Senior QC Analyst - Pharma

Oxford Global Resources; Amsterdam; On-site; EUR 42,000 - 54,000; Full time

Job summary

Oxford Global Resources is seeking a Senior Chemical Analyst to lead non-routine QC activities in our Amsterdam lab. You will contribute to process improvements, support method validations, and handle OoS investigations alongside the Lab Manager and QA team.

You will work with HPLC, GC, UV, IR and other techniques, support GMP-compliant operations, and participate in automation and lab improvement projects in a vibrant, small-team environment.

Qualifications

• BSc or MSc in analytical chemistry or another relevant field.
• Several years of experience in pharmaceutical QC.
• Experience with deviation handling, method validation, SOP writing.

Responsibilities

• Handle deviations and OoS investigations from the QC end.
• SOP writing.
• Method validation.
• Continuous improvement.
• Work under GMP guidelines.
• Involvement in automation projects and lab improvements.
• Chemical analysis using a wide range of techniques.

Skills

Deviation handling

SOP writing

Method validation

Continuous improvement

GMP compliance

Laboratory automation

Education

BSc or MSc in Analytical Chemistry

Tools

HPLC

GC

UV

IR

Titrations

Dissolution testing

Grain size

Job description

We are looking for a Senior Chemical Analyst to pick up all non-routine aspects on the QC-lab and to work on improvement processes.

Job description

You are working in a relatively small team as a Senior QC Analyst focused on improving the processes and handling non-routine events with the Lab Manager and QA-team. The lab team tests hundreds of raw materials and final products, which means regular method validations, occasional out of specs and deviations and a lot of variety. Outside of the non-routine aspects, you are a senior member of the analytical team and do HPLC, GC, UV, IR, titrations, physical testing, dissolution testing, grain size, and much more. The lab will have many modernization projects over the coming year that you will be heavily involved in, so the time to join is now!

Responsibilities

• Handle deviations and OoS investigations from the QC end
• SOP writing
• Method validation
• Continuous improvement
• Work under GMP guidelines
• Involvement in automation projects and lab improvements
• Chemical analysis using a wide range of techniques

Profile

• BSc or MSc degree in analytical chemistry or another relevant field
• Several years of experience in pharmaceutical QC
• Experience with deviation handling, method validation, SOP writing

Benefits and practical information

• Long term position, start through Oxford
• Salary range: €3800,- to €4800,- gross monthly
• Full-time role on site, 32 hours is possible
• Region: Amsterdam
• Vacaturenummer: 27594