Contract HPLC/GC SME — Pharma Method Development

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

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.