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Pilot Production Technician III
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Pilot Production Technician III : MedImmune, LLC.
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| Job Number |
01989 |
| Employee Type |
Full Time |
| Company Name |
MedImmune, LLC. |
| Location |
Gaithersburg
Maryland
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| Salary (year) |
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| Start Date |
1/18/2010 |
| Industry |
Biotech |
| Job Type |
Development-Manufacturing-Sciences |
| Relocation |
Not Required |
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MedImmune, LLC.
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| What Does Your Boss Say About You? |
| Description |
Description
Title: Pilot Production Technician III
Location: MD, Gaithersburg - Corporate Headquarters
Req: 01989
Position Summary: Responsible for executing pilot-scale processes for the manufacture of biologics (recombinant proteins or virus-based vaccines) for use in various pre-clinical studies such as toxicology, formulation and viral clearance
About the Organization
My company shares my
passion for helping to improve human health around the world."
"This is My MedImmune."
Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc.
Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world.
Company Information
MedImmune, LLC. is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law.
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| Requirements |
Position Requirements
Major Duties and Responsibilities (including supervising others):
Proficient in the operation and cleaning of all area specific production equipment such as centrifuges, filtration devices, chromatography equipment, washers and autoclaves.
Weigh and check raw materials, assemble and clean process equipment, monitor processes.
Complete and/or review production documentation and maintain clean working environment.
Submit samples for analytical testing.
Edit and/or author production documentation and job aids/Standard Operating Procedures as needed to accurately reflect process steps and capture process changes.
Possess sound scientific knowledge and understanding of manufacturing processes and uses this skill set to routinely monitor manufacturing processes and recognize potential process issues as they arise.
Provide training and operational guidance to junior staff and also serves to mentor junior staff in manufacturing techniques.
Communicate with co-workers across Development organizations and assist, as requested, in planning of process operations.
Demonstrate good interpersonal skills, pay close attention to detail, and function successfully in a team environment. Discuss challenges and offer potential resolutions with colleagues and senior personnel.
Maintain a professional and productive relationship with supervisor and co-workers
Educational Requirements
Requirements/Qualifications:
Education/Experience: Requires B.S. in science or equivalent experience/degree; Associates degree in a scientific discipline with 3 - 4 years relevant experience or a high school diploma with a minimum of 5 years relevant experience would be considered. Prior GMP experience is preferred but not required.
Special Skills/Abilities: Prior GMP experience is preferred but not required. Prior process development experience preferred but not required.
Job Complexity: Work on routine manufacturing assignments as well as other assignments that are complex in nature where considerable judgment and initiative are required in resolving problems, trouble shooting and making recommendations.
Supervision: Work under minimal supervision from the area supervisor. Perform routine work with minimal instruction and new assignments with general instruction. Act independently to develop manufacturing methods and procedures.
MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune¡¦s approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune¡¦s approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency.
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