QC Analyst (HPLC/GC) - Pharma Quality Control

Bausch Health; Ksawerów; On-site; PLN 60,000 - 90,000; Full time

Benefits offered by this job

Growth opportunities

Training programs

Employee benefits

Job summary

Bausch Health in Poland seeks a Quality Control professional to conduct finished product and raw material testing with emphasis on HPLC and GC methods. You will prepare analytical documentation, support method transfers, and contribute to method validation and validation activities.

The role requires a chemistry/pharmacy degree, at least 1 year in QC labs, and strong knowledge of GMP/GLP. Proficiency in Excel is expected; OpenLab and SAP QM are a plus.

Qualifications

• Bachelor's degree in Chemistry, Pharmacy or related field.
• At least 1 year of experience in aQuality Control laboratory in pharma.
• Practical knowledge of HPLC and GC analyses.
• Good understanding of GMP/GLP requirements.
• Proficiency in Microsoft Excel; OpenLab and SAP QM are plus.

Responsibilities

• Perform quality control testing of finished products and raw materials, focusing on HPLC and GC analyses.
• Prepare and maintain analytical documentation.
• Participate in analytical method transfers.
• Support analytical method validation and cleaning validation activities.
• Investigate and document OOS and OOT results.
• Assess deviations and non-conformities.
• Supervise reference standards and lab reagents; coordinate waste management.
• Oversee sample retention and archiving processes.
• Monitor and maintain laboratory equipment.

Skills

Analytical thinking

Problem solving

Teamwork

Attention to detail

Excel

Education

University degree in Chemistry, Pharmacy, or related

Tools

HPLC

GC

OpenLab

SAP QM

Job description

Bausch Health in Poland seeks a Quality Control professional to conduct finished product and raw material testing with emphasis on HPLC and GC methods. You will prepare analytical documentation, support method transfers, and contribute to method validation and validation activities.

The role requires a chemistry/pharmacy degree, at least 1 year in QC labs, and strong knowledge of GMP/GLP. Proficiency in Excel is expected; OpenLab and SAP QM are a plus.