Atyab International Services Required Microbiologist ( Food and Water )  Details are provided below  Atyab International Services, the first International conformity assessment body from the Sultanate of Oman providing comprehensive services in testing, inspection and certification is currently seeking a qualified Microbiologist for their team.  The ideal candidate will have a strong background in Microbiology specifically in Food and Water Testing and possesses the necessary qualification and experience to uphold the highest standards in laboratory testing and ensure compliance with International regulations including ISO 17025 1. Qualifications -  -Bachelor’s or Master's Degree in Microbiology, Food Science, Environmental Science or a related scientific discipline or  equivalent - Knowledge of ISO 17025 standards and laboratory accreditation process  2. Experience-  a. 5 + Years in Microbiological testing of Food and Water  b. Strong...

Exciting Career Opportunity for R and D at Erba Transasia  Details are provided below  1. Position- Executive/ Sr. Executive R and D  2. Qualification- M. Sc / Ph. D. ( Microbiology/ Biotechnology/ Biochemistry)  3. Experience-  a. M. Sc. With 3 to 5 Years experience  OR Ph. D Freshers/ 1 to 2 Years in Immunoassay development  b. Hands on experince with Fluorescence Technology  4. Key Responsibilities-  a. Development of Immunoassays  b. Reagent Development- Synthesis and bio conjugation of Nano materials for assay Development  c. Execution of experiment for development and validation of Fluorescence based kits  d. Testing and clinical validation of developed immunoassays  e  Compile daily experimental reports and update team lead. 5. Job Location- .Mumbai  6. Apply on - careers@transasia.co.in 

Vacancy in Biotenic Pharma Private Limited  The Biotenic Pharma Private Limited Genetic Toxicology team is seeking for a Senior Research Scientist in the Genetic Toxicology Department  Details are provided below  1. Position- Senior Research Scientist  2. Educational Qualification- M. Pharma/ M. Sc. / M. Tech / Ph. D. / Life Sciences ( Pahrma / Biotechnology/ Biochemistry/ Other Biology Field)  3. Experience- Experience in Genetic Toxicology studies specifically with OECD TG 471 , 473, 474, 475 and 476.  4. Technical Skills- Proficient in conducting bacterial reverse mutation assays , in Vitro chromosomal aberrations , in vivo micronucleus assays , slide reading , microscopy , animal handling , data analysis software,  and laboratory instruments.  5. Knowledge- In depth understanding of genotoxicity mechanisms and regulatory requirements in Toxicology  6. Communication Skills - Excellent verbal and written communication skills...

URGENT HIRING ALERT  Vacancy at IPL Biologicals Limited  IPL Biologicals Limited actively seeking applications from passionate VAM Manager Candidates to join dynamic team at Biologicals Limited Haridwar  Job Description-  a. Lead the development of VAM including strain , cultivation and Formulation  b. Conduct testing to optimize the VAM process  c. Collaborate with R and D teams to explore product quality  d.  Identify innovative Methodologies and technologies to increase VAM production efficiency and monthly / yearly production targets  e.  Oversee the entire production cycle of VAM from inoculum development to packaging  f. Develop and maintain a robust quality assurance program for VAM production  g.Conduct regular quality tests and Analyses on VAM products.  h. Implement Corrective actions for quality issues and ensure products meet regulatory standards  Mandatory Skills -  VAM , VAM process , Fo...

Hiring  For Upstream Department Candidate required for Upstream in Classical Fermentation bulk Production for API Pharma. Designation – Senior Executive Experience – 8+ Years Qualification – B.Tech/M.sc/B.sc (Biotechnology) Location - Pithampur - SEZ Responsibilities: 1. Preparing, reviewing and approving the instruction for the production of intermediates and APIs according to written procedure. 2. Production of APIs and intermediates according to pre-approved instruction. 3. Reviewing all production batch records ensuring these are completed and signed. 4. Ensure that the production deviations are reported and evaluated, Critical deviation are investigated and conclusions to be recorded. 5. Ensure that the production facilities are clean and ensure schedule of cleaning 6. Ensure that the necessary calibration is performed and records kept. 7. Ensure that validation protocols and reports are reviewed and approved. 8. Ensure that the premises and equipment are mainta...

  Urgent Requirement for Microbiology Department at Natco Pharma Formulation division Kothur (Near Shadnagar) Department: Microbiology (Formulations) Qualification: M. Sc (Microbiology) Experience: 3 to 8 Years Work Location: Kothur (50 KM from Hyderabad city) Job Requirements Positions - Assistant Officer / Officer 1. Experience in Water Sampling & Testing. 2. Experience in Media Preparation & Method Validations. Positions: Executive / Senior Executive 1. Review and approval of Microbiological analysis reports 2. Preparation of SOPs related to QC Microbiology. 3. Implementation of Good Microbiological Laboratory Practices at Work. 4. Review of microbial test results of water samples as required. 5. Maintenance of laboratory area and related monitoring records as applicable Interested candidates can share CVs at jaganmohan.p@natcopharma.co.in Click Here For Details

Join Biosimilar Manufacturing Team at Kwality Pharmaceuticals Ltd.   Kwality Pharmaceuticals Ltd.  are expanding our team and seeking talented professionals to be part of our Biosimilar Manufacturing Plant in Amritsar. If you're passionate about biologics and biosimilar production,  have exciting opportunities for you! Open Positions and Requirements: 1. QA Specialist – Qualification (4-6 years) -Expertise in equipment qualification (IQ, OQ, PQ) and utilities validation in view of biologics manufacturing. -Ability to prepare and review qualification protocols and reports. -Track periodic calibrations and validations. 2. QA Officer – Regulatory Submission (1-3 years) -Experience in preparing regulatory submissions for biosimilars (e.g., CTD, ACTD). -Understanding of domestic and global regulatory guidelines (RCGM, DCGI, etc.). -Proficiency in compiling and reviewing quality and technical documents for submissions. -Familiarity with post-submission activities ...