Cleaning Validation Engineers

VTI Life Sciences; Raleigh (NC); On-site; USD 70,000 - 130,000; Full time

Job summary

VTI Life Sciences is seeking two Cleaning Validation Engineers to work onsite at a pharmaceutical manufacturing facility in Raleigh, NC. The roles require strong knowledge of Cleaning Validation processes and the ability to collaborate across various functions. Successful candidates will participate in key validation activities and ensure compliance with industry regulations while working in a dynamic team environment.

Benefits

Competitive compensation

Excellent benefits

Matching 401K

Professional development and training

Qualifications

• 4+ years for Cleaning Validation Engineer, 8+ years for Senior Engineer.
• Experience in a CDMO or drug product facility is needed.
• Current industry knowledge of Cleaning Validation required.

Responsibilities

• Document strategy for Cleaning Validation execution.
• Write and review cleaning and sanitization procedures.
• Liaise with operational teams and third-party contractors.

Skills

Cleaning Validation

Knowledge of Autoclaves

Cross-functional Collaboration

Tools

Kneat

Job description

3 days ago Be among the first 25 applicants

VTI Life Sciences (VTI) Is Seeking Forward-thinking And Ambitious Engineers Looking To Accelerate Their Career In The Pharmaceutical, Biotechnology And Medical Device Industries. We Offer An Opportunity To Help Support Our Teams Of Industry Subject Matter Experts And Thought Leaders While Consulting With Some Of The Biggest Companies In The Life Sciences Industry. We Are Looking For 2 Cleaning Validation Engineers To Work Onsite At Our Client's Pharmaceutical Manufacturing Facility In The Raleigh, NC Area. One (1)CleaningValidation Engineer And One (1) SeniorCleaningValidation Engineer. Job Title

CleaningValidation Engineer Industry: Pharmaceutical Manufacturing Level of Experience:

4+ years Location: North Carolina, USA (On-Site) Duration: Through the end of the year (Initial Contract) Job Title: SeniorCleaningValidation Enginee r Industry: Pharmaceutical Manufacturing Level of Experience:

8+ years Location: North Carolina, USA (On-Site) Duration: Through the end of the year (Initial Contract) Job Description Looking for a Cleaning Validation Engineer,specifically for drug product parts washers . Past work in a CDMO or a drug product facility is needed. Strong working knowledge ofKneat. The candidate needs to have current industry Cleaning Validation knowledge, including autoclaves, for drug products. The candidate needs to be able to work across functions and departments Participate in CV conversations for CQV but including all necessary functions such as, but not limited to,operations, QA, QC, process support, supply chain, etc and gain alignments as needed. Liaise with the operational readiness team and third-partycontractors, as applicable, to build the connection and define interactions with operations as it relates to cycle development and hold times Document a strategy for how CV will be executed at the site. Write and review cleaning and sanitization procedures and maintainthe Cleaning Validation Master Plan Work with CV team at their sister site in Europe to clone where possible from SOPs, methods, etc. and develop a plan for the localization of these at their North Carolina facility Define roles and responsibilities during CV and gain alignment from supporting teams Together with the CV lead,develop a communication strategy to ensure the site is informed about CV and work with the head of CQV to launch Work with project managers to develop tracking tools and visibility to CV activities Ensure our plan aligns with all necessary regulations and will support successful qualification and future site regulatory inspections SME for presentation of cleaning validation to Regulatory (FDA), internal and external auditors. Identify all necessary SOPs and need by dates and work with owning functions to ensure delivery Work in partnership with QC teams to determine the appropriate CV methods and sampling strategies Work in partnership with the Supply Chain teams to develop a material resourcing and storage strategy to support CV activities, as needed Develop a strategy in collaboration with QC and Operations, for ensuring the training of personnel ahead of executing CV on site Work with the CQV leads, CV lead, REs, and QA on the implementation of the CV strategy in their respective areas Develop a high-leveldocumentation plan and work with the Kneat leads to ensure templates are ready for the execution of these documents Localize documents and applicable CV related SOPs to the client site Perform investigation of deviations and/or discrepancies VTI Life Sciences strives to maintain and inspire professional excellence by providing Commissioning, Qualification, Quality Engineering, Automation and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries. VTI offers professional development, training, competitive compensation, excellent benefits, a matching 401K, plus a stimulating and collaborative work environment. We are committed to providing exciting career opportunities in a work environment that values trust, respect, openness, teamwork, creative talent, enthusiasm and diligence. As one of the leading global Commissioning, Qualification and Validation Services organizations, VTI is always looking for innovative, talented and experienced validation professionals for our multinational and global offices. We offer some of the best salary and benefit packages in the industry for our full-time/permanent employees. www.validation.org

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Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Biotechnology

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