Quality Control Analyst III

Integrated Resources, Inc

Lexington, Massachusetts

Apply

JOB DETAILS

JOB TYPE

Contractor

SKILLS

Analysis Skills, Biological Assay, Clinical Research, Drug Manufacturing, Drug Products, GMP (Good Manufacturing Practices), High Performance Liquid Chromatography (HPLC), Information Technology & Information Systems, Laboratory Operations, Manufacturing Operations, Operational Support, Operations, Product Testing, Quality Assurance, Quality Assurance Methodology, Quality Control, Rehabilitation Nursing, Testing

LOCATION

Lexington, Massachusetts

POSTED

1 day ago

Quality Control Analyst IIIContractCompany DescriptionIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionClient: Direct ClientLocation: Lexington, MAJob Title: QC AnalystDuration: 1 yearResponsibilities• Primary duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations/validation/or development studies.• Testing may include but not limited to samples from drug substance and drug product manufacturing, stability, raw materials and various protocol studies using test methods derived from the various compendial and non-compendial sources.• May assist in sampling activities.• This position is expected to maintain operational and GMP readiness of the QC areas.• In addition, the individual may participate in more complex projects, operational excellence initiatives, and various quality systems with general supervision.QualificationsExperience Required:• Specific QC Focus Areas:• Product Testing: Area focuses on techniques such as HPLC, SDS-PAGE, Capillary Electrophoresis, Potency and Bioassays.• GMP and HPLC Experience 100% Necessary• At least 2 years in a QC Environment• Performing Analytical testing• Oversight of general QC Lab activity• Quality System experience a plus• Candidates need minimum of 2 yrs QC analytical HPLC experience.• Works under general supervision. Work is reviewed for soundness of judgment and overall adequacy and accuracy.• Contributes to the completion of organizational projects and goals. Errors in judgement or failure to achieve results would normally require a moderate expenditure of resources to rectify.

Quality Control Analyst III

Integrated Resources, Inc

Lexington, Massachusetts

About the Company

Integrated Resources, Inc

Similar Job Searches