Randstad Quality Assurance Inspector in Swiftwater, Pennsylvania

Quality Assurance Inspector

job details:

  • location:Swiftwater, PA

  • salary:$22.62 - $26.61 per hour

  • date posted:Thursday, November 29, 2018

  • experience:3 Years

  • job type:Contract

  • industry:Professional, Scientific, and Technical Services

  • reference:27158

job description

Quality Assurance Inspector

job summary:

Authoring and resolution of deviations in order to meet production and product release requirements.

location: Swiftwater, Pennsylvania

job type: Contract

salary: $22.62 - 26.61 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

  • Identification and facilitation of interdepartmental process improvements.

  • Utilize root cause analysis techniques during deviation investigational process

  • Work cross functionally, to develop and implement continuous process improvements

  • Support production needs and continuous improvement including change control, deviation writing / review, CAPA implementation, and operational optimization.

  • Collaboration with Technical Writers to write, review, revise and prepare manufacturing documents (BPR, SOP, SWI, etc) in accordance with cGMP and regulatory guidelines.

  • Communicate across multiple groups and levels to obtain consensus in order to facilitate deviation closure

  • Manage multiple priorities either independently or part of a team in order to meet key deadlines and communicate issues and progress across all levels of organization

  • Accurately communicate (both written and verbal) progress and updates across multiple levels of the organization and regulatory agencies.

  • Will be responsible for performing administrative tasks such as gathering and preparing documentation to support investigations and or change controls/capas

qualifications:

  • Bachelor Degree and 3-5 years' experience.

  • Working knowledge of cGMP's is required.

  • Must have knowledge of continuous improvement techniques and problem solving skills.

  • Previous experience working within a production department of a pharmaceutical company.

  • Technical Writing experience preferred.

  • Candidate must be able to work extended and flexible hours (including weekends) when needed.

skills: SOP, CAPA, 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.