Role: Associate Director, Quality Assurance – Pharma

Location: El Paso, Texas

Alcott Global has been retained by a leading global organization in the pharmaceutical and medical device manufacturing sector. This leadership role is responsible for providing strategic direction and oversight for Quality Assurance across pharmaceutical manufacturing operations, while ensuring compliance with FDA regulations (21 CFR Parts 210, 211, and 820), EU GMP, ISO 13485, and other global quality standards. As a key member of the site Quality Leadership Team, the Associate Director will drive quality strategy, regulatory readiness, risk-based decision-making, and continuous improvement initiatives aligned with both global and site objectives.

The role will lead Quality Assurance oversight across pharmaceutical manufacturing processes including formulation, filling, Triton, and Cascade Water Sterilization (CWS), ensuring robust quality systems, contamination control, product disposition, sustainable compliance, and operational excellence. The individual will also work closely with Manufacturing, Supply Chain, Engineering, Regulatory Affairs, EHS, R&D, and other cross-functional teams to support compliant pharmaceutical manufacturing operations, strengthen quality culture, and enable business objectives.

What we are looking for:

The ideal candidates will bring strong experience in pharmaceutical manufacturing, with a proven track record in Quality Assurance, Sterile Manufacturing, Formulation, Filling Operations, Contamination Control, cGMP Compliance, Regulatory Inspections, Risk Management, CAPA, Deviations, Change Control, Root Cause Investigations, Product Disposition, and Quality Systems.

Key Responsibilities:

• Lead end-to-end Quality Assurance oversight across pharmaceutical manufacturing operations, including formulation, filling, Triton, and Cascade Water Sterilization (CWS), ensuring manufacturing activities are adequately supported, operationally efficient, and fully compliant with cGMP (21 CFR Parts 210/211), QSR (21 CFR Part 820), ISO 13485, EU GMP, and global quality standards.
• Serve as the site Subject Matter Expert (SME) for Pharmaceutical Manufacturing Quality, providing strategic oversight of production quality, in-process controls, batch record review, product disposition, contamination control strategies, and risk-based decision-making while ensuring manufacturing operations remain inspection-ready.
• Provide strategic oversight of Quality Systems, ensuring effective management of deviations, CAPAs, change controls, complaints, investigations, verification of effectiveness (VoE), and sustainable corrective actions while driving continuous improvement across pharmaceutical manufacturing operations.
• Lead Quality Compliance and Regulatory Readiness by ensuring compliance with FDA, EU GMP, ISO 13485, and global quality requirements, acting as the site QA lead during FDA inspections, regulatory audits, customer audits, and regulatory responses, including support for 483 observations and Warning Letter remediation activities.
• Drive Quality Risk Management and Operational Excellence by leveraging data-driven analysis, root cause investigations, quality metrics, trend analysis, and quality risk management principles to identify systemic issues, strengthen quality systems, and improve manufacturing performance.
• Build and develop a high-performing Quality Assurance organization by providing leadership, coaching, and technical mentorship, fostering a culture of accountability, ownership, urgency, execution, continuous learning, and a strong quality mindset while ensuring appropriate capability across pharmaceutical operations and quality systems.
• Drive strategic quality initiatives through effective collaboration with Manufacturing, Supply Chain, Engineering, Regulatory Affairs, EHS, R&D, and cross-functional stakeholders to support business continuity, validated manufacturing processes, contamination control, supply reliability, and operational excellence.

Candidate Profile:

• 10+ years of relevant experience in Quality Assurance within pharmaceutical manufacturing.
• 5+ years of leadership experience managing Quality teams, pharmaceutical manufacturing quality functions, or site-level quality operations.
• Strong knowledge of FDA regulations (21 CFR Parts 210/211/820), EU GMP, ISO 13485, cGMP, sterile manufacturing, contamination control, Quality Systems, Risk Management, and regulatory inspection requirements.
• Experience supporting regulatory inspections and interactions, including FDA inspections, 483 observations, Warning Letters, customer audits, and regulatory remediation activities.
• Strong ability to lead cross-functional teams, drive accountability, strengthen compliance culture, and support operational excellence.
• Pharmaceutical manufacturing experience is mandatory, with experience supporting sterile manufacturing and aseptic operations strongly preferred.
• Experience with Lean/Six Sigma methodologies, SAP, Microsoft Office, and enterprise Quality Management Systems is preferred.

Role: Associate Director, Quality Assurance – Surgery

Location: El Paso, Texas

Alcott Global has been retained by a leading global organization in the pharmaceutical and medical device manufacturing sector. This leadership role is responsible for providing strategic direction and oversight for Quality Assurance across Surgery manufacturing operations, while ensuring compliance with FDA regulations (21 CFR Parts 210, 211, and 820), EU GMP, ISO 13485, and other global quality standards. As a key member of the site Quality Leadership Team, the Associate Director will drive quality strategy, regulatory readiness, risk-based decision-making, and continuous improvement initiatives aligned with both global and site objectives.

