Associate Quality Control at AstraZeneca

Frederick, Maryland, United States -

Full Time

Start Date

Immediate

Expiry Date

21 Mar, 26

Salary

89370.0

Posted On

21 Dec, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Control, GMP, Critical Thinking, Attention To Detail, Documentation, Data Entry, Laboratory Testing, Calibration, Team Collaboration, Problem Solving, Communication, Self-Motivated, Multi-Tasking, Good Manufacturing Practices, Good Laboratory Practices

Industry

Pharmaceutical Manufacturing

Description

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! Accountabilities - 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. Essential Skills/Experience - BS (0-5 years) preferably in pharmaceutical industry Desirable Skills/Experience - 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. 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! The annual base pay (or hourly rate of compensation) for this position ranges from $59,580.00 to $89,370.00 Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. Date Posted 18-Dec-2025 Closing Date Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

Responsibilities

As an Associate Quality Control, you will conduct in-process and finished product testing, ensuring compliance with standard operating procedures. You will also maintain laboratory equipment and documentation while collaborating with your team.