Compliance Manager

|Scientific & Pharmaceutical - Quality Assurance & Regulatory|Wellington

About the Company: Our client is a prominent and successful player in the animal health industry with their state-of-the-art manufacturing site, based in the Hutt Valley. With substantial ongoing investment in their facilities, they are poised for significant growth and exciting opportunities.

The Role: In response to increasing workloads, we are seeking an experienced Compliance Manager to join our client’s team. As a Compliance Manager, you will play a key role in supporting the Site Quality Head and managing the Quality Compliance Department. Your focus will be on driving continuous improvement of quality systems at a busy manufacturing site. You’ll also take on responsibilities related to team management, staff training and development, auditing, and overseeing various quality-related systems.

Key Responsibilities:

Quality Systems Oversight:

  • Manage and enhance quality systems including Stability, Seed Management, Quality Training, Auditing, AHQM, and Qualifications/Validations
  • Oversee compliance programs such as periodic product quality reviews, sample retention programs, auditing programs, and real-time trend analysis.

    Team Management:

    • Support team development and management, ensuring effective staff training and performance.

    Auditing & Compliance:

    • Conduct and oversee internal and external audits.
    • Manage and resolve compliance issues, ensuring all processes align with regulatory and quality standards.

       
      You, the Ideal Candidate: To excel in this role, you should possess the following qualifications and experience:

      • Educational Background: Bachelor’s degree or higher in a science-based discipline (Microbiology, Biology, Chemistry preferred).
      • Industry Experience: Minimum of 10 years in Quality Assurance or Quality Control within a GMP/GLP environment.
      • Management Skills: Proven experience in leading a technically diverse team.
      • Technical Expertise: Experience in method validation/verification, validation/qualification (including software systems), customer complaints, quality risk management, and stability reports.
      • Knowledge: In-depth understanding of QA systems, Good Laboratory Practice (GLP), and Good Manufacturing Practice (GMP) requirements.
      • Attention to Detail: Strong ability to review technical documentation for accuracy and completeness.
      • Communication Skills: Excellent written and verbal communication skills with a positive influence.
      • Computer Proficiency: High level of proficiency in Excel, Word, Access, Outlook, and SAP.
      • Problem-Solving: Sound and logical approach to problem-solving.

       
      Why Apply? Join a global leader dedicated to saving and improving lives worldwide. Our client values their employees and offers a comprehensive benefits package, including insurance benefits, enhanced KiwiSaver contributions, and much more. This is your chance to be part of a dynamic organization with significant growth potential.

      Ready to make an impact?
      Apply now and take the next step in your career with a leading organization in the animal health sector!
      To apply, please select the relevant ‘Apply’ button, or alternatively, forward your CV to maya@trs.co.nz