Pharma Bidding Analyst — Regulatory Specs Expert

Zuellig Pharma Corporation; Parañaque; On-site; PHP 400,000 - 650,000; Full time

Job summary

Zuellig Pharma is seeking a detail-oriented professional to review and validate technical specifications for government bids. You will ensure all medicine specifications meet regulatory criteria, identify correct pharmacological classifications, and reflect only compliant offerings in bid submissions.

Responsibilities include thorough documentation management, internal bidding, and ensuring completeness of all bid packages.

Qualifications

• Bachelor's Degree in Pharmacy with strong knowledge of pharmaceutical products, drug regulations, healthcare compliance, and medication management.
• Complex knowledge of documentation management and therapeutic class of medicines.
• Familiarity with government bidding processes and regulatory requirements is a plus.

Responsibilities

• Review, validate, and identify accurate technical specifications of pharmaceutical products for government bids.
• Ensure all medicine specs, regulatory requirements, and product offerings comply with bidding criteria.
• Achieve Bid qualification to contribute to government channel sales targets.
• Analyze procurement requirements and validate technical specs (generic/brand names, dosage, route, packaging, storage, shelf-life).
• Compare bid specs with company portfolio to ensure compliance and eligibility.
• Review pharmacological classifications and therapeutic equivalence for accurate bid matching.
• Ensure bids adhere to ABC and exclude non-compliant submissions.
• Ensure document completeness and validity; remove incomplete or expired documents.

Skills

Pharmaceutical knowledge

Documentation management

Bid/tender knowledge

Regulatory compliance

Pharmacy operations

Education

BS Pharmacy

Job description

Zuellig Pharma is seeking a detail-oriented professional to review and validate technical specifications for government bids. You will ensure all medicine specifications meet regulatory criteria, identify correct pharmacological classifications, and reflect only compliant offerings in bid submissions.

Responsibilities include thorough documentation management, internal bidding, and ensuring completeness of all bid packages.