QA/ QC/ Microbiology Executives-Pharma

Role & responsibilitiesAnalytical Method Validation (AMV): Perform method validation activities, including designing validation protocols, executing validation studies, and documenting results for analytical methods used in raw materials, in-process testing, and finished product testing.Method Transfer: Participate in the transfer of analytical methods from...

**Job Summary** **Key Responsibilities** - Conduct real-time inspection of products on the production line to ensure they meet specified quality standards. - Verify product dimensions, appearance, and functionality using appropriate measuring tools and inspection techniques. - Monitor production processes and identify any deviations from quality standards,...

Responsible for manufacturing and monitoring of batches in Tablet, Capsules, Liquid Oral, Ointment departments.Must have sound knowledge and experience in formulations.Must have experience in granulation and compression.To maintain the GMP, personnel safety and hygienic practices on shop floor.To ensure the online completion of documents.To provide the...

Documentation, QMS Documentation, Validation, qualification, deviation, change control etc MFR/SOP/AMV (analytical Method Validation), ACTD/CTD, Dossier Preparation. Knowledge of COPP. Having a sound knowledge of BMR preparation and filing, FR&D Documentation, PV ETC Monitoring of process validation activity with preparation of protocol and report. ...

Civil and Structural - Site Manager - Diploma / Degree in Civil Engineering - 10-15 Years Experience in Industrial Construction. Working Experience of 5 years with PMC / Consultancy Company preferred. - Supervising Civil and Structural work of contractor - ⁠Co ordination with client too Management - ⁠Co ordination with Consultants Design Office in...

Roles and ResponsibilitiesKnowledge of proper operation and cleaning of Machine & Area related to Granulation, Compression, Coating and Capsule Filling.The persons having knowledge of handling change control, deviation insident, market complaint. Having knowledge of GMP and GDP.The persons having knowledge of BMR/BPR preparation and SOP preparation.The...

Role & responsibilities* Receiving and GRM preparation at Engineering/ QC Chemicals/ RM & FG* Coordinate with Purchase Head Office team w.r.t. Materials and documents.* Handling of damaged / Expired/ Obsolete Engg./ Consumable/ Misc./ QC Chemicals* Stock taking and inventory control of Engg./ Consumables/ Misc./ QC Chemicals.* SAP T-codes knowledge for...

Civil and Structural - Site Manager - Diploma / Degree in Civil Engineering-10-15 Years Experience in Industrial Construction.Working Experience of 5 years with PMC / Consultancy Company preferred.Supervising Civil and Structural work of contractor⁠Co ordination with client too Management⁠Co ordination with Consultants Design Office in...

Role & Responsibilities:Monitor the Server Room and ensure proper functioning of systems and operations.Handle time synchronization of production and QC (Quality Control) equipment.Perform maintenance and troubleshooting of IT-related equipment, including:Desktops, Laptops, Servers, Printers, and Scanners.Computer networks, attendance machines, and access...

**Responsibilities: - ** **Document Control Management**: Oversee the creation, revision, approval, distribution, and archiving of quality and manufacturing-related documents, including Standard Operating Procedures (SOPs), batch records, specifications, protocols, and reports. **GMP Compliance**: Ensure that all documentation processes align with Good...