Director of Quality - Biologicals and Chemicals Division

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office

Job Description

Position Summary

TheDirector of Quality - Biologicals and Chemicals Divisiony provides global quality leadership across the Cell Culture Media Network, spanning multiple manufacturing sites (e.g., Grand Island, Inchinnan, Miami). Reporting to the Sr. Director of Quality, this role is accountable for the performance, compliance, and continuous improvement of the Manufacturing Quality function across the network. The Director ensures consistent application of Quality Management Systems, ensures product quality, drives harmonization across sites, and aligns quality strategy with business objectives, customer expectations, and regulatory requirements.

Key Responsibilities

• Lead and execute the network-wideManufacturingQuality strategy aligned with BCD Quality operating model

• Provide end-to-end Quality leadership across multiple manufacturing sites, ensuring compliance to ISO 13485, FDA 21 CFR 820, MDSAP, and applicable global standards

• Drive harmonization and standardization of Quality processes, systems, and metrics across the network

• Own networkproductQuality performance, includingprimaryKPIs related to complaints,cost ofpoor quality(COPQ),and manufacturing health, and other metricsasrequiredto ensure the health of manufacturing quality processes.

• Lead and develop a global team across Quality Engineering, QMS, laboratories, and product release functions

• Partner with Operations, R&D, Regulatory Affairs, and Commercial teams to ensure successful product lifecycle management

• Drive proactive quality engineering strategies and continuous improvement initiatives (e.g.,LeanSix Sigma)

• Oversee and governcomplaint and nonconformance managementacrossthe media networksites

• Serve as escalation point for critical quality issues and ensuretimelycontainment and resolution

• Lead customer and regulatory interactions, including audits, inspections, and issue resolution

• Enable execution readiness for regional capacity expansion and new product introductions

• Establish andmaintaina strong culture of quality, accountability, and continuous improvement across the network

Leadership & Governance

Maintain centralized Quality governance across the network while supporting site-level execution through matrix leadership. Ensure consistent decision-making, escalation pathways, and performance management across regions. Drive Management Review processes at network level and ensure alignment with enterprise quality objectives.

Qualifications

• Bachelor’s degree in Science, Engineering, or related field (advanced degree preferred)

• 10+ years of Quality experience in regulated industries

• 5+ years of leadership experience in multi-site or global quality organizations

• Deep knowledge of GMP, ISO standards, FDA regulations, and global quality systems

• Demonstrated experience leading cross-functional and multi-site initiatives

• Strong leadership, communication, and decision-making skills

• Experience in continuous improvement methodologies (Six Sigma, Lean)

• Ability tooperatein a global, matrixed organization

Compensation and Benefits

The salary range estimated for this position based in New York is $175,000.00–$205,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

• A choice of national medical and dental plans, and a national vision plan, including health incentive programs

• Employee assistance and family support programs, including commuter benefits and tuition reimbursement

• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

• Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.