CRAMSN RESEARCH PARK IS ORGANISING WALK IN INTERVIEW Details are provided below 1. Department: Research & Development 2. Job Location: CRAMSN Research Park, Pashamylaram, Patancheru, Hyderabad 3. Qualification: M.Sc 4. EXPERIENCE:1-3 Years -Must be from CDMO / API Industry. -Skills in route scouting, feasibility studies, optimization and experience in process safety data evaluation. -Knowledge of scale-up activities, interpretation of analytical results and regulatory understanding. -Familiarity with crystallization techniques, impurity profiling, genotoxic & nitrosamine assessment. -Utilization of ChemDraw and associated tools of R&D 5. How to Apply: Reach at : Mani Shankar, manishankar.dadi@msnlabs.com Please Note Candidates Are Requested to Bring Resume, Photo Copy of Educational Certificates, Latest Increment Letter, Last Three Months Pay Slips, Last Six Months Bank Statements, Passport Size Photographs, Aadhar Card Copy WALK-IN ...
Required Executive/ Sr. Executive for Upstream Manufacturing - Biologics- M.Sc./B.Tech. in Biotechnology- 04 Positions
Aragen is hiring for Executive/ Sr. Executive for Upstream Manufacturing Biologics department.
Details are provided below
1. Position: Executive/ Sr. Executive
2. Department: Upstream Manufacturing - Biologics
3. Role: Upstream Manufacturing
4. Experience: 2-6 Years
5. Qualification: M.Sc./B.Tech. in Biotechnology
6. Work Location: Bommasandra, Bengaluru
7. Number of Openings: 04
8. Skills Required:
-Upstream - Manufacturing
Execute, monitor, and optimize mammalian cell culture processes to support the production of biologics.
-Operate and maintain single-use bioreactors, including system setup, process monitoring, and troubleshooting during manufacturing runs.
-Collaborate with cross-functional teams to support process development, scale-up activities, and contribute to process characterization and validation.
-Ensure adherence to Good Manufacturing Practices (GMP) and internal quality standards, including performing in-process testing and maintaining accurate documentation.
-Perform qualification activities for upstream process equipment in compliance with regulatory requirements.
-Maintain comprehensive and accurate records of manufacturing processes, procedures, and results to ensure traceability and audit readiness
-Upstream - QMS & Documentation
-Initiate and document deviations related to upstream processes in compliance with GMP requirements.
-Prepare, review, and submit batch manufacturing records (BMR), ensuring accuracy, completeness, and compliance.
-Prepare, revise, and maintain Standard Operating Procedures (SOPs) in alignment with regulatory and company standards.
-Prepare qualification documents for upstream equipment and processes, ensuring proper documentation and compliance.
-Ensure all documentation is maintained as per regulatory requirements and internal quality standards. Support investigations, root cause analysis, and follow-up actions related to deviations and process non-conformances.
9. How to Apply:
Mail ID:
PrashanthCherugad@aragen.com
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