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BSc Quality Assurance Jobs at B Braun – Apply Online

Executive – Quality Assurance & Regulatory Affairs

Company: Oyster Medisafe Pvt. Ltd.

Job Posting Location: IN-Hyderabad

Functional Area: Regulatory Affairs

Working Model: Onsite

Requisition ID: 1278

Job Summary:

We are seeking a highly skilled and experienced Executive for our Quality & Regulatory Affairs team. The ideal candidate will be responsible for document management (digitally), ensuring compliance with regulatory requirements. This role involves managing documentation, handling quality systems, and liaising with local and central drug authorities in India to ensure our products meet all necessary regulations.

Key Responsibilities:

  • Regulatory Compliance: Ensure compliance with ISO 13485, CE marking, and other relevant regulatory standards.
  • Documentation Management: Act as the document controller, maintaining and managing all quality and regulatory documentation in the digital documentation system.
  • Quality Systems: Oversee the implementation and maintenance of GMP and quality management systems.
  • Liaison with Authorities:
    • Communicate with drug authorities and other regulatory bodies to ensure product compliance.
    • Liaise with regulatory authorities to obtain various certificates and licenses.
  • Audits and Inspections: Prepare for and support internal and external audits and inspections.
  • Training and Development: Provide training to staff on quality and regulatory requirements and best practices.
  • Continuous Improvement: Identify
    areas for improvement in quality and regulatory processes and implement necessary changes.
  • Artwork Management:
    • Responsible for creating/updating printing artworks in compliance with various regulatory requirements.
    • Liaise with internal/external service providers for artwork management.

Job Requirements:

  • Education:
    • Bachelor’s degree in a relevant field (e.g., Bio Engineering, Life Sciences, Engineering, Quality Management).
  • Experience:
    • Minimum of 3-5 years of experience in quality and regulatory affairs, preferably in the medical device or pharmaceutical industry.
  • Certifications:
    • Preferable to have internal auditor certification in ISO 13485.
    • Awareness of Indian Medical Device Rules and EU Medical Device Regulations.
  • Knowledge:
    • Strong understanding of regulatory requirements and standards, including ISO 13485, CE marking, EU MDR 2017/745, and Indian Medical Device Rules & Regulations.
  • Skills:
    • Excellent document management and system handling skills.
    • Strong communication and interpersonal skills.
  • Attention to Detail:
    • High level of accuracy and attention to detail in all tasks.

APPLY ONLINE HERE

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