Quality Control Chemist I – Pharma Lab Start-up

Lever, Inc.; Bend (OR); On-site; USD 60,000 - 85,000; Full time

Benefits offered by this job

Paid time off

Retirement plan

Health plans

Life and disability insurance

Employee Assistance Program

Pet insurance

Job summary

Serán BioScience in Bend, Oregon is expanding its GMP manufacturing footprint, hiring a Commercial Quality Control Chemist to support the start-up of a new QC laboratory and ongoing analytical testing for commercial products.

You will operate HPLC, GC, dissolution, UV-Vis, FTIR and related instruments, document results under cGMP and GDocP, and contribute to investigations and CAPAs as part of a quality-focused team.

Qualifications

• Bachelor’s degree in a scientific discipline with hands-on lab experience preferred.
• Master’s degree in a scientific discipline with hands-on lab experience preferred.
• Experience in pharmaceutical commercial QC testing preferred.

Responsibilities

• Perform routine and non-routine analytical testing of commercial pharmaceutical products.
• Execute facility testing, finished product release, stability, in-process control, raw material testing, and other QC testing.
• Operate analytical instruments (HPLC, GC, dissolution, UV-Vis, FTIR) as qualified.
• Prepare samples, standards, reagents, and solutions per procedures.
• Document results accurately within testing timelines and in compliance with cGMP and GDocP.

Skills

cGMP knowledge

GDocP

Analytical chemistry

Laboratory techniques

Data integrity

Problem solving

Attention to detail

Time management

Cross-functional collaboration

Effective communication

Education

Bachelor’s degree in a scientific discipline

Master’s degree in a scientific discipline

Tools

HPLC

GC

Dissolution

UV-Vis

FTIR

Job description

Serán BioScience in Bend, Oregon is expanding its GMP manufacturing footprint, hiring a Commercial Quality Control Chemist to support the start-up of a new QC laboratory and ongoing analytical testing for commercial products.

You will operate HPLC, GC, dissolution, UV-Vis, FTIR and related instruments, document results under cGMP and GDocP, and contribute to investigations and CAPAs as part of a quality-focused team.