Cleaning Validation Engineer

MedPharm Ltd; Durham (NC); On-site; USD 90,000 - 120,000; Full time

Job summary

MedPharm Ltd. is seeking a Cleaning Validation Engineer to lead site‑wide validation programs across product lifecycles, ensuring cGMP and FDA compliance in a multi‑product facility.

You will drive CVMP development, risk‑based approaches, and robust validation strategies for CIP, COP, and manual cleaning. The role emphasizes inspection readiness, data analysis, and collaboration with Manufacturing, QA, and Regulatory teams.

Qualifications

• Bachelor’s or Master’s degree in Engineering or related discipline.
• 5–8+ years of experience in cleaning validation and CQV in pharma/biopharma/CDMO environments.
• Experience supporting regulatory inspections and lifecycle cleaning validation programs.

Responsibilities

• Develop and maintain the Cleaning Validation Master Plan (CVMP) aligned with FDA, ICH Q9, EU Annex 1.
• Lead CQV activities for CIP, COP, and manual cleaning systems.
• Design and execute validation studies (swab/rinse sampling, recovery studies).
• Develop risk‑based sampling strategies and worst‑case scenarios.
• Ensure ongoing compliance through trend analysis, inspections support, and CAPA management.

Skills

Cleaning Validation

CIP/COP

Risk assessment

DOE

Regulatory knowledge

Education

Bachelor’s or Master’s in Engineering

Tools

IQ/OQ/PQ

WFI/clean steam

Job description

Position Summary –

The Cleaning Validation Engineer oversees the development, maintenance, and governance of MedPharm’s site-wide cleaning validation program across the full product lifecycle, from development through commercialization, ensuring compliance with cGMP, FDA, and global regulatory requirements.

Supporting MedPharm’s growth into a late-stage, commercialization-focused CDMO, this role provides technical leadership, risk‑based strategy, and operational discipline to ensure inspection readiness, prevent cross‑contamination in a multi‑product environment, and optimize manufacturing throughput. The role serves as an SME in CIP, COP, and manual cleaning processes, driving robust, efficient, and compliant validation strategies aligned with client expectations and business growth.

Essential Functions

Cleaning Validation Program Ownership & Strategy

• Develop and maintain the Cleaning Validation Master Plan (CVMP) in alignment with FDA, ICH Q9, ASTM E2500, and EU Annex 1
• Establish lifecycle validation strategies (Stages 1–3, including CPV)
• Define MACO and PDE‑based acceptance limits using risk‑ and toxicology‑based approaches

Validation Execution & Technical Leadership

• Author, review, and approve validation protocols and reports (including IQ/OQ/PQ as applicable)
• Design and execute validation studies (swab/rinse sampling, recovery studies, riboflavin coverage, CHT/DHT/CEHT)
• Develop risk‑based sampling strategies and worst‑case scenarios based on equipment and contamination risk
• Lead CQV activities for CIP, COP, parts washers, and manual cleaning systems

Cleaning Optimization & Troubleshooting

• Optimize cleaning cycles using key parameters (flow, temperature, detergent, contact time)
• Perform system performance analysis (spray coverage, flow distribution, conductivity return)
• Investigate failures (TOC, residues, riboflavin) and implement CAPAs
• Apply data‑driven and DOE approaches to improve consistency and effectiveness

Compliance & Lifecycle Management

• Ensure ongoing compliance through periodic review and trend analysis (TOC, conductivity, residues)
• Support and represent cleaning validation during inspections and audits
• Maintain inspection readiness through documentation, deviation, and CAPA management
• Support change control and FMEA‑based risk assessments

Collaboration & Training

• Partner cross‑functionally (Manufacturing, Quality, Engineering, Analytical, PM) to align strategies
• Review GMP documentation (URS, FRS, P&IDs, equipment designs)
• Train staff on cleaning procedures, inspection expectations, and sampling
• Provide mentorship and technical leadership within the function

Standardization & Continuous Improvement

• Develop and maintain SOPs, templates, and validation procedures
• Drive standardization of cleaning validation practices
• Implement improvements to enhance efficiency, consistency, and risk control

Supervisory responsibilities

• May provide technical leadership and mentorship to junior validation engineers or contractors
• Lead training initiatives related to cleaning validation processes and compliance

Key Relationships

• Manufacturing Operations
• Quality Assurance & Quality Control
• Analytical Development / Laboratories
• Engineering & Facilities
• Project Management
• Regulatory Affairs
• Clients / External Auditors

Travel requirements

• Minimal travel required; occasional travel for client meetings, audits, or regulatory inspections

Education and Experience

• Bachelor’s or Master’s degree in Engineering (Mechanical, Chemical, or related discipline)
• 5–8+ years of experience in cleaning validation and CQV within pharmaceutical, biopharmaceutical, or CDMO environments
• Strong experience in multi‑product GMP manufacturing environments, preferably including topical, semi‑solid, or aseptic/fill‑finish operations
• Demonstrated experience supporting regulatory inspections and lifecycle cleaning validation programs

Knowledge, Skills, and Abilities

• Subject matter expertise in Cleaning Validation (CIP, COP, manual cleaning systems) and lifecycle validation
• Strong knowledge of regulatory requirements (FDA, cGMP, ICH Q9, ASTM E2500, EU Annex 1, GAMP 5, ALCOA+)
• Expertise in:
  • MACO & PDE calculations and toxicological risk assessments
  • Cleaning cycle development, optimization, and troubleshooting
  • Swab and rinse sampling strategies and recovery studies
  • Cross‑contamination control strategies in multi‑product facilities
  • Data analysis and trending (TOC, conductivity, residue monitoring)
• Experience with:
  • CIP system performance analysis (flow dynamics, spray coverage, conductivity return)
  • Equipment qualification (IQ/OQ/PQ) and utilities (WFI, clean steam, HVAC)
  • Cleaning validation for process, fill‑finish, and packaging equipment
• Strong technical writing skills for protocols, reports, and SOPs
• Excellent problem‑solving and root‑cause analysis capabilities
• Ability to manage multiple priorities in a fast‑paced, growth‑oriented environment
• Strong communication and cross‑functional collaboration skills

Physical Demands and Work Environment

May be required to stand for extended periods within manufacturing environments; occasional lifting of materials or equipment (up to 20 kg); exposure to GMP manufacturing areas including cleanrooms, laboratories, and production suites; may be exposed to varying temperatures, chemicals, and moderate noise levels in manufacturing settings.

Other Duties

You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.

Limitations and Disclaimer

The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.