Stanford Laboratories

Job Title : Assistant General Manager (AGM)Experience : 15-25 YearsLocation : Una, Himachal PradeshQualification : MSc/Post graduation degree in related fieldJob descriptionRole & responsibilities :- Lead the QC department (raw materials, in-process, finished products, stability, and microbiology) in line with cGMP and international quality standards.-...

Role & responsibilitiesResponsible for ensuring that all pharmaceuticals products developed with the R&D Department meet the highest quality standards.Prepare and review regulatory dossier documents for DCGI, ROW and Export market business.Ensure all the documents meet regulatory requirements and guidelines including quality.Implement and maintain quality...

Role & responsibilitiesMust have knowledge of dispensing of RM/PM.In-process quality checksReview BMR/BPR, regulatory books, online entries, sampling techniques.Calibration of IPQA instruments.Control sample and stability sample handling procedure.Preferred candidate profileMust have experience in OSD plant.Perks and benefits

Role & responsibilitiesSupervise and coordinate security and ensure all the protocols are in line with the organization.Ensure all updates on local, state, and federal laws concerning security and safety, along with industry best practices.Conduct a regular inspections of the premises.Monitoring access points, surveillance systems, and other security...

Job descriptionPrimarily responsible for supervision of Formulation & Development area and to monitor / Supervision and control over the operator / assistant operator in their designated premises at the site.Literature search, patents search and review the same as per product requirement.Innovator/ market sample characterization.Day to – day execution...

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...

Roles and Responsibilities:Should Know cGMP practices and Documentation.Handled USFDA Audits Should be able to enter data in BMR BPR independently Should be able to manage area independently Ready to work in shiftsMachines :HVAC, Capsule Filling & AutocartonatorDesired Candidate ProfileQualification : ITI /+ 2 with 2 to 6 years of experience in Tablet...

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...

Roles & Responsibilities:-Preparation, Review and Issuing control of BMR and BPR-Handling of Change control, Deviation, CAPA, and Investigation in shop floor.-Preparation and Review of SOP and All formets of manufacturing and packing.-Preparation and control of Validation protocol and involving in process validation.-In process monitoring during Dispensing,...

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...

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. ...

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...