Role: Associate Director, Quality Assurance – Vascular

Location: El Paso, Texas

Alcott Global has been retained by a leading global organization in the pharmaceutical and medical device manufacturing sector. This leadership role is responsible for providing strategic direction and oversight for Quality Assurance across Vascular manufacturing operations, while ensuring compliance with FDA regulations (21 CFR Parts 210, 211, and 820), EU GMP, ISO 13485, and other global quality standards. As a key member of the site Quality Leadership Team, the Associate Director will drive quality strategy, regulatory readiness, risk-based decision making, and continuous improvement initiatives aligned with both global and site objectives.

Role: Associate Director - Computer System Validation 

Location: El Paso, Texas

Role: Microbiology Associate Director

Location: El Paso, Texas

Alcott Global has been retained by a leading global organization in the pharmaceutical and medical device manufacturing sector. This leadership role is responsible for providing strategic direction and oversight for Quality Control, including Microbiology, Incoming Materials, and Chemical Laboratory operations, while ensuring compliance with FDA regulations (21 CFR Parts 210, 211, and 820), EU GMP, EU Annex 1, ISO 13485, and other global quality standards. As a key member of the site Quality Leadership Team, the Associate Director will drive quality strategy, regulatory readiness, and continuous improvement initiatives aligned with both global and site objectives.

The role will lead microbiological control, incoming material testing, chemical analysis, contamination control strategy (CCS), laboratory operations, data integrity, and regulatory readiness, ensuring robust quality systems, timely product disposition, and operational excellence. The individual will also work closely with Manufacturing, Supply Chain, Engineering, EHS, and other cross-functional teams to support compliant manufacturing operations, strengthen quality culture, and enable business objectives.

What we are looking for:

The ideal candidates will bring strong experience in pharmaceutical and/or medical device manufacturing, with a proven track record in Microbiology, contamination control, environmental monitoring, sterility assurance, water systems, incoming materials testing, chemical laboratory oversight, and data integrity.

Key Responsibilities: 

• Lead end-to-end laboratory operations across Microbiology, Incoming Materials Inspection & Testing, and Chemical/Analytical Laboratories, ensuring laboratories are adequately resourced, operationally efficient, and fully compliant with GMP (21 CFR Parts 210/211), ISO 13485, EU Annex 1, and global quality standards.
• Serve as the site Subject Matter Expert (SME) for Microbiology and Contamination Control, driving the site's Contamination Control Strategy (CCS), with oversight of Environmental Monitoring (EM), sterility, bioburden, water systems (PW/WFI), cleanroom qualification, cleaning validation, microbiological investigations, trending, and risk mitigation.
• Provide strategic oversight of Incoming Material Quality, ensuring robust sampling plans, testing strategies, supplier quality alignment, risk-based material release processes, and continuous improvements in testing efficiency while maintaining regulatory compliance.
• Lead Chemical and Analytical Laboratory excellence, overseeing analytical and microbiological method validation, verification and transfer, stability programs (where applicable), laboratory investigations (OOS, OOT, deviations), and ensuring the reliability, integrity, and regulatory compliance of analytical data supporting product quality and submissions.
• Drive Quality Systems, Regulatory Compliance, and Data Integrity, ensuring effective management of Deviations, CAPAs, Change Control, Risk Management (ICH Q9), ALCOA+ principles, LIMS and computerized laboratory systems, 21 CFR Part 11 compliance, CSV lifecycle activities, and acting as the laboratory lead during FDA, EU, and Notified Body audits, inspections, and regulatory responses.
• Build and develop a high-performing laboratory organization by providing leadership, coaching, and technical mentorship, fostering a culture of accountability, ownership, urgency, execution, continuous learning, and a strong quality mindset while ensuring appropriate microbiology and analytical expertise across the function.
• Drive continuous improvement and strategic initiatives to strengthen laboratory performance through improved cycle times, enhanced investigation effectiveness, robust microbiological control programs, implementation of automation and digital solutions, and alignment with site and global quality strategies through close collaboration with Manufacturing, Supply Chain, Engineering, EHS, and cross-functional stakeholders.

Candidate Profile:

• 10+ years of relevant experience in Quality Control, Microbiology, Laboratory Operations, Pharmaceutical Manufacturing, Biotech, or Medical Device Manufacturing
• 5+ years of leadership experience managing teams, programs, or site-level quality functions
• Strong knowledge of FDA, EU GMP, ISO 13485, cGMP, 21 CFR 210/211/820, Annex 1, and data integrity expectations
• Experience supporting regulatory inspections and interactions, including FDA inspections, 483s, and warning letter responses
• Strong ability to lead cross-functional teams, drive accountability, strengthen compliance culture, and support operational excellence
• Pharmaceutical manufacturing experience is strongly preferred or required for select roles
• Bilingual proficiency is preferred