Senior Quality Consultant – Person-in-Plant

🔥 0 minutes ago

🌐 United Kingdom, Sweden, +3 more countries – Remote

🇬🇧 United Kingdom – Remote 🇸🇪 Sweden – Remote 🇭🇷 Croatia – Remote 🇩🇪 Germany – Remote 🇳🇱 Netherlands – Remote

⏰ Full Time

🟠 Senior

💼 Consultant

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

ProPharma

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 2001

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

💰 $8.6M Venture Round on 2020-10

Healthcare • Logistics • Manufacturing

ProPharma is a leading research consulting organization in the life sciences industry. The company specializes in providing custom solutions across the full product lifecycle, from early discovery to post-market monitoring. ProPharma's services include regulatory sciences, clinical research solutions, quality and compliance services, pharmacovigilance, medical information, and R&D technology. Known for its deep domain expertise, ProPharma assists clients in the pharmaceuticals, biotechnology, and medical device sectors with regulatory support, clinical development, and quality management. ProPharma's global team supports a wide range of therapeutic areas including oncology, cardiovascular, and rare diseases, among others, ensuring effective and efficient delivery of life-saving therapies.

📋 Description

• Lead and manage routine Quality Management Reviews (QMRs) • Provide quality oversight and support during Process Performance Qualification (PPQ) activities for clinical and commercial products • Perform key audits related to quality findings • Coordinate and deliver mock inspection readiness activities, including preparation, coaching, documentation review, and inspection simulations • Perform QMS tasks including CAPAs and deviations • Support inspection and audit readiness initiatives across clinical and commercial manufacturing operations • Collaborate with cross-functional stakeholders to address and resolve quality risks • Review and evaluate quality systems, documentation, and manufacturing activities for GMP compliance and company quality standards • Act as a quality subject matter expert for assigned projects and quality-related initiatives • Provide guidance on compliance expectations and quality system requirements • Provide overall QA Lead support for Person-In-Plant activities

🎯 Requirements

• Must be educated to a BSc or higher within a life-sciences discipline • Thorough experience working in Quality Assurance within the life-sciences industry • Previous experience working as a Person-in-Plant or supporting Person-in-Plant activities • Previous experience managing CDMO partners highly preferred • Fluent in English • Currently based within the UK or EU • Ability to perform the project as designated within the job description

🏖️ Benefits

• Short-term three-month project initially • Full-time 1.0 FTE (40 hours a week) • Remote working supported • Hybrid working encouraged for new hires based within a reasonably short commute of an office, as agreed with the manager • Equal Opportunity Employer workplace committed to diversity, equity, and inclusion