Quality Control Investigation Writer

Job overview

The Quality Control Investigation Writer role is onsite in High Point, NC, with pay up to $36.00 per hour. The role supports a biotechnology company’s GMP-regulated pharmaceutical manufacturing operations through scientifically sound, compliant laboratory investigations.

What you'll do

• Lead and author investigations involving out-of-specification and out-of-trend results, environmental monitoring excursions, and laboratory deviations
• analyze laboratory data and supporting records to determine root cause and product impact
• facilitate investigation meetings
• prepare reports and quality records including CAPAs and change controls
• review records for accuracy and compliance
• support Quality Assurance reviews
• and participate in inspections and audits.

What we're looking for

Skills & competencies

quality control investigation writer

high point nc

genesis10

up to $36/hr

gmp

laboratory investigations

oos

oot

environmental monitoring

capa

change controls

pharmaceutical manufacturing

Work arrangement

• Weekend coverage required

Benefits & perks

• Medical, dental, vision, and sick pay where applicable.

Why this role

Requires at least two years in a GMP-regulated pharmaceutical, biotechnology, or biologics environment and at least one year authoring and leading QC laboratory investigations.

About the employer

Genesis10 is hiring for this role. Industry: Research and Development in Biotechnology (except Nanobiotechnology). Sector: 54.