Quality & Regulatory Affairs Rockville MD 20850 12 + months contract with high possibility of extension
Experis is seeking for Quality & Regulatory Affairs to join one of our Fortune 500 life science clients in Rockville MD 20850. Position Summary and Responsibilities : Roles that are responsible for the analysis, development, and operation of quality and risk management systems.
Activities include developing standards for quality, documentation, and processes as well as continuous improvement and preventive activities.
Includes jobs which are not directly specialized in one of the other defined Quality job families or which are fully responsible for the whole functional area.
IMPACT: Impacts the results of own team with own contributions.
COMPLEXITY: Performs routine assignments using existing procedures OR works autonomously within established procedures and practices that require knowledge of concepts and procedures within a job discipline OR specialized technical expertise within an analytical/scientific method or operational process.
ACCOUNTABILITY/ INDEPENDENCE: Accountable for the quality of own work.
Receives instruction, guidance, and direction from more senior level roles.
EXPERIENCE: Typically, graduate background with little professional experience.
Non-graduate jobholders require a substantial amount of professional experience and additional qualifications that also provides exposure to fundamental theories, principles, and concepts.
EXPERIENCE: Typically reports to a manager role, Project Manager role for a defined period based on organizational set-up (there is not necessarily a difference in role level between a manager and its direct reports - same level or lower-level reporting is possible, provided job scope and responsibilities are clearly distinct); typically, no direct reports.
Minimum Qualifications: BS or AS degree and 1-2 yrs experience, or HS Diploma/equivalent and 5+ yrs experience We are looking for the candidates who are eligible to work with any employers without sponsorship.
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