Qualified Person Associate — Growth & Mentorship

Q-support; Belgique; Hybrid; 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
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:

• O versee 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 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
• We seek a colleague with 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)

IF YOU ARE INTERESTED:

• Provide your application and CV to [e-mail]

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