Pharma Bidding Analyst - Compliance & Bid Strategy

Zuellig Pharma; Hinoba-an; Hybrid; PHP 446,000 - 781,000; Full time

Job summary

Zuellig Pharma in Sta. Rosa, Philippines, is seeking a Bidding Analyst responsible for reviewing, validating and identifying accurate technical specifications of pharmaceutical products for government bids, ensuring compliance with bidding criteria and regulations.

Focus on technical specification review, analysis of procurement requirements, alignment with product portfolio, and ensuring completeness of documents. Strong knowledge of drug regulations and documentation management is expected.

Qualifications

• Strong knowledge of pharmaceutical products, drug regulations, healthcare compliance, and medication management.
• Complex knowledge of documentation management and therapeutic class of medicines.

Responsibilities

• Review, validate and identify accurate technical specifications for government bids.
• Ensure medicine specifications, regulatory requirements, and product to offer comply with bidding criteria.
• Analyze procurement requirements for pharmaceutical products.
• Identify and validate the correct technical specifications of medicines (generic/brand, dosage, route, packaging, storage, shelf-life).
• Compare bid specifications with company portfolio to determine compliance and eligibility.
• Review pharmacological classifications and therapeutic equivalence to ensure accurate bid matching.
• Remove incomplete or expired documents from submissions.

Skills

Pharmaceutical knowledge

Regulatory compliance

Documentation management

Education

Bachelor's Degree in Pharmacy (BS Pharmacy)

Job description

Zuellig Pharma in Sta. Rosa, Philippines, is seeking a Bidding Analyst responsible for reviewing, validating and identifying accurate technical specifications of pharmaceutical products for government bids, ensuring compliance with bidding criteria and regulations.

Focus on technical specification review, analysis of procurement requirements, alignment with product portfolio, and ensuring completeness of documents. Strong knowledge of drug regulations and documentation management is expected.