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Weekend Cleaning Validation Engineer Jobs (NOW HIRING)

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Cleaning Validation Specialist We are looking for a resource to support the development and ...

Validation & Engineering Group, Inc

PR

Day shift with the possibility of randomly working extended hours and/or weekends and Holidays ... Experience supporting various manufacturing equipment and/or systems, as well as Cleaning ...

Gilead

Cleaning Validation Engineer II

La Verne, CA · On-site

$99K - $129K/yr

Lead and execute cleaning validation activities for a multiproduct facility , including parenteral ... Occasionally support night, weekend, and off-shift schedules as needed based on business demands ...

Intellectt INC

"cleaning validation"

Holly Springs, NC · On-site

Role:CQV Engineer - Cleaning Validation Location: Holly Springs, NC Key Responsibilities: * Execute and document cleaning validation protocols per FDA/ICH guidelines (ALCOA principles). * Apply ...

Intellectt INC

Validation Engineer II

Bothell, WA · On-site

Validation Engineer II (Onsite) Location: Bothell, WA Overview: We are looking for a CQV ... Cleaning validation experience * Exposure to PPQ * Utilities/facility qualification experience

Validation & Engineering Group, Inc

PR

This role ensures that cleaning and sterilization systems are installed, tested, and qualified in ... Available to work extended hours, possibility of weekends and holidays. At Validation & Engineering ...

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Weekend Cleaning Validation Engineer information

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$51

$78

How much do weekend cleaning validation engineer jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for weekend cleaning validation engineer in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Weekend Cleaning Validation Engineer, and why are they important?

To thrive as a Weekend Cleaning Validation Engineer, you need a solid background in engineering or life sciences, knowledge of GMP regulations, and experience in cleaning validation processes. Familiarity with validation protocols, data analysis software, and document management systems is typically required, along with certifications like Six Sigma or relevant industry training. Strong problem-solving skills, attention to detail, and effective communication are essential soft skills for this role. These skills ensure that cleaning processes meet strict regulatory standards, maintain product safety, and support continuous manufacturing operations during weekend shifts.

What is a Weekend Cleaning Validation Engineer?

A Weekend Cleaning Validation Engineer is a specialized professional who works primarily on weekends to ensure that cleaning processes in manufacturing or laboratory environments meet regulatory and safety standards. They validate and document cleaning procedures, analyze samples for contaminants, and ensure compliance with industry guidelines such as GMP (Good Manufacturing Practice). Their work helps prevent cross-contamination and ensures product quality, particularly in industries like pharmaceuticals, biotech, and food processing. Weekend schedules often support continuous operations or minimize downtime for critical cleaning activities.

How to become a cleaning validation consultant?

To become a cleaning validation consultant, professionals typically gain experience in pharmaceutical or biotech manufacturing, focusing on cleaning processes and validation protocols. Relevant certifications, such as those in Good Manufacturing Practices (GMP) or validation, along with strong knowledge of regulatory requirements, are important. Developing skills in process validation, risk assessment, and documentation helps establish credibility in this consulting role.

What does a cleaning validation engineer do?

A cleaning validation engineer is responsible for developing, executing, and documenting cleaning procedures to ensure that manufacturing equipment meets safety and quality standards. They verify that cleaning processes effectively remove contaminants, often using analytical methods and validation protocols, to prevent cross-contamination in regulated industries like pharmaceuticals or biotech. The role typically requires knowledge of regulatory requirements, validation techniques, and attention to detail.

What are the unique challenges of working as a Cleaning Validation Engineer on weekends, and how can I prepare for them?

As a Weekend Cleaning Validation Engineer, one unique challenge is operating with reduced onsite support and resources, since many departments may have limited staffing during weekends. You’ll need to be proactive in planning your validation activities, ensuring all necessary materials and documentation are prepared in advance. Communication skills are vital, as you may need to coordinate with off-shift or on-call teams to resolve issues promptly. Adapting to a quieter work environment can also present opportunities for focused, uninterrupted work, allowing you to complete validations efficiently.

Are validation engineers in demand?

Validation engineers, including those specializing in cleaning validation, are in demand due to the regulated nature of industries like pharmaceuticals and biotechnology. They are valued for their expertise in ensuring compliance with industry standards, often requiring knowledge of validation protocols, quality systems, and relevant regulations. The demand is expected to grow as companies prioritize quality assurance and regulatory compliance.

What is the hourly rate for product validation expert?

The hourly rate for a product validation expert, including a Weekend Cleaning Validation Engineer, typically ranges from $30 to $60 depending on experience, location, and industry. Professionals with specialized skills or certifications may earn higher rates, especially in regulated environments like pharmaceuticals or food manufacturing. Rates can vary based on project scope and employer size.

What is the difference between Weekend Cleaning Validation Engineer vs Weekend Quality Assurance Technician?

