Job description
Matrix Recruitment are currently recruiting for a Technology Transfer Engineer to join the team in Louth.
What you need to know:
Our Engineers help ensure that internal and external manufacturing operations remain operational, continuously improve, and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities, and Validation.
Your New Job:
We are seeking a skilled Technical Specialist to support Drug Product manufacturing operations. This role will contribute to the success of multiple production areas, provide technical leadership, drive process improvements, and ensure our commercial processes operate to the highest GMP and regulatory standards. The position requires strong collaboration across cross-functional teams and hands-on support for routine operations, technology transfer, and site readiness activities.
Key Duties and Responsibilities:
What are we looking for?
Apply for this job now or get in touch with Brenda on 087-4343544
By applying, you are giving consent for Matrix Recruitment to contact you about this job. We collect your data for recruitment purposes only and will retain it for the duration required as outlined in our privacy policy. All CVs are kept confidential and will not be submitted to any clients without your knowledge and permission. Please note that due to the expected high volume of applications we can only reply to applicants suitable for the position.
We Value Your Trust.
What you need to know:
Our Engineers help ensure that internal and external manufacturing operations remain operational, continuously improve, and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities, and Validation.
Your New Job:
We are seeking a skilled Technical Specialist to support Drug Product manufacturing operations. This role will contribute to the success of multiple production areas, provide technical leadership, drive process improvements, and ensure our commercial processes operate to the highest GMP and regulatory standards. The position requires strong collaboration across cross-functional teams and hands-on support for routine operations, technology transfer, and site readiness activities.
Key Duties and Responsibilities:
- Partner closely with internal departments to deliver on production and business objectives.
- Provide day-to-day technical support across Drug Product operations including formulation, filling, lyophilisation, capping, and automated visual inspection.
- Serve as the process SME, taking ownership of assigned processes and demonstrating deep technical understanding and problem-solving capability.
- Lead and support technical activities for commercial manufacturing, such as writing change controls, managing process improvement initiatives, conducting statistical evaluation of process performance, and investigating atypical or non-conforming events.
- Contribute to technology transfer activities by preparing and/or reviewing GMP documentation such as master batch records, protocols, qualification documents, change controls, reports, and regulatory submissions.
- Provide on-the-floor support during commercial batches and technology-transfer campaigns, including Person-In-Plant (PIP) coverage as needed.
- Interpret and apply GMP and regulatory requirements, helping to develop standardised procedures and work practices in collaboration with Operations and Quality teams.
- Support inspection readiness efforts for routine regulatory inspections and for new product introductions or transfers, partnering with Operations, Quality, and Regulatory Affairs.
- Participate in the development, sharing, and adoption of best practices, continuous improvement initiatives, and business process enhancements across the site.
What are we looking for?
- Minimum of 3 years post-bachelor's degree experience in a GMP functional area or support of a GMP functional area, such as Operations, Technical Operations, Technology, Engineering, and/or Maintenance.
- Bachelor’s degree in chemical/Biochemical Engineering, Pharmaceutical Science, or Chemistry/Biology, or other related science or engineering field.
- Proven expertise in aseptic operations, analytical testing, process development and tech transfer.
- Knowledge of USP1790 and industry/ regulatory requirements such as Annex 1 desirable
- Experience with lyophilized products advantageous
- Experience in start-up facility advantageous
- Demonstrated ability to independently manage projects/work to schedule/deadlines
- Statistics experience (including Proactive Process Analysis and Continuous Process Verification)
- Experience in deviation management and/or change control and/or equipment support and/or equipment qualification, and/or project management.
Apply for this job now or get in touch with Brenda on 087-4343544
By applying, you are giving consent for Matrix Recruitment to contact you about this job. We collect your data for recruitment purposes only and will retain it for the duration required as outlined in our privacy policy. All CVs are kept confidential and will not be submitted to any clients without your knowledge and permission. Please note that due to the expected high volume of applications we can only reply to applicants suitable for the position.
We Value Your Trust.
