Cleaning Validation Specialist

Unicon Pharma Inc; North Carolina; On-site; USD 61,992 - 82,656; Full time

Job summary

A pharmaceutical company in North Carolina is seeking a Cleaning Validation Support specialist for a contract role lasting over 6 months. The position involves authoring technical documentation, developing protocols, and supporting regulatory submissions. Candidates should have relevant experience and be prepared to work onsite full-time during first shifts. This position provides a competitive hourly pay rate between $45.00 and $60.00.

Qualifications

• Act as the Cleaning Validation Specialist within a cross‑functional team.
• Author and review technical documentation including SOPs and validation reports.
• Develop and execute Cleaning Validation Protocols.

Responsibilities

• Support regulatory submission preparations.
• Oversee contractors involved in system qualifications.
• Provide regular updates on qualification activities.

Job description

1 week ago Be among the first 25 applicants

This range is provided by Unicon Pharma Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$45.00/hr - $60.00/hr

Direct message the job poster from Unicon Pharma Inc

Recruiter at Unicon Pharma | Quality & Compliance | Validation

*Skills, experience, and other compensable factors will be taken into account when determining pay rate. The pay range provided in this posting is a reflection of a W2 hourly rate; other employment options may be available that may result in pay outside of the provided range.

*Due to client requirement, applicants must be willing and able to work on a w2 basis

Title: Cleaning Validation Support

Duration: 6+ months (likely extensions)

Location: NC - onsite

Hours: 40 hours/week - 1st shift

Start: 1-2 weeks from offer

Interview Process: 1-2 rounds

*Looking for various years of experience - more than one position available

Job Responsibilities:

• Act as the Cleaning Validation Specialist within a cross‑functional team and provide subject matter expertise during the planning, design, and execution phases of projects.
• Author and review technical documentation, including cleaning cycle development reports, SOPs, system lifecycle documentation, protocols, and validation reports.
• Develop and execute Cleaning Validation Protocols, ensuring timely identification and resolution of any deviations or non‑conformances.
• Support regulatory submission preparations and represent validation deliverables during regulatory inspections as the SME.
• Oversee contractors involved in system qualifications and ensure the quality and compliance of deliverables.
• Provide regular updates on qualification activities and project progress to the leadership team.

Seniority level

Mid-Senior level

Employment type

Contract

Job function

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