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Process Validation Jobs in New Jersey (NOW HIRING)

Actalent

Validation Manager

Cherry Hill, NJ

$90K - $155K/yr

Lead the end-to-end planning, coordination, and execution of process and product validation projects across the site. * Manage a portfolio of validation, qualification, and technology transfer ...

Rocket Pharmaceuticals

NJ · On-site

$118 - $158/hr

Develop critical validation documentation required to support the PPQ program planned for Q2 2027, including PPQ protocols, Process Validation Master Plans, microbial validation documentation ...

Rocket Pharma

NJ · On-site

$118 - $158/hr

Develop critical validation documentation required to support the PPQ program planned for Q2 2027, including PPQ protocols, Process Validation Master Plans, microbial validation documentation ...

Leiters Inc

Validation Engineer

Buena, NJ · On-site

$97K - $121K/yr

This includes commissioning and qualification of the equipment, process validation, facilities qualification, utilities qualification, electronic system validation, shipping validation, and program ...

New

Jobtailor

Process Supervisor - 2nd Shift

Cherry Hill, NJ · On-site

$90 - $120/hr

Process Validation * Inventory Turnover Management * Regulatory Commitment Management Soft Skills * Leadership * Conflict Resolution * Employee Feedback * Communication * Team Building #J-18808 ...

New

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Process Validation information

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How much do process validation jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for process validation in New Jersey is $40.14, according to ZipRecruiter salary data. Most workers in this role earn between $23.41 and $52.21 per hour, depending on experience, location, and employer.

What is process validation?

Process validation is a documented procedure used in industries, especially pharmaceuticals and manufacturing, to ensure that a process consistently produces a product meeting its predetermined specifications and quality attributes. It involves planning, conducting, and analyzing studies that provide evidence the process is reliable and reproducible. Regulatory agencies like the FDA require process validation to guarantee product safety and efficacy. Process validation typically includes design, qualification, and continued monitoring stages. This ensures that any variations in the process do not affect the final product's quality.

What are some common challenges faced by professionals in process validation, and how can they be addressed?

Professionals in Process Validation often encounter challenges such as managing tight project timelines, ensuring compliance with evolving regulatory standards, and resolving unexpected deviations during validation runs. Effective communication with cross-functional teams—such as Quality Assurance, Manufacturing, and R&D—can help address these issues quickly. Staying proactive with documentation, maintaining a robust risk assessment process, and continually updating knowledge on industry regulations are key strategies to overcoming these challenges and ensuring successful validation outcomes.

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

To thrive as a Process Validation Specialist, you need a strong background in engineering, life sciences, or a related field, along with expertise in validation protocols and regulatory guidelines such as GMP. Familiarity with validation software, data analysis tools, and documentation systems like LIMS is typically required, and certifications such as Six Sigma or ASQ may be advantageous. Attention to detail, analytical thinking, and effective communication are crucial soft skills for this role. These skills ensure that manufacturing processes consistently produce products that meet quality standards and regulatory compliance, which is essential for patient safety and product efficacy.

What is the difference between Process Validation vs Quality Assurance Specialist?

AspectProcess ValidationQuality Assurance Specialist
CredentialsGMP, ISO certifications, technical trainingGMP, ISO certifications, auditing training
Work EnvironmentManufacturing, pharmaceutical, biotech facilitiesQuality departments, manufacturing sites
Employer & Industry UsageUsed in regulated industries to ensure process consistencyEnsures product quality through audits and compliance

Process Validation focuses on confirming that manufacturing processes consistently produce quality products, while Quality Assurance Specialists oversee overall quality systems, audits, and compliance. Both roles are essential in regulated industries but serve different functions in maintaining product integrity.

What skills are needed for process validation?

Process validation professionals need strong analytical skills, attention to detail, and knowledge of manufacturing processes and quality systems. Familiarity with regulatory requirements such as GMP, validation protocols, and proficiency with data analysis tools are also important. Effective communication and documentation skills are essential for ensuring compliance and successful validation activities.

What are popular job titles related to Process Validation jobs in New Jersey?

For Process Validation jobs in New Jersey, the most frequently searched job titles are:

What job categories do people searching Process Validation jobs in New Jersey look for?

The top searched job categories for Process Validation jobs in New Jersey are:

Process Validation jobs near you
Infographic showing various Process Validation job openings in New Jersey as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $83,490 per year, or $40.1 per hour.

Process Validation Engineer

Katalyst Healthcares and Lifesciences

Newark, NJ • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

Job Description:
  • We are seeking an experienced Process Validation Engineer to support new pharmaceutical manufacturing projects within a sterile GMP environment. This role will focus on process validation, technology transfer, and qualification activities for pre-filled syringe (PFS) manufacturing lines. The ideal candidate will have strong experience with aseptic processing, PPQ execution, and cross-functional collaboration to ensure successful project delivery and regulatory compliance.
Responsibilities:
  • Develop and execute process validation strategies for new and existing sterile manufacturing processes.
  • Lead Process Performance Qualification (PPQ) activities for pre-filled syringe (PFS) fill lines.
  • Support technology transfer projects, ensuring seamless implementation of manufacturing processes across production lines.
  • Coordinate and evaluate aseptic media fill studies to verify process performance and compliance.
  • Perform process revalidation activities and maintain validated manufacturing processes.
  • Support smoke studies and qualification activities for automated visual inspection systems.
  • Collaborate with Manufacturing, Quality, Validation, Engineering, and external partners throughout project execution.
  • Prepare and review validation protocols, reports, risk assessments, and technical documentation.
  • Ensure compliance with cGMP, FDA regulations, and industry best practices.
  • Provide technical support for investigations, process improvements, and continuous improvement initiatives.
Requirements:
  • Bachelor's degree in engineering, Life Sciences, or a related discipline.
  • Experience in Process Validation within a pharmaceutical or sterile manufacturing environment.
  • Hands-on experience with Technology Transfer and PPQ execution.
  • Strong knowledge of aseptic manufacturing, media fills, and sterile processing.
  • Experience supporting smoke studies and qualification activities.
  • Excellent technical writing, communication, and cross-functional collaboration skills.
  • Working knowledge of FDA regulations, cGMP, and validation lifecycle requirements.

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