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Pilot Production Technician I - BPD

Местоположение Гейтерсберг, Мэриленд, США Идентификатор вакансии R-084479 Дата публикации 06/15/2020

As a pilot production associate 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 through hands-on training.  You will join a collaborative and driven team in a world class biopharmaceutical company that is driving disruptive innovation in the industry.

Qualifications

Pilot Production Technician I: Bachelors degree and 0+ years experience OR Associates degree and 1-2 years experience OR high school diploma and 5+ years experience. 

Pilot Production Technician II:Bachelors degree and 2+ years experience OR Associates degree and 3-4 years experience OR high school diploma and 7+ years experience

Principal Duties

  • Operates bio-pharmaceutical manufacturing equipment such as: incubators, stainless steel and disposable single-use bioreactors, depth filtration skids, LN2 dewars, chromatography skids, single-use mixers, centrifuges, washers, autoclaves, tanks and in-process testing instruments.
  • Performs SIP, CIP and manual cleaning and sanitization of equipment
  • Monitors critical process parameters and troubleshoots equipment during processing.
  • Performs daily manufacturing tasks per Standard Operating Procedures and Manufacturing Production Records.
  • Documents all manufacturing activities clearly and accurately per cGMP and regulatory requirements.
  • Prepares for processing by ensuring equipment and materials necessary are adequate and available.
  • Ensures all production activities are completed in an aseptic, safe and compliant manor. 
  • Interacts regularly with co-workers, senior personnel and supervisors in dynamic team environment to improve quality and process efficiency

Purification Technical Principal Duties

  • Introductory knowledge of Column Chromatography process operations, column packing TFF (Tangential Filtration Flow) and basic analytical testing (e.g. Protein concentration, osmolarity, pH etc.)


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 authorisation and employment eligibility verification requirements.

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Отличная корпоративная культура, отличные рабочие условия, поддерживающий менеджмент. Возможность ротации внутри компании. Они ценят инклюзивность и разнообразие.