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Assistant Cleaning Validation Engineer Jobs (NOW HIRING)

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 ...

BioPhase Solutions

Validation Engineer

Los Angeles, CA

$115K/yr

Execute Process Validation and Cleaning Validation: Identify critical process parameters, establish ... Bachelors in engineering, chemistry, or related field * Certifications related to GMP compliance ...

Moriah Engineering

PR · On-site

Collaborate with cross-functional teams, including Quality Assurance, Manufacturing, and Engineering, to define cleaning validation requirements and processes. Develop and implement protocols for ...

Intellectt INC

Validation Engineer

San Diego, CA · On-site

Validation Engineer Location: San Diego, CA Duration: Longterm Job Summary: A Validation Engineer ... Execute validation protocols for equipment qualification, process validation, cleaning validation ...

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

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All JobsAssistant Cleaning Validation Engineer Jobs

Assistant Cleaning Validation Engineer information

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$33K

$88.8K

$134.5K

How much do assistant cleaning validation engineer jobs pay per year?

As of Jun 25, 2026, the average yearly pay for assistant cleaning validation engineer in the United States is $88,754.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $104,500.00 per year, depending on experience, location, and employer.

What is the difference between Assistant Cleaning Validation Engineer vs Cleaning Validation Engineer?

AspectAssistant Cleaning Validation EngineerCleaning Validation Engineer
CredentialsTypically requires a bachelor's degree in life sciences or engineering; certifications like ASQ or GMP training are commonRequires similar qualifications; often more experience or advanced certifications
Work EnvironmentSupports validation activities in pharmaceutical or biotech manufacturing facilitiesLeads validation projects, performs complex testing, and reviews validation protocols
Employer & IndustryPharmaceutical, biotech, or medical device companiesSame industries, with more senior responsibilities

The Assistant Cleaning Validation Engineer typically supports validation tasks under supervision, focusing on executing protocols and data collection. In contrast, the Cleaning Validation Engineer oversees validation processes, reviews results, and ensures compliance. Both roles are essential in maintaining product quality and regulatory standards in pharmaceutical manufacturing.

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What cities are hiring for Assistant Cleaning Validation Engineer jobs? Cities with the most Assistant 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:
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Assistant Cleaning Validation Engineer jobs near you
Infographic showing various Assistant Cleaning Validation Engineer job openings in the United States as of June 2026, with employment types broken down into 59% Full Time, 39% Part Time, 1% Temporary, and 1% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $88,754 per year, or $42.7 per hour.
Sr. Engineer, Cleaning Validation

Sr. Engineer, Cleaning Validation

Hikma Pharmaceuticals PLC

Columbus, OH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago

Hikma Pharmaceuticals rating

7.8

Company rating: 7.8 out of 10

Based on 29 frontline employees who took The Breakroom Quiz

39th of 72 rated pharmaceutical

Job description

Job Title: Sr. Engineer, Cleaning Validation
Location: Columbus, OH
Job Type: Full time
Req ID: 10915
About Us:
As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' mission is to bring Better Health. Within Reach. Every Day.® for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 800 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our 32 manufacturing plants, eight R&D centers, and 9,500+ employees worldwide, we are always hard at work creating high-quality medicines and making them accessible to the people who need them.
Description:
We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Sr. Engineer, Cleaning Validation to join our team.
In this role, you will be responsible for developing, maintaining, and approving the cleaning validation requirements ensuring compliance to the applicable business and regulatory standards. Develop and maintains site cleaning and cleaning validation processes from product development through product lifecycle. Review and approve the cleaning procedures and support the process to educate those performing the cleaning on the expectations and intent of cleaning, inspection, and cleaning verification sampling. Defines testing strategies and document the performance and compliance of the cleaning validation program. Interfaces with regulatory inspections, investigations and site projects.
Key Responsibilities:
  • Develops and approves validation deliverables, which comply with regulatory guidelines and business requirements. Represent CV during regulatory inspections.
  • Conduct periodic reviews of the compliance of cleaning processes to the validated state and to ensure the effectiveness of the cleaning validation program.
  • Revise and approve procedures for cleaning processes utilized in operations including cleaning, inspection, and cleaning verification work instructions.
  • Support the implementation of the optimization and improvements in a consistency and effectiveness ways of cleaning processes.
  • Support employee training to ensure compliance to procedure and process effectiveness.
  • Establishes and/or participates in the creation of policies, procedures, guidelines, and templates in the area of validation. Provide leadership and direction to manage the testing approach and cleaning swab sample locations on new equipment and/or for new products, with the appropriate direction on the alignment with the philosophy defined by the Cleaning Validation engineering team.
  • Lead, define and manage the mentoring and training of Cleaning Validation colleagues on policies and procedures including the cleaning validation process.

Qualifications:
We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:
  • Bachelor's degree in engineering or related scientific discipline.
  • Minimum of eight (8) years of pharmaceutical industry experience in quality, production, engineering or a laboratory setting.
  • 5+ years specific cleaning validation experience in a pharmaceutical environment. Three years of that experience by a combination of equipment qualification, process validation, or cleaning validation is acceptable.
  • Experience with the authoring and execution of Quality documentation including validation documentation, technical protocols and/or technical reports. Strong knowledge of FDA Current Good Manufacturing Practices (cGMP), ISPE's Risk-Based Manufacture of Pharmaceutical Products, and ICH Q9 Quality Risk Management. Experience and Inspection interaction with FDA, EMA or other regulatory agencies required.
  • Ability to define a problem; collect, statistically analyze, and interpret data; contribute to development of corrective and preventative actions (CAPA) and implementation plans.
  • Demonstrated knowledge of project management skills and techniques, ability to prepare time lines and schedules to ensure projects are executed on time. Excellent organization skills with demonstrated ability to manage multiple projects and deadlines simultaneously. Self-directed individual.
  • Demonstrated skills in multitasking in an environment of high volume projects. Proven ability to shift thought processes quickly and accurately from one project to another.
  • Demonstrated ability to apply critical thinking skills to identify problems. Experience is preferred to use the statistical analysis of data and trends to recognize symptoms, causes, and alternate solutions and makes timely sound decisions even under risk and uncertainty.
  • Demonstrated ability for independent work that requires multi-tasking and a high level of attention to detail.
  • Demonstrated ability to facilitate and/or be an active participant on teams.
  • Demonstrated proficiency in interpersonal communications, both written (technical writing required) and verbal.
  • Demonstrated successful communication/collaborative skills, influencing skills, and negotiation skills to manage conflicting and/or multiple demands, opinions, and expectations including ability to facilitate meetings as well as present to various levels within an organization.
  • Demonstrate the ability to influence/persuade individuals to gain acceptance of an idea or plan is preferred.
  • Demonstrated proficiency in computer skills as a business tool, specific work experience using Microsoft applications (Word, Excel, PowerPoint). Knowledge of application software such as Change control system, SAP, Document Management system or Laboratory information system required.

Preferred Qualifications:
  • 3+ years related experience in project or people management role preferably in a regulated environment.
  • Quality experience in the pharmaceutical industry.

What We Offer*:
  • Annual performance bonus, commission, and share potential
  • Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 4% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute
  • A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries
  • 3 personal days (prorated based on hire date)
  • 11 company paid holidays
  • Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
  • Employee discount program
  • Wellbeing rewards program
  • Safety and Quality is a top organizational priority
  • Career advancement and growth opportunities
  • Tuition reimbursement
  • Paid maternity and parental leave

*Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.
Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
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