Quality Control Specialist | Growth & Training

Bausch Health

Ksawerów

On-site

PLN 120,000 - 170,000

Full time

4 days ago
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Benefits offered by this job

Training programs
Professional technical support
Friendly working environment

Job summary

Bausch Health's EMO-FARM Sp. z o.o. in Ksawerów, Poland, seeks a QC Specialist to join the Quality Control team.

You will prepare analytical documentation, develop schedules, and maintain spreadsheets while ensuring regulatory compliance across validated methods and testing procedures. The role requires a university degree in chemistry or pharmacy, at least 2 years of QC analytical experience, GMP knowledge, and English at B2 level.

Qualifications

  • University degree in Chemistry, Pharmacy, or related field.
  • Minimum 2 years in an analytical QC role.
  • Knowledge of GMP and regulatory guidelines.
  • English proficiency at B2 or higher.
  • Strong analytical and collaborative skills.

Responsibilities

  • Prepare and update required analytical documentation.
  • Develop schedules and oversee execution.
  • Create and maintain spreadsheets with qualification and validation.
  • Evaluate analytical method performance.
  • Review validated methods and validation documentation for compliance.
  • Oversee laboratory equipment including HPLC/GC systems.
  • Monitor ICH guideline updates and quality system procedures.
  • Initiate change controls and quality events.
  • Plan and execute lab purchases for consumables and equipment.
  • Oversee waste management and MSDS documentation.
  • Act as Key User for SAP, Trend Complex, and PharmaComplex systems.

Skills

Analytical thinking
Team player
Organizational skills
Advanced Excel

Education

University degree in Chemistry or Pharmacy

Tools

OpenLab
SAP QM
Trend Complex
PharmaComplex
Microsoft Excel

Job description

Bausch Health's EMO-FARM Sp. z o.o. in Ksawerów, Poland, seeks a QC Specialist to join the Quality Control team.

You will prepare analytical documentation, develop schedules, and maintain spreadsheets while ensuring regulatory compliance across validated methods and testing procedures. The role requires a university degree in chemistry or pharmacy, at least 2 years of QC analytical experience, GMP knowledge, and English at B2 level.

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