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Required Junior Research Fellow- Masters in a Virology/Microbiology Biotechnology/Brochemistry/Life Sciences / Genetics

Department of Virology Post Graduate Institute of Medical Education & Research, Sector 12A, Chandigarh-160012 NOMPS/ANRF/25/27 Date: 02/08/2025 Recruitment Notice Applications are invited from eligible candidates for an Extramural (funded by DST-ANRF; Project ID: CRG/2023/007689) research project entitled "Nevel neurovascular organoids to understand the neuropathogenesis of non-polio enterovirus" at Department of Virology at PGIMER, Chandigarh on a tenure basis. The following post will be filled up on a purely contractual basis. 1. Sr No.: 1 2. Name of the Post:Junior Research Fellow 3. No.  Of Post  : 01 4. Qualification:  Essential qualification: a) Masters in a Virology/Microbiology Biotechnology/Brochemistry/Life Sciences / Genetics from recognised institution with first class aggregate b) Scholars who are selected through eligibility Tests-CSIR-UGC NET, (including national Cat-1, II and III), GATE or any National level examination conducted by Central...
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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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