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Cleaning Validation Engineer Jobs in Edison, NJ (NOW HIRING)

3B Staffing LLC

Validation Engineer

Plainsboro, NJ · On-site

Validation Engineer III_US Location (On-site, Remote, or Hybrid?): Plainsboro, NJ (onsite ... Gown qualification is a plus, with an understanding of clean room practice and cGMP environments.

3B Staffing LLC

Validation Engineer

Plainsboro, NJ · On-site

Validation Engineer III_US Location (On-site, Remote, or Hybrid?): Plainsboro, NJ (onsite ... Gown qualification is a plus, with an understanding of clean room practice and cGMP environments.

AbbVie

Validation Engineer II

Branchburg, NJ

An engineering professional that works with project engineers, stakeholders, and other project team ... Support site Cleaning Validation program. * Process and complete work order demand maintenance ...

AbbVie

Validation Engineer II

Branchburg, NJ · On-site

$75K/yr

An engineering professional that works with project engineers, stakeholders, and other project team ... Support site Cleaning Validation program. * Process and complete work order demand maintenance ...

AbbVie

Validation Engineer II

Branchburg, NJ · On-site

An engineering professional that works with project engineers, stakeholders, and other project team ... Support site Cleaning Validation program. * Process and complete work order demand maintenance ...

GenScript/ProBio

(Sr.) Validation Engineer

Hopewell, NJ · On-site

$80K - $120K/yr

Support facility, utility, equipment, process, cleaning, and computer system validation (CSV ... Coordinate validation activities with Manufacturing, Engineering, QA, QC, Automation, and external ...

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All JobsCleaning Validation Engineer JobsCleaning Validation Engineer Jobs in Edison, NJ

Cleaning Validation Engineer information

See Edison, NJ salary details

$23

$53

$80

How much do cleaning validation engineer jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for cleaning validation engineer in Edison, NJ is $53.83, according to ZipRecruiter salary data. Most workers in this role earn between $40.82 and $65.43 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a cleaning validation engineer, and why are they important?

To thrive as a Cleaning Validation Engineer, you need a strong background in chemical engineering, microbiology, or a related field, often complemented by experience in GMP-regulated industries. Familiarity with validation protocols, analytical testing methods, and documentation tools (such as LIMS or QMS software) is essential, and certifications like Six Sigma or ASQ may be advantageous. Strong attention to detail, analytical thinking, and effective communication are key soft skills for success in the role. These capabilities are crucial to ensure regulatory compliance, product safety, and effective cross-functional collaboration in pharmaceutical or biotech manufacturing environments.

What is a cleaning validation engineer?

A Cleaning Validation Engineer ensures that manufacturing equipment and processes meet regulatory standards for cleanliness in industries like pharmaceuticals, biotech, and medical devices. They develop validation protocols, conduct tests, analyze data, and document results to confirm that cleaning procedures effectively remove contaminants. This role involves collaborating with quality assurance, production, and regulatory teams to maintain compliance with FDA, GMP, and other industry regulations.

What are the main challenges faced by cleaning validation engineers in the pharmaceutical industry?

Cleaning Validation Engineers in the pharmaceutical industry often face challenges such as staying up-to-date with evolving regulatory requirements, troubleshooting complex cleaning failures, and thoroughly documenting all validation activities. Balancing the needs for robust contamination control with operational efficiency requires analytical thinking and strong problem-solving abilities. Collaboration with manufacturing, quality assurance, and laboratory teams is frequent, as cleaning validation projects require input and support from multiple departments. Successfully managing these challenges ensures product safety, regulatory compliance, and continuous process improvement within manufacturing operations.

What are popular job titles related to Cleaning Validation Engineer jobs in Edison, NJ? For Cleaning Validation Engineer jobs in Edison, NJ, the most frequently searched job titles are:
What job categories do people searching Cleaning Validation Engineer jobs in Edison, NJ look for? The top searched job categories for Cleaning Validation Engineer jobs in Edison, NJ are:
Cleaning Validation Engineer jobs near you
Infographic showing various Cleaning Validation Engineer job openings in Edison, NJ as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Hybrid job distribution, with an average salary of $111,965 per year, or $53.8 per hour.

Validation Engineer II

Medvacon Life Sciences LLC

East Windsor, NJ • On-site

Full-time

Re-posted 27 days ago

Job description

POSITION OVERVIEW:
The Validation Engineer II ensures compliance and operational excellence by managing validation processes across sterile and non-sterile manufacturing. It oversees multiple projects, develops documentation, and collaborates with teams to enhance efficiency, support product development, and drive continuous improvement aligned with our mission to provide high-quality, accessible medications.
ESSENTIAL JOB FUNCTIONS:
  • Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site Acceptance Testing, Installation Qualification, Operational Qualification, Performance Qualification, and Process Qualification for sterile and non-sterile manufacturing.
  • Oversees multiple validation projects, ensuring timely budget-compliant completion while driving continuous improvement to boost manufacturing efficiency.
  • Prepares, reviews, and approves technical documents, including Standard Operating Procedures and current Good Manufacturing Practice (cGMP) records, while managing change control, Corrective and Preventive Action, and quality investigations.
  • Operates and manages critical equipment, executing cleaning, sterilization, and lyophilization cycles.
  • Provides training, supports Research and Development and product development, manages contractors for Commissioning, Qualification, and Validation (CQV) activities, and assists with audits to ensure compliance.

QUALIFICATIONS:
  • Bachelor of Science degree in a scientific or engineering discipline.
  • 7 years Validation experience in the pharmaceutical or biotechnology industries.
  • Advanced knowledge of cGMP, CQV, sterilization process validation, and regulatory compliance, including Good Automated Manufacturing Practice and 21 Code of Federal Regulations Part 11.
  • Strong problem-solving, project management, and attention to detail, with proficiency in Microsoft Office Suite, Quality Management Systems, and experience in Computer System Validation and Cleaning Validation preferred.

KEY COMPETENCIES:
  • Customer Focus: Ability to build strong customer relationships and deliver customer centric solutions.
  • Optimizes Work Processes: Know the most effective and efficient processes to get things done, with a focus on continuous improvement.
  • Collaborates: Builds partnerships and works collaboratively with others to meet shared objectives.
  • Resourcefulness: Secures and deploys resources effectively and efficiently.
  • Manages Complexity: Makes sense of complex, high quality, and sometimes contradictory information to effectively solve problems.
  • Ensures Accountability: Holds self and other accountable to meet commitment.
  • Situational Adaptability: Adapts approach and demeanor in real time to match shifting demands of different situations.
  • Communicates Effectively: Develops and delivers multi-mode communications that convey a clear understanding of the unique needs of different audiences.

VALUES:
  • People: Our people define who we are as a company, and we believe that understanding and addressing the needs of our team, clients, and community is fundamental to fostering a culture of support and growth.
  • Quality: Quality stands at the core of our mission, reflecting our commitment to excellence in every medication we produce.
  • Service: We are here to serve others. Every interaction with our patients, providers, employees, and other stakeholders comes from a place of service.
  • Innovation: By continuously exploring new methodologies and embracing technology, we ensure that every solution we offer is at the forefront of pharmaceutical care.

SUPERVISORY RESPONSIBILITIES:
This position does not have supervisory responsibilities.
CERTIFICATES, LICENSES, REGISTRATIONS:
Certified Quality Engineer Preferred.
Important Notice: Protecting Your Information
Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to jobs@medvacon.com.

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