PV/RA Manager (Zaventem, BE)

Zaventem, Belgium Type not listed
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Chiesi Farmaceutici is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

PV/RA Manager

Are you an experienced Pharmacovigilance and Regulatory Affairs professional ready to take ownership of the daily PV/RA operations? Do you combine in-depth expertise with a hands-on mentality and the ability to guide and develop others?

At Chiesi, you will independently manage the day-to-day PV/RA activities across the Benelux. You work closely with the department manager, who remains responsible for the strategic direction, and provide operational leadership to the PV/RA Specialist and the Medical Information & PV Officer.

We would love to meet you!

Why this role stands out

Independently run the daily PV/RA operations.

Combine hands-on PV/RA work with the operational leadership of two colleagues.

Act as the first point of contact for operational questions and decisions.

Contribute directly to patient safety, compliance and the availability of medicinal products.

What will you do?

As PV/RA Manager, you coordinate, oversee and execute the daily Pharmacovigilance and Regulatory Affairs activities within Chiesi Benelux. You set priorities, safeguard quality and compliance and ensure smooth collaboration with Chiesi Global, authorities and external partners.

You will:

Lead, coach and support the PV/RA Specialist and Medical Information & PV Officer in their daily work.

Act as Affiliate Pharmacovigilance Person for Chiesi Global and Local Contact Person for Pharmacovigilance towards the relevant Benelux authorities.

Maintain and continuously improve the local PV and RA Quality Systems.

Oversee the review, registration, reporting and follow-up of safety information and adverse-event reports.

Coordinate PV training, agreements, reconciliations, service providers and Risk Management Plans.

Lead the preparation and follow-up of audits, inspections and CAPA activities.

Ensure that current and future products comply with regulatory requirements across the Benelux.

Coordinate registration dossiers, product information and packaging materials in close cooperation with Chiesi Global.

Monitor regulatory developments and translate them into clear operational actions.

Optimise working processes and identify opportunities to improve quality, efficiency and business continuity.

We offer you

Join a passionate, Italian family-owned company where our values and behavior truly matter!

As family-owned company we focus on making impact for patients, the planet, people and all that with shared prosperity. Our activities have been externally validated as B Corp certified. At Chiesi, we believe in continuous growth and development. Your personal and professional journey matters to us!

In addition to our focus on professional success, we place great importance on team connection and collaboration. That’s why we organize several internal offsite business events to foster connection, feedback and collaboration.

An attractive salary in line with your responsibilities and experience.

Performance-based bonus structure linked to individual objectives and company result.

13th month of salary

32 holidays per year, including 20 legal holidays and 12 RWH-days (Reduced Working Hours)

Lease car

Hybrid working model: everyone is working at least 3 days per week in the office. The other days you are free to work remotely.

Workation: option work from another location for up to three weeks per year, giving you the freedom to balance work and life in a way that suits you best.

Allowances: internet allowance, cost allowance & meal vouchers

Group insurance with no employee contribution and coverage in case of death and disability, ensuring you and your family are always well protected.

DKV hospitalization is fully paid by the employer for you and your family.

Outpatient care insurance.

Family travel insurance is fully paid by the employer for you and your family.

C-Fit Program: Track your well-being in our app, enjoy a shared healthy lunch at the office, and participate in well-being activities that combine fun with colleagues while helping you achieve a healthy lifestyle.

Annual budget of € 1.000 that you can use for learning or well-being opportunities, helping you grow professionally and personally.

Who are we looking for?

A senior PV/RA professional who can work autonomously, make sound operational decisions and keep the department moving forward. You enjoy working hands-on and bring positive energy, drive and a genuine passion for PV and RA. You may already have leadership experience or be ready to grow into this responsibility.

You bring:

A master’s degree in biomedical or pharmaceutical sciences, or an equivalent level gained through experience.

At least five years of relevant experience within both Pharmacovigilance and Regulatory Affairs.

The ability to independently manage daily PV and RA activities.

Strong knowledge of Good Pharmacovigilance Practices and medicinal product lifecycle management.

Experience with Health Authority inspections and audits.

Experience as an LCPV or in a comparable pharmacovigilance-responsible role is preferred.

Excellent written and spoken communication skills in Dutch, French and English.

A proactive, positive and solution-oriented mindset.

People-management or coaching experience, or the ambition and potential to develop in this area.

Chiesi uses diversity and inclusion as a source of innovation and creativity. Therefore, we welcome all applications regardless of ethnic origin, age, gender, disability, sexual identity, ideology or religion.

Interested?

Nice! We are looking forward to receiving your application. Click on the ‘Apply now’ button and upload your CV and motivation letter, and we will contact you.

Questions? Please contact Femke Roze at f.roze.ext@chiesi.com.

About Chiesi

Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 7,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. Discover more here.

At Chiesi we are thinking generations ahead, driving sustainable innovation with purpose. This fosters a culture of reliability, transparency, and ethical behaviour at every level. As a Benefit Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact.

Diversity and inclusion are at the heart of who we are. We believe our differences make us stronger. We are a vibrant ecosystem of passionate, talented individuals united by strong values, each bringing unique perspectives that help us to continuously challenge the status quo for the better.

PV/RA Manager

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Job details

Seniority
Manager
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Zaventem, Belgium
Employment type
Not listed

How this role compares

Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.

We currently track 41 comparable Manager Pharmacovigilance roles across 22 biopharma companies.

41Comparable roles tracked
37Currently active
22Companies hiring similar roles
14Countries represented

Salary context

7 of 41 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Manager, Pharmacovigilance Case Processing (Boston, MA, US) · Servier $131,000/yr – $150,000/yr
Peer group range $140,500 – $205,000 (median $186,375)

Where these roles are based

Top locations among the 41 comparable roles

United States14
India6
Poland4
France3
Japan3
China2

+ 8 more countries

Seniority mix

41 of 41 peers have a known seniority level

Manager29
Associate Director9
Associate3

Therapeutic area mix

0 of 41 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

45%similar
Mylan AB Solna, Sweden Manager
Same function Same seniority
45%similar
BMS Services Sp. z o.o. Warsaw, Poland Manager
Same function Same seniority
45%similar
Amgen Inc. Remote, United States Manager
Same function Same seniority
45%similar
Amgen Inc. Remote, United States Manager
Same function Same seniority
45%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority
45%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

45%
Senior Manager PV Sweden & Affiliate Safety Representative
Mylan AB · Solna, Sweden · Manager
Function Therapeutic area Seniority Country
45%
Global Pharmacovigilance Safety, Senior Manager- Obesity
Amgen Inc. · Remote, United States · Manager
Function Therapeutic area Seniority Country
45%
Drug Safety Specialist/Non-Line Manager or Staff/Patient Safety and Pharmacovigilance (Shinagawa, Japan, Tokyo)
Boehringer Ingelheim · Shinagawa, Japan · Manager
Function Therapeutic area Seniority Country
45%
Senior Product Manager, Clinical Safety and Pharmacovigilance Systems
ModernaTX, Inc. · Cambridge, United States · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.