About this role
Position Summary:
The R&D Specialist supports and gives assistance to the R&D Team and collaborate with her/his co-worker on all products developed and formulated products, performance of daily R&D activities, maintains and monitor all documents related to the R&D processes.
Job Scope:
Assists in the research and development of new products and protocolsMaterial Qualification and AccreditationProduct CostingPerform SAP (Systems Application Product) transactions as required to support SBUs directly linked to R&D processesConsolidation and safe-keeping of researches and related studiesRe-formulation of products and redirection of manufacturing processes as neededGeneration/ Preservation and Revision (if needed) of Master Production DocumentsTrouble Shooting of problems regarding materials, processes, products and other related activities
Duties & Responsibilities:
In-charge of the manufacturing process trouble-shooting activities such as but not limited to:
Re-processing with advance under-studies product formula and recommends pertinent percentage inclusion level to the original formulation for commercial process manufacturingEnsures that the following parameters are satisfied within the covered monitoring:Chemical analysis recovery is within the specified requirementPhysical and testing conformityCommercial batching conform the re-processing guide;Stability, if necessaryCompilation of test result/s and monitoring intactPerform the SAP (Systems Application Product) transactions required for raw material reservation/requisition for developmental products and trial batchesConducts study, review and pre-qualification of alternative source/s of applicable raw material substitution to existing component in the product formulation/s as a resolution to the identified trouble-shooting made and recommends accordinglyPerforms research activities, the collation and orderly safe-keeping of the researched data information, hand-outs, or related dossiers that supports the commercial trouble-shooting or the recommended product enhancement or fortification of the existing product formulaConducts supporting trial testing parallel to the commercially-identified trouble to rule out root-cause and recommends appropriate corrective actions/ Support on answering and investigation on product complaintPrepares Master Production Documentation of all Re-processing formulation and the applicable registration to the Document Control Center (DCC)Conducts pilot scale and production scale batch trials and technology transfer for new products developedPlays vital role for the developmental project’s first three (3) commercial process validation protocol run and the applicable documentation and change controlResponsible for preparing the documents required by Regulatory for Product RegistrationSOP Creation and Revision if neededCollation and Preparation of Product Quality ReviewResponsible for the updating of file record of the Master Batch Production Record (MBPR) and assures the complete attachment of the relevant supporting documents of the product dossier per envelopeResponsible for the requisition of the office and laboratory supplies pertinent to the department’s activitiesIn-charge of the Monthly Developmental Progress Reporting and the need to call for any related coordination meeting with the manufacturing related departmentsEnsures safe-keeping and the corresponding inventory management of glass wares and RPDD Laboratory Equipment plus its preventive maintenance and calibration requirementsAuthorized signatory for the following documents in the absence of the RDD Manager such as: Product Label, Costing Approval, MBPR/MPDR or its BPR/PDR approval, and any Raw/Packaging Material’s accreditationRepresents the Department for scheduled and unscheduled meetings and other technical presentation/ trainings or suppliers’ product presentation in the absence of R&D Manager Preferably a graduate of B.S. Chemistry, B.S. Chemical Engineering, B.S. Pharmacy, Industrial Pharmacy Other science related courses may also apply but with 2 years relevant R&D experience on Pharmaceutical and Veterinary Industry A professional board license would be an advantage.
Skills: Basic knowledge of computer operations and softwares, cGMP and ISO principles and implementation
Other: Must be responsible, hardworking, analytical, resourceful, result oriented, honest and trustworthy. Must be pro-active and adapts to all types of situation and personalities. Above average oral and written communication skills. Possess leadership and supervisory skills
Experience: Preferably with 3 years of relevant work experience in a pharmaceutical / veterinary laboratory doing related product study and development of processes and up to its commercial processing He must know the validation processes from start to en
Our Manufacturing processes brings out the best taste in food products through our flavors, herbs, and spices. That add nutritional value through our vitamins and minerals. We customize powder and liquid flavor mixes, seasoning mixes, and vitamins premixes according to our client’s requirements and guarantee the best value and satisfaction to our clients.