Randstad Quality Control Specialist in Rockville, Maryland

Quality Control Specialist

job details:

  • location:Rockville, MD

  • salary:$21.56 - $25.36 per hour

  • date posted:Wednesday, December 5, 2018

  • experience:3 Years

  • job type:Contract

  • industry:Professional, Scientific, and Technical Services

  • reference:27196

job description

Quality Control Specialist

job summary:

  • The analytical support specialist supports the operation and performance of key business information systems critical to the Quality Control Organization.

  • Supports delivery of strategic IT programs to Quality Control Organization.

  • Works with key business personnel at the site as well as above site support in implementing programs that align with the needs and efforts of the Quality Control Organization.

  • This includes business needs assessments, risk and priority assignment, and project justification and approval skills and experience.

location: Rockville, Maryland

job type: Contract

salary: $21.56 - 25.36 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

  • Serve as system administrator on laboratory systems to identify, analyze, and troubleshoot problems.

  • Assist with development of system administration process

  • Deliver user, process, and technical specifications and design documents.

  • Assess laboratory systems for regulatory compliance requirements.

  • Implement solutions to ensure laboratory systems compliance

  • Develop and report key usage and performance metrics for systems.

  • Provide user training and support.

  • Manage efforts throughout the life-cycle of laboratory equipment. From planning thru decommissioning.

  • Assist with development of laboratory system life-cycle management process

  • Author, revise, and review SOPs as necessary.

qualifications:

  • Minimum Level of Education* BS degree in scientific discipline

  • Laboratory system experience and general GMP

  • Preferred Level of Education BS/ MS

  • 3-5 years experience managing information systems in a GxP regulated environment

  • Strong interpersonal and leadership skills. Solid team player able to function within a team based organization.

  • Strong verbal and written communication skills.

  • Able to interact with peers and senior personnel in a multidisciplinary environment including validation, production and IT

  • Ability to prioritize and decide appropriate course of actions. Effective at implementing decisions and multi-tasking.

  • Fully versed in GMP's, NIH, ICH Guidelines, FDA and other regulatory agency requirements for validation and operations of analytical and stability functions.

skills: Quality control, SOP, ICH Regulations, GMP (Good Manufacturing Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.