StellenbeschreibungppJoin a dynamic quality team where you'll collaborate with global stakeholders and manufacturing partners to drive product quality and support the successful delivery of innovative therapies. /p pProclinical is seeking a Quality Product Associate to oversee the quality and compliance of pharmaceutical and biologic products. This role focuses on ensuring timely delivery of high-quality products while maintaining compliance with local, divisional, and global regulations. You will collaborate with internal teams and third-party manufacturers to support product transfers, manage quality records, and contribute to new product launches. /p pPlease note that to be considered for this role you must have the right to work in this location or hold an EU passport. /p h3Responsibilities: /h3 ul liAct as the primary quality lead for assigned projects, ensuring on-time quality deliverables. /li liPerform final quality batch record reviews for products manufactured by third-party manufacturers. /li liEnsure alignment and fulfilment of Quality and Technical Agreements with legal contracts. /li liEstablish and maintain open communication with third-party manufacturers, affiliates, and internal teams to address quality concerns and identify potential projects. /li liCommunicate and negotiate with external quality organizations to minimize compliance risks while balancing operational costs. /li liManage quality records, including Change Controls, Exception Reports, CAPAs, and Complaints, in a timely manner. /li liSupport quality assurance activities for new product launches, including coordination with third-party manufacturers. /li liFacilitate investigations into complaint trends and manage exception documents and corrective actions. /li /ul h3Key Skills and Requirements: /h3 ul liDegree-qualified in Life Sciences, Engineering, a technical field, or possess equivalent relevant industry experience. /li liProven experience within Quality Assurance Operations, with a solid understanding of pharmaceutical and/or biologics manufacturing processes. /li liKnowledge of a range of pharmaceutical dosage forms, including sterile biologics, ointments, tablets, capsules, modified-release products, and active pharmaceutical ingredients (APIs). /li liStrong analytical and critical thinking skills, with the ability to prioritise and manage multiple complex projects simultaneously. /li liExcellent communication and stakeholder management skills, with the ability to operate effectively as a leader, collaborator, or independent contributor. /li liHighly organised, detail-oriented, and able to work with pace and urgency in a dynamic, fast-moving environment. /li /ul pIf you are having difficulty in applying or if you have any questions, please contact Molly Colclough at /p /p #J-18808-Ljbffr