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    Regulatory Affairs Executive - Vadodara, India - PR Flexmake

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    Full time
    Description

    PR Flexmake Private Limited (P+caRe) is hiring for Executive - Quality Control & Regulatory Affair

    Experience : 1 - 3 years

    Location : Vadodara

    Website :

    Mob. :

    Email :

    JOB DESCRIPTION

    Maintenance of QM, SOP, Device and Plant Master Files, Quality certification audits, documentation, Manufacturing license for medical devices (Class A&B), Inspecting the final output, model, specifications and design and approving the final products

    REQUIRED CANDIDATE PROFILE

    1-3 Years of experience in similar profile

    Qualification: B.Sc. / M. Sc. / B. Pharma

    Medical Device Rules 2017

    Can do Independently license application

    Role : QA / QC Executive

    Industry Type : Medical Devices & Equipment

    Functional Area : Quality Assurance

    Employment Type : Full Time, Permanent

    Role Category : Production & Manufacturing

    Education - UG :B.Sc in Any Specialization, B.Pharma in Any Specialization

    KEY SKILLS

    Medical Devices, ISO 13485, Quality Control Management, Inspection Quality Management and Regulatory Compliance

    COMPANY BRIEF :

    Founded in 2017 by the team of industry professionals as a Medical Device company specializing in Orthopaedic Aids and Rehabilitation Products, entered market in 2020 with 225 plus specialized range of products with commitment to help people who suffer from movement disorder and improve their quality of life.

    We are in process of becoming an innovative manufacturer and a leading supplier of non-invasive orthotic and rehabilitation solutions in India as well as overseas countries. We specialize in helping people who suffer from movement disorders.

    PRODUCT CATEGORIES:

    1. Cervical 2. Spine 3. Shoulder 4. Wrist 5. Finger 6. Elbow 7. Hip 8. Knee 9. Calf/Thigh 10. Ankle 11. Leg 12. Heel

    (Each category comprises of its own unique varients)



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