External Manufacturing Operations (on site)

A fantastic opportunity has arisen for an External Manufacturing Operations – Senior specialist 12 Month Contract . Our vision as a Manufacturing & Supply Division is to be the most trusted supplier of biopharmaceuticals & Vaccines worldwide. We have created a reliable global manufacturing network that’s devoted to delivering a high quality, reliable supply to customers and patients on time, every time. Come join us if this aligns with your values and goals! Why you should apply! You will: • Drive excellence in Compliance, Supply, Continuous Improvement & Cost to meet customer demand at the Contract Manufacturing Organization (CMO)• Support and guide new project support as well as commercial oversight between our Manufacturing Division and the CMO. • Be part of a cross-functional team (Supply Chain, Quality, Technical Ops, Procurement…) who are accountable for delivering daily/weekly/monthly/annual requirements at their external partner(s). Bring energy, knowledge, innovation to carry out the following: • Ensure compliance: Maintain up-to-date knowledge of regulatory requirements and industry standards pertaining to both aseptic manufacturing and cold chain logistics, participating in regulatory inspections as needed (Quality Risk management, Deviation Management, Product Release, Change Control); • In-Plant Support: Provide on-site support at the CMO facility, ensuring alignment with production goals and quality standards. Facilitate communication between the CMO and internal stakeholders.• Aseptic Manufacturing Oversight: Oversee and support aseptic processing activities, including sterile filling, lyophilization, and packaging, ensuring adherence to Good Manufacturing Practices (GMP) and regulatory requirements.What skills you will need: In order to excel in this role, you will more than likely have: • Bachelor’s degree preferably in the Engineering, Science or Business • Minimum 4 years’ relevant experience in the pharmaceutical industry and/or manufacturing (sterile operations, quality, technical) with a thorough knowledge of global GMP and regulatory requirements. • Sterile Drug Product and /or Vaccines operations experience would be a distinct advantage. • Ability to work collaboratively on issue resolution and management of events (quality/ supply etc) • Ability to achieve compliance goals, Responsabilità:
We offer a 12 months fixed term contract. Annual salary 50k -