Swisher International, Inc

Laboratory Quality Control Senior Manager

Swisher International, Inc • $100K — $120K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a relevant scientific field (Chemistry, Analytical Chemistry, etc.)
  • 8-10 years of experience in analytical or quality control laboratory environments
  • 2+ years of leadership experience managing laboratory personnel
  • Experience with equipment qualification, SOPs, and quality control processes
  • Strong leadership, organizational, and problem-solving skills
  • Demonstrated commitment to laboratory safety and regulatory compliance
  • Limited travel availability for lab operations and support.

Responsibilities

  • Lead the transfer and setup of analytical testing methods to the Swisher QC lab
  • Implement and manage day-to-day operations of the centralized quality control lab
  • Partner with internal stakeholders to finalize lab space and operating requirements
  • Coordinate procurement, installation, and qualification of laboratory equipment
  • Establish and maintain laboratory quality systems and controlled test methods
  • Lead personnel management, training, and workflow coordination for a multi-shift operation
  • Investigate lab events and ensure compliance with regulatory standards.

Benefits

  • Medical, dental, and vision insurance effective on hire date
  • Generous 401(k) plan
  • Defined Contribution Plan
  • Paid vacation and paid holidays
  • Tuition reimbursement program.
Full Job Description
The Laboratory Quality Control Manager leads the implementation, operational readiness, and day-to-day management of Swisher's centralized quality control laboratory for finished-product release testing. This role establishes and maintains the people, methods, equipment, procedures, quality systems, and external partnerships needed to generate accurate, reliable, traceable, and defensible data for product disposition in a regulated manufacturing environment.

KeyResponsibilities

Laboratory Startup & Centralization

  • Lead the transfer of analytical testing methods and capabilities from third-party laboratories to the Swisher QC laboratory, including transfer protocols, knowledge transfer, training, documentation, and resolution of technical issues
  • Lead implementation and operational readiness of the centralized quality control laboratory, including startup planning, workflow design, and coordination of readiness activities through go-live
  • Partner with Quality Assurance, Research and Development, Engineering, Facilities, EHS, Operations, Procurement, and other stakeholders to finalize laboratory space, utilities, layout, safety, and operating requirements
  • Coordinate the selection, procurement, installation, commissioning, qualification, calibration, and operational readiness of HPLC/UHPLC systems and other laboratory equipment
  • Establish laboratory quality systems, including controlled test methods, SOPs, forms, training records, data-review practices, investigation processes, and document controls
  • Coordinate method qualification, validation or verification, personnel qualification, and parallel testing with third-party laboratories; assess comparability results and support go-live decisions for in-house product-release testing
  • Support the recruitment, onboarding, training, and qualification of laboratory personnel, and establish staffing, coverage, and workflow plans for a multi-shift testing operation
  • Establish capacity, inventory, vendor, service, equipment-redundancy, and contingency plans to support current testing demand, future growth, and continuity of product-release testing
  • Maintain qualified third-party laboratory relationships for overflow, contingency, specialized testing, calibration, and technical support as testing capabilities transition in-house


