Analytical method development of API and itermediate. Handling of HPLC, GC, Karlfisher, potentiometry titration. Preparation of specification and STP. Titration expertise. Daily work reporting, literature search and trouble shooting in QC Labs.
Preparation of DMFs for different markets in CTD and eCTD formats. Coordination with cross-functional dept to manage the documents. Supporting marketing team & QC/QA/R&D in various capacity. Preparation of Declarations and other supporting docs. Perks and benefits Transportation Canteen PF Medical Insurance
Analytical method development of API and itermediate. Handling of HPLC, GC, Karlfisher, potentiometry titration. Preparation of specification and STP. Titration expertise. Daily work reporting, literature search and trouble shooting in QC Labs.
Handle End to End Recruitment. Handling Statutory Compliance. Prepare attendance for Payroll. Contract Labour Management. Training and Development. Plant Administration.
Preparation of DMFs for different markets in CTD and eCTD formats. Coordination with cross-functional dept to manage the documents. Supporting marketing team & QC/QA/R&D in various capacity. Preparation of Declarations and other supporting docs.
QMS documents and issuance of docs. Review of Docs. Identify and report quality issues and deviation. Handling of change control, incidents & deviation. Line clear & dispatch activities. Document distribution and control.
Handle End to End Recruitment. Handling Statutory Compliance. Prepare attendance for Payroll. Contract Labour Management. Training and Development. Plant Administration. Perks and benefits PF ESIC
Analytical method development of API and intermediate. Handling of HPLC, GC, Karlfisher, potentiometry titration. Preparation of specification and STP. Titration expertise. Daily work reporting, literature search and trouble shooting in QC Labs. Required Candidate profile Must worked in ADL department of API industry for at least 5 Years. Perks and benefits PF Transportation Canteen
Preparation of DMFs for different markets in CTD and eCTD formats. Coordination with cross-functional dept to manage the documents. Supporting marketing team & QC/QA/R&D in various capacity. Preparation of Declarations and other supporting docs. Perks and benefits PF CANTEEN TRANSPORTATION
Handling chemical reaction, column chromatography. Organic synthesis of API drug. Documentation work, Literature work. Handling of hydrogenation reaction, bromination. Knowledge of pilot plant and validation batches.
Handling chemical reaction, column chromatography. Organic synthesis of API drug. Documentation work, Literature work. Handling of hydrogenation reaction, bromination. Knowledge of pilot plant and validation batches. Required Candidate profile Must have 4+ years of R&D Experience and preferred in API - Pharma.
Preparation of DMFs for different markets in CTD and eCTD formats. Coordination with cross-functional dept to manage the documents. Supporting marketing team & QC/QA/R&D in various capacity. Preparation of Declarations and other supporting docs. Required Candidate profile Candidate from Pharma - API industry and should have 8+ Years of Experience in Regulatory Affairs. Perks and benefits Canteen Transportation Health Insurance
Lead & represent the QC department during internal, external, and regulatory audits by ensuring laboratory compliance, presenting documentation, addressing auditor queries. Ensure compliance with cGMP, WHO and other applicable regulatory guidelines. Required Candidate profile Must have 10+ Years of experience in QC and have Managerial experience of more than 5+ Years and Candidate should have Pharmaceutical - API background.
Handling chemical reaction, column chromatography. Organic synthesis of API drug. Documentation work, Literature work. Handling of hydrogenation reaction, bromination. Knowledge of pilot plant and validation batches.
Executing trials to optimize manufacturing processes. Conducting studies to determine the product's lifespan and stability over time. Analyzing experimental data, interpreting results, using this info for product improvements and troubleshooting.
Maintain Live Contact with existing customers & Networking. Days to day enquiry / Query response to the clients. Maintain sales that meet Organizations' sales Budget. Customer Visit. Conducting market research & develop marketing strategies.
Maintain all safety Records, Records & Certificate as required under the safety norms Risk assessment, construction safety, fire safety, occupational health etc... Safety Training, safety audit etc Coordinate and implement of effective EHS policies. Required Candidate profile PDIS is must.
Handling Quality management system and regulatory support & reviewer. Change control, CAPA,OOS,APQR. Compliance verification at Site. Dispatch compliance. BMR and Work sheet compliance before release. Document and Data control and training.
Responsible for marketing and sales of Bulk drugs (API’s) and Pharmaceutical intermediates. Acquiring new customers for the purpose of expanding the current business. Enable long term supply contracts and pricing agreements with key customers. Required Candidate profile Must have experience and knowledge of API Pharma.
Preparation of DMFs for different markets in CTD and eCTD formats. Coordination with cross-functional dept to manage the documents. Supporting marketing team & QC/QA/R&D in various capacity. Preparation of Declarations and other supporting docs. Required Candidate profile Candidate from Pharma - API industry and should have 8+ Years of Experience in Regulatory Affairs. Perks and benefits Transport Canteen PF Health Insurance
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