QA Officer

at  Quantum Pharmaceutical

Are you passionate about innovation and quality in the pharmaceutical industry? Do you thrive in a dynamic and supportive work environment? Quantum Aseptic Services, part of the Target Healthcare Group, is looking for talented individuals to join our team and help us achieve our mission.

TRANSFORM HEALTHCARE WITH US!

At Quantum Aseptics, we’re revolutionising the delivery of aseptic medicines, and we are seeking passionate Quality Assurance Officer to join our mission.

WHY TOP TALENT CHOOSES US

Impact - Ensure the safety and efficacy of life-saving medicines.
Innovation - Work with cutting-edge technology and groundbreaking processes in a rapidly growing environment.
Career Growth - Enjoy unparalleled opportunities for continuous learning and professional advancement.
Collaborative Excellence - Be part of a passionate, international team dedicated to making a real difference in healthcare.
Competitive Rewards - Receive a top-tier salary, comprehensive benefits, and enjoy a balanced work-life environment.
If you are passionate about quality and aspire to make a significant impact in healthcare, we want you on our team. Join Target Healthcare Group and become a key player in our mission to transform healthcare.
Our Quality Assurance department is the heart of our operation, ensuring every product meets the highest standards of Good Manufacturing Practices. As we expand, we are seeking a meticulous and dedicated Quality Assurance Officer to join our elite team.

AS A QUALITY ASSURANCE OFFICER YOUR DUTIES WILL INCLUDE, ALTHOUGH ARE NOT LIMITED TO:

• Managing quality assurance activities such as Deviation and CA/PA management, Change Management while assuring compliance with established standards, regulations, specifications, and SOPs.
• Ensuring that documentation follows current Good Manufacturing Practices, current Good Documentation Practices, and external regulations. Assure the safety and quality of the products, processes, and systems.
• Developing and maintaining procedures, and policies to assure compliance with cGMP’s. Ensuring all documents are created, distributed, stored, and archived in line with regulatory requirements.
• Ensuring all systems, operations, products, processes, procedures, and documentation for adequacy and effectiveness to ensure Quality and Regulatory Compliance to related CAPA.
• Leading, participating in, and reviewing all types of investigations, Root Cause Analysis and Quality Risk Management.
• Applying problem solving logically and in an organized manner. Must have experience with Root Cause Analysis tools and the ability to apply tools.
• Leading and assisting with both internal and external audits and audit reports.
• Assessing and implementing regulatory changes.
• Identifying any relevant quality-related training needs, provide training tools and deliver training.

TO BE SUCCESSFUL IN THIS ROLE, YOU MUST SHOULD BE ABLE TO DEMONSTRATE:

• Experience of operating in a similar role is desirable.
• Bachelor’s degree with 2 or more years’ experience in Quality, Manufacturing, or related field.
• Ability to communicate efficiently verbally and in writing with all levels of the organization and with external clients.
• Detailed knowledge of applicable regulations and standards. Strong analytical/problem solving skills.
• Knowledge of Scilife (eQMS) will be advantageous.
• Demonstrable experience of working autonomously and making decisions with minimal direction.
• Ability to travel to other sites and for vendor audits.
• Experience working in pharmaceutical / healthcare / life sciences industry advantageous.
• English and Mathematics GCSE grades A-C (or equivalent).
• High computer literacy; experience operating with all Microsoft Office software.