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Logistics Quality Specialist

Job Field:
Regulatory and Drug Safety Jobs
Pharmacovigilance Jobs, QA Jobs
Contract Type:
Salary Description:
Job Ref:

Do you want to be part of an award-winning clinical research organisation who is positively working towards improving the health and lives of millions?

At Clintec, we know where people’s lives are involved there is way more to be done. That is why every person working on a Clintec project is working hard to find innovative ways to overcome obstacles. It’s this unwavering determination that keeps us delivering excellence every time!
We have an excellent career opportunity for a determined and motivated Logistics Quality Specialist who strives for excellence to join our North American team on a full time basis.

Responsibilities of the Logistics Quality Specialist

Interface with Quality department in managing NOE’s/CAPA’s/Change Controls for Logistics
Author NOE’s/CAPA’s/Change Controls – including conducting investigation
Develop and report on Key Quality metrics for Logistics
Serve as a backup to Inventory Control, Warehouse and Shipping Operations


Bachelor’s Degree or 3-5 years’ experience in warehouse/distribution operations
Extensive cGMP and GDP Quality experience in the pharmaceutical industry
Microsoft Office experience
SAP Experience
Knowledge of basic mathematics

Why Work For Clintec?

At Clintec, we believe our people are our greatest asset and understand that the best performance comes from individuals who know they are part of a valued team. You can expect to receive expert training and guidance throughout your career with us, with the opportunity to develop, progress and travel globally.

We can offer you:

A competitive salary, car allowance, 25 days annual leave, medical, dental and vision cover, health reimbursement arrangement (HRA), flexible spending accounts, pension plan, life assurance and a friendly and social working environment!
The opportunity to work with various global pharmaceutical leaders on the some of the most prestigious, ground-breaking and challenging drug development projects
Real career development opportunities and a life-long career with an innovative, forward-thinking clinical research company

Company Info

Clintec (an IQVIA company), established for 22 years, is an award-winning, full-service global clinical research organisation. Our head quarter office is based in Scotland, UK and we have operations across 50+ countries worldwide.
We differ from other players in the clinical research industry as we combine the agility and flexibility typical of smaller CROs with the global coverage and management associated with large CROs.
We provide clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries, assisting with key product development and managing clinical trials across all major therapeutic areas, with expertise in Oncology and Rare Disease studies.

Application Details

To be considered for this role, please click the APPLY NOW button. Alternatively if you want to know more about job opportunities at Clintec or our company, please visit our website or contact our internal recruitment team directly at


Clinical Research / Clinical Trials / Clinical Research Professionals / Clinical Research Career / GMP / Supply Chain / Logistics / Global CRO

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