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Validation Director (08-008)
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Country: USA
Location: Maryland-Anne Arundel County Annapolis, MD 21401
Total applied: 40 Job Category:Biotech/R&D/Science
Location:Annapolis, MD 21401
Status:Full Time, Employee
Occupations:Biological/Chemical Research;Pharmaceutical Research
Career Level:Manager (Manager/Supervisor of Staff)
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Validation Director (08-008)
At PharmAthene, our commitment is reflected in all that we do. We are a company driven by the desire to make a difference and recognize that our success depends on the creativity, dedication and performance of our team.
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PharmAthene’s primary objective is the development of effective countermeasures to a range of potential biological and chemical weapons. We aim to recruit talented scientists and management to lead its programs and oversee the outsourcing of various program activities with an urgency to develop these countermeasures as rapidly as possible.Â
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In any organization, it is the people who make it all happen and that is especially true at PharmAthene. We offer prospective employees exciting challenges, unique opportunities for career growth and a fast-paced environment that emphasizes innovation and achievement.  Â
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Currently, PharmAthene is searching for qualified candidates for the position noted below. If you believe your credentials meet our expectations, apply today!
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Validation Director (08-008)
The Validation Director generates and revises Validation Master Plans for PharmAthene products. Responsibilities/Duties: Responsibilities include writing protocols and reports, revalidation strategies, master plans, and standard operating procedures. Protocol execution including sample collection, analytical testing, statistical data analysis, report preparation, and presentation of results.Requirements include:Bachelors Degree in Chemistry, Biology, Engineering and/or related discipline required; Masters Degree preferred. 8+ years of experience in biotechnology, pharmaceutical, and/or biomedical industry. Minimum 5 years experience interfacing with regulatory agencies (e.g. FDA, EU). Highly proficient in application of cGMP regulations (US, Canada, and EU). Strong interpersonal skills and sense of business management ethics.
As PharmAthene’s operations are focused in biodefense, which is subject to special restrictions under International Traffic in Arms Regulations, U.S. Citizenship or U.S. Permanent Resident status may be required. PharmAthene offers a challenging, dynamic environment with growth opportunity, competitive compensation and a full benefits program. Only those candidates meeting the requirements noted below and selected for an interview will be contacted.PharmAthene provides equal employment opportunities to employees and applicants for employment in accordance with applicable federal, state and local laws.    EEO
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