Engineer III, QA

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Greenville, NC
In-Office
Biotech
Our Mission is to enable our customers to make the world healthier, cleaner and safer.
The Role

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Job Summary:

We are seeking an experienced and meticulous QA Engineer III to join our Quality Assurance team as a Quality Validation Specialist. The ideal candidate will have a strong background in quality validation processes, excellent analytical skills, and a dedication to maintaining the highest standards of product quality. Typical work hours are Monday - Friday from 8a - 5p, but the role also requires this individual to be available if needed for urgent off-hours questions.

Key Responsibilities:

  • Quality Validation: Govern validation activities for equipment, processes, computer software, and cleaning validation, ensuring compliance with industry standards and regulatory requirements.

  • Test Planning: Approve comprehensive test plans, test cases, and test scripts based on product requirements and specifications.

  • Execution and Reporting: Ensure oversight for execution of validation protocols and test cases, and provide approval.

  • Continuous Improvement: Continuously review and improve validation processes and procedures to enhance efficiency and effectiveness.

  • Alignment: Ensure all validation activities align with company policies, industry standards, and regulatory requirements.

  • Collaboration: Work closely with multi-functional teams, including development, validation, engineering, product management, and regulatory affairs, to ensure quality objectives are met.

  • Training and Mentorship: Provide guidance and mentorship to junior QA engineers and contribute to the development of the QA team.

Qualifications:
  • Education: An Associate's degree is minimally required; A Bachelor’s degree in Computer Science, Engineering, or a related field, or an advanced degree is highly preferred.

  • Experience: Minimum of 5-7 years of experience in quality assurance in a pharmaceutical or similar GMP environment, with at least 3 years in a quality validation role.
     

  • Technical Skills: Proficiency in validation tools and methodologies, experience with automated testing frameworks, and strong understanding of software development life cycle (SDLC).
     

  • Analytical Skills: Excellent problem-solving skills and attention to detail.

  • Communication: Strong verbal and written communication skills, with the ability to effectively convey complex information to diverse collaborators.

  • Industry Knowledge: Familiarity with relevant industry standards and regulations (e.g., ISO, FDA, GMP) is highly desirable.

  • Certifications: Relevant certifications (e.g., ISTQB, ASQ) are a plus.

We offer competitive salary, an annual incentive bonus plan, 401K with company match up to 6%, tuition reimbursement and a range of other employee benefits! We foster an exciting company culture that encourages innovation, forward-thinking, and an outstanding career and development prospects. Come be a part of the team!

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The Company
HQ: Waltham, MA
100,000 Employees

What We Do

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

Why Work With Us

You will join a company which every colleague has the opportunity to create possibilities, for oneself, for our customers and patients. There is no more exciting place to be than at the forefront of solving problems which help improve lives around the world. As a company, we are committed to supporting your career aspirations and your journey.

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