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    QC Metrologist - New Brunswick, United States - Sun Pharmaceutical Industries

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    Description
    COME WORK FOR US - INVESTING IN YOU AS A SUN PHARMA EMPLOYEE


    • Medical, Dental, Vision Benefits
    • Health Savings Account (HSA), Flexible Spending Account (FSA)
    • Prescription Drug Coverage
    • Telehealth and Behavior Health Services
    • Income Protection - Short Term and Long Term Disability Benefits
    • Retirement Benefits - 401k Company Match on Day One (100% vesting immediately)
    • Group Life Insurance
    • Wellness Programs
    • Corporate Discounts on personal services: Cellular phones, Entertainment, and Consumer Goods

    Sun Pharma Vision:
    Reaching People And Touching Lives Globally As A Leading Provider Of Valued Medicines

    Sun Pharmaceutical Industries Ltd.

    (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of over $ 4.5 billion US Dollars.

    Supported by more than 40 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe including the United States.

    Sunology is a combination of Sun Values and Ideology and is the way of life at Sun Pharma. Sunology is Humility.
    Integrity.
    Passion.
    Innovation. It represents our promise to all stakeholders including patients, physicians, and employees.

    Our Code of Conduct

    Our Global Code of Conduct governs every aspect of our operations.

    Sun Pharma is a family of thousands of people, working across many countries, speaking multiple languages, and all united, with one common purpose:
    to make good health accessible and affordable to local communities and society at large.

    Through active fieldwork, dedicated research teams, and in recognition of the efforts who work behind the scenes to combat illness and disease, the Sun Pharmaceutical Group helps as many people as possible, to secure their right to good health.

    The way we work every day is important to us.


    DOWNLOAD OUR CODE OF CONDUCT


    Perform or assist with all essential tasks including preventative maintenance, calibration, and qualification of laboratory instruments in accordance to all applicable SOP to ensure adherence to cGMP in support of the laboratory operation.

    Assist with instrument maintenance and schedule outside contractor where necessary.


    • Preparation of master Preventive Maintenance/Calibration schedule.
    • Planning, execution and review of instrument calibration/qualification related activities as per the calibration master plan.
    • Draft and review of instrument operation, maintenance and calibration procedures.
    • Initiate change controls for new and existing instrument and its procedures.
    • Concurrent documentation of all the raw data, observations in the notebook or applicable documents.
    • Notify to the supervisor any anomalous or OOC results. Notify the management for any observations or deviations.
    • Adhere to cGMP and safety procedures.
    • Review and report any applicable calibration/qualification documents.
    • Logging and attending instrument repair requests.
    • Scheduling visit for outside contractors for preventive maintenance or repair.
    • Placing "out of service tag" on instrument due for calibration, instrument requiring a repair or on a new instrument.
    • Opening the investigations and conduct primary investigation under direct guidance from management.
    • Ensure adequate labeling of all instruments and ensure instrument calibration status.
    • Order and maintain spare parts for major instrument to ensure continuous support of the analysis.
    • Verify the expiry date of chemicals, reagents, primary calibrators prior to use.
    Qualifications


    • Minimum BS or equivalent degree in Chemistry or related discipline.
    • Minimum of four (4) years of Pharmaceutical Industry Laboratory experience
    • In depth knowledge of analytical instrumentation such as HPLC, GC, FTIR, UV and practice.
    • Practical problem solving skills for instrumentation troubleshooting.
    • Knowledge of ICH and FDA regulatory guidance.
    • Must be familiar with cGMP/GLP practices for analytical laboratories and EHS/OSHA safety regulations.
    • Excellent written and verbal communication skills and working knowledge of Microsoft Office Applications.
    • A self-starter with a hands-on approach and a can-do attitude.
    • The requirement for English language proficiency for this job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).
    • Able to lift and carry 50lbs
    • While performing the duties of this job, the employee is frequently required to sit; use hands to finger, handle objects, or feel objects, tools, or controls; and reach with hands and arms.
    • The employee is occasionally required to stand, stoop, kneel and crouch.
    • Specific vision abilities required of this job include close vision, distance vision, color vision and the ability to adjust focus.

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