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Job Field: Office Jobs
Location: SALT LAKE CITY, UT
Job Type: Full Time

JOB SUMMARY:

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Supervisor, Manufacturing October 30, 2012 - December 31, 2012 Location: Salt Lake City, UT Salary Range: DOE Exempt/Non-Exempt: Exempt Benefits: Yes Employment Type: Full Time Employer: Cephalon, Inc. Description: Overview This position will be filled by a person who, as a result of education or experience in a relevant industry, possesses the knowledge and skills necessary to provide direct supervision to a team of pharmaceutical Production Technicians in performance of daily work assignments to meet pharmaceutical manufacturing and packaging production schedules, insure training and governmental compliance, track production using an automated data system, perform process investigations, and write operating procedures. Duties: Requirements ? Provides direct supervision of Pharmaceutical Manufacturing / Packaging Technicians involved in the production of commercial drug products and clinical supplies produced in the Salt Lake City facilities. ? Configures daily work assignments and supervises technicians working in the Manufacturing and Packaging Operations Areas. ? Responsible for ensuring production schedules and performance goals are met. ? Evaluates work-in-progress and makes real-time decisions concerning actions to be taken in response to unexpected Production Area events. ? Trains all subordinates on cGMPs. ? Ensures all actions in area of responsibility are conducted in accordance with FDA, MHRA, and EMEA GMP; also ensures Area compliance with regards to other Government agencies such as OSHA, EPA, DEA, etc. ? Enters Production data into automated Operations Management system used to track production activities, record material usage, labor allocations, production yields, etc. Oversees the flow of batch paperwork and reviews all completed records for accuracy, completeness, and legibility. ? Works as a liaison between Quality Assurance /Quality Control and Production when conducting investigations into production anomalies and laboratory results that do not meet expected standards. ? Works as a liaison between the Production Areas and Warehouse to resolve issues regarding materials inventory usage, inventory control, and end of lot assignments. ? Writes, edits, and reviews Area Standard Operating Procedures and any other work instructions that may be required for compliant operation of the Production Areas. ? Responsible for ensuring a safe and healthy work environment by adhering to and enforcing all Area Safety Policies and Procedures. Responsible for ensuring subordinate staff is trained in most current Safety policies, programs, and procedures. ? Responsible for ensuring subordinate staff training on all Company policies and procedures as directed by Corporate Management. ? Responsible for tracking subordinate staff attendance, vacation, and personal time off. Responsible for initiating disciplinary actions, if necessary, in response to violations or abuse of employee time off guidelines. ? Other duties as assigned by Area Management. Qualifications: Qualifications Requires a Bachelor s degree in a scientific discipline or minimum of five years pharmaceutical experience. Provides direct supervision to nonexempt employees. Works on problems of moderate scope where analysis of data requires evaluation of identifiable factors. Exercises judgment within generally defined practices and policies in selecting methods and techniques for completing required manufacturing and packaging operations. Frequently interacts with subordinates and functional peer groups at various management levels. Interaction normally requires the ability to gain cooperation of others while presenting technical information concerning specific projects/schedules, etc. Click Here to Download Complete Job Description

KEY REQUIREMENTS:

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