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Third Party Manufacturing - R&D Associate, Sligo
Client: Cpl
Location: Sligo, Ireland
Job Category: Other
EU work permit required: Yes
Job Reference: [Reference Number]
Job Views: 107
Posted: 21.01.2025
Expiry Date: 07.03.2025
Job Description:
Our client is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
Primary Functions:
Establish effective working relationships with Third Party Manufacturers (TPM), Commercial and Nutrition Supply Chain (NSC) Divisional functions including Regulatory, Medical, Tech Centre and Quality to provide support for product moves and New Product Introductions. A logical thinker, the R&D Associate will bring technical and scientific expertise to all matters pertaining to the delivery to market of new powder and liquid nutritional products produced at Third Party Manufacturers in Asia and Europe. An ‘innovation oriented’ contributor with excellent attention to detail and communication skills, the R&D Associate will have the ability and inquisitiveness to comprehend the details behind processes and transactions beyond his/her direct area of responsibility to ensure compliance with both regulatory and product design requirements.
Scope Includes:
1. Product Development: Design new products or variations of existing products. Re-formulate existing nutritional products for manufacture at TPM sites to meet new regulations or market requirements. Support the qualification of new ingredients and suppliers. Support the development of manufacturing processes for new and existing products at various TPMs.
2. Documentation Development: Draft new document packages for new list numbers. Revise existing documentation as needed. Create Raw Material Specification documents for new ingredients and advise QA on Raw Material testing Program requirements.
3. Technical Expertise: Support assessment of new suppliers and ingredients. Draft finished product testing requirements. Troubleshoot formulation and manufacturing issues. Support QA function of the TPM group with investigation of complaints, deviations, and Exceptions Reports.
4. Project Activities: Support the development of project scope, trial, and budget requirements. Attend project meetings for all R&D activities and provide technical leadership to multi-disciplinary project teams.
5. Stability Data: Maintain repository of stability data for TPM products. Oversee product testing and stability program requirements.
Education: BSc in food science or engineering preferred.
Experience: Minimum of 3 to 5 years of prior experience in formulation and manufacturing processes of powder and liquid nutritional products in the Nutritional industry.
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