What are the responsibilities and job description for the Quality Technician position at Randstad Life Sciences?
Job Description
Job DescriptionCompany Description
Quality Technician III
Duration: 1 year contract, can be extended
Location: Onsite in Marlborough, MA
Pay Rate: $20 - 27.57
Must Haves:
- This is a lab role - skills experience with basic instruments are required (calipers, rulers, microscopes, X-ray machine, laser consoles), etc.
- There will be a lot of writing - must be accurate and a good communicator
Job Summary
The CIS Quality Technician III is responsible for day-to-day activities of returned complaint products. This individual will assist and support Engineers who perform in-depth complaint analysis & investigations: root cause analysis, returned product analysis, and investigation closure for BSC manufactured and OEM products.
Job Responsibilities
- Perform returned product analysis: visual inspection, dimensional, mechanical, and electrical testing
- Maintain CIS laboratory in compliance with governing regulations and standards.
- Maintain work instructions related to the labs and returned product.
- Disposition returned product, including retention and storage of returned product according to documented procedures.
- Maintain test equipment used in labs
- Perform x-ray analysis for CIS and additional departments (R&D and DQA)
- Work is supervised and completed according to specific, documented instructions.
- Contacts are primarily with immediate supervisor, Lab tech, CIS Engineers, vendors and other personnel in the section or group.
Education & Qualifications
Required
- Education & Training: Quality Technician Certification and/or 2-year degree required with 3-5 years job related experience.
- Skills: Outlook, Microsoft Word, Excel are a must, and SAP is beneficial. Also, must be able to perform basic mathematical calculations.
- **Must have demonstrated Lab experience.
- Excellent writing and verbal communication skills are the key to success in this role.
- Demonstrated ability to balance multiple priorities against strict deadlines while maintaining a high degree of quality and customer service.
- Working knowledge of CGMPs and GLPs, the ability to read product drawings and to document product analysis results in compliance with Good Documentation Practices.
- Experienced with the use of various types of measurement equipment.
- Excellent organizational skills, strong teamwork orientation, and handle work of a highly confidential nature.
- Requires attention to detail. Must possess strong analytical skills and problem-solving abilities.
- Experience with Complaint System platform. (i.e., Trackwise System or comparable)
Preferred
- Experience with medical device products preferred
- Experience working with products that have been contaminated
- Flexibility to travel to Quincy location when required
- Technical writing experience is a plus
Supportive work environment and excellent culture!
Company Description
Supportive work environment and excellent culture!
Location/Region: Marlborough, MA
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