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    Job · 10779283

    INDORE · FULLTIME

    Executive

    Rubicon Research logo

    Rubicon Research

    Indore · onsite · Posted 71d ago

    Sourced fromFoundit
    Not disclosed6–8 yrsfulltimeIndore

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    Section · 01

    About this role

    Purpose

    To support Lab (Analytical) for maintaining Quality and compliance as per the GMP norms

    Position / Job Title

    Executive

    Department

    Quality Assurance – Analytical Lab Quality Assurance

    Reporting To

    Senior General Manager –Quality Assurance

    Location

    Pithampur

    Years Of Experience

    6 Years to 8years

    Dosage Form

    Solid Oral / Cream and Ointment experience is must

    Job Responsibilities / Deliverables

    Requirements For The JOB

    Well versed in the analytical review of documents, which includes those from GLP section.

    Handling of OOS, OOT, Events, Change control and CAPA.

    Review and ensure compliance of Column management, Standard management, glassware management and chemical management.

    Responsible for Retention samples management and review of stability sample and stability study management. To review of stability protocol/summary sheet.

    Review Computer system validation, calibration & qualification of instruments. Review of audit trails from the computerized systems.

    Ensure QC laboratory compliance at all times, participate in Lab check rounds.

    Preparation & review of OOS/OOT/Events trending.

    Review of analytical documents, chromatograms related to AMT/AMV protocols and reports.

    Preparation of SOPs

    To review the Analytical reports in support of Batch release activities

    To review and approve the batches with generation of Certificate of Analysis for Finished Product

    Review Analyst qualification data

    Qualifications & Pre-requisites

    Must-Have Skills:

    Should be Graduate/Postgraduate in Science or Pharmacy

    Must have knowledge on handling HPLC, GC, KF, Dissolution. FTIR, FTNIR is preferable.

    Exposure to various regulatory bodies like US FDA, MHRA, TGA

    Exposure to specific dosage forms like OSD (preferred)

    Expertise in Qualification of CSV instrument documents verification

    Expertise in Method validation and Analytical method transfer process

    Exposure to expertise towards handling of QMS records

    Additional Notes

    Role is expected to work in all shifts.

    Expected to visit Satara/Thane sites at least twice a month on need basis.

    Sourced from foundit

    Section · 02

    Skills

    ftirkfdissolutionMethod ValidationHPLCGCFTNIRAnalytical Method Transfer

    Section · Company

    About Rubicon Research

    Rubicon Research logo

    Rubicon Research

    Pharma

    1.1k+

    employees

    1999

    27 years old

    Atlanta,Georgia

    United States

    About

    Rubicon has built and expanded on strong strategic partnerships primarily regarding Development, Manufacturing, and Regulatory Support of Pharmaceutical Products.

    Industries

    PharmaInternet

    Employee ratings

    375 reviews

    3.4/ 5

    Culture

    3.2

    Career growth

    3.0

    Work-life

    3.1

    Employees rate it well for

    Work Culture34Senior Management28Learning26Salary25HR Policies23

    Find them on

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    Executive · waiting for your command