QA Supervisor

QA Supervisor Greenville, NC Job Details Full-time 19 hours ago Benefits Paid parental leave Paid holidays Health insurance Dental insurance Tuition reimbursement Paid time off Parental leave Vision insurance 401(k) matching Employee discount Benefits from day one Opportunities for advancement Referral program Qualifications Resource allocation Financial planning Pharmaceutical regulatory compliance SAP Laboratory information management systems GMP Change management Team development Supervising experience Bachelor's degree Budget planning Continuous improvement Task prioritization Staff training Batch records Pharmaceutical plant experience Organizational skills Quality audits Quality assurance within manufacturing Employee engagement Senior level Document management systems Leadership 2 years Implementing cost-saving initiatives Team motivation (leadership skill) Communication skills Staffing management Regulatory compliance management Organizational budget management Time management Staff development Performance evaluation Full Job Description Work Schedule First Shift (Days) Environmental Conditions Office Job Description 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. Excellent Benefits Package Review our company's Total Rewards Medical, Dental, & Vision benefits-effective Day 1 Paid Time Off & Holidays 401K Company Match up to 5% Tuition Reimbursement - eligible after 90 days! Employee Referral Bonus Employee Discount Program Recognition Program Charitable Gift Matching Company Paid Parental Leave Career Advancement Opportunities Group/Division Summary The Drug Product Division - North America (DPD-NA) is one of the five divisions within the Pharma Services Group. With approximately 4,400 colleagues across six sites, the division specializes in advancing sterile injectable and oral solid dose drug products from development through commercialization. Discover Impactful Work The Quality Assurance (QA) Supervisor plays a critical role in ensuring product quality and regulatory compliance. This position oversees QA activities including auditing, batch record review, product release, document management, complaints, investigations, and quality system oversight. The role also provides leadership to QA staff, fostering a culture of quality, accountability, and continuous improvement. A Day in the Life Promote a strong quality culture by guiding staff in applying policies, procedures, and controls Lead, coach, and empower team members to support organizational change and build effective teams Drive employee engagement and support career development while aligning with business objectives Supervise QA staff responsible for audits, batch record review, and final product release Ensure compliance of manufacturing and testing activities through thorough batch record review and adherence to procedures Support continuous improvement initiatives in quality systems and team capabilities Manage resources, including staffing and budgeting, to meet operational needs Participate in financial planning and cost-saving initiatives Conduct performance management activities, including goal setting, reviews, and addressing performance issues Provide training and development opportunities to enhance team performance and growth Keys to Success Education Bachelor's degree required, preferably in a scientific discipline Experience Minimum 5 years of experience in a cGMP manufacturing or QA environment At least 2 years of experience in manufacturing operations (pharmaceutical, food, or cosmetic preferred) Minimum 2 years of supervisory or demonstrated leadership experience Knowledge, Skills, Abilities Strong knowledge of cGMP regulations and their application Familiarity with systems such as SAP, TrackWise, eDMS, and LIMS is preferred Understanding of batch release processes and quality assurance practices Ability to lead teams, solve complex technical problems, and drive results Strong organizational skills and attention to detail Ability to work independently in a fast-paced, multi-tasking environment High level of integrity, confidentiality, and professionalism Effective time management and prioritization skills Strong interpersonal and communication (written and verbal) skills Competencies Leadership and team development Quality and compliance mindset Accountability and ownership Effective communication Continuous improvement orientation Physical Requirements Ability to move within office and manufacturing environments Capability to stand, walk, stoop, kneel, and crouch for extended periods Ability to lift and carry 10-35 pounds Manual dexterity for computer and equipment use Visual acuity for reading and operating equipment Ability to sit, reach, talk, and hear for prolonged periods Use of PPE as required (e.g., safety glasses, lab coat, gloves, respirator)