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    Analytical Researcher Ii

    Teva Pharmaceuticals
    6-9 years
    Not Disclosed
    Ambernath
    10 Nov. 22, 2024
    Job Description
    Job Type: Remote Education: MSc./M. Pharm/PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    About Us

    At Teva Pharmaceuticals, we are on a mission to make good health affordable and accessible for millions worldwide. Operating in nearly 60 countries with a rich diversity of nationalities and backgrounds, we are proud to be the world’s leading manufacturer of generic medicines. Our products feature on the World Health Organization’s Essential Medicines List, and every day, 200 million people globally take our medicines.

    We are committed to innovation and continuously seek new ways to improve healthcare, and we’re looking for talented individuals to join us on this journey.

    Job Opportunity: Analytical Chemist – Nitrosamines Projects

    Role Overview:
    Support Global R&D sites in Nitrosamines-related projects by performing routine analytical method development, validation, and transfer activities. Work includes testing APIs, intermediates, and finished products under the guidance of a supervisor.

    Key Responsibilities

    Analytical Activities

    • Execute daily tasks related to Nitrosamine impurities, ensuring timely completion based on project priorities.
    • Develop, validate, and transfer methods for Nitrosamines in drug substances and products.
    • Perform troubleshooting of analytical instruments to resolve operational challenges.
    • Conduct instrument calibration as part of routine activities.
    • Compile analytical data, ensuring compliance with Good Laboratory Practices (GLP) and quality standards.

    Laboratory Operations

    • Manage and reconcile global analytical samples from in-house FRD and Teva sites.
    • Maintain laboratory inventory, including columns, standards, chemicals, spares, and consumables.
    • Prepare laboratory documentation such as Standard Test Procedures (STPs) and analytical Standard Operating Procedures (SOPs).
    • Conduct literature searches to support analytical method development.

    Compliance and Safety

    • Ensure adherence to data integrity standards, pharmaceutical quality systems, and GLP.
    • Actively participate in implementing EHS policies to maintain a safe working environment.

    Qualifications

    Education:

    • M.Sc. or M.Pharm in Analytical Chemistry or related field.
    • Ph.D. candidates are also eligible.

    Experience:

    • 6–9 years of relevant experience for Master’s degree holders or 3–6 years for Ph.D. holders.
    • Proven expertise in analytical method development and validation for Nitrosamine impurities.
    • Hands-on experience with advanced mass spectrometry technologies, including:
      • LC-MS/MS
      • GC-MS/MS
      • LC-HRMS

    Knowledge:

    • Familiarity with regulatory requirements for major markets (e.g., US, EU, Canada).
    • Strong understanding of ICH guidelines and pharmaceutical quality systems.

    Personal Attributes

    • Basic communication skills and ability to work in a matrix structure.
    • Honest, trustworthy, and respectful.
    • Culturally aware, self-motivated, and adaptable.

    Equal Employment Opportunity

    Teva Pharmaceuticals is committed to equal opportunity in employment. We ensure equal treatment regardless of age, race, religion, gender, or any other legally protected status. We foster a diverse and inclusive workplace and are dedicated to providing accommodations during the recruitment process to support candidates with specific needs.

    Join us at Teva Pharmaceuticals and help make a difference in global healthcare!

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