AstraZeneca-posted 4 days ago
Full-time • Entry Level
Onsite • Frederick, MD
5,001-10,000 employees

Our Frederick Manufacturing Center (FMC) creates life-changing medicines for people around the world and has been recognized by our local community as being a Top 50’ Business in Frederick and awarded Frederick County’s ‘Best Place to Work’. This distinctive biologic manufacturing facility, with over 800 employees, makes a direct contribution to treating people with cancer, respiratory and autoimmune conditions across the globe. We work hard to deliver life-changing medicines to patients, and we take time to have fun and celebrate our accomplishments. From catered site festivities to competitive events, community outreach activities, environmental and wellness showcases and team-building functions, we take time to recognize our achievements and celebrate our diversity. We are dedicated to creating a culture of inclusion and collaboration and are committed to continuous learning by offering ongoing skill building and training for our staff. Fueled by our aspiration to deliver accelerated growth for our company and to make people’s lives better, there’s never been a more exciting time to join the team and shape the future of AstraZeneca Operations. Are you ready to take on diversified tasks with a global team? We are looking for a Quality Control Analyst to join our Operations team. This role offers the opportunity to work on multiple projects, while partnering with knowledgeable colleagues across multiple business functions. Be exposed to new ways of thinking, helping us to grow collectively and as individuals. This is a place where you will feel included in the conversation. Every voice is heard and matters! Shift - 1st Shift M-F Are you ready to step into a role where your critical thinking and attention to detail can make a real impact? As an Associate Quality Control, you'll be at the heart of laboratory operations, ensuring precision and accuracy in every experiment. You'll maintain meticulous records and work collaboratively within a team, all while enhancing your independence over time. If you have QC or GMP experience, that's a plus! At AstraZeneca, we are driven by a commitment to excellence, constantly innovating and trialing new models and technologies to enhance reliability in our processes. Our proactive, science-based approach empowers us to foresee risks and act swiftly, ensuring that every batch we certify meets the highest standards. Here, you'll find an inclusive community where collaboration is key, offering you the chance to grow your career amidst exciting opportunities from new products and technologies. Ready to make a difference? Apply now and join us in our mission to improve patient outcomes!

  • Conduct in-process and finished product testing according to standard operating procedures.
  • Complete documentation supporting testing procedures, including data capture forms, equipment logbooks, and inventory forms.
  • Enter data evaluated for compliance to specifications and report abnormalities.
  • Calibrate and maintain laboratory equipment according to standard operating procedures.
  • Maintain lab instrumentation according to maintenance schedules.
  • Ensure supply levels support performance of assigned duties.
  • Read, understand, and follow SOPs and comply with cGMPs.
  • Apply critical thought to solving problems.
  • Apply knowledge of good manufacturing practices and good laboratory practices daily.
  • Adhere to Company safety procedures and guidelines daily.
  • Follow all safety regulations as indicated in the MedImmune Policies and Procedures.
  • Perform laboratory testing as assigned and per schedule. Example possible testing duties: pH, osmolarity, UV/Vis, ELISA.
  • Maintain training >95% completed on time, with 100% completed prior to performing any related analysis.
  • BS (0-5 years) preferably in pharmaceutical industry
  • Hands-on experience with balances, pipetting, pH, osmolarity, UV/Vis, ELISA desired.
  • Self-motivated. Multi-tasking, excellent written and oral communication skills desired.
  • GMP experience.
  • qualified retirement program [401(k) plan]
  • paid vacation and holidays
  • paid leaves
  • health benefits including medical, prescription drug, dental, and vision coverage
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