", "identifier": { "@type": "PropertyValue", "name": "Randstad", "value": "3164" }, "datePosted" : "2019-01-03", "employmentType" : "FULL_TIME", "hiringOrganization" : { "@type" : "Organization", "name" : "Randstad" }, "jobLocation" : { "@type" : "Place", "address" : { "@type" : "PostalAddress", "addressLocality" : "Swiftwater", "addressRegion" : "PA", "postalCode" : "18370", "addressCountry": "US" } } } }
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Quality Assurance Inspector

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.

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