Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow.
Our mission is to work side by side with our customers in order to improve patients' lives by bringing new biopharmaceuticals to market.
Main activities:
- Support MSAT and Development units in activities related to QA and GMP Compliance;
- Be responsible for activities related to Change Controls, Deviations and CAPA for MSAT and PD units;
- Support MSAT and Development for internal document management;
- Support MSAT in equipment and material scouting and, URS definition and material flow definition.
**Requirements**:
- Fluent communication in English
- Effective interpersonal and communication skills
- Knowledge of GMP principles and Quality requirements for viral vectors and cell manufacturing operations
- Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork.
Our core values stem from our team members and are embedded into our DNA.
They provide a common language and understanding of how we as an organization are connected across three continents.
Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe._- LinkedIn _
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- AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement.
AGC Biologics is an equal opportunity employer.
All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances._