Commissioning, Qualification, And Validation Specialist - 1843056
🚀 Job Opportunity: Validation / C&Q Specialist 🚀
📍 Location: In one of our client's facilities in Puerto Rico (100% Onsite Work Availability)
Embark on a rewarding career journey in Pharmaceuticals and Medical Devices as a Validation / C&Q Specialist! This exciting role is offered through a contract with ProQuality Network at one of our distinguished clients in Puerto Rico.
🌐 About ProQuality Network:
ProQuality Network is a collective of industry Subject Matter Experts (SME’s) who have successfully navigated their career paths and united to serve our sector, comprehending its unique needs and opportunities. Attuned to industry standards, regulatory expectations, and well-versed in its challenges, we become your optimal choice when resource constraints, expertise gaps, or a desire to direct in-house resources towards core business activities arise.
As seasoned Quality Experts with unmatched expertise in the Biosciences/Life Science Manufacturing realm, we provide Top-Tier Consultants, Advisors, and Specialists, all dedicated to addressing the Industry quality-centric challenges: Quality Systems, Quality Risk Management, Proactive Compliance Enhancement, Compliance Remediation, Quality-Driven Project Management, and Strategic Consulting.
🌐 Explore all job openings at ProQuality Network by visiting our website: ProQuality Network Job Openings https://www.proqualitynet.com/
Summary:
We are seeking an experienced and meticulous Validation Consultant to join our team. In this role, you will be responsible for leading validation activities for pharmaceutical processes, equipment, and systems, ensuring compliance with regulatory requirements and industry standards.
Key Responsibilities:
- Lead and manage Commissioning and Qualification (C&Q) projects.
- Develop and execute validation protocols (IQ, OQ, PQ) and reports.
- Collaborate with cross-functional teams, including quality assurance, engineering, and manufacturing, to ensure successful project execution.
- Conduct Risk Assessments and develop mitigation strategies to address potential validation issues.
- Provide technical expertise and guidance to junior team members and clients.
- Ensure all validation documentation is accurate, complete, and compliant with regulatory standards.
- Stay current with industry trends and regulatory changes to ensure best practices are followed.
Qualifications:
- Bachelor’s degree in Engineering, Life Sciences, or a related field. Advanced degree preferred.
- Minimum of three (3) years of experience in validation within the pharmaceutical industry.
- Strong knowledge of SDLC and regulatory requirements, including FDA, EMA, and GMP guidelines.
- Proven track record of successfully managing validation projects.
- Excellent problem-solving and analytical skills.
- Strong communication and interpersonal skills.
- Ability to work independently and as part of a team.
⬇️ Apply through the link below ⬇️
Join our network of industry experts at ProQuality Network as we shape the future of healthcare through excellence and innovation. 🌐🛠️
🌐 Explore all job openings at ProQuality Network by visiting our website: ProQuality Network Job Openings https://www.proqualitynet.com/
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