Chemist I

Do you have expertise in, and passion for, manufacturing in a high performing pharmaceutical environment?  Would you like to apply your expertise to impact the well-being of patients in a company that follows the science and turns ideas into life changing medicines? We have future Operator opportunities in Formulation and Packaging. See below for specific responsibilities and qualifications for each group.

At AstraZeneca, we work together across global boundaries to make an impact and find answers to challenges. We do this with the utmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people’s exceptional skills with those of people from all over the globe.

The Mt. Vernon site was established in 1972 and is the flagship site delivering innovative, life changing oral solid medicines. At the site we formulate and pack OSD tablets, capsules for over 60+ markets. The Mt Vernon site is the largest AZ production site in the US and is located in the southwest corner of the state of Indiana, approximately 15 miles from Evansville, Indiana – the third largest city in the state of Indiana. The Mt. Vernon site is dedicated to creating a culture of inclusion and collaboration. We host yearly Inclusion and Diversity conferences and have an employee resource group devoted to promoting diversity and inclusion and enhancing employees' professional development through interactive and engaging events and initiatives.

Are you ready to make a difference in the world of pharmaceuticals? As a Chemist I, you'll be at the forefront of ensuring the quality and efficiency of our products. Dive into routine qualitative and quantitative analytical chemistry testing and data review on pharmaceutical raw materials, components, and finished products. Your work will be pivotal in maintaining high standards and driving innovation in our processes. This role may include shift work, offering you a dynamic and engaging work environment.

Shift: 2nd Shift (Tuesday to Friday 12pm to 10:30pm) or 3rd Shift (Monday to Tuesday, 10pm to 8:30am)

Accountabilities:
- Perform data review activities as required.
- Participate in and potentially lead QC Team Discussions.
- Maintain adequate inventories of reagents, glassware, and other supplies.
- Keep current, complete, legible notebooks and laboratory records in compliance with good scientific and regulatory practices.
- Write and execute laboratory investigations for known lab errors and Out of Specification (OOS) results using the current electronic deviation system and/or other QC procedures.
- Participate in investigations for PET process areas related to QC processes or data.
- Train QC employees in good analytical techniques, methods, and instrumentation based on expertise.
- Troubleshoot methods and processes.
- Execute laboratory processes in compliance with GMPs, site and corporate policies, standard operating procedures (SOPs), and test methods. Immediately report deviations that have the potential to compromise product quality.
- Perform testing on a range of samples, including chemical raw materials, components (including packaging materials), finished products, stability samples, water, and environmental samples.
- May perform sampling activities of various types in the facility (e.g., swabs).
- Dispose of flammable materials in the <90 day accumulation container.
- Maintain and troubleshoot testing equipment.
- Provide and follow up on ideas for continuous improvements in laboratory processes.
- Perform project work.
- Train QC employees in GMP, SHE, QC methods, and processes.
- May serve as an expert in a specific area of laboratory equipment, process, or system.

Essential Skills/Experience:
- Bachelor's degree with 0 to 3yrs of relevant experience or a minimum of 3 years of demonstrated relevant experience in Quality Control lab setting in lieu of a degree.

Desirable Skills/Experience:
- Bachelor of Science degree, preferably in Chemistry or a related discipline.
- 2 years laboratory experience.
- High level of knowledge and competence with a specific piece of laboratory equipment, or a QC/QA process or system.

AstraZeneca offers an environment where you can work on diversified tasks with a global team. Collaborate on multiple projects while partnering with knowledgeable colleagues across various business functions. You'll be exposed to new ways of thinking, fostering growth both collectively and individually. Here, every voice is heard and matters, creating an inclusive atmosphere where you feel part of the conversation.

Ready to take the next step in your career? Apply now to join our team and make an impact!

Date Posted

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.