Manufacturing Technology Associate II
The Manufacturing Technology Associate II core responsibilities include supporting the design of validation sampling/test plans, performing development studies, generating validation protocols, executing validation studies, resolving technical issues encountered during study execution, and preparing validation final reports for cleaning, sterilization, process, manufacturing/analytical equipment, and utility system qualifications. Projects are typically small or part of larger projects. Projects are assigned by management.
The Manufacturing Technology Associate II also supports technology transfer activities tracked in the site change control system, method validation/method transfer, filter validation, shipping qualification, and FAT/SAT/Commissioning activities. The individual may assist with validation master plans. The individual should possess strong technical skills and experience with biopharmaceutical unit operations and equipment.
The position may require off-shift and weekend work as well as infrequent travel.
Knowledge: Full use and application of principles, theories, concepts and techniques in a limited area or field.
Problem Solving: Develops solutions to problems within job scope where precedents exist. Depending upon ability, may determine individual approach to devising solutions to problems.
Discretion/Latitude: Works under general supervision to meet project goals. Work is reviewed for soundness of technical approach.
Impact: Recommendations consistently result in project advancement. Contributes to technology development or support programs. Effectively functions as a member of one or more project teams.
Interpersonal Communications: Primary interaction is within the organization. Has some internal customer or outside supplier contacts on routine matters. Has established working relationships and credibility with department members and others within the company.
Typical Education: B.S./B.A./M.S. in Engineering, Biological/Physical Sciences, or equivalent focus of study.
MedImmune, LLC. is an Equal Opportunity/Affirmative Action 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.
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.
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.
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