
Description
Senior Quality Manager
Location: Lancaster South Carolina
Schedule: Monday-Friday 8am-5pm
Direct Hire, Full relocation package available
Salary: $110,000-$125,000/year plus discretionary bonus potential of 12%-15% of YTD earnings
Job Summary:
This role is responsible for developing and overseeing quality systems within manufacturing environments, including close coordination with laboratory functions to ensure procedures align with applicable regulations, industry best practices, and internal standards. The position collaborates across departments to support compliant, efficient operations in both in-house and external manufacturing sites.
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Apply in-depth knowledge of GMP regulations relevant to the manufacturing of regulated products, including food and dietary supplements.
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Oversee and ensure implementation of quality processes related to production and packaging, including cleaning protocols and documentation.
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Work closely with operations to ensure consistency between batch records, on-the-job training, and work instructions across various production types (e.g., tablets, liquids, powders, chews).
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Help establish quality standards where needed and support alignment across facilities.
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Coordinate with supply chain teams to manage the release and availability of raw materials for production.
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Lead or support internal and external audits, particularly those involving laboratory operations, and contribute to corrective action strategies.
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Lead or oversee investigations of quality-related issues within manufacturing operations.
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Serve as Quality Management Representative when required.
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Support the deployment and maintenance of quality systems (e.g., CAPA, process control) to ensure product and process compliance.
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Oversee compliance activities for contract manufacturers.
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Collaborate with other departments and contribute in a cross-functional team setting.
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Perform additional responsibilities in support of broader organizational goals.
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Strong understanding of both Quality Assurance and Quality Control systems.
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Working knowledge of regulatory standards (e.g., FDA, USP, AOAC, ICH) and experience in implementing GMP or GLP systems in regulated manufacturing settings.
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Strong problem-solving abilities and cross-functional communication skills.
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Experience building and motivating teams across departments.
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Bachelor's degree in Chemistry, Microbiology, or a related scientific discipline.
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At least 10 years of experience in Quality roles within the pharmaceutical, nutritional supplement, or similar regulated manufacturing industries.
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Prior experience in laboratory management is required.
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Responsible for supervising quality team members.
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Enforce safe work practices and ensure employees are trained to identify and report unsafe conditions.
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Address and correct hazardous situations promptly or implement interim safeguards when immediate correction isn't possible.
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Ensure incident response procedures are followed, including injury response, reporting, investigation, and corrective action.
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Collaborate on root cause analyses (e.g., 5 Whys) and contribute to the development and implementation of effective corrective actions.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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