Reference: Posted: Location: Worcester, MassachusettsCompany: Planet Pharma GroupContact: ApplicationsEmail: PR Range: 19-26/hr DOEThe Associate Data Reviewer supports the data review team within a fast paced GMP environment in support of one or more of the following areas; raw material, environmental monitoring, in-process, final bulk, stability or validation. The coordinator will complete review of assays, data mining projects, and archiving of data. Works under the guidance of a supervisor but is able to manage time efficiently in achieving timely completion of assigned dutiesMajor Responsibilities:
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
* Archiving of data in the RIMS system
* Performs Routine Review of Lab test data including On-the-Floor Review, and Off-the-Floor Review for low complexity test methods.
* Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements
* Understand, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements
* Accepts responsibility to complete assigned tasks as committed. Works with other to maintain a positive atmosphere to accomplish business objectives
* Supports the review team with administrative tasks such as logbook management and scanning/filing of data.
* Participates in training of other employees, but focused on demonstration and not management of training deliveryQualifications:
List required and preferred qualifications (up to 10). Include education, skills and experience.
* Bachelor’s Degree OR High School Diploma with 5+ years of combined experience in manufacturing, QA, QC in pharmaceutical or biologics industry
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
* Archiving of data in the RIMS system
* Performs Routine Review of Lab test data including On-the-Floor Review, and Off-the-Floor Review for low complexity test methods.
* Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements
* Understand, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements
* Accepts responsibility to complete assigned tasks as committed. Works with other to maintain a positive atmosphere to accomplish business objectives
* Supports the review team with administrative tasks such as logbook management and scanning/filing of data.
* Participates in training of other employees, but focused on demonstration and not management of training deliveryQualifications:
List required and preferred qualifications (up to 10). Include education, skills and experience.
* Bachelor’s Degree OR High School Diploma with 5+ years of combined experience in manufacturing, QA, QC in pharmaceutical or biologics industry
Associate Data Reviewer in worcester at Unknown Company
This position is listed as full time and onsite.