QA Supervisor (1 Day Shift & 2 Night Shift Positions)

Thermo Fisher Scientific • Greenville, NC

1d • Onsite

About The Position

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. As part of the Drug Product Division (DPD), the Greenville, North Carolina site is a multi-purpose pharmaceutical development, manufacturing, and packaging campus. The Drug Product Division - North America (DPD-NA) is one of the five divisions that make up the Pharma Services Group. We are made up of approximately 4400 colleagues across six sites who specialize in taking sterile injectable and oral solid dose drug products from development to commercialization. This position has 3 openings: one day shift/12-hour (6am-6pm), and two night shift/12-hour (6pm-6am on a 3-2-2 rotation). Flexibility to work overtime as needed. Join our Quality Assurance team at Thermo Fisher Scientific, where you'll contribute to ensuring product quality and regulatory compliance. As a QA Supervisor, you'll lead and develop a team of quality professionals while overseeing quality operations including batch record review, quality monitoring, and continuous improvement initiatives. You'll collaborate with cross-functional teams to enhance quality excellence and maintain our high standards for product safety and compliance. This position offers the opportunity to contribute by helping ensure the quality of products that enable our customers to make the world healthier, cleaner and safer.

Requirements

• BS degree required
• Advanced Degree plus 2 years of experience, or bachelor's degree plus 3-5 years of experience in quality assurance in a regulated manufacturing environment required
• 2 -5 years of supervisory/leadership experience required
• Experience with batch record review, deviation management, and CAPA systems
• Experience developing and delivering quality-related training
• Experience hosting regulatory inspections and customer audits
• Comprehensive knowledge of cGMP regulations, ISO standards, and quality systems
• Strong understanding of quality risk management principles and tools
• Demonstrated success in implementing quality improvements and leading change initiatives
• Expertise in quality documentation systems and electronic quality management tools
• Excellent project management and organizational skills
• Strong analytical and problem-solving abilities
• Excellent written and verbal communication skills
• Ability to build relationships and collaborate across all organizational levels
• Proficiency with quality management software systems (e.g., TrackWise, SAP)
• Comprehensive understanding of validation principles and requirements
• Demonstrated ability to support quality culture and continuous improvement
• Strong decision-making skills with focus on risk-based approaches
• Ability to effectively manage multiple responsibilities in a deadline-oriented environment

Nice To Haves

• Preferred Fields of Study: Biology, Chemistry, Engineering
• Advanced degree preferred
• Professional certifications (e.g., CQE, ASQ) desirable
• Experience in pharmaceutical, medical device, or related industry

Responsibilities

• Lead and develop a team of quality professionals
• Oversee quality operations including batch record review, quality monitoring, and continuous improvement initiatives
• Collaborate with cross-functional teams to enhance quality excellence and maintain high standards for product safety and compliance
• Help ensure the quality of products that enable our customers to make the world healthier, cleaner and safer

Benefits

• Competitive remuneration
• Annual incentive plan bonus scheme
• Healthcare
• Range of employee benefits
• Employment with an innovative, forward-thinking organization
• Outstanding career and development prospects
• Exciting company culture that stands for integrity, intensity, involvement, and innovation
• Reasonable accommodation for individuals with disabilities to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Number of Employees: 5,001-10,000 employees