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    Sr. QC Compliance Specialist - New Brunswick, United States - Sun Pharmaceutical Industries

    Sun Pharmaceutical Industries
    Sun Pharmaceutical Industries New Brunswick, United States

    2 weeks ago

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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
    Independently manages laboratory compliance activities for assigned functions and projects. Author Laboratory method, specification. Perform and write laboratory, CAPAs, Lab Event/Out-of-Specification and Out-of-Trend investigations, deviations. Author laboratory SOP's accordingly to company's standards and FDA /ICH guidelines.


    • Writes technical documents such as methods, specifications, method validation protocols and reports, method transfer protocols and reports based on corporate policies and SOP's, compendia, ICH and FDA regulatory guidance.
    • Evaluate Sun global documents (GQS and GSOP) against site-specific procedures and update the site procedure accordingly.
    • Generates change requests required for analytical documents, and routes documents for review and approval. Maintains hard copies and electronic file of technical documents.
    • Timely provide the QC documents required for CBE, PAS and ANDA submission to RA.
    • Collaborates with colleagues and external partners to achieve individual and department goals.
    • Perform and author laboratory Lab Event/Out-of-Specification and Out-of-Trend investigations and ensure they and closed on a timely fashion.
    • Perform root cause analysis using various investigation tools and develop appropriate CAPA.
    • Perform the gap assessment with laboratory SOP and Global documents.
    • Conduct unplanned deviation investigation, impact assessment and appropriate CAPA.
    • Track and perform the activity related to Global CPAP.
    • Ensure continuous laboratory compliance by adopting best industry practice and complying with procedure requirements.
    Qualifications


    • Minimum BS or equivalent degree in Chemistry or related discipline.
    • Minimum of eight (8) years of experience in the pharmaceutical industry.
    • Excellent computer skills, and competence with Microsoft Office (Word, Excel, PowerPoint) and Access.
    • Must have an understanding of FDA guidelines, ICH guidance and DEA regulations. Ensures compliance with cGMPs, DEA regulations, safety and site operating procedures under the direction of Management.
    • Must be familiar with proper cGMP practices for analytical laboratories and working knowledge of basic laboratory instrumental analysis and wet chemistry skills.
    • Must have cGMP compliance knowledge and experience.
    • Collaborates with colleagues and external partners to achieve primary Department goals.
    • Works in coordination with project plans and goals as assigned by Management.
    • Demonstrated excellent communication: verbal, written and presentation skills.
    • A self-starter with a hands-on approach and a can-do attitude.
    • A team building champion driving innovative cross functional synergies.
    • Excellent project management and problem solving skills.
    • 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).
    IND123
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