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Required Freshers and Experienced- Microbiology Trainee , Officer Microbiology Testing, Officer Microbiology Environmental Monitoring

Required Microbiology Trainee , Officer Microbiology Testing,  Officer Microbiology Environmental Monitoring  Anthea Pharma Organizing Walk In Interview For Microbiology for Trainee Microbiology , Officer Microbiology Testing and for Officer Microbiology Environmental Monitoring  About Company-  Anthea Pharma, established in 2019 is a Budding, R&D focused Injectables firm, backed by the prestigious Yashoda Group. Based out of Hyderabad, India, Anthea Pharma has a well equiped R&D facility, and an injectable manufacturing facility, currently capable of manufacturing liquid Vials, Emulsions, PFS, Lyophilized Vials and Ampoules. Anthea Pharma envisions to manufacture for the world and be a global firm focused on injectables needs with consistent supply of highest-quality products across therapeutic segments. Details of Job availability are Provided below  A. Section- Microbiology  1. Position- Trainee Microbiology Environmental Monitoring 2...

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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