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  • Posted 2 months ago
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Job Description

PurposeRecruitment of New Position.Position / Job TitleAssistant Manager (Supervisor).DepartmentQuality Control Reporting ToSr. Manager (P4) / AGM (M1) LocationAmbernath Years of Experience8 to 12 years.Dosage FormSolid Oral / Nasal / Liquid Job Responsibilities / Deliverables

  • He is Responsible to leading LCMS instrumental team (Approx 5 members) with planning and execution for RM, Finished Product Samples and Stability Samples testing. He is primary responsible and main role to arrange the Extractable, Leachable, Nitrosamine-NDSRI impurity, other organic impurity etc testing on LCMS (Sciex).
  • Responsible for arranging a review of analytical raw data for correctness and completeness and to ensure final data submission to QA or other respective departments as per specified timelines.
  • He is responsible for arranging the method validation, verification, method transfer activity as when applicable on LCMS and train-qualified the people on LCMS testing.
  • The candidate should have handling experience in LCMS (Sciex), HPLC (Shimadzu) and other instruments like UV, IR, GC instruments will add advantages.
  • He is responsible to care-taker, calibration and PM of LCMS (Sciex).
  • He is responsible for QMS handling (incidences, investigations, OOS, OOT, CC, CAPA etc.) and closing within stipulated timeline with proper root cause of his section.
  • He is responsible for facing the Audit (USFDA/MHRA/Client etc.)
  • He Should have good written and communication skills.
  • Responsible for adherence of GLP and Health, Safety Environment system in Laboratory.

Qualifications & Pre-Requisites

Preferably have following skill but not limitas mentioned below;

  • Master Degree of Science / Pharma.
  • The candidate should have handling experience and theoretical knowledge on LCMS (Sciex), HPLC (Shimazu), UV, IR and requires knowledge of data review.
  • He should have experience of QMS Handling and know about GLP-GMP standard of analytical work.
  • The candidate having experience in US-FDA/MHRA approved company is preferable.
  • Knowledge of Chromeleon 7.2 software & Sciex OS 3.3 will be an added advantage.

Additional Notes

  • Role is expected to work in all shifts.
  • If required, the candidate should be ready to travel to all plant locations on work priority as per company policy.
  • Responsible to ensure compliance to GLP, Health, Safety and Environment. requirement.

More Info

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Job ID: 139984345

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