Director of Quality Control

Kaye/Bassman International; Ohio; On-site; USD 150,000 - 190,000; Full time

Benefits offered by this job

Relocation assistance

Job summary

Kaye/Bassman International is seeking a Director of Quality Control in central Ohio to lead two sterile injectable QC labs, guiding analytical, microbiology, sterility and environmental monitoring programs across operations and R&D.

The ideal candidate has 12+ years in pharma manufacturing with 8+ years in management, strong cGMP/GLP knowledge, and a proven track record in regulatory audits and CAPAs.

Qualifications

• BS in Life Sciences required at minimum; advanced degree preferred.
• 12+ years’ experience in the pharmaceutical manufacturing industry with at least 8 years in management.
• Experience with regulatory inspections/audits and cGMP/GLPs.

Responsibilities

• Lead QC laboratories supporting sterile injectable manufacturing across two central Ohio sites.
• Oversee analytical, microbiology, sterility, bioburden and environmental monitoring programs.
• Manage and mentor laboratory personnel; drive CAPAs and deviations.
• Collaborate with Regulatory Affairs, Engineering and QA Compliance on new tech and processes.

Skills

QC leadership

Sterility testing

Microbiology

Environmental monitoring

Regulatory audits

TrackWise

Lighthouse

People management

Education

BS Life Sciences

MS/PhD preferred

Tools

TrackWise

Lighthouse

MS Office

Job description

This is a well-established U.S. manufacturer of sterile injectables with more than 50 years in the market, operating as part of a global pharmaceutical group. The company has built its reputation on developing and delivering complex, hard-to-manufacture injectables and drug-shortage medicines that hospitals and clinics rely on every day. It continues to invest significantly in expanding and modernizing its U.S. manufacturing footprint — a rare combination of stability, scale, and forward momentum for quality professionals.

2. The Role They Will Play

The Director, Quality Control is the laboratory leader standing between commercial sterile injectable production and the patients who receive it. The role directs analytical, microbiology, sterility, bioburden, and environmental monitoring programs across two central Ohio manufacturing facilities, in support of both operations and R&D. Recently elevated from a senior manager position to Director, it carries leadership of a QC laboratory of approximately 50 chemists and microbiologists and reports directly to the Vice President of Quality Assurance — a visible, high-impact seat in a quality organization that is actively building.

Key Responsibilities

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

• Manage the day-to-day activities in the laboratories in support of both operations and R&D functions as well as Environmental Monitoring Technicians in manufacturing at the company’s two central Ohio manufacturing facilities.
• Manage testing programs including analytical, sterility, bioburden and microbiological tests as necessary.
• Manage, identify and introduce new testing methodologies for applicable testing procedures.
• Manage and perform trend analysis for all operations.
• Provide support in front of regulatory agencies eg: FDA/ CDER-CBER, customer audits, corporate auditors, Health Canada, EMA, internal audits and as required.
• Supervise the certification of laboratory technicians on various test procedures per USP, FDA, PDA and EU guidelines.
• Hire, train and manage performance of existing and future laboratory personnel and technicians.
• Write, review, and approve validation and qualification SOPs.
• Provide expertise in EMPQ qualifications, new sterile filler qualifications, new water systems qualifications, new laboratory space qualifications and disinfectant study qualifications.
• Ensure laboratories maintain compliance with cGMPs/GLPs, support validation, regulatory filing, R&D, Metrology, Engineering, QA, manufacturing and formulation operations.
• Identify, evaluate, purchase and qualify laboratory equipment.
• Direct, perform and resolve out-of-specification investigations, deviations and implement CAPAs.
• Have knowledge of and support the Sterility Assurance Utilities process, Cleaning & Disinfection process and Traffic & Gowning process of sterile manufacturing.
• Train, coach, mentor and supervise direct reports.
• Oversee, trouble shoot and investigate outsourced testing for products and components.
• Partner with Production, Regulatory Affairs, Engineering, and QA Compliance to strategize and organize implementation of new technology, processes, and products.
• Identify and facilitate process improvements to increase efficiencies in systems, operations, and personnel.
• Ensure all work is performed and documented in accordance with existing Company policies and procedures, as well as cGMP and health and safety requirements.
• Position has responsibilities at multiple locations in central Ohio and provide input, as requested, with the company’s New York manufacturing site on microbiology issues.
• Perform any other tasks/duties as assigned by management.

The ideal candidate is an accountable, hands-on QC leader who has personally run a cGMP laboratory supporting commercial sterile injectable manufacturing — owning the outcomes, not simply supporting or participating in them.

• Expertise in leading cGMP QC laboratories supporting injectable manufacturing, with strong knowledge of contamination control, disinfection, microbiology, sterility assurance and aseptic processing.
• 12+ years’ experience in the pharmaceutical manufacturing industry, including a minimum of 8 years’ management experience (exceptions may be considered for outstanding candidates with proven expertise).
• Exposure to Trackwise for Deviations, CAPAs and CR process.
• Working knowledge of Lighthouse, or equivalent, environmental monitoring systems, including implementation and operation.
• BS in Life Sciences required at minimum; advanced degree preferred.

Additional Qualifications

• Experience with method development, in microbiology and/or analytical methods is desired.
• Strong knowledge of MS-Office software and PC Skills required.
• Excellent leadership, communication, organizational, interpersonal and communication skills (oral and written).
• Proven record of people and program management skills.
• Ability to work independently and deliver timely results.
• Ability to work off hours and weekends as needed.

Physical Environment and Requirements

• Employee must be able to occasionally lift and/or move up to 25 pounds.
• Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential for the health and safety of employees.

Location & Relocation

• Full relocation assistance.
• On-site role in central Ohio (Columbus area), with responsibilities across multiple local facilities.