QA Supervisor (1 Day Shift & 2 Night Shift Positions)
Greenville, North Carolina, United States · On-site
Senior$20B raised
Work Schedule 12 hr shift/nights Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail …
Skills: Batch Record Review, Deviation Management, CAPA Systems, cGMP Regulations, ISO Standards
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Mid level
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Greensboro, North Carolina, United States · On-site
Mid level
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Charlotte, North Carolina, United States · On-site
Senior+
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Wilmington, North Carolina, United States · Hybrid
$94k–$156k/yr
Mid level$2.6B raised
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Salisbury, North Carolina, United States · On-site
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Greensboro, North Carolina, United States · On-site
Senior+
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Jacksonville, North Carolina, United States · On-site
Senior+
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Lead Product Development Engineer - Power Electronics
Raleigh, North Carolina, United States · Hybrid
$105k–$154k/yr
SeniorVisa sponsorship$12B raised
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Morrisville, North Carolina, United States · On-site
Senior+
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Kannapolis, North Carolina, United States · On-site
Mid level
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Founded in 1956, the Jacuzzi® Brand has grown to become the modern-day Jacuzzi Group-- the premier manufacturer of functional products for the home and outdoor space found in more than 60 countries. Jacuzzi Bath Remodel …
Founded in 1956, the Jacuzzi® Brand has grown to become the modern-day Jacuzzi Group-- the premier manufacturer of functional products for the home and outdoor space found in more than 60 countries. Jacuzzi Bath Remodel …
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Full-time
bachelor degree, postgraduate degree, professional certificate
Competitive Remuneration, Annual Incentive Plan Bonus Scheme, Healthcare
Posted 44d ago
~36 hrs/week
Responsibilities
Lead and develop a team of quality professionals while overseeing quality operations including batch record review and quality monitoring. Collaborate with cross-functional teams to ensure product safety, regulatory compliance, and continuous improvement initiatives.
Requirements
Requires a BS degree in Biology, Chemistry, or Engineering with 3-5 years of QA experience in a regulated manufacturing environment and 2-5 years of leadership experience. Proficiency in cGMP, ISO standards, and quality management software like TrackWise or SAP is essential.
Full job description
Work Schedule
12 hr shift/nights
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Warehouse
Job Description
Title: QA Supervisor (Day Shift & Night Shift Openings)
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.
Division/Site Specific Information
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 is day shift/12-hour Say Shift (6am-6pm), and two are night shift/12-hour Night shift from 6pm-6am on a 3-2-2 rotation. Flexibility to work overtime as needed.
Discover Impactful Work:
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.
A Day in the Life:
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.
Keys to Success:
Education
BS degree required.
Preferred Fields of Study: Biology, Chemistry, Engineering
Advanced degree preferred.
Professional certifications (e.g., CQE, ASQ) desirable.
Experience
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 (pharmaceutical, medical device, or related industry preferred).
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.
Knowledge, Skills, Abilities
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
Benefits
We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.
Related keywords
cGMPISO StandardsCAPATrackWiseSAPPharmaceuticalMedical DeviceQuality AssuranceBatch Record ReviewValidationCleanroomPPERegulatory ComplianceCQEASQDrug Product Division
About Thermo Fisher Scientific
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.
For more information, please visit www.thermofisher.com.
Offices: 168 Third Avenue, Waltham, MA, US
Analytical InstrumentsLaboratory Supply Chain Programs and eCommerceLaboratory EquipmentLab ServicesSpecialty DiagnosticsLife SciencesPharma Servicesand CDMOElectronicsHealth Care
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