AspectWeekend Cleaning Validation EngineerWeekend Quality Assurance Technician
CredentialsRelevant engineering or validation certifications, GMP knowledgeQuality assurance certifications, GMP familiarity
Work EnvironmentManufacturing/cleanroom validation settingsQuality control labs and production areas
Industry UsageCommon in pharmaceutical and biotech manufacturingUsed across similar manufacturing sectors

The Weekend Cleaning Validation Engineer focuses on validating cleaning processes to ensure compliance with industry standards, while the Weekend Quality Assurance Technician oversees overall quality checks and documentation. Both roles require GMP knowledge and are vital in maintaining product safety during weekend shifts in manufacturing environments.

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Weekend Cleaning Validation Engineer jobs near you
Infographic showing various Weekend Cleaning Validation Engineer job openings in the United States as of July 2026, with employment types broken down into 61% Full Time, 38% Part Time, and 1% Temporary. Highlights an 100% Physical job distribution, with an average salary of $108,152 per year, or $52 per hour.

Cleaning Validation Engineer

Eliquent Life Sciences, Inc

Montrose, CA • On-site

Full-time

Posted 21 days ago

Job description

About Company:

Who Are We?

ELIQUENT Life Sciences is a leading global consulting group delivering regulatory affairs, pharmacovigilance, quality, and compliance solutions that support pharmaceutical, biotechnology, medical device, and combination product companies across therapeutic modalities, phase-based pathways, and major global markets.


Why explore your future at ELIQUENT?

ELIQUENT Life Sciences is a trusted global consulting firm helping life sciences companies navigate regulatory complexity and bring breakthrough therapies to market. Founded by former regulators and industry experts, we offer end-to-end support in regulatory affairs, pharmacovigilance, and quality compliance. Our team is driven by a shared mission to improve global health through innovation, collaboration, and integrity. At ELIQUENT, you will be part of a purpose-led organization where your expertise contributes to meaningful impact and your growth is supported every step of the way.


About the Role:

The Cleaning Validation Engineer plays a critical role in ensuring that pharmaceutical manufacturing equipment and processes meet stringent cleanliness standards to guarantee product safety and regulatory compliance. This position is responsible for designing, executing, and maintaining cleaning validation protocols that confirm the effective removal of contaminants and residues from manufacturing systems. The engineer collaborates closely with cross-functional teams including quality assurance, production, and engineering to develop scientifically sound validation strategies aligned with industry best practices and regulatory requirements. By analyzing data and continuously improving cleaning processes, the role helps to minimize risks of cross-contamination and supports the overall integrity of pharmaceutical products. Ultimately, the Cleaning Validation Engineer ensures that all cleaning activities are validated, documented, and compliant with FDA, EMA, and other relevant regulatory bodies, thereby safeguarding patient health and company reputation.

Minimum Qualifications:

  • Bachelor’s degree in Pharmaceutical Engineering, Chemical Engineering, or a related scientific discipline.
  • Demonstrated experience in cleaning validation within pharmaceutical manufacturing environments.
  • Strong knowledge of Sterilize-In-Place (SIP) systems and pharmaceutical manufacturing processes.
  • Familiarity with regulatory requirements such as FDA, EMA, and ICH guidelines related to cleaning validation.
  • Proficiency in developing and executing validation protocols and technical reports.

Preferred Qualifications:

  • Advanced degree (Master’s or higher) in Pharmaceutical Engineering or related field.
  • Experience with automation and control systems used in pharmaceutical manufacturing.
  • Certification in validation or quality assurance (e.g., ASQ Certified Quality Engineer).
  • Hands-on experience with analytical techniques such as HPLC, TOC, or ATP bioluminescence for cleaning verification.
  • Strong project management skills and experience leading cross-functional validation projects.

Responsibilities:

  • Develop, review, and execute cleaning validation protocols and reports in accordance with cGMP and regulatory guidelines.
  • Perform risk assessments and establish acceptance criteria for cleaning processes based on product and equipment characteristics.
  • Collaborate with manufacturing and quality teams to identify critical cleaning parameters and optimize cleaning procedures.
  • Conduct sampling, analytical testing, and data analysis to verify the effectiveness of cleaning processes.
  • Maintain comprehensive documentation and ensure all validation activities are audit-ready and compliant with regulatory standards.
  • Investigate and resolve deviations or non-conformances related to cleaning validation activities.
  • Stay current with industry trends, regulatory changes, and emerging technologies to continuously improve cleaning validation practices.

Skills:

The required skills such as expertise in SIP systems and pharmaceutical manufacturing processes are applied daily to design and optimize cleaning validation protocols that ensure equipment cleanliness and product safety. Pharmaceutical engineering knowledge enables the engineer to understand complex manufacturing systems and develop scientifically robust validation strategies. Analytical skills are essential for interpreting test results and making data-driven decisions to improve cleaning procedures. Preferred skills like familiarity with advanced analytical techniques and automation systems enhance the engineer’s ability to implement innovative solutions and increase validation efficiency. Effective communication and project management skills facilitate collaboration with multidisciplinary teams and ensure timely completion of validation projects in compliance with regulatory standards.