Junior QC Analyst

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

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact.

Job Responsibilities

• Performing quality control testing of finished products and raw materials, with a particular focus on HPLC and GC analyses.
• Preparing and maintaining analytical documentation.
• Participating in analytical method transfers.
• Supporting analytical method validation and cleaning validation activities.
• Investigating and documenting OOS (Out-of-Specification) and OOT (Out-of-Trend) results.
• Assessing deviations and non-conformities.
• Supervising reference standards and laboratory reagents, and coordinating waste management activities.
• Overseeing sample retention and archiving processes.
• Monitoring and maintaining laboratory equipment.

Requirements

• University degree in Chemistry, Pharmacy, or a related scientific field.
• Minimum 1 year of experience in a Quality Control laboratory within the pharmaceutical industry.
• Practical knowledge of analytical techniques, particularly HPLC and GC.
• Good understanding of GMP and GLP requirements.
• Proficiency in Microsoft Excel.
• Knowledge of OpenLab software and SAP ERP (QM module) will be considered an advantage.
• English language skills sufficient to understand scientific and technical documentation.
• Strong analytical thinking and problem-solving skills.
• Good organizational skills, attention to detail, and reliability.
• Ability to work effectively in a team and build positive working relationships.

We Offer

• Opportunities for professional growth and continuous development.
• Training programs and professional technical support.
• A strong organizational culture.
• A friendly and supportive working environment.
• An attractive employee benefits package.

We are an Equal Opportunity Employer. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.