Validation & Engineering Group, Inc.

Cleaning Validation Specialist

Validation & Engineering Group, Inc.  •  Greenville, SC (Onsite)  •  4 hours ago
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Job Description

Pinnaql is a trusted consulting partner to regulated life sciences companies, providing deep technical, validation, and quality expertise across every stage of the product lifecycle. We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity, accelerate project timelines, and maintain a strong state of compliance and audit readiness.

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

  • Cleaning Validation Specialist

Description:

We are seeking a Cleaning Validation Specialist to support full lifecycle cleaning validation activities at a regulated manufacturing site in Greenville, SC. This role is part of a broader initiative to strengthen cleaning validation practices and ensure compliance with current regulatory and site standards.

The position requires both technical ownership and hands on execution. The ideal candidate can independently lead cleaning validation efforts, from strategy through final report, while also performing sampling and execution activities in alignment with production schedules.

Key Responsibilities:

  • Develop cleaning validation strategies, master plans, and validation plans, including product and equipment grouping and worst case selection
  • Establish or support residue acceptance limits (MACO, HBEL/PDE, and cleaning agent limits)
  • Author cleaning validation protocols, reports, and supporting risk assessments
  • Execute cleaning validation protocols, including swab, rinse, and visual inspection
  • Coordinate sampling and testing activities with the laboratories
  • Lead or support deviation investigations, root cause analysis, and CAPA related to cleaning validation
  • Train operators and staff on cleaning procedures, sampling techniques, and protocol execution
  • Provide technical guidance on cleaning processes, including cleaning agents, solvents, CIP and COP, and manual cleaning methods
  • Collaborate with Quality, Manufacturing, and Laboratory teams to ensure successful and timely execution
  • Support other Commissioning, Qualification, and Validation activities as needed based on project demands

Required Qualifications:

  • Bachelor’s degree in Engineering, Chemistry, Biology, or a related science
  • 5+ years of cleaning validation experience in a regulated environment (pharmaceutical, biotech, or medical device)
  • Proven experience with the full cleaning validation lifecycle: strategy, protocol development, execution, and reporting
  • Hands on experience with swab and rinse sampling techniques
  • Strong knowledge of GMP requirements and applicable guidance (FDA, EU Annex 15, ICH Q7 and Q9)
  • Excellent technical writing skills
  • Ability to work independently with minimal supervision
  • Experience in sterile or ophthalmic manufacturing
  • Experience with CIP systems and automated cleaning processes
  • Experience with electronic validation systems (for example, Kneat)
  • Candidates must be authorized to work for any employer in the United States without visa sponsorship, we are not able to sponsor a visa or work on a C2C basis for this opportunity.

Work Requirements:

  • On site position in a manufacturing environment
  • Flexibility to work early, late, off shift, and weekend hours to support sampling based on production schedules
  • Ability and willingness to enter confined spaces, including tanks and similar equipment, to perform inspections, measurements, and sampling in compliance with site safety procedures

At Pinnaql, 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.

Pinnaql 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.

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Validation & Engineering Group, Inc.

About Validation & Engineering Group, Inc.

Validation & Engineering Group, Proudly serving our clients since 1997.

Our Mission states in part: "provide our clients with the best resources to meet their needs". In our search for the best talent, we are inclusive and do not discriminate. V&EG is proud to be an equal opportunity workplace and is an affirmative action employer.

Validation & Engineering Group provides world-class service and expertise to the pharmaceutical, medical device and biotechnology industries. We offer our clients: Validation, Control System Solutions, Instrumentation, Training, Equipment Rentals, and Regulatory Compliance Services to ensure adherence to Federal and European regulatory agencies. Our group had serve in solid dosages, liquids, creams, lyophilizers, and parenteral dosage.

Our agility in responding to our clients’ needs, access to the best pool of talent, and the combined experience and technical expertise of our resources make Validation & Engineering Group a leader in the pharmaceutical, medical devices, and biotechnology industries.

At Validation & Engineering Group we provide professional expertise in the areas of:

•Audit and Assessment

•Automated Process Control System Qualification

•Equipment and Facilities Qualification

•Facilities Start-Up and Commissioning

•GAP Analysis

•Information Systems Computer Validation

•Packaging and Process Analysis

•Process & Cleaning Validation

•Project Management

•Quality Systems

•Risk Based Approach

•Regulatory Compliance

•Standard Operating and Maintenance Procedures

•Training

•Utilities Support and Qualification

In addition we offer Equipment Rentals and training to your workforce such as: Temperature & Relative Humidity, Electrical, Process, Environmental, and. Analytical.

Our Offices:

Puerto Rico:

Centro Internacional de Mercadeo I 100 Carr. 165 Ste 703, Guaynabo, 00968 Puerto Rico

Phone: (787) 622-0996

United States:

2180 Satellite Blvd, Suite 400Duluth, Georgia 30097 United States

Phone: (770) 403-5802

Industry
Architecture & Engineering
Company Size
51-200 employees
Headquarters
Guaynabo, PR
Year Founded
1997
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