Research & Development Specialist ( Animal Health)

7 days ago

, Philippines Blaine Corporation Full-time ₱600,000 - ₱800,000 Contract

Research & Development Specialist (Animal Health)

Full‑time position.

Position Summary

The R&D Specialist supports and collaborates with the R&D Team on product development and formulation, performs daily R&D activities, and maintains and monitors all documents related to the R&D process.

Job Scope

  • Assist in the research and development of new products and protocols
  • Material qualification and accreditation
  • Product costing
  • Perform SAP transactions as required to support SBUs directly linked to R&D processes
  • Consolidation and safe‑keeping of research and related studies
  • Re‑formulate products and redirect manufacturing processes as needed
  • Generate, preserve, and revise master production documents as necessary
  • Troubleshoot problems regarding materials, processes, products, and related activities

Duties & Responsibilities

  • Lead manufacturing process troubleshooting activities, including re‑processing with advanced product formulas and recommending appropriate inclusion levels for commercial production
  • Ensure that monitoring parameters such as chemical analysis recovery, physical and testing conformity, commercial batch conformance to re‑processing guides, stability (if necessary), and compilation of test results are met
  • Perform SAP transactions for raw material reservation/requisition for developmental products and trial batches
  • Conduct studies, reviews, and pre‑qualification of alternative raw material sources to existing product components, recommend resolutions, and document recommendations
  • Conduct research activities and organize researched data, hand‑outs, and dossiers that support commercial trouble‑shooting or product enhancement
  • Perform supporting trial testing parallel to commercial trouble‑shooting to identify root causes and recommend corrective actions, and assist in product complaint investigation
  • Prepare master production documentation for re‑processing formulations and their registration with the Document Control Center (DCC)
  • Conduct pilot‑scale and production‑scale batch trials and technology transfer for new products developed
  • Play a vital role in the developmental project’s first three commercial process validation runs, including documentation and change control
  • Prepare documents required by regulatory authorities for product registration
  • Create and revise SOPs as needed
  • Collate and prepare product quality reviews
  • Maintain the Master Batch Production Record (MBPR) file and ensure all supporting documents are attached
  • Requisition office and laboratory supplies pertinent to departmental activities
  • Report monthly developmental progress and coordinate meetings with manufacturing departments
  • Maintain inventory management of glassware and RPDD laboratory equipment, including preventive maintenance and calibration
  • Act as authorized signatory for documents in the absence of the R&D Manager, such as product labels, costing approvals, MBPR/MPDR approvals, and raw/packaging material accreditation
  • Represent the department at scheduled and unscheduled meetings, and conduct technical presentations or supplier product presentations in the absence of the R&D Manager

Preferred Qualifications

  • Graduate of B.S. Chemistry, B.S. Chemical Engineering, B.S. Pharmacy, or Industrial Pharmacy; other science related courses may apply with at least 2 years of relevant R&D experience in the pharmaceutical and veterinary industries. A professional board license is an advantage.

Skills

  • Basic knowledge of computer operations and software
  • Knowledge of cGMP and ISO principles and implementation

Other Requirements

  • Responsible, hardworking, analytical, resourceful, result‑oriented, honest, and trustworthy
  • Pro‑active and adaptable to all types of situations and personalities
  • Above average oral and written communication skills
  • Leadership and supervisory skills

Experience

  • Preferably 3 years of relevant experience in a pharmaceutical/veterinary laboratory performing product study, process development, and commercial processing. Must understand validation processes from start to end.

Job Location

Location details available upon request.