Pharma Bid Analyst – Regulatory Specs & Compliance

Zuellig Pharma; Carmen; On-site; PHP 600,000 - 900,000; Full time

Job summary

Zuellig Pharma is seeking a qualified Pharmacy graduate to review and validate technical specifications of pharmaceutical products for government bids. You will ensure compliance with regulatory requirements, correct pharmacological classifications, and alignment with ABC bidding criteria.

In this role, you will assess dosage strength and form, route of administration, packaging, storage needs, and shelf-life, while maintaining complete and up-to-date documentation across submissions.

Qualifications

• Bachelor's degree in Pharmacy required with strong knowledge of drug regulations.
• Experience with documentation management is preferred.
• Familiarity with government bidding and regulatory requirements.

Responsibilities

• Review and validate technical specifications of pharmaceutical products for government bids.
• Ensure compliance with bidding criteria and ABC guidelines.
• Analyze procurement requirements and verify correct pharmacological classifications.
• Identify and validate dosage forms, strengths, routes, packaging, storage, and shelf-life.
• Review documents for accuracy and remove incomplete or expired submissions.
• Compare bid specifications with product portfolio to ensure eligibility.
• No overbidding and ensure bid submissions are complete and valid.

Skills

Pharmaceutical products knowledge

Drug regulations

Healthcare compliance

Medication management

Education

Bachelor's Degree in Pharmacy (BS Pharmacy)

Job description

Zuellig Pharma is seeking a qualified Pharmacy graduate to review and validate technical specifications of pharmaceutical products for government bids. You will ensure compliance with regulatory requirements, correct pharmacological classifications, and alignment with ABC bidding criteria.

In this role, you will assess dosage strength and form, route of administration, packaging, storage needs, and shelf-life, while maintaining complete and up-to-date documentation across submissions.