Farmaprojects, part of Polpharma Group B.V., is a B2B Pharmaceutical Laboratory company offering a broad Portfolio of Generic Pharmaceutical Products and Value Added Medicines.
For our Laboratory in Barcelona, Farmaprojects is looking for a new Quality Control Analyst to join our Quality Department in January 2025. This position will report directly to the Quality Control Manager.
At Farmaprojects, you can expect:
* To be part of the transformation of the business
* Continuous learning opportunities
* A rapidly expanding company
* A multicultural environment open to new ideas
* A company culture that is a reflection of shared values
You will be part of an exciting team contributing to the business whilst enjoying the following corporate benefits:
* Flexible working hours
* Commuter benefits
* Ticket Restaurant
* Health Insurance
* Annual learning & development
* Mental healthcare support and services
* Team-driven celebrations and events
* and more!
RESPONSIBILITIES:
* To carry out the analysis and control functions necessary to effectively cover the needs of the Quality Control department.
* Carry out the appropriate tasks to optimize and make the necessary processes profitable.
* Ensure compliance with GMP (Good Manufacturing Practices) standards.
* Carry out technical reviews and calculations generated in the laboratory.
* Perform physicochemical analyses in relation to the products under study.
* Carry out stability analyses of the products under study.
* Collaborate in the investigation of analytical deviations and out-of-specification results.
* Responsible for the operation and calibration of assigned devices and installations.
* Collaborate in the qualification, calibration, and verification of the same.
* Comply with quality, safety, prevention and environmental standards.
* Collaborate in the drafting and updating of SOPs, standard operating procedures. Work in accordance with the guidelines described in the SOPs.
* Maintain the archive of all generated documentation up to date.
Requirements:
* ·Experience in a GMP environment.
* Experience in a similar position within the chemical-pharmaceutical industry.
* Proficiency in HPLC Waters (Empower)
* Experience with other analytical techniques for finished products will be valued (Dissolution Test, Karl Fischer, Spectrophotometer, Disintegration Test, etc.).
* Secure handling of common MS Office programs, databases, excellent knowledge, and handling of data sources
* Fluency in English (written and oral).