Sorry, the offer is not available,
but you can perform a new search or explore similar offers:

Customer Services Representative

Job Description & ResponsibilitiesAs part of our Client Services group, you will liaise with Interactive Brokers' clients from around the globe, including bu...


From Interactive Brokers - Illinois

Published 13 days ago

Investor Relations Manager

Reddit is looking for someone to help support our Investor Relations strategy and initiatives. You will support the Head of Investor Relations in the develop...


From Reddit - Illinois

Published 13 days ago

Content Author Lead

We're seeking an inspired, motivated, and experienced Content Author Lead to join our team. The Content Author Lead is responsible for leading a team of cont...


From Critical Mass - Illinois

Published 14 days ago

Web Chat Specialist - Remote Work

Job Description: Commercial Metals is seeking a part-time Web Chat Specialist to join our team remotely from Chicago, Illinois. As an Entry Level Web Chat S...


From Commercial Metals - Illinois

Published 12 days ago

Qa Specialist Handling

Qa Specialist Handling
Company:

(Confidential)


Details of the offer

Full job description *Job Title: QA Specialist I (Complaint handling/DHR/CAPA/GMP) *Location: North Chicago, IL 60064 (Onsite) *Duration: 12 months contract, Full-Time * Employment Type: W-2 Job Description: Description: Perform sampling, inspecting, and physical testing of incoming commodities per appropriate product specification in a laboratory environment. Applies scientific knowledge to daily operations, data management, and problem solving. Understands and follows documentation. Analyzes basic/simple data, evaluates results, forms conclusions, and recommends process and/or document improvements. Recognizes deviation from normal operating procedures. Recognizes and troubleshoots instrumentation and/or work order problems and routine operational issues.
Responsibilities : Responsible for performing routine testing on incoming materials in accordance with approved specifications and procedures. Disposition incoming material for use in manufacturing. Maintains certification in assigned job responsibilities and completes training on-time. Participates in complaint handling, failure investigations, and CAPA documentation. Understands, implements, and maintains the quality policy and ensures compliance to site level policies and procedures. Develops knowledge of products and technologies. Interacts on a necessary basis with internal and external support groups to perform core skills. Participates in team activities and area metric tracking. Responsible for supporting Operations efforts in meeting established production schedule. Reports problems in a timely and accurate manner. Seeks additional guidance or advice when problem is beyond scope of training or knowledge. Skill qualifications : 4+ years of overall work experience. Previous experience in Quality Assurance. 2+ Experience in a manufacturing/finishing environment is desired. Previous knowledge of GMP regulations and standards affecting pharmaceutical products is desired. Have an understanding of material/product traceability and Device History Records. Good understanding of basic math. Good clerical skills is required. Computer skills proficiency including word processing, spreadsheets, instrumentation related and network systems. Educational qualifications: High School Diploma required; Bachelor's degree preferred. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit
Recruiter Details:
Name: Shivangi Shivpuri
Email:
Internal Reference Id: 24-08639
Job Types: Full-time, Contract
Salary: $25.00 - $30.00 per hour
Schedule:
8 hour shift Work setting:
In-person Application Question(s):
Do you have the required experience in Quality Assurance? Do you have experience in complaint handling, failure investigations, and/or CAPA documentation? Do you have previous experience and knowledge of GMP regulations? Do you have knowledge of pharmaceutical products? Do you have an understanding of material/product traceability and Device History Records? Ability to Relocate:
North Chicago, IL: Relocate before starting work (Required) Work Location: In person


Source: Grabsjobs_Co

Requirements

Qa Specialist Handling
Company:

(Confidential)


Built at: 2024-05-18T02:58:33.108Z