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Weekend Cleaning Validation Engineer Jobs (NOW HIRING)

Validation & Engineering Group, Inc

PR · On-site

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 ...

Validation & Engineering Group, Inc

PR · On-site

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 ...

Validation & Engineering Group, Inc

PR · On-site

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 ...

Validation & Engineering Group, Inc

PR · On-site

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 ...

Validation & Engineering Group, Inc

PR · On-site

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 ...

Actalent

Validation Engineer

Sacramento, CA

Cleaning validation experience is considered a plus. The Validation Engineer supports sterile pharmaceutical manufacturing with a strong focus on aseptic sterile fill operations, automated equipment ...

Catalent Pharma Solutions

Validation Engineer

Chelsea, MA · On-site

$89K - $110K/yr

The Validation Engineer is responsible for executing validation activities within a GMP ... Provide technical support to key site programs, including the cleaning program (cleaning validation ...

Catalent, Inc.

Validation Engineer

Chelsea, MA · On-site

$89K - $110K/yr

The Validation Engineer is responsible for executing validation activities within a GMP ... Provide technical support to key site programs, including the cleaning program (cleaning validation ...

Validation & Engineering Group, Inc

PR

Available to work extended hours, possibility of weekends and holidays. At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ...

Cencora

Cleaning Validation Specialist

Juncos, PR

Bachelor's in science,Pharmacy or Engineering Preferred Qualifications: * Minimum of 5 years of professional experience in cleaning validation in the pharmaceutical and biotechnology industries.

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Available to work extended hours, possibility of weekends and holidays. Responsibilities: * Develop ...

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Available to work extended hours, possibility of weekends and holidays. Responsibilities: * Develop ...

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Available to work extended hours, possibility of weekends and holidays. Responsibilities: * Develop ...

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All JobsWeekend Cleaning Validation Engineer Jobs

Weekend Cleaning Validation Engineer information

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$22

$51

$78

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

As of Jun 25, 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.

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.

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.

More about Weekend Cleaning Validation Engineer jobs
What cities are hiring for Weekend Cleaning Validation Engineer jobs? Cities with the most Weekend Cleaning Validation Engineer job openings:
What are the most commonly searched types of Cleaning Validation Engineer jobs? The most popular types of Cleaning Validation Engineer jobs are:
What states have the most Weekend Cleaning Validation Engineer jobs? States with the most job openings for Weekend Cleaning Validation Engineer jobs include:
What job categories do people searching Weekend Cleaning Validation Engineer jobs look for? The top searched job categories for Weekend Cleaning Validation Engineer jobs are:
Weekend Cleaning Validation Engineer jobs near you
Infographic showing various Weekend Cleaning Validation Engineer job openings in the United States as of June 2026, with employment types broken down into 97% Full Time, 1% Part Time, 1% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Specialist (Cleaning-In-Place)

Validation & Engineering Group, Inc

PR • On-site

Full-time

Posted 6 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Validation Specialist - CIP

Summary:
The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and Sterilization-In-Place (SIP) systems within a biotech manufacturing environment. This role ensures that cleaning and sterilization systems are installed, tested, and qualified in compliance with GMP, FDA, EMA, and ASTM E2500 standards, supporting readiness for process validation and commercial manufacturing.

Key Responsibilities:
Commissioning & Qualification Execution:

  • Review and approve vendor FAT/SAT protocols for CIP/SIP equipment.
  • Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam sterilization cycle qualification, and temperature mapping.
  • Oversee the qualification of utilities supporting CIP/SIP systems (Clean Steam, WFI, Process Air).
  • Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity.


Documentation & Compliance:

  • Generate and review URS, FAT/SAT, IOQ, and PQ documentation in compliance with ASTM E2500 and GAMP 5.
  • Ensure traceability from design specifications through executed testing.
  • Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.
  • Prepare summary reports for Quality Assurance approval.


Cross-functional Collaboration:

  • Collaborate with Process Engineers, Automation, QA, and Manufacturing to ensure successful integration of CIP/SIP operations with process equipment.
  • Support operations during process validation batches and cleaning validation campaigns.
  • Provide training and technical guidance to CQV engineers and contractors executing test protocols.


Qualifications:

  • Bachelor’s degree in Chemical, Mechanical, or Biochemical Engineering (or equivalent).
  • Minimum 7–10 years of experience in CQV within biotech or pharmaceutical manufacturing environments.
  • Experience in generating and executing documentation for CQV activities.
  • Strong knowledge of cleaning validation, sterilization principles, and automation integration.
  • Familiarity with DeltaV, SCADA, or PLC systems for CIP/SIP recipe management.
  • Expertise in ASTM E2500, ISPE Baseline Guides, GAMP 5, and FDA/EMA guidelines.
  • Proficiency in reviewing P&IDs, piping isometrics, and functional design specifications.
  • Experience executing or overseeing FAT/SAT, IOQ, PQ activities.
  • Knowledge of data integrity, 21 CFR Part 11, and electronic validation systems (e.g., Kneat, ValGenesis).
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Available to work extended hours, possibility of weekends and holidays.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.