Cleaning Validation Specialist Job at Veranova in West Deptford Township
Veranova, West Deptford Township, NJ, United States
Quality Assurance - Cleaning Validation Specialist
Who We Are: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to quality, compliance, safety, and excellence in delivery shapes everything we do. We seek innovative individuals with a growth mindset who want to make a difference.
Veranova is a global leader in developing and manufacturing complex APIs for pharma and biotech clients. We support innovation through technical expertise and flexible solutions. Join us in our mission to improve and save lives through therapeutics.
Role Overview:
The Cleaning Validation Specialist is the site SME responsible for coordinating cleaning validation activities related to intermediate and API manufacturing, including facility surfaces and equipment. This role collaborates with multiple departments to ensure compliance with regulatory and customer standards, implementing effective cleaning strategies. It also manages environmental and purified water monitoring programs to ensure product quality and safety.
Core Responsibilities:
- Develop, execute, and validate cleaning procedures for equipment, lines, and facilities.
- Write and review validation protocols and reports in line with regulations, ensuring residue-free cleaning.
- Conduct sampling and testing to validate cleaning effectiveness.
- Maintain validation schedules to meet deadlines.
- Review data, ensure it meets acceptance criteria, and recommend improvements.
Qualifications:
Required:
- At least 7 years of QA experience with a relevant degree.
- Minimum 3 years in contamination control, cleaning validation, environmental monitoring, or purified water systems, preferably in pharma/biotech manufacturing.
- Leadership experience in FDA-regulated industries.
- Strong knowledge of cGMP, FDA, EMA, ICH standards.
- Experience with microbiological sampling, environmental monitoring, and water testing.
- Proficiency with risk assessment tools like FMEA.
- Experience in cross-functional projects and metrics development.
- Excellent communication skills.
- Hands-on experience with cleaning validation, TOC, and bioburden reduction.
- Detail-oriented with a solid understanding of cGMP regulations.
- Ability to manage complex projects independently.
- Certification in contamination control (e.g., PDA).
- Knowledge of risk-based validation approaches and continuous improvement methodologies like Lean or Six Sigma is a plus.
- Familiarity with environmental monitoring equipment and water system validation.
Our Commitment:
- Health & Wellness: Benefits, mental health resources, PTO, and holidays.
- Financial Wellness: Competitive salary, pension, bonuses, 401(k) match.
- Professional Development: Learning opportunities, tuition assistance.
- Inclusive Culture: We value diversity and inclusion for a thriving workplace.
How to Apply:
Visit www.veranova.com to view roles and join our Talent Community. We encourage applications from diverse backgrounds and those who want to contribute to improving patient lives. For accommodations, email talentacquisition@veranova.com with your request.
Additional Information:
Applicants must be authorized to work in the US. Veranova does not accept unsolicited agency resumes and is committed to a scam-free recruitment process. All communication will come from official Veranova email addresses.
We are an Equal Opportunity Employer, respecting all characteristics protected by law. Your data will be handled confidentially according to our privacy notice.
Job Details:
- Seniority level: Mid-Senior level
- Employment type: Full-time
- Job function: Quality Assurance
- Industry: Pharmaceutical Manufacturing