Vendor Quality Control Analyst jobs in the United States

Accountabilities:

As a Quality Control Senior Analyst, your role will extend beyond the scope of QC Analyst. You will perform a broad spectrum of routine tasks in your functional area, review documented information, prepare and execute protocols, and author technical reports. You will also own complex minor investigations, change controls, and CAPAs. Your role will involve preparing documentation for presentation to Regulatory Agencies and applying critical thinking to solving problems of advanced scope. You will also provide direction and training to analysts and represent QC on site committees.

Essential Skills/Experience:

- Bachelor’s degree in a Scientific / Biotech / Pharmaceutical field of study.

- 4 years of experience performing PCR and PCR Lab Operations.

The annual base pay (or hourly rate of compensation) for this position ranges from $74,778 - $112,166. 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. 

When we put unexpected teams in the same room, we encourage bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work our entire shift onsite, but that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

At AstraZeneca, we are driven by our aspiration to deliver accelerated growth for our company and to make people’s lives better. We are at an exciting time of new products and launches, making it the perfect time to join our Supply Chain and shape our future with a big contribution to life-changing medicines. We foster an encouraging, positive environment where ideas are welcomed and rewarded. If you are self-driven, thrive at pace, continuously learning and proactively taking on more, then this is the place for you.

Are you ready to make a big impact? Join us at AstraZeneca and contribute to life-changing medicines. Apply now!

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.