The Manufacturing Sciences team, based in Gaithersburg, Maryland, is a fully integrated process scale-up and cGMP biomanufacturing function. At our Pilot Plant Facilities, our dynamic clinical manufacturing team performs bioprocessing operations for novel molecules to support the development of new medicines. We produce pre-clinical and early through late-stage clinical drug products that advance AstraZeneca's biologics pipeline.

Our integrated team collaborates with our counterparts in technical process development; manages and assures the supply of raw materials; performs non-conformance identification and resolution activities; and provides engineering, technical service, and process automation functions.

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.

This role will provide an opportunity to support the startup of a new manufacturing facility. Once startup activities are completed in 2027 it will transition to 12-hour shift structure in support of a 24/7 operating model for cGMP clinical manufacturing execution.

Main Duties & Responsibilities:

• Operates bio-pharmaceutical manufacturing equipment such as incubators, stainless steel and disposable bioreactors, depth filtration skids, chromatography skids, 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 of experience

Required Skills:

All stream

• Introductory knowledge of cell culture operations including Biosafety Cabinet Operation, Bioreactor Operations, aseptic technique and harvest.

• Introductory knowledge of chromatography, filtration and basic analytical testing (e.g., Protein concentration, osmolarity, pH etc.)

• Familiarity with basic biology & 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.

• Independent and self-starting. Ability to work with minimal supervision.

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 Posted
23-Jun-2026

Closing Date
30-Jun-2026