QA Operations Specialist
Gdańsk
Boost your career with us:
Polpharma Biologics is a state-of-the-art biological R&D and manufacturing facility, one of the most modern in Europe. We have a fantastic, international team of experienced experts and dynamic young scientists with common goals and values. Biotechnology is our passion.
Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
Your role:
In this role, you will have an opportunity to take part in the whole life cycle of biopharmaceutical product development and production. You will be responsible for risk assessments, investigations related to deviations, proper documentation management, and preparations for audits and inspections.
Your responsibilities:
- Ensuring cGMP and regulatory compliance of operations leading to biological Drug Substance and Drug Product
- Supporting that all aspects of handling and manufacturing of biopharmaceutical products at our site comply with the requirements that meet all relevant cGMP regulatory and legislative requirements
- Ensuring that a high quality of products is achieved through qualification and validation based on quality risk analyses, product quality assessments, and ongoing verification
- Supporting the whole life cycle management of a manufacturing facility, up to and including GMP compliant market production
- Ensuring that all processes and products at the site meet all internal and external requirements
- Establishment, implementation, and supervision of the required quality processes in product development, manufacturing, testing, storage, and distribution
- Batch records’ and all related documentation review
- Participation in investigations on deviations and complaints, OOS/OOT, recalls and escalations
- Supporting change control requests, assuring GMP and regulatory compliance
- Participation in risk assessments
- Supporting all product and process-related activities e.g. process transfers, process validations, and continuous process verification (including e.g. stability studies, hold time studies, approval of protocols and reports)
- Supporting the preparation of Annual Product Quality Reviews
- Preparation and review of required GMP documentation – assisting in coordination and preparation of Polpharma Biologics for inspections, audits, and controls
- Participation in internal and external audits
- Support establishment of Quality Management System documentation in accordance with the requirements of Polpharma Biologics and the HA requirements in reference to diverse market areas
- Ensuring correctness and data integrity of all regulatory and manufacturing data
If you have:
- University degree (Biology, Chemistry, Pharmacy, Biotechnology or related)
- 3 years of working experience in the pharmaceutical industry, incl. 2 years in Quality Control and/or Quality Assurance of pharmaceutical products
- Excellent knowledge of GMP requirements and pharmaceutical laws and regulations
- Understanding of analytical technologies related to the evaluation of biopharmaceutical products, knowledge of sterile pharmaceutical production
- Understanding of issues and needs related to qualification and validation processes in biopharmaceutical manufacturing
- Knowledge of Quality Management Systems
- Experience in Biotechnological manufacturing or commercial production
- Fluent English