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Sandoz

Leader in generic and biosimilar medicines

Operational Quality Assurance Specialist

Regulatory & Quality (Life Sciences)Updated on Nov 12
Full-timeWarsaw, PolandPLN7.3k - PLN13.7k /moIn-person

About the Job

Requirements

  • A higher education qualification is preferred in pharmacy, biotechnology, chemistry, chemical technology, chemical and process engineering, or production engineering.
  • At least two years of pharmaceutical-industry experience in Quality Assurance, Quality Control, or production.
  • Knowledge of Good Manufacturing Practice requirements and pharmaceutical law.
  • Ability to conduct and evaluate investigations into deviations and nonconformities.
  • Practical knowledge of Microsoft Office.
  • English proficiency at B1/B2 or higher to work with documentation and communicate in a business context.
  • Analytical thinking and risk-assessment skills.
  • Ability to work independently and take responsibility for decisions.
  • Good work organization and ability to prioritize.
  • Communication and interdepartmental collaboration skills.
  • Accuracy and attention to detail.
  • Proactive approach to solving quality problems.
  • Openness to professional development and expanding specialist knowledge.

Responsibilities

  • Oversee the compliance of medicinal-product packaging processes with Good Manufacturing Practice, pharmaceutical law, and the internal Quality Management System.
  • Review, assess, and approve quality documentation, procedures, and instructions related to medicinal-product packaging processes.
  • Participate in change control, assess the impact of changes, and oversee their implementation.
  • Conduct and approve activities related to deviations, complaints, and Corrective and Preventive Actions.
  • Review production documentation for compliance with registration requirements and Good Manufacturing Practice.
  • Contribute to quality risk analyses.
  • Support process and cleaning validation and the qualification of premises and equipment.
  • Participate in internal audits, customer audits, and inspections by regulatory authorities.

Desired Qualifications

  • Experience in validation, qualification, and change management is an advantage.
  • Knowledge of SAP and other quality systems is an advantage.

About the Company

Sandoz

Leader in generic and biosimilar medicines

What does the company do? Sandoz is a global leader in generic and biosimilar medicines, with a broad portfolio of about 1,300 products that address diseases from the common cold to cancer. How does its product work? The medicines are off-patent (generics) or biosimilars that match the reference brands in safety, quality, and efficacy, offering affordable treatment options to patients and helping healthcare systems save money while expanding access. How is it different from competitors? Sandoz emphasizes scale, a long heritage dating back to 1886, and a sizeable global workforce dedicated to broadening patient access, aiming for large social impact and substantial healthcare savings. Its leadership in biosimilars and the breadth of its portfolio set it apart in the market. What is the company's goal? To pioneer access for patients by making high-quality medicines more affordable and widely available worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1886

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