Compliance Enhancement Program (CEP) || Pharma || Ahmeadabad

3 - 8 years

7 - 12 Lacs

Posted:2 weeks ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

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Email id: renu.kumari@adecco.com

Contact : 6364920532 ( Watsapp)

Qualification:

Professional as part of Compliance enhancement program

Key Responsibilities

1. Project Management & Oversight

  • Lead the planning, execution, and monitoring of

    key site-related projects

    , ensuring alignment with regulatory requirements and business goals.
  • Collaborate with site

    cross-functional teams

    to manage project deliverables, resources, and timelines effectively.
  • Proactively identify risks and implement mitigation plans to ensure project success.

2. Operational Excellence

  • Champion a

    culture of continuous improvement

    by identifying inefficiencies and driving initiatives to improve productivity and quality.
  • Apply

    Lean Six Sigma

    and other best practices to

    streamline processes

    and eliminate Non-Value-Added (NVA) activities.
  • Establish and track site-level improvement metrics.
  • Ensure the policy Vs Practice

3. Cross-Functional Collaboration

  • Work closely with stakeholders from

    Manufacturing, QA, QC, R&D, Engineering, Regulatory Affairs

    , Other Supporting services and leadership to design and implement Strategies to enhance the

    compliance standards and performance strategies

    .
  • Act as a liaison to ensure alignment across departments and foster transparent communication, Policy Vs Practice and simplification of policy for easy understanding and effective implementation.

4. Reporting & Dashboard Development

  • Develop and maintain

    project dashboards

    and reports to monitor KPIs, project status, and compliance metrics.
  • Present project updates and improvement recommendations to

    plant leadership and senior management

    .

Desired Candidate Profile

  • Strong project management and cross-functional coordination skills.
  • Demonstrated experience in

    operational excellence, regulatory compliance, and quality systems

    within a pharmaceutical or manufacturing setup.
  • Proficiency in

    Lean, Six Sigma, or continuous improvement tools

    .
  • Strong analytical, problem-solving, and communication skills.
  • Proficient in MS Office, Excel, PowerPoint; familiarity with project management tools (e.g., MS Project, Power BI) is an advantage.
  • Good communication, and problem-solving skills.
  • Familiarity with Good Laboratory / Good Documentation / Laboratory Safety
  • Ability to communicate effectively with cross-functional stakeholders.
  • Organized, analytical, and quality-focused mindset with attention to regulatory detail.

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