LSC has an exciting opportunity for a TSMS Dry External Manufacturing representative to join a leading pharmaceutical company in Cork. This is is a chance for you to work with a global company that strives for excellence in every aspect of its operation and has a huge reputation for its diverse working culture. If you have a minimum of 3 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: Organization Overview: Join the energetic and growing Dry - External Manufacturing Organization (DRY-EM) that delivers a diverse portfolio of medicines essential to our patients around the world. The DRY-EM TS/MS (Technical Services / Manufacturing Science) Scientist will provide technical and scientific expertise within a dynamic external manufacturing environment. The Scientist is responsible for providing technical support to achieve the reliable and compliant manufacture of spray dry dispersion and solid dosage manufacture at external contract manufacturing groups to predetermined global quality standards. This person interacts daily with a wide variety of people, primarily external partners team members and site management. The candidate will be responsible for supporting ongoing manufacturing at our External Partners through tasks such as process monitoring, response to issues, and improvements where necessary. This is a Small Molecule position. The position requires knowledge of cGMPs, applicable global regulatory manufacturing guidance, and the corporate/industry standards Responsibilities: Provide technical oversight for spray dry and solid dosage manufacturing processes, leveraging a strong technical foundation and previous experience supporting these processes. Participate in resolution of technical issues including those related to control strategy and manufacturing. Possess excellent technical writing capabilities including authoring of deviations and change controls. Employ excellent communication skills to manage internal and external relationships. Build and maintain relationships with development and central technical organizations. Ensure that processes are compliant, capable, in control, and maintained in a validated or qualified state. Understand, justify and document the state of validation with data that evaluate the capability of the manufacturing process to meet its stated purpose. Maintaining processes in a state of compliance with US and global regulations Operate with 'Team Lilly' in mind Basic Requirements: Bachelors (minimum) in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering 3+ years of demonstrated hands on working experience and proficiency with spray dry/or solid dosage manufacturing and working knowledge of regulatory expectations. Additional Preferences: Strong understanding of regulatory requirements and their application in a manufacturing environment Proficient in data management practices across manufacturing operations Demonstrates adaptability, a collaborative mindset, and a positive attitude toward change Proven ability to effectively communicate and influence across diverse technical and business teams Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects Additional Information: Some flexibility may be required to support 24/7 operations and issue resolution with external partners in different time zones. Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a valid Stamp 1G/Stamp 4 visa to apply! Apply via this advert or contact Siobhan Cummins at LSC on if you have any more questions about this role!
TPBN1_IJ