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Manager

2+ years
Not Disclosed
10 Oct. 24, 2024
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

We are Growing, Grow with Us!
Are you looking for a dynamic company with daily challenges and opportunities? Pharmalex is your next career move! As one of the leading service providers for the pharmaceutical industry globally, we specialize in all aspects of drug and medical device approval, market development, and effective product maintenance.

Position: Manager

Your Role

  • Document Management:
    Evaluate, prepare, and compile documents related to pharmaceutical quality, including Active Substance Master Files, Certificates of Suitability, Investigational Medicinal Product Dossiers, and Quality Overall Summaries/Expert Reports for marketing authorization dossiers. Emphasize compliance with technical and regulatory requirements as well as customer-specific demands.

  • Project Strategy and Planning:
    Collaborate with the Business Development team to strategize for new and ongoing projects, supporting the preparation of client proposals.

  • Project Management:
    Ensure project quality, adherence to timelines, and customer satisfaction. Conduct gap analyses of documents based on requirements.

  • Regulatory Support:
    Provide regulatory guidance throughout the product lifecycle management.

  • Coordination and Communication:
    Facilitate communication among project teams, customers, internal departments, suppliers, local partners, and regulatory bodies for all essential operational procedures.

  • Process Optimization:
    Assist in optimizing internal departmental processes.

  • Knowledge Sharing:
    Present and distribute relevant technical knowledge and conduct SOP training based on organizational and client needs.

  • Additional Tasks:
    Undertake any regulatory-related tasks for all types of products across various markets.

Your Profile

  • Education:
    Graduate, Post-graduate, or Doctorate degree in life sciences, Pharmacy, Medical sciences, or equivalent.

  • Experience:
    Minimum of 5 years in regulatory affairs within the pharmaceutical industry.

  • Work Style:
    Autonomous, focused, and capable of delivering high-quality work.

  • Team Collaboration:
    Strong sense of responsibility and ability to work effectively in a team.

  • Language Skills:
    Excellent command of English.

  • Regulatory Knowledge:
    Sound understanding of current legal and regulatory requirements in developed markets (Japan, USA, EU).

  • Organizational Skills:
    Ability to manage and prioritize multiple tasks, especially under tight timelines.

  • Communication Skills:
    Strong organizational and communication skills with a high degree of social competence. Experience in virtual teams and matrix organizations is a plus.

How to Apply

If you are interested in joining our Pharmalex team for this exciting opportunity, please submit your application, including your earliest possible starting date, any visa requirements, and salary expectations. We look forward to hearing from you!