CareerPlan

QC Analyst II

Kundl, ATFull-time€48k–€73k2026-10-19 → 2026-11-10

Core

Perform, evaluate, and document analytical tests in a GMP-regulated QC lab to ensure timely release of raw materials, in-process controls, and finished products.

Role type

Quality Control Analyst

Builds

Analytical test results and quality documentation for pharmaceutical manufacturing

Domain

Pharmaceutical manufacturing / Quality Control

Required skills

GMP compliance, analytical testing methods, OOS/OOT investigation, data integrity, deviation handling, method validation support, environmental monitoring, audit support

Preferred skills

Chemistry/Biochemistry/Pharmacy background, GxP experience, laboratory equipment operation, continuous improvement initiatives

Technologies

Laboratory Information Management Systems (LIMS), analytical instruments

Responsibilities

Conduct and document analytical tests per GMP; Review raw data and lab records; Investigate OOS/OOT results; Support method validations and transfers; Participate in internal/external audits and inspections; Monitor environmental conditions; Collaborate with cross-functional teams

Seniority

Mid-level, hands-on IC