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    Job · 21049327

    AHMEDABAD · FULLTIME

    QC Chemist

    Medicare Hygiene Limited

    Medicare Hygiene Limited

    Ahmedabad · onsite · Posted 8d ago

    Sourced fromFoundit
    Not disclosed2–4 yrsfulltimeAhmedabad

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    Section · 01

    About this role

    Company Description

    Medicare Hygiene Limited is an Ahmedabad-based manufacturer of surgical dressings and wound care products, trusted by hospitals, nursing homes and healthcare professionals across India. We are expanding our Quality team and looking for a QC Chemist.

    Role Description

    This is a full-time, on-site role at our Ahmedabad facility. You will handle testing and inspection of raw materials, packing materials and in-process products, maintain laboratory systems, and support quality release in line with ISO 13485:2016.

    Experience: 2-3 years

    Qualification: B.Sc / M.Sc (Chemistry)

    Preferred industry: Chemical / Medical Device / Pharma

    Key Responsibilities

    • Sampling, testing and inspection of raw materials and packing materials as per specification.
    • Follow-up of supplier test reports.
    • Monitoring and preservation of residual samples.
    • Report generation with protocol.
    • Preparation of chemicals and lab reagents; standardization of lab solutions.
    • Daily lab monitoring: room temperature and humidity, daily balance and pH meter calibration, distilled water preparation and checking.
    • Maintaining chemical stock records.
    • Follow-up and monitoring of instrument calibration.
    • In-process checks as per quality plan and specification.
    • Identifying, raising and following up in-process non-conformities until closure.
    • Line clearance.
    • Verification of codes, labels and packing quantity until finished goods release and warehouse transfer.
    • BMR verification and online documentation.
    • ISO 13485:2016 system management, audit support and NCR closure.
    • Monitoring rejection reports until disposition.
    • Supporting QC release verification.
    • Ensuring correct Approved / Rejected / Under Test labels, floor item identification and traceability.
    • Raising change notes and suggestions.
    • Coordination of external product testing and reports.
    • Active participation in continuous improvement and new product development activities.
    • Artwork preparation and checking.
    • Any additional tasks assigned by the QA/QC Head and Management.

    Requirements

    • B.Sc / M.Sc in Chemistry with 2-3 years of relevant experience.
    • Background in medical device, pharma or chemical industry preferred.
    • Understanding of ISO 13485:2016 & CE EU MDR 2017/745.
    • Hands-on experience with lab instruments.
    • Strong documentation skills and attention to detail.

    How to Apply

    • Apply through LinkedIn or share your CV at [HIDDEN TEXT]. Shortlisted candidates will be contacted for an interview.

    Sourced from foundit

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    Section · 02

    Skills

    lab instrumentsDocumentation SkillsISO 13485:2016

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