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Apply online for the Manufacturing Manager position and advance your career in the Biotech industry today.
Manufacturing Manager : MedImmune, LLC.
Job Number 02568
Employee Type Full Time
Company Name MedImmune, LLC.
Location Philadelphia
Pennsylvania
Salary (year)
Start Date 6/12/2010
Industry Biotech
Job Type Manufacturing
Relocation Not Required
MedImmune, LLC.  
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Description

Description
Title: Manufacturing Manager (Day) Location: PA, Philadelphia Req: 02568 Position Summary: Responsible for the daily Manufacturing Department activities including, material preparation, thaw, blend, aseptic filling, and contract packaging. Supports the commercial production plan by providing assistance with technical issues which arise in Manufacturing.
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/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.
Requirements

Position Requirements
Essential Job Functions: Responsible for implementation of new initiatives and process improvements within Manufacturing. Responsible for overseeing technology transfer of new products to the facility. Collaborates with many other functions within the organization (e.g., QA, QC, Development, Validation, etc.). Participates in CBER/Team Bio inspections as a Process SME. Manages the Supervisors and manufacturing employees on Day/Night Shifts Critical review and revision of Standard Operating Procedures, Batch Records, and other documentation Directs thaw, blend, filling, equipment preparation, EM and facility cleaning Ensures accurate completion of all Documentation. Ensures Safety and Compliance on the Day/Night Shifts. Evaluates technician and Supervisor competency. Performs formal reviews, and ensures completion of required training within the Day/Night Shift Prepares work rosters and leads shift change. Issues shift notes to the site. Administration of corrective actions, investigates deviations and executes closure in Trackwise. Author/Reviewer in Aegis Continued vigilance for areas of improvement. Leads and closes deviation investigations, implements/closes appropriate CAPAs
Educational Requirements
Education: Bachelor’s degree in engineering, biological sciences or equivalent field of study from a four-year college or university Experience: 7 - 10 years related experience or training 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.
Contact Info
Apply online at company website
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