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Weekend Cleaning Validation Engineer Jobs (NOW HIRING)

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

$99.71K - $129.03K/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 ...

kindeva

Validation Engineer II

Saint Louis, MO

This role assists with equipment qualification, aseptic process validation, cleaning validation ... Bachelor's degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related ...

kindeva

Validation Engineer II

Saint Louis, MO

This role assists with equipment qualification, aseptic process validation, cleaning validation ... Bachelor's degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related ...

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

As of May 29, 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 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 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 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
Cleaning Validation Engineer

Cleaning Validation Engineer

Sterling Engineering Inc.

Crystal Lake, IL

$95K - $105K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago

Job description

Job Title: Cleaning Validation Engineer
Location: Crystal Lake
Hire Type: Direct Hire
Compensation: $95,000–$105,000/year
Benefits: PTO, paid holidays, medical/dental/vision, retirement plan
Position Summary:
We are seeking a Cleaning Validation Engineer to support cleaning validation activities within a GMP-regulated pharmaceutical manufacturing environment. This role is responsible for developing, executing, and maintaining cleaning validation programs to ensure manufacturing equipment and processes meet regulatory and quality standards.
The ideal candidate will have experience with cleaning validation protocols, technical documentation, GMP compliance, and cross-functional collaboration within pharmaceutical manufacturing.
Key Responsibilities:
  • Lead cleaning validation activities for new equipment, process changes, and continuous improvement projects
  • Develop and execute cleaning validation protocols, sampling plans, and final reports
  • Evaluate validation data to ensure cleaning effectiveness, repeatability, and compliance
  • Support change controls, deviations, investigations, and CAPAs related to cleaning validation
  • Partner with Manufacturing, Engineering, QA, QC, and Regulatory teams on validation initiatives
  • Assist with residue limits, recovery studies, and acceptance criteria development
  • Maintain validation documentation, SOPs, and quality standards
  • Support internal and external regulatory inspections as a cleaning validation SME
  • Review and approve controlled documents within area of expertise
  • Support training and mentoring of validation personnel as needed
Qualifications:
  • Bachelor’s degree in Engineering, Chemistry, Biology, or related scientific discipline preferred
  • 3+ years of validation experience in pharmaceutical manufacturing
  • Direct cleaning validation experience strongly preferred
  • Strong understanding of cGMPs, validation principles, and regulated manufacturing environments
  • Experience writing and executing validation protocols and reports
  • Excellent technical writing, analytical, and problem-solving skills
  • Ability to manage multiple priorities in a fast-paced environment
  • Strong communication and cross-functional collaboration skills


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.