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Check with seller Quality Specialist III Milwaukee

Published date: April 3, 2022
  • Location: Milwaukee, Wisconsin, United States

Join the Thermo Fisher team in Milwaukee, WI. We are rapidly growing this site to provide R&D, manufacturing and operations support for catalog and custom TheraPure components.

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.

What will you do?

The primary goal of the Quality Specialist III position is to maintain and continually improve the quality management systems of the site to achieve the proper balance between fulfilling customer needs and business objectives.

Key Responsibilities:
Provide Quality review and approval of all investigations, deviations, change controls, validation protocol and reports (IQ/OQ/PQs), SOPs, and in-process controls in support of manufacturing
Drive complaints from internal and/or external customers to resolution in a timely manner
Investigate, analyze and correct non-conformances (internal, external and systemic issues)
Provide training to associates, foster achievement of goals as coach for team members and act as role model in implementation and improvement of safety practices/procedures
Work as a member of New Product Introduction teams, assuring design quality elements are maintained and compliant with applicable regulations
Analyze trends and collaborate with Manufacturing to investigate trends, conduct root cause analysis and lead corrective actions for processes and products, ensuring their effectiveness
Collect, analyze, and present Quality data to create and implement projects for improvement
Recommend product revisions, process changes, and/or testing procedures to assure that QMS standards are being attained
Create quality documents aligned to QMS standards and practices, revises quality documentation to better define, improve, or clarify practices, process and/or product quality
Participate as internal auditor for ISO 9001, and participate in external audits
Assume leadership role in managing projects, develop technical recommendations with significant impact, and use influence to drive ongoing improvement of quality and compliance
Operate with minimal level of direct supervision
Support and actively participates in the continuous improvement processes.
Other duties apparent or assigned

What do we offer?

A choice of national medical and dental plans, and a national vision plan that start on day one
Tuition reimbursement offered, with opportunity to grow your career
Regular site activities, snacks, and lunches
A wellness program, and valuable health incentive opportunities for company contributions to a Health Reimbursement Account (HRA) or Health Savings Account (HSA)
Tax-advantaged savings and spending accounts and commuter benefits
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, short- and long-term disability, and volunteer time off in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

Minimum Requirements/Qualifications:
B.S. in Biology, Chemistry, Biochemistry, a related science, or quality engineering
Minimum of 5 years of experience in operational and/or quality assurance position in a manufacturing organization
Makes sound judgments and decisions and provides proper advice on issues of work product quality nature and/or QMS compliance
Must be self-motivated, proactive, organized, and detail oriented
Strong analytical and problem-solving skills with attention to details and the ability to find creative solutions that meet both QMS and business requirements
Ability to effectively organize and present information to groups of employees, site leadership, and customers
Two years analyzing systems through the use of auditing and process flow tools
Understanding of ISO9001 or equivalent quality system principles
Ability to verbally communicate, read and write in English
Ability in the use of electronic systems (e.g., computer) and MS office (Word, Excel) knowledge
The employee is occasionally required to walk, sit, stoop, bend, kneel, crouch, and crawl

At Thermo Fisher Scientific, each one of our 90,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.

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