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.
Are you a diligent and detail-oriented QA Scientist? Then you may be the colleague that AGC Biologics is looking for now to join us in this 9 months maternity cover. Become a part of the QA Mammalian team and our truly unique culture! We are an exceptionally collaborative and supportive group where tasks are prioritized together. You'll find a strong sense of belonging and an inclusive spirit where every member is valued both professionally and personally.
The QA Department:
QA Operations consists of two sub teams with the main responsibility of quality assurance of manufacturing activities and batch release of mammalian recombinant manufacturing of drug substances (API) and cellbanks. AGC Biologics is a CDMO and covering international pharma customers. We manufacture a big range of drug substances from clinical to commercial. The two sub teams are scientists and senior scientists with various professional backgrounds and years of experience.
The department has an open communication with a focus on a high level of professionalism. We are open-minded and have a high service level for our colleagues in the rest of the AGC Biologics organization - and not least for our international customers. The QA Operations team is characterized by positive and proactive colleagues meeting deadlines through committed and friendly collaboration.
We actively work within our field of understanding- and interpreting legislation to ensure manufacturing is in compliance with current standards for GMP production, i.e., EU GMP, 21 CFR and ICH guidelines. Continuously we improve our standards within quality- and manufacturing processes, innovate with modern technology and our common value chain with internal stakeholders.
Role & Responsibilities:
The QA Scientist provides customer service, with the highest integrity, focused on quality and compliance with partnership with AGC Biologics. You will help ensuring resolution of significant quality issues with the client through coordination and collaboration of internal functional resources to identify, proposing and carrying out an efficient plan to settle the issue, while protecting product quality and patient’s safety. You will be responsible for the overall QA review and approval of all technical documents including but not limited to:
- Batch production records (BPR).
- Change controls
- Deviations
- CAPAs
- DS specifications
- Master Production Records
- Risk Assessments
- Support the generation of new, as well as improvement of, existing department SOPs
- Support delivery of AGC projects
- Work with management to resolve project issues and resource constraints within the team
- Support client audits as necessary
- Assist with negotiation terms of Quality agreements with the client as required
- Liaise with the internal and external stakeholders to resolve and clarify any point of issue
- Assist with the generation of APQR (Annual Product Quality Review)
Your Profile:
We are looking for a colleague with relevant educational background and GMP experience:
- You have >2 years of experience with Quality Assurance or >5 years relevant GMP experience.
- A science-based Master’s degree or equivalent.
- Substantial experience working in or directly supporting manufacturing within a drug substance/product manufacturing site.
- Previous biopharma experience is preferred.
- Strong working knowledge of the principles and guidelines for GMP.
It is of utmost importance to have a self-motivating personality with a pragmatic attitude and approach to the daily work - without compromising quality. The environment is dynamic and challenging, which requires the ability to find solutions, deliver on promises and give our customers a positive experience. Other personal characteristics relevant to this role are:
- Strong decision making and ‘can do’ attitude.
- Excellent written and verbal communication skills in English to internal and external stakeholders.
- Ability to work in a fast paced, matrix environment essential.
- Capable of working to deadlines and prioritizing multiple tasks.
- Flexibility to meet the changing needs and priorities of the business.
Your Application & Our Interview Process:
Send your application as soon as possible, and no later than the 13th of January. We treat the applications as we receive them, and conduct interviews with qualified applicants.
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.
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook!
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.
Similar Jobs
What We Do
AGC Biologics offers deep industry expertise and uniquely customized services for the scale-up and cGMP manufacture of protein-based therapeutics (using mammalian and microbial systems), mRNA, pDNA, viral vector and cell therapy products, from pre-clinical to commercial production, including our proprietary CHEF1TM Expression System for efficient protein production with CHO cells. Our company DNA drives us to provide innovative solutions to partner with our customers in helping them reach their goals and accelerate their projects at our cGMP-compliant facilities in the US, Europe and Japan, as well as to facilitate approval and manage spending during the product lifecycle. We forge exceptionally strong partnerships with our customers and we never lose sight of our commitment to deliver reliable and compliant drug substance. Visit www.agcbio.com to learn more.








