QA CMOs Specialist

Research and Development & Drug Product Manufacturing Carrer de Castelló, 1, 08830 Sant Boi de Llobregat Barcelona, Spain
Job details
At Synthon you will have a great experience, in an excellent work environment, and surrounded by highly talented and motivated people, where you will be able to contribute by collaborating with the rest of the team to achieve the Company's results, and develop professionally and personally.

Job details

Reporting to the Department Manager, this person will be assigned the following functions:
Review and issuance of documentation necessary for batch certification.
Entering data into the Lims system
Support documentation requests from Holding sites and through Request to QP
Management of sending documentation to the contracted Contract manufacturers for their correct manufacturing.
Department Database Maintenance
Maintain the GXP documentation system in both electronic and paper formats when required.
Administrative tasks supporting batch release
Our offer
At Synthon, we provide our employees with a working environment that emphasizes trust, pride, and joy. This approach has earned us recognition as a Great Place to Work® in 2017 and 2019. As a company, we recognize our impact on the wider world, including the economic, social, and environmental aspects. Our values are rooted in caring for one another, our partners, patients, and society at large. We actively support various educational initiatives and contribute to charitable causes, as well as working to develop the communities to which we belong worldwide.

We offer our employees:
Be part of a dynamic work environment, based on trust and transparency.
Flexible schedule: (Monday to Friday: arrival between 07:00 and 10:00; Monday to Thursday: departure between 16:00 and 19:00 – 30 minutes to 1 hour of lunch; Friday: departure between 15:00 and 19:00 – 30 minutes to 1 hour of lunch.

Indefinite contract
Attractive salary package, flexible remuneration plan and social benefits package.
Requirements

Our requirements are:
CGFS in Analysis and Control, Manufacturing of Pharmaceutical Products, Administration or Health
English – intermediate level
Knowledge of Office automation and SAP is valued.
1-2 years of experience in similar roles in Quality Assurance departments in the Pharmaceutical Industry or in production or packaging (finished product) departments.

We are looking for people with attention to detail, pro-activity and communication and teamwork skills.
Application
Apply now
If you are interested in this position and would like to grow professionally within Synthon, we look forward to your application. You can send it until December 5, 2023.

Work with us

Working together for patients worldwide

Our mission is to create access to high-quality generic medicines for all patients. We believe in our trusted partnerships to achieve our goals. If you would like to discuss partnering opportunities, get in touch.

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