia dissolution and statistical evaluation, its report preparation and interpretation of data.
m. Hands on experience on Preparation of STPs for API, Excipients, KSM, Intermediate,
n. In-process and Formulation for all tests.
o. Well versed with instrunient Calibrations and GLP Practices.
p. Understanding of ICH guidance and Regulatory expectations is much appreciated.

Interview Details 
1. Date 
9th MARCH, 2025 (Sunday)  
2. Venue - 
ROYAL ORCHID GOLDEN SUITES, PUNE
Golden Nest, Opp. Cerebrum IT Park Kalyani Nagar Pune-411014
3. Time: 10:00 AM to 5:00 PM

NOTE - Candidates interviewed during last 6 months need not apply

In case of any Query you may contact
devalmodi@torrentpharma.com |
vilshashah@torrentpharma.com |nitinsingh@torrentpharma.com
(M) +91 6359621127

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