Consultant

ProPharma; Oregon (WI); On-site; USD 166,000 - 277,000; Part time

Job summary

ProPharma in Oregon is seeking a HPLC/GC SME for a 1.5–2 month contract onsite. You will help lead analytical development to support the synthetic team and validate HPLC methods for small molecule API manufacturing.

The role requires 10–20 years of relevant experience, with emphasis on analytical method development and qualification/validation activities. This onsite contract offers an opportunity to impact critical development milestones.

Qualifications

• 10–20 years of experience in pharma analytics or development.
• Expertise in HPLC method development and validation.
• Experience supporting small molecule API QC and analytics.

Responsibilities

• Lead analytical development for the synthetic team.
• Develop and validate HPLC methods to support API manufacturing.
• Plan and execute qualification/validation activities for methods.

Skills

HPLC method development

Analytical method qualification

QC for small molecules

Job description

This is a 1.5 to 2-month contract onsite in Oregon.

Project Start Date: September 14, 2026

Job Title: HPLC / GC SME

Description: Needing someone who can help do/lead analytical development to support their synthetic team. This person will need to be experienced with both HPLC development of methods to support small molecule API manufacturing and the qualification/validation of those methods

Required skillset: Small molecule pharma QC or Analytical method development

Years of Experience: 10 - 20 years of experience