QA Specialist (QP Delegate)

Fertin Pharma Group; Vejle; On-site; DKK 550,000 - 700,000; Full time

Job summary

Fertin Pharma Group is seeking a QA Specialist (QP Delegate) to join our quality team in Denmark. This role focuses on day-to-day quality activities, investigations, and continuous improvement, working closely with Quality and Operations to prevent issues through stronger processes.

You will contribute to deviation investigations, product release, GMP support, and change controls, while ensuring compliance and robust quality management across manufacturing operations.

Responsibilities

• Supporting and approving deviation investigations, including root-cause analysis and CAPAs
• Participating in the release process of our pharmaceutical products
• Providing GMP and quality support to pharmaceutical manufacturing
• Reviewing and approving manufacturing documentation
• Participating in change controls, risk assessments, and quality improvement activities
• Contributing to the simplification of our Quality Management System
• Supporting inspection and audit readiness
• Participating in cross-functional projects where quality expertise is needed

Job description

Full details of the job.

Job Title of Vacancy

Job Title of Vacancy QA Specialist (QP Delegate)

Vacancy No

Vacancy No VN2432

Category

Category Quality and Compliance

Contract Type

Contract Type Permanent

Contract Duration

Full Time / Part Time

Full Time / Part Time Full Time

Job Advert

Do you have a passion for pharmaceutical quality, but also believe that Quality should be about more than compliance?

At Fertin Pharma, we develop and manufacture pharmaceutical and nutraceutical products in partnership with leading global and regional brands, combining pharmaceutical expertise with innovative oral delivery technologies.

We are looking for a QA Specialist who wants to work close to our pharmaceutical operations and help us ensure the quality of our products and continuously strengthen the way we manufacture. You will become part of an environment where GMP, manufacturing, and continuous improvement come together.

About the role:

As QA Specialist, you will collaborate closely with colleagues across Quality and Operations. Your role will combine day-to-day quality activities with investigation, problem solving, and continuous improvement. You will have the opportunity to influence how we work with quality and help move from simply reacting to quality issues towards preventing them through stronger processes and effective collaboration.

• Supporting and approving deviation investigations, including root-cause analysis and CAPAs
• Participating in the release process of our pharmaceutical products
• Providing GMP and quality support to pharmaceutical manufacturing
• Reviewing and approving manufacturing documentation
• Participating in change controls, risk assessments, and quality improvement activities
• Contributing to the simplification of our Quality Management System
• Supporting inspection and audit readiness
• Participating in cross-functional projects where quality expertise is needed

Who are you?

Your exact educational background is less important than your ability to understand processes, challenge constructively and turn complex quality issues into practical solutions. We imagine that you:

• Have a relevant scientific, engineering, or pharmaceutical background
• Preferably have experience from pharmaceutical or other highly regulated industry
• It would be considered a strong advantage if your educational background and professional experience meet the requirements for acting as a delegated Qualified Person (QP Delegate) according to Danish requirements
• Understand GMP and preferably have practical experience working within a pharmaceutical Quality Management System
• Can balance compliance, risk and operational reality
• Have experience with, or an interest in, deviations, CAPA, root-cause analysis and risk management
• Is curious and comfortable asking why
• Communicate clearly and collaborate naturally across functions

If you are motivated by making quality work in practice, not simply administering it, we would like to hear from you.

Interviews will be conducted on an ongoing basis.

Special Conditions:

As part of our recruitment process, we conduct background checks on all candidates who accept an offer of employment with Fertin. A satisfactory background check is a condition of employment. The background check is a standard and important part of our hiring process and is carried out in accordance with applicable laws and regulations, as well as Fertin’s internal compliance and integrity requirements.