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About Dow Pharmaceutical Sciences, Inc.:
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Dow Pharmaceutical Sciences, Inc. is a privately held, dynamic and growing independent contract drug development and consulting company, specializing in dermatological, opthalmic, and other topical products. We provide individual or integrated services to clients including formulation development, analytical and stability, clinical trial materials and regulatory and clinical affairs. Pharmaceutical development employees at Dow Pharmaceutical Sciences, Inc. are experienced, highly qualified team players, essential to the success of our company.
Click here to go to the Dow Pharmaceutical Sciences, Inc. website.
For details about Dow Pharmaceutical Sciences, Inc., click here.
About the Opportunity/Requirements:
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Position will manage Quality Assurance and Compliance functions including documentation reviews, in-process and product release, testing data review, preparing complete documentation packages, participation in internal and external audits, and training support. Ensure the functional responsibilities are GXP compliant with the regulations.
Responsibilities will include: Familiarity with the manufacturing operations, knowledge of the requirements of a document management system, participation in the GXP training programs, support of internal audits and reporting of findings to management, participation in external audits, contributions to quality system improvements, conducting and contributing to OOS and deviation investigations, participating in client and regulatory audit/inspections, effective communication with departments, and ensuring timeliness, accuracy and integrity of the work product. The position will require keeping current with international compendia regulations. Supervision of staff activities.
The position requires experience supervising staff, a working knowledge of GMP and quality systems, working knowledge of various analytical and microbiology methodologies, effective communication skills, team work, problem solving skills, good judgment, excellent writing skills, attention to detail, organization skills, and ability to multitask and meet demanding timelines. The position requires fluency with Microsoft Office software.
A minimum of a Bachelor’s degree in a scientific or life sciences field with at least five to seven years working experience in the pharmaceutical industry including a minimum of three to five years in a quality area or equivalent experience or a Masters degree in Chemistry, Biology, or Health Sciences with a good working knowledge of pharmaceutical GMP and at least three years in a quality function. If you are interested in becoming a team member of our expanding and dynamic organization, please submit your cover letter and resume through the link provided, or visit our website at www.dowpharmsci.com for additional information.
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