Benefits

• Extensive training and development.
• Opportunity for project management and leading laboratory improvements.
• 4 reward yourself days off.

About the company
This organization is a renowned global leader in the healthcare and life sciences industry. With a rich history spanning over a century, located in Wellington, New Zealand. This organization has consistently been at the forefront of medical innovation, dedicated to inventing life-saving medicines and vaccines for some of the world's most formidable diseases.

About the opportunity
As the Quality Control Systems Specialist, you will be reporting into the Site Quality Head, you will be required on-site to provide technical oversight for the quality control laboratory systems and to ensure testing is compliant with the current requirements. You will assist with the implementation of new test methods, systems, processes, and equipment to guarantee quality control testing is adhering to the local regulatory requirements and the organization’s global quality policies. To excel in this role, you will need to communicate effectively, along with possessing extensive laboratory management experience, a strong focus on process improvement, and excellent organizational and project management skills.

This role is located in New Zealand, relocation opportunities from Australia or International. 

Duties

• Assessing vendors for new equipment while ensuring equipment validation aligns seamlessly with the Method Robustness program.
• Overseeing troubleshooting, calibration and maintenance updates of the equipment and analytical instruments.
• Continuous review of test methods used in the labs.
• Conducting internal and external audits and generate report findings.
• Developing data integrity and software improvements, implementations, and providing training and support to all staff members.
• Participating in the review of policies and procedures, EHS and workplace risk assessments.
• Ensuring all documentation and reports are compliant with company and notified bodies’ quality standards.
• Managing change controls and CAPA’s ensuring they’re carried out in a timely manner.

Skills and Experience

• Master’s or doctoral degree in a Science related field.
• Experience with accredited laboratories, method development, validation, health & Safety Ex: VICH, ICH guidelines.
• Over 5 years of experience as a Senior QC Analyst or Laboratory Supervisor leading technical improvements.
• Utilizing proactive methods of planning, developing, and implementing policies or use of resources.
• Efficient technical writing and computer skills using Microsoft word, excel, PowerPoint.
• Managing, supporting, and motivating staff.
• A Highly motivated, independent, and proactive individual, Ability to multi-task and adapt as required.

Culture
This organization fosters an environment that encourages intellectual curiosity and personal growth, where your talents and skills will be nurtured as part of their ever-evolving team.

How to Apply
Click apply or contact Tamara El Husseini by sending your resume to telhusseini@hpgconnect.com to schedule in a confidential discussion.