Responsible Person Associate

Q Support; Town of Belgium (WI); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Attractive salary package

Mentorship with experienced professionals

Flexible work environment

Frequent Team Events

Job summary

Q Support in Belgium is seeking a Qualified Person / Responsible Person (Associate). You will oversee compliance with GMP and GDP standards, handle multiple projects, and maintain quality management systems. The ideal candidate has a Master’s degree in pharmacy and a strong background in Quality Assurance.

This role offers significant responsibility with opportunities for professional development, mentorship, and a flexible work environment, including homeworking options.

Qualifications

• Minimum 2 years of professional experience in Quality Assurance.
• Registered by the Belgian Authorities as Qualified Person (is a plus).

Responsibilities

• Oversee quality and compliance aspects related to GMP and GDP.
• Maintain the QMS of clients and handle multiple RP projects.
• Provide impeccable service to clients.

Skills

Knowledge of Good Manufacturing Practice (GMP)

Knowledge of Good Distribution Practice (GDP)

Proficiency in MS Office

Strong problem-solving mindset

Multilingual: NL/FR/EN

Education

Master’s degree in pharmacy

Job description

Responsible Person Associate

Q-SUPPORT IS LOOKING FOR:

Qualified Person / Responsible Person (Associate)

WHO ARE WE?

• Partner of pharmaceutical companies providing expertise in RP/QP/RIP matters
• Located in Dilbeek – Nice Coworking space Fosbury & Sons
• Team of enthusiastic professionals willing to bring excellence to our client as well as internally
• Tailored services for the life science industry
• Provide the best service to our customers (expertise, pro‑activity & communication)
• Build Strong partnerships with our customers
• 100% satisfied clients

RESPONSIBILITIES OF THE QUALIFIED PERSON/RESPONSIBLE PERSON:

• Oversee all quality and compliance aspects related to Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) in Belgium and the Netherlands.
• Endorse all the RP responsibilities in the context of clients’ activities (audit, implementing and maintaining QMS, Quality Agreements, inspection, supplier qualification…) with the support of our Senior Expert Consultant (Coach)
• Juggle between different RP projects on a weekly basis.
• Maintain the QMS of our clients
• As part of Q‑support you will also be involved in various internal tasks to make Q‑support the best place to work (technical publication for our social media, internal procedure and processes…)
• Provide an impeccable service to the clients entrusted to you

THE PROFILE WE ARE LOOKING FOR:

• Master’s degree in pharmacy
• Minimum 2 years of professional experience in Quality Assurance
• Registered and approved by the Belgian Authorities as Qualified Person in accordance with the Royal Decree of 14 December 2006 (is a plus but not a mandatory)
• Knowledge of Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP)
• (Willing to obtain) strong knowledge of the legislation and guidelines (Eudralex volume 4, Belgian Law of 25 March 1964, RD 14 December 2006, Good Distribution Practices)
• High level of independence, yet supervised by Senior Expert consultant
• Demonstrated proficiency in MS Office
• Strong problem solving mindset and attention to details
• NL/FR/EN (English and NL is mandatory, FR is a plus)

WHAT’S IN IT FOR YOU:

• A role with a lot of responsibility and the chance to work self‑organized in a dynamic & positive environment
• Being able to develop yourself (training, coaching)
• Mentorship with experienced QPs/RPs/RIP within the company
• Learn & Grow with your peers
• Attractive salary package
• Frequent Team Event
• Flexible work environment (homeworking, flexible hours)