Pilot Production Technician I - Gaithersburg, MD | Biospace
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Pilot Production Technician I

MedImmune, LLC

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Location:
Gaithersburg, MD
Posted Date:
7/21/2017
Position Type:
Full time
Job Code:
R-010595
Salary:
Required Education:
Bachelors Degree
Areas of Expertise Desired:

Job Description

                             
                                       Location:Gaithersburg, Maryland, United States
Job reference: R-010595

Posted date: Jul. 10, 2017

                                                     
                           


 

   If you’re inspired by the possibilities of science to change lives and you thrive when making brave decisions – join us.  

   MedImmune is the worldwide biologics research and development arm of AstraZeneca. Here, you’ll have the opportunity to make a difference in people’s lives every day. As one of the world’s premier biotechnology companies, our mission is centered on delivering life-changing products that advance world health, and help fight and cure disease.  As a Pilot Production Technician I in Gaithersburg, MD, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives.  

 

   We’re constantly pushing the boundaries of science to deliver life-changing medicines to patients, with a passion for discovery and a pipeline to show for it. We’re pioneering innovative research and exploring novel pathways across key therapeutic areas including oncology, respiratory, inflammation and autoimmunity, cardiovascular and metabolic disease, and infection and vaccines. And we’re industry-leading in immunology, protein engineering and translational science. We offer a unique and strong collaborative network as part of the AstraZeneca family, as together we explore synergies between small and large molecules.  

 

   MedImmune has a dynamic environment that fosters collaboration and innovation. We attract top minds, and we nurture and build top talent.  

   Position Summary  

 

   The Pilot Production Technician is responsible for the operation of equipment according to established Standard Operating Procedures and Master Production Records for the manufacture of therapeutic proteins and vaccines in accordance with Current Good Manufacturing Practices (cGMP’s).  

   Principal Duties  

 

   Operates production equipment such as bioreactors, centrifuges, filtration devices, chromatography equipment, washers, autoclaves, tanks.  

 

   Weighs and checks raw materials, assembles and cleans process equipment, monitors processes  

 

   Performs SIP, CIP and manual cleaning and sanitization of equipment  

 

   Demonstrates aseptic technique  Completes production records  

 

   Maintains clean room environment to comply with regulatory requirements  

 

   Ensures a safe work environment in accordance with Medimmune’s standards  

 

   Basic understanding of cGMP documentation standards for SOP’s MPR and SPR’s  

 

   Adheres to Good Manufacturing Practices and standard operating procedures.  

 

   Regularly works on routine manufacturing assignments  

 

   Learning and executing basic troubleshooting techniques on equipment and process  

 

   Works under direct supervision  

 

   Receives instructions, as needed, on routine work and more detailed instructions on new assignments  

 

   Support Services Technical Principal Duties  

 

   •             Perform SIP, CIP and manual cleaning and sanitization of equipment  

 

   •             Preparation and filtration of production scale buffer and media solutions.  

 

   •             Operate area specific production equipment such as glass washers, autoclaves, fixed and portable stainless steel tanks, etc.  

   Interacts regularly with co-workers, senior personnel and supervisor in dynamic and team environment.  

   Qualifications  

 

   Bachelor’s degree in the Sciences and 0+ years relevant experience.  

   *LI-MEDI  

   Next Steps – Apply today!  

 

   To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience – it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity.  If you know someone who would be a great fit, please share this posting with them.  

 

   AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.  

 

   If you’re inspired by the possibilities of science to change lives and you thrive when making brave decisions – join us.  

Requirements

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