As an associate specialist in the Clinical production team within Biopharmaceutical Development, you'll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry. In this role you will take an adaptable, science driven approach to everything you do.
You will become an integral part of process development, accelerating product candidates into the clinic and gaining knowledge and experience in cell culture, purification and critical support activities. Under the supervision of highly trained personnel, you will gain the process knowledge and skillsets to perform large scale clinical development activities. You will join a collaborative and driven team in a world class biopharmaceutical company.
Main Duties & Responsibilities:- Operates bio-pharmaceutical manufacturing equipment such as: incubators, stainless steel and disposable bioreactors, single-use mixers, centrifuges, washers, autoclaves, tanks and in-process testing instruments.
- Performs steam sterilization, clean in place, manual cleaning and sanitization of equipment
- Records manufacturing activities clearly and accurately within approved current good manufacturing practices (cGMP) documents and regulatory requirements.
- Prepares for processing by ensuring equipment and materials necessary are adequate and available.
- Ensures a safe and environmentally sustainable work environment in accordance with AstraZeneca standards
- Ability to utilize MS Office tools and AZ enterprise systems
Education & Experience Requirements:Bachelor's degree in a science field with 0-4 years' experience
Required Skills: - Introductory knowledge of cell culture operations such as Biosafety Cabinet Operation, cell banking, Bioreactor Operations, depth filtration, and Centrifuge Harvest Operations.
- Ability to work with others in a team environment
- Familiarity with area specific production equipment such as parts washers, autoclaves, fixed and portable stainless-steel tanks, etc.
- Familiarity with basic chemistry concepts.
- Introductory knowledge of raw material weigh-out and media/buffer preparation.
- Ability to work with others in a team environment
Desired Skills: - Demonstrates a high level of drive and initiative.
- Logic and decision-making abilities, critical thinking and troubleshooting skills.
- Demonstrates flexibility and willingness to change ways of working/identify opportunities to improve processes within cGMP clinical manufacturing environment.
So, what's next! Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours.
The annual base pay (or hourly rate of compensation) for this position ranges from $65,081.60 - $97,622.40 USD Annual. 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 Posted26-Oct-2026
Closing Date29-Oct-2026
