R&D Product Introduction & Validation Specialist

Square Pharmaceutical, Inc; Carmona; On-site; PHP 600,000 - 900,000; Full time

Job summary

Square Pharmaceutical, Inc is seeking a qualified professional to drive product introduction and technology transfer to production. The role focuses on pilot batches, process characterization, and packaging material development to support new product launches.

You will prepare process validation plans, execute characterizations, generate reports, and ensure GMP compliance across all activities, while identifying improvements using current technologies.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering, or Biochemistry.
• Proficient with Microsoft Office, technical writing, analytical/troubleshooting skills.
• Experience in product development or process validation preferred.

Responsibilities

• Introduce new products and facilitate technology transfer to production.
• Execute product introduction activities such as pilot batch compounding and process characterization.
• Develop and monitor packaging materials for new products.
• Prepare process validation controls and sampling plans.
• Execute process characterization and validation of all products.
• Prepare validation reports and align process-related concerns with Master BPRs/PDRs.
• Prepare cleaning validation protocols and reports.
• Improve formulation and process of existing products using current technology.
• Create technical specifications for new raw materials and packaging materials; improve existing specs.
• Meet targets and deliver results through planning, organizing and task completion.
• Ensure GMP compliance at all times.

Skills

Problem-Solving

Analytical Thinking

Technical Writing

Process Improvement

Education

Bachelor's Degree in Pharmacy

Tools

Microsoft Office

Technical Writing

Analytical Troubleshooting

Job description

Square Pharmaceutical, Inc is seeking a qualified professional to drive product introduction and technology transfer to production. The role focuses on pilot batches, process characterization, and packaging material development to support new product launches.

You will prepare process validation plans, execute characterizations, generate reports, and ensure GMP compliance across all activities, while identifying improvements using current technologies.