Quality Specialist / Document Control

Industry

Science and Research

Advert ID

BBBH5468926

Location

Foster City

Job Type

Permanent

Hours

Full-Time

Salary Range

USD33.50 - USD41.75 per hour

No. of Openings

1

Branch Information

Silicon Valley, CA - (USA) 3031 Tisch Way 110 Plaza West CA San Jose , CA 95128

ContactNumber

408-577-1258

Job Description

Quality Specialist - $33.50-41.75/hr





Our client in Foster City, CA is looking for hardworking, motivated talent to join their team. Or client is a genomics pioneer specializing in DNA sequencing. They are looking for candidate with experience in QA and document control roles within the Biotech Field. Don't wait… apply today!





What's in it for you?





* $33.50-41.75/hr

* Monday-Friday, 8am-5pm

* Paid training

* Full time hours

* Clean and safe work environment

* Opportunity for growth



What will you be doing?





* Manage the document control program as well as suggest and implement improvements to existing process

* Monitor change activities approval/implementation and be able to resolve issues of varying complexity



* Interface with internal and external customers to convey requirements and resolve issues to drive efficient and effective process

* Write, edit, review and maintain procedural documentation including, but not limited to, department policies, procedures and guidance documentation

* Manage the training program as well as suggest and implement improvements to existing process

* Support the track and review of competency assessments and training records review process

* Perform trending analysis (Quality Metrics) on an as needed basis, including using statistical process control methods

* May assist in the investigation and resolution of nonconforming events and CAPA projects

* Perform other duties as assigned

* Prioritize and coordinate tasks and projects within a fast-paced environment



What do you bring?





* Positive, can-do attitude

* MUST HAVE DOCUMENT CONTROL EXPERIENCE IN RELATED FIELD

* MUST HAVE QA EXPERIENCE IN RELATED FIELD

* 2-4 years of direct work experience in QA, including all aspects of device/diagnostic quality systems

* Extensive experience working in and/or managing document control systems (electronic preferred) is required

* Experience working in an ISO 13485 or CAP/CLIA regulated environment

* Excellent problem solving and analytic skills

* Effective interpersonal and communication skills and capable of supporting cross-functional project goals

* An understanding of GDP, FDA Quality System Regulations, CLIA and/or ISO Standards (ISO 13485 and ISO 14971) is a plus



Why should you choose Manpower?





* Free training to upgrade your skills, including a free college tuition program

* Medical, dental, vision, 401k

* Weekly pay with direct deposit

* 24/7 Manpower customer care support

* Dedicated Career Partner to help you achieve your career goals

* Voted #1 best places to work by Glassdoor 2022



Are you Interested?

Stop your job search and apply today! A recruiter will be in touch within 24 hours.

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ManpowerGroup recognizes the importance of providing an accessible and barrier-free environment. We are committed to creating a welcoming, fair and inclusive environment by offering equal opportunity to access our services. At ManpowerGroup, we are committed to providing accommodations, and will work with you to meet your needs.