integrated resourcesLexington, MA
Quality Control Analyst III
Quality Control Analyst III
Quality Control Analyst III
integrated resourcesLexington, MA
today
Quality Control AnalystsQuality Control Systems ManagersInspectors, Testers, Sorters, Samplers, and Weighers
Apply for this role (opens in a new tab)Quality Control Analyst IIIA Few Words About Us Integrated 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 Description
Client: Direct Client
Location: Lexington, MA
Job Title: QC Analyst
Duration: 1 year
Responsibilities:
- 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.
Qualifications
Experience 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.
Also on the board Same function, level within a rung
Level
Senior
Location
Lexington, MA
Occupation
Quality Control Analysts
Industry
Pharmaceutical Preparation Manufacturing
Posted
today