Analytical Scientist Microbiology

Job Summary
We are seeking a dynamic and experienced Analytical Scientist in Microbiology to design and execute experiments analyse and interpret data and report the results. Able to maintain laboratory equipment troubleshoot instrumentation and ensure accurate record keeping. And maintain the safety compliance and efficient functioning of the microbiology laboratory by complying with all safety standards and regulatory requirements. Regular communication with the team lead and continuous improvement of procedures and protocols for the overall success of the laboratorys operations.

Roles & Responsibilities

• You will be responsible to organize the microbiology laboratory for safety and good laboratory compliances. Report discrepancies in procedures/ products/ materials/people practices/ systemic issues/ any other abnormalities to microbiology team lead.
• You will be responsible to initiate and implement updated procedures as per lab requirement. Online documentation will be required.
• You will be responsible for planning the daily activities for microbiology testing and ensure availability of worksheets for all the microbiology samples and tracking timely planning and testing.
• You will be responsible to ensure that the Standard Operating Procedures /Standard Test Procedures are replaced in their designated place after completion of the analysis.
• You will be responsible for timely submission of daily status report to team lead.
• You will be responsible to execute the periodical environmental monitoring of the aseptic area as per procedures.
• You will be responsible to ensure the Good Laboratory Practice (GLP) compliance for all instruments/Equipments located at Microbiology lab.
• You will be responsible for analysis of finish product raw material and excipient Microbial Limit Test method developments and method validations.
• You will be responsible for Antimicrobial Efficacy Test method development and method validation and batch analysis.
• You will be responsible for various validation methods like Sterility method validation and Bio-burden method validation for batch analysis by open method and closed method.
• You will be responsible for Identification of microorganism through Vitek-2 compact.
• You will be responsible for Bacterial endotoxin test method validation and batch analysis by Gel clot method and kinetic method Chromogenic and Chromogenic and Turbid metric method.
• You will be responsible for Microbial kill rate study as per the Food and Drug Administration (FDA) requirements and Microbial potency assay method development and method validation study.
• You will be responsible for Media preparation and reconciliation culture handling and culture maintains and stock maintenance.
• You will be responsible for Handling of steam sterilizer Laminar Airflow (LAF) Biological Safety Cabinet (BSC) and Isolator.
• You will be responsible for Environmental monitoring in aseptic areas and purified water Water for injection (WFI) analysis and trends preparation. Also adhere to the safety and quality aspects.
• You will be responsible for Operation of Laboratory Information Management System (LIMS) software Operation of International Caries Detection and Assessment System (ICDAS) and Allyone software. 

Qualifications :

Educational qualification: . in Microbiology/Biotechnology

Minimum work experience: 2-3 years of experience 

Skills & attributes:  
Technical Skills

• Experience in Medical Laboratory technology (MLT) method developments and method validations and batch analysis.
• Experience in Antimicrobial test method development and validation and batch analysis.
• Experience in Sterility method validation and batch analysis by open method and closed method.
• Experience in Bio-burden method validation and batch analysis for in process samples.
• Knowledge on Microbial kill rate study as per the Food and Drug Administration (FDA) requirements.
• Knowledge on Microbial potency assay method development and method validation study.
• Experience in Bacterial endotoxin test method validation and batch analysis by Gel clot method and kinetic method Chromogenic and Chromogenic and Turbidity metric method.
• Expertise on Microbiology Lab related Instrument/Equipment calibration (Balance pH meter).
• Experience in Preparation of Method validation protocol and report.
• Experience in Preparation of Standard Operating Procedures /Standard Test Procedures.
• Knowledge on aseptic process and behaviour.
• Knowledge on Deviation Incidents with investigation and associated CAPA.
• Experience in handling of regulatory audit.

Behavioral Skills

• Excellent communication and interpersonal skills.
• Ability to work with cross functional teams.
• Strong analytical and problem-solving abilities. 

Additional Information :

About the Department

Integrated Product Development Organisation                                         

We integrate our deep science capabilities and cutting-edge technology to develop innovative accessible and affordable therapies for patients worldwide. We are a science-driven innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API Formulations Clinical Intellectual Property and Regulatory Affairs. We are serving 55 markets including USA Canada Europe China LATAM ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API) Oral formulations Parenteral (Injectables Opthalmics) & Other dosages
Our product development efforts drive a portfolio of more than 1000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates we have filed 1071 patents and also published over 1000 papers for peer review over the years.

Benefits Offered
At Dr. Reddys we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddys are on par with the best industry standards. They include among other things and other essential equipment joining & relocation support family support (Maternity & Paternity benefits) learning and development opportunities medical coverage for yourself and your family life coverage for yourself.

Our Work Culture
Ask any employee at Dr. Reddys why they come to work every day and theyll say because Good Health Cant Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations but as a means to help patients lead healthier lives and were always attuned to the new and the next to empower people to stay fit. And to do this we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system they can make magic.
For more details please visit our career website at

Remote Work :

No

Employment Type :

Full-time