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(Senior) Manager, Technical Regulatory

3+ years
Not Disclosed
10 Jan. 2, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Job Title: Regulatory Affairs Specialist - CMC
Location: Not specified
Category: Regulatory Affairs


About Roche:
Roche fosters a culture of diversity, equity, and inclusion, reflecting the communities we serve. In the global healthcare landscape, diversity is key to success, and we believe inclusion helps us understand the varied healthcare needs of people everywhere. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.


The Position:

General Position Summary:
As a Regulatory Affairs Specialist in CMC (Chemistry, Manufacturing, and Control), you will coordinate and prepare document packages for regulatory submissions, ensuring alignment with local and regional registration requirements and Roche's internal policies. You will compile materials required for submissions, license renewals, and annual registrations, while also recommending changes for labeling, manufacturing, marketing, and clinical protocols for regulatory compliance. Your role will involve monitoring and improving tracking systems, staying updated on regulatory changes, and engaging with regulatory agencies on defined matters. You will work independently and provide functional guidance to colleagues with less experience.

Your Opportunity:

  • Prepare high-quality CMC regulatory documents for global/local products, ensuring compliance with Roche corporate standards and health authority regulations.
  • Manage regulatory aspects of change control, ensuring effective communication with stakeholders regarding technical changes.
  • Provide regulatory support for quality systems, such as change control, discrepancy management, and Health Authority inspections as needed.
  • Interact with regulatory agencies on specific matters related to submissions and approvals.
  • Keep internal teams (TRL, CTP, and stakeholders) informed about project status, submission risks, and regulatory timelines.
  • Contribute to regulatory excellence by identifying opportunities, mitigating risks, and supporting continuous improvements.
  • Collaborate with technical partners and stakeholders to facilitate the "One Regulatory Voice" for regulatory submissions across the product lifecycle.

Who You Are:

  • Education:

    • Master's Degree in life sciences or a related discipline (preferred).
  • Experience:

    • 3+ years of experience in the pharmaceutical, biotechnology, or related industries in areas like CMC, Regulatory Affairs, Quality, R&D, Manufacturing, or related fields.
    • Experience with generating technical registration dossiers for China, EU, or USA markets is preferred.
    • Experience in analytical development, MSAT, manufacturing process development, or supply chain would be a plus.
    • Experience in Regulatory Affairs filing is an advantage.
  • Knowledge/Skills/Competencies:

    • Proficient in ICH, WHO, and China regulations and guidelines; knowledge of FDA and EMA regulations is an advantage.
    • Expertise in handling a wide range of data and information related to CMC, clinical, and non-clinical matters.

Who We Are:
At Roche, over 100,000 people across 100 countries are pushing the boundaries of healthcare. Working together, we've become one of the world’s leading research-focused healthcare groups, driven by innovation, curiosity, and diversity.