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And Validation Recruitment Area Jobs (NOW HIRING)

CYNET SYSTEMS

Validation Engineer 1

Austin, TX · On-site

$43 - $45/hr

Defining and executing validation strategies, enablement of features and unit test plans ... DC metro area, Cynet Systems Inc. is a leading staffing and recruiting powerhouse. Proudly ...

CYNET SYSTEMS

Validation Engineer 2

Austin, TX · On-site

$56 - $59/hr

Defining and executing validation strategies, enablement of features and unit test plans ... DC metro area, Cynet Systems Inc. is a leading staffing and recruiting powerhouse. Proudly ...

Qualcomm

SoC/Validation Engineer

San Diego, CA · On-site

$129K - $147K/yr

Job Area: Engineering Group, Engineering Group > ASICS Engineering General Summary: This individual ... To all Staffing and Recruiting Agencies : Our Careers Site is only for individuals seeking a job at ...

Intel

Mixed Signal validation engineer

Folsom, CA · On-site

$122K - $172K/yr

... area goals are met. Key Responsibilities * Define, develop, and perform pre-silicon functional ... Your recruiter can share more about the specific compensation range for your preferred location ...

Lancesoft

Validation Engineer II

Carlsbad, CA · On-site

$30 - $32.47/hr

Minimum 2-3 years of related work experience with a good understanding of specified functional area ... Has a broad knowledge Meet Your Recruiter Abhinav Garipally

Intel

Mixed Signal validation engineer

Santa Clara, CA · On-site

$122K - $172K/yr

... area goals are met. Key Responsibilities * Define, develop, and perform pre-silicon functional ... Your recruiter can share more about the specific compensation range for your preferred location ...

Qualcomm

PST Validation Engineer

San Diego, CA · On-site

Job Area: Engineering Group, Engineering Group > ASICS Engineering General Summary: ASICS ... Staffing and recruiting agencies and individuals being represented by an agency are not authorized ...

OneBlood

Donor Recruitment Supervisor

Charlotte, NC

Assists with all Donor Recruitment activities in a specific geographic area. Accountable for ... Valid driver's license and clear driving record. KNOWLEDGE, SKILLS AND ABILITIES: * Ability to read ...

OneBlood

Donor Recruitment Supv

Charlotte, NC · On-site

Assists with all Donor Recruitment activities in a specific geographic area. Accountable for ... Valid driver's license and clear driving record. KNOWLEDGE, SKILLS AND ABILITIES: * Ability to read ...

OneBlood

Donor Recruitment Supervisor

Charlotte, NC

Supervises the recruitment of blood donors in a defined collection area. Assists with all Donor ... Valid driver's license and clear driving record. KNOWLEDGE, SKILLS AND ABILITIES: * Ability to read ...

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As of Aug 5, 2026, the average hourly pay for and validation recruitment area 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.
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Infographic showing various And Validation Recruitment Area job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $108,152 per year, or $52 per hour.

Cleaning Validation Specialist

BioPhase Solutions

Los Angeles, CA

$100K/yr

Full-time

Re-posted 28 days ago

Job description

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Cleaning Validation Specialist to work for a leading Greater Los Angeles area contract development and manufacturing organization.

Salary: $90-100k+/year depending on experience

Responsibilities:
  • Develop, write, and review cleaning validation protocols, reports, and standard operating procedures (SOPs) in accordance with GMP regulations and global procedures.
  • Establish acceptance criteria for cleaning validation based on product residues, cleaning agents, and microbial contaminants.
  • Plan and execute cleaning validation studies, including surface sampling, rinse sampling, and swabbing of equipment and facilities.
  • Conduct analytical testing associated to cleaning validation, to include Total Organic Carbon (TOC) testing
  • Coordinate with production and quality control to schedule and perform validation activities.
  • Analyze cleaning validation data to ensure compliance with established acceptance criteria.
  • Prepare detailed validation reports summarizing findings, deviations, and corrective actions.
  • Ensure all cleaning validation activities comply with relevant GMP guidelines, including FDA, EMA, and other regulatory bodies.
  • Align local site-based procedures with global SOP’s.
  • Stay current with regulatory updates and industry best practices related to cleaning validation.
  • Identify opportunities for process improvements in cleaning procedures and validation practices.
  • Participate in root cause analysis and implement corrective and preventive actions (CAPAs) for cleaning validation deviations.
  • Provide training to production and quality staff on cleaning procedures and validation requirements.
  • Maintain comprehensive and up-to-date documentation of all cleaning validation activities.
  • Work collaboratively with production, quality assurance, quality control, and regulatory affairs to ensure cleaning validation requirements are met.
  • Site representative for the global cleaning validation team to align on bets practices, globally
  • Support internal and external audits related to cleaning validation processes.
Experience/Requirements:
  • BA/BS in Chemistry, Microbiology, Engineering, or a related field; advanced degree preferred
  • 3-5+ years of experience in cleaning validation within a GMP-regulated pharmaceutical manufacturing environment
  • Strong understanding of GMP regulations, cleaning validation principles, and pharmaceutical manufacturing processes
Please send resumes to tiffany@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities!!!