Sahar Rehman

Project Coordinator
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Profile Views 48

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Last Seen: 22 September 2022 2:39 PM

Skills
SAP ERP LIMS Team management Microsoft SOP Labsolution Review Specification Project Coordinator Follwup Customer-oriented Deviation Change Contorl CAPA Market complaints
  • Experience
    4 Years
  • U.A.E Experience
    Fresh
  • Industry
    Pharmaceutical
  • Nationality
    India
  • Visa status
    Visit Visa in UAE
  • Qualification
    Matric - Biotechnology, Microbiology, Cell biology, Biochemistry, Immunology, Marketing and communication
  • Driving License:
Other Matching Titles/Position
NULL
Industry Titles
Pharmaceutical
Facility Management
General

Summary of Career

Work Experience (Employment History)

Experience as Project Coordinator

  • Employer

    The Himalaya drug company

  • From

    18 August 2021

  • To

    To date

  • Detail

    Review domestic and export artworks as per country wise regulation.
    Coordinate with marketing operators, FD, packaging, QA for product requirements and related queries.
    Follow up for new product development and plan accordingly.
    Coordinate between departments and marketing for product artwork clearance.
    Review change control, deviation, OOS, review customer complaints, compare risk analysis.

Experience as Quality Assurance- Reviewer

  • Employer

    Stabicon Lifescience

  • From

    03 December 2018

  • To

    16 August 2021

  • Detail

    Document control.
    Review lab Protocol, Method Validation, Verification and routine workstreams.
    Stability Protocol and Study Approval. COA preparation. BMR, BPR Review
    Actively involved in the plant Quality Management system activities.
    Monitoring stability study conducted in accordance with the requirement specified in respective SOP.
    Check and maintain the efficiency of Product. Review Lab error, OOS, OOT and Deviation.

Experience as Quality Assurance

  • Employer

    Wirksam Pharma

  • From

    02 March 2018

  • To

    22 October 2018

  • Detail

    QMS Qualification and Document control (URS, IQ, OQ, PQ and Validation) and review Data Master File.
    Control Sample Handling Maintenance, Issuance and control of Master documents and logbooks.
    Review OOS, OOT, Deviation.
    Issuance a number of forms, Protocol, Specifications,
    Breakdown forms, PM schedules and Calibration schedules. BMR, BPR & Artwork review.

Academic Qualification

Matric 30 May 2016

Biotechnology, Microbiology, Cell biology, Biochemistry, Immunology, Marketing and communication
Certifications
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