Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

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. 

Location/Division Specific Information

Greenville, NC

How will you make an impact?

This role offers technical challenges and a collaborative atmosphere, allowing you to make a significant impact on our operations and contribute to our mission of improving global health and safety. Typical shift hours are 8:00am–5:00pm, Monday through Friday with overtime expected.

Key Responsibilities

Review work order documentation meticulously to ensure flawless execution of all procedures.Ensure compliance with cGMPs, Standard Operating Procedures (SOPs), and regulatory requirements through detailed follow-ups and evaluations.Serve as a GMP resource to Production and other internal teams, strictly preventing any regulatory liabilities or client dissatisfaction.Provide technical and regulatory expertise to aid Production in competing at the highest levels of efficiency and accuracy.Perform detailed analysis on batch record data, tracking errors and process flow to determine areas for improvement and successfully implement enhancements.Commit to working in a safe and responsible manner to maintain an injury-free and incident-free workplace.Adhere to all job-related safety protocols and training requirements.Perform additional duties as assigned to support the continuous improvement of our operations.

How will you get there?

Education:

High school diploma or equivalent is minimally required.

Experience:

4 years of proven experience required in Quality Assurance within a GMP environment.

Equivalency

Equivalent combinations of education, training, and meaningful work experience may be considered.

Knowledge, Skills, Abilities:

Strong analytical skills to track and improve batch record accuracy and process efficiency.Outstanding attention to detail and thoroughness in all tasks.Ability to collaborate effectively with cross-functional teams.Dedication to upholding high standards of safety and compliance.

Qualifications

Proven experience in Quality Assurance within a GMP environment.Strong analytical skills to track and improve batch record accuracy and process efficiency.Outstanding attention to detail and thoroughness in all tasks.Ability to collaborate effectively with cross-functional teams.Dedication to upholding high standards of safety and compliance.

What We Offer

Compensation

Competitive hourly pay rateAdditional shift differentialAnnual performance-based bonusAnnual merit performance-based increase

Excellent Benefits

Benefits & Total Rewards | Thermo Fisher ScientificMedical, Dental, & Vision benefits-effective Day 1Paid Time Off & Designated Paid HolidaysRetirement Savings PlanTuition ReimbursementEmployee Referral BonusCareer Advancement Opportunities