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Pharmaceutical Project Manager: Clinical Supply Quality Management Redesign
Ref No.: 18-02635
Location: West Point, Pennsylvania
Position Type:Contract
Job Category:Biotech/Pharmaceutical
Benefits:401K, Dental Insurance, Medical Insurance
*1 year contract position, with additional opportunity based upon performance and continued busines need*

The company: Our client is a global healthcare company. The Company offers health solutions through its prescription medicines, vaccines, biologic therapies and animal health products. It operates through four segments: Pharmaceutical, Animal Health, Healthcare Services and Alliances. The Company's Pharmaceutical segment includes human health pharmaceutical and vaccine products marketed either directly by the Company or through joint ventures. Human health pharmaceutical products consist of therapeutic and preventive agents, generally sold by prescription, for the treatment of human disorders. The Company sells its human health pharmaceutical products primarily to drug wholesalers and retailers, hospitals, government agencies and managed healthcare providers, such as health maintenance organizations, pharmacy benefit managers and other institutions. Vaccine products consist of preventive pediatric, adolescent and adult vaccines, primarily administered at physician offices.

Primary Skills - Document Life Cycle Management / Required Education & Skills - * Bachelor’s Degree in an appropriate scientific or business field of study * Minimum of six (6) years’ experience in the Pharmaceutical or equivalent industry * Strong technical knowledge, skills and experience in communications / Preferred Education & Skills - * Excellent verbal and written communication skills as well as presentation skills * Strongly developed cross-functional teamwork and collaboration skills * Experience directly related to the development of Quality Standards and core requirements for Market Supply and / or Clinical Supply * Experience directly related to Quality Assurance or Quality Control 

SOP Management Contractor Description: Primary Responsibilities include: * Serve as document life cycle manager for QMS Quality Standards, Global Procedures and Local Procedures. * Work closely with the Clinical Supply QMS Redesign Team to ensure successful implementation of new QMS * Support appropriate and timely documentation review and approval cycles * Perform documentation review to ensure consistency (e.g. language, formatting, etc.) within the Redesign Team and across the Clinical Supply network 

Pay Rate: $52 - $56 per hour
Drug and background screenings required

On-Board Services provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, national origin, age, disability or genetics.