Quality Specialist, Contamination Control

Job not on LinkedIn

🕒 4 days ago

🇮🇪 Ireland – Remote

⏱ Part Time

🟡 Mid-level

🟠 Senior

✨ Quality Specialist

👻 Ghost score 12%

What it means: the chance that no one is really hiring for this job.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

Pharmalliance Consulting Ltd

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2019

💼 Consulting

💊 Pharmaceuticals

🏥 Healthcare

Consulting • Pharmaceuticals • Healthcare

Pharmalliance Consulting Ltd. appears to be a consulting firm serving the pharmaceutical and healthcare sectors. The available text provided was website/CSS markup with no substantive content, so the description below is inferred from the company name rather than the supplied content. Pharmalliance Consulting Ltd. likely provides professional consulting services (such as regulatory, clinical, quality, commercial or strategic advice) to pharmaceutical, biotechnology or broader healthcare organizations, although specific services and scale are not provided in the available data.

📋 Description

• Set up and build client contamination control projects on the CCbD platform • Gather, organise and enter site and process information, including cleanroom areas and grades, and personnel, material and equipment flows • Map manufacturing and support processes step by step to identify contamination risks and existing controls • Support contamination control risk assessments and gap assessments against EU GMP Annex 1 (2022) • Collate client data, including environmental monitoring data, into Excel trackers and summaries • Draft, format and check reports, SOPs and assessment records • Track project actions and open items and maintain up-to-date project records • Support client presentations and cGMP training materials linked to CCbD projects • Work alongside senior consultants on client contamination control projects

🎯 Requirements

• Degree in a science or engineering discipline, such as microbiology, biotechnology, pharmaceutical science, chemistry or chemical engineering • Understanding of contamination control principles, including cleanroom classification, gowning, cleaning and disinfection, and environmental monitoring • Good process knowledge and ability to understand manufacturing or cleanroom processes step by step • Strong attention to detail in documents, data and records • Good Microsoft skills: Word, Excel, PowerPoint and Outlook • Clear written and spoken English • Ability to work to deadlines and manage own time in a part-time schedule • Knowledge of EU GMP Annex 1 (2022) and contamination control strategy requirements • Placement, internship or project experience in a GMP, laboratory or cleanroom environment • Familiarity with quality risk management tools such as FMEA (ICH Q9) • Comfort working in web-based software platforms

🏖️ Benefits

• Part-time schedule of 10–20 hours per week • Fully remote work • Immediate start • Opportunity to work alongside senior consultants • Opportunity to learn contamination control practices and cGMP compliance • Exposure to client contamination control projects and CCbD, an Annex 1-aligned platform

📊 Check your resume score for this job

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

Upload Resume