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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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FRESENIUS KABI ONCOLOGY LIMITED- MULTIPLE OPENINGS IN QUALITY ASSURANCE, PRODUCTION AND QUALITY CONTROL MICROBIOLOGY DEPARTMENT

WALK IN INTERVIEW 
FRESENIUS KABI ONCOLOGY LIMITED BADDI ( HP) - MULTIPLE OPENINGS IN QUALITY ASSURANCE, PRODUCTION AND QUALITY CONTROL MICRO DEPARTMENT 
Details are provided below 

Walk In Interview- 17 November 2024
 ( Sunday) 
Time - 09.30 AM To 04.00 pm 
Criteria - 2 to 8 Years 
Designations - Officer / Executive/ Sr. Executive 
Interview Venue - Hotel Spice , NH 72 , Selaqui Industrial Area , Selakui, Shankerpur, Hakumatpur, Uttarakhand 
Contact Person - Shikha Sharma ( 1785- 667815/251315)
E mail - Shikha.sharma@fresenius-kabi.com 
Note - Candidates are requested to carry updated CV , one passport size photo  and latest salary slip. 

1. Department- Quality Assurance 
2. Qualification- B. Pharm/ M. Pharm 
3. Skills - 
a. Preparation anf review of risk assessment 
b. Investigations , evaluations and implementations of CAPA and effectiveness check evaluation 
c. MQA operations change  control , actions items and internal audits and response 
d. Tracking and trending of deviations/ events, shop floor MQA compliance,
e. Review of batch documents, protocols , reports , SOPs and trend reports etc 
f. Cleaning and process validation protocol /reviews/oversight/ trainings 
g. Global SOP implementation plan and compliance verification 

1. Department- Production 
2. Qualification- Diploma/ B  Pharm 
3. Skills- 
a. Filling Process 
Experience and knowledge of aseptic operations, media filling , cleaning and disinfection , depyrogenation , sterilization, area monitoring etc 
b . Lyophilization Process 
Experience and knowledge of Lyo preparation, Lyo loading and uploading, basic troubleshooting, handling of aseptic Interventions etc 
c. Compounding Process 
Experience and knowledge of bulk preparation, CIP and SIP of Vessels, component preparation, Autoclave Operations, cleaning and sanitatization , area monitoring. 
d.  QMS 
Experience of QMS Activities in Sterile Manufacturing that is change control, deviations, risk assessment, CAPA and compliance 

1. Department- Quality Control Microbiology 
2. Qualification- M  Sc. Microbiology/ Biotech
3. Skills - 
a. Proficient in environment monitoring in all three methods of viable and non viable 
b. To be proficient in water System, Sampling and testing ( Microbial physicochemical) of all types of pharmaceutical water types. Should be knowing the requirements and specifications of different water systems used in pharmaceutical purposes 
c. Proficient in Bioburden , TVAC, TYMC and Microbial Limit Tests with pharmacopial requirements and have performed method sutaibility studies for different test methods 
d.  Media Preparation, management and sterilization proficiency is basic requirement with ability to perform and manage media relaase and discard process. Proficient in antibiotic assays will be an added advantage. 

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