QC Officer/r/Executive

We Are Urgently Required QC (HPLC) Sr.Officer/Executive Pharmaceutical injectable plant (USFDA Approved) ( Only Female Candidates Can apply) Exp: 3 to 8 YrsSalary:- depends on interview HR /

We Are Urgently Required QC (Wet.Lab) OfficerFor Pharmaceutical API manufacturing plant(USFDA approved) Exp: 2 to 5 YrsSalary:- depends on interview HR /

Role Overview:The Lab QA/QC Reviewer will be responsible for the comprehensive review and approval of analytical data generated by the QC laboratory.This role ensures data integrity, compliance with regulatory guidelines, and facilitates resolution of quality investigations related to lab incidents.Key Responsibilities:Perform detailed analytical data review...

Job Description • Define productivity metrics and align operating definitions with QC teams.• Simplify and digitize data for reporting QC productivity metrics.• Publish monthly QC productivity metrics reports for all labs.• Identify improvement levers for QC productivity and develop action plans to address them, reporting progress regularly.•...

Job Description • Define productivity metrics and align operating definitions with QC teams.• Simplify and digitize data for reporting QC productivity metrics.• Publish monthly QC productivity metrics reports for all labs.• Identify improvement levers for QC productivity and develop action plans to address them, reporting progress regularly.•...

Candidate should have good exposure of Analytical Data Review and electronic data review of QC instruments (LCMS/HPLC/ GC/ Dissolution, Malvern 3000 etc) .Should have Strong knowledge of QC investigations (Lab incidents, OOS/OOT etc).

Job Description• Define productivity metrics and align operating definitions with QC teams.• Simplify and digitize data for reporting QC productivity metrics.• Publish monthly QC productivity metrics reports for all labs.• Identify improvement levers for QC productivity and develop action plans to address them, reporting progress regularly.• Manage...

Role & responsibilities :This position will be responsible for planning, coordinating, and monitoring production activities to ensure optimal inventory levels and timely delivery of products.Lead and optimize the production planning process for injectable products.Efficient coordination with procurement, artwork development, CQA, and other relevant stake...

Process Validation:Plan and execute process validation activities for sterile injectable products as per cGMP and regulatory expectations.Prepare and review validation protocols and reports, ensuring compliance with internal SOPs and global regulatory guidelines (e.g., USFDA, EU-GMP, WHO).Cleaning Validation:Develop and implement cleaning validation...

RESPONSIBILITIESDaily planning of analytical activities, resource management and work allocation.Plan and execute sampling and analysis for raw materials, packaging materials, intermediates & finished products.Review and /or Approval & Implementation of Standard operating procedureReview and /or Approval of Implementation analytical protocol and analytical...