Sign upLog in

Scientist-I

Integrated Resources, Inc

Lititz, Pennsylvania

Apply
JOB DETAILS
JOB TYPE
Full-time
SKILLS
Analysis Skills, Assays, Clinical Research, Computer Systems, Corporate Policies, Current Good Manufacturing Practice (cGMP), Documentation, Federal Laws and Regulations, GMP (Good Manufacturing Practices), Government Regulations, Government Requirements, Information Technology & Information Systems, Laboratory, Laboratory Testing, Maintain Compliance, Materials Testing, Order Supplies, Physical Chemistry, Quality Assurance Methodology, Record Keeping, Regulations, Regulatory Requirements, Rehabilitation Nursing, State Laws and Regulations, Team Lead/Manager, Test Plan/Schedule, Testing, Time Management
LOCATION
Lititz, Pennsylvania
POSTED
Today
Scientist-IIntegrated 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 DescriptionUnder routine supervision, performs physical and chemical testing of raw materials, materials in process and finished product to assess conformance to applicable standards. Adheres to Company policies, governmental and regulatory requirements and maintains adequate lab supplies.Duties & Responsibilities:Performs laboratory testing of raw materials, materials in-process and finished products using classical wet methods and validated instrumental methods of analysis, in accordance with company test methods.Assures that instruments used in analytical methods are calibrated and performing properly.Performs investigational testing of complaint samples using appropriate analytical methods.Performs standardization of solutions and instruments as required and records results in official logs.Records all results of testing in logbooks, directly on report forms or into the laboratory computer system using proper documentation. Maintains records in accordance with cGMP.Embraces and demonstrates the company's values on an on-going basis.Performs other duties as assigned and directed.Additional Responsibilities:(Define key accountabilities and/or activities.) Under limited supervision and in accordance with all applicable federal, state and local laws/regulations, the Companies' policies, procedures and guidelines, this position:Communicates potential problems and issues to the Team Leader in a timely manner. Review unusual assay results with the Team Leader to determine the method of solution, suggesting appropriate alternative tests.Initiates and completes analytical laboratory investigations in a timely manner.Acquires, maintains and applies current professional knowledge and skills associated with the job.Demonstrates competent computer use (entry/retrieval).Orders laboratory supplies as needed.Adheres to regulatory, company and departmental requirements.Ensure quality and compliance in all my actions by:Attend GMP training on the schedule designated for my role and as appropriate for my role.Adhere to strict compliance with procedures applicable to my role.Exercise the highest level of integrity in the tasks that I perform.In a timely and prompt manner, identify, report and seek correction for deviations noted in my workplace.Embrace a behavior of employee involvement and commitment to doing the job right the first time.

About the Company

I

Integrated Resources, Inc

Resume Resources

Free Resume TemplatesFree Resume Builder