Ongoing Laboratory Operations

  • Lead daily laboratory operations, including workflow, staffing, prioritization, and shift coverage, to meet testing and product-release requirements
  • Manage, coach, train, and develop laboratory personnel; assign work, monitor performance, set expectations, and maintain documented personnel qualifications
  • Develop, implement, maintain, and continuously improve laboratory procedures, controlled test methods, SOPs, and supporting records
  • Oversee routine analytical testing and technical review to ensure the accuracy, integrity, traceability, and reliability of laboratory data and results
  • Maintain transferred analytical methods after go-live through ongoing qualification, verification, validation, comparability assessment, and controlled change management
  • Manage the laboratory equipment lifecycle, including selection, procurement support, installation, qualification, calibration, preventive maintenance, troubleshooting, service coordination, and readiness of HPLC/UHPLC systems and related equipment
  • Investigate out-of-specification, out-of-trend, failed system-suitability, data-integrity, calibration, and other laboratory events; ensure timely documentation, root-cause analysis, corrective action, escalation, and closure
  • Maintain inspection and audit readiness by ensuring compliance with applicable regulatory requirements, quality systems, laboratory practices, safety expectations, and document-control standards
  • Monitor laboratory capacity, turnaround time, workload, supply usage, and operational performance; identify trends, risks, and constraints and communicate them to management
  • Manage laboratory supplies, standards, reagents, reference materials, consumables, and inventory, including vendor coordination and appropriate storage and control
  • Evaluate and recommend technologies, methods, equipment, and process improvements that enhance quality, reliability, efficiency, scalability, and cost management
  • Partner with Quality Assurance, Operations, Research and Development, Engineering, EHS, Procurement, and external laboratories to support testing, investigations, method transfer, overflow, contingency planning, and laboratory readiness
  • Support departmental planning and budget administration, including staffing and resource needs, equipment and supply costs, vendor relationships, and approved operating priorities
  • Maintain a safe, organized, and compliant laboratory environment, and ensure required safety procedures and training are consistently followed


Qualifications

  • Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Chemical Science, or a related scientific field
  • 8-10 years of experience in an analytical or quality control laboratory, including significant experience in a regulated laboratory or manufacturing environment
  • 2+ years of experience leading laboratory personnel and managing day-to-day laboratory operations
  • Experience managing equipment qualification and calibration, SOPs and controlled methods, data integrity, investigations, training, and laboratory readiness
  • Working knowledge of quality control testing, method validation and verification, laboratory result review and reporting, precision measurement, and quality-improvement practices
  • Strong leadership, coaching, organizational, analytical, problem-solving, and decision-making skills
  • Ability to communicate technical information clearly, manage competing priorities, meet deadlines, and collaborate effectively across functions
  • Demonstrated commitment to laboratory safety, accurate documentation, ethical data practices, and regulatory compliance
  • Limited travel may be required for method transfer, vendor coordination, training, or site support


Preferred Qualifications

  • Master's degree in Chemistry, Analytical Chemistry, Biochemistry, Chemical Science, or a related scientific field is preferred
  • Experience establishing, scaling, centralizing, or launching an analytical or quality control laboratory, including equipment readiness, quality-system implementation, personnel qualification, and go-live support
  • Experience in a regulated industry, such as pharmaceuticals, tobacco or nicotine, food and beverage, dietary supplements, medical devices, consumer goods, or a similar FDA-regulated manufacturing environment
  • Experience with HPLC/UHPLC laboratory operations, chromatographic testing, laboratory data systems, analytical troubleshooting, and analytical method transfer
  • Experience supporting finished-product release testing and product-disposition decisions
  • Formal training in GMP, GLP, ISO 17025, data integrity, laboratory quality systems, or related disciplines
  • Experience managing a multi-shift laboratory and coordinating with external laboratories for overflow or contingency testing


What We Offer

  • Base salary and bonus program
  • Medical, dental, vision, life insurance effective on date of hire
  • Generous 401(k) Plan
  • Defined Contribution Plan
  • Paid vacation and paid holidays
  • Tuition reimbursement


Official Contact Information

  • Email: All official emails will come from an @Swisher.com address
  • Website: Verify job listings and contact details on https://careers.swisher.com


Important: We will never contact you via Teams, Zoom, or Google Meets. If you qualify for an interview the proper meeting method will be shared with you beforehand. Confidential information should only be shared through secure methods outside of email.

About Swisher International, Inc

Swisher International, Inc is a tobacco company that produces cigars and smokeless tobacco products. The company was founded in 1861 and is headquartered in Jacksonville, Florida. Swisher International, Inc has a portfolio of brands such as Swisher Sweets, Optimo, and Kayak. The company has manufacturing facilities in Florida, West Virginia, and the Dominican Republic. In 2015, Swisher International, Inc was acquired by a group of investors led by Justin Kennedy.
Learn more about Swisher International, Inc
Size
1,000 employees
Industry

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