Local Contact Person for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA)

Ergomed; Lisboa; Híbrido; EUR 30 000 - 50 000; Tempo integral

Resumo da oferta

A pharmacovigilance service provider in Portugal is seeking a Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs. In this role, you will ensure compliance with local regulatory requirements and manage pharmacovigilance activities. Candidates should have a Bachelor's degree in Life Sciences or similar and at least 3 years of experience in the pharmaceutical industry. Strong knowledge of ICH GVP and proficiency in English and Portuguese are essential. Opportunities for career development and a supportive work environment are offered.

Serviços

Training and career development opportunities

Friendly, supportive working environment

Opportunity to work globally

Qualificações

• Minimum 3 years' experience in pharmaceutical or CRO industry or regulatory authority.
• Minimum 2 years in LCPPV role or pharmacovigilance experience.
• Pharmacovigilance training and relevant professional background as required.

Responsabilidades

• Act as primary contact with local regulatory authorities for compliance.
• Collect and report locally suspected ADRs or ICSR.
• Review local Product Information and Mock-ups.

Conhecimentos

Knowledge of ICH GVP

Proficiency in English

Proficiency in Portuguese

Strong skills in Microsoft Office

Formação académica

Bachelor's Degree in Life Sciences, Chemistry, Nursing or equivalent

Descrição da oferta de emprego

Company Description

PrimeVigilance (part of Ergomed Group), is a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.

PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.

We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.

Come and join us in this exciting journey to make a positive impact in patient’s lives.

Job Description

The Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) serves as the primary local representative to ensure compliance with national pharmacovigilance and regulatory requirements. This dual-role position is responsible for executing PV and RA activities at the local level, supporting the Marketing Authorisation Holder (MAH) in maintaining product compliance throughout its lifecycle.

Main responsibilities

• Primary contact person with local regulatory authorities for Regulatory Affairs and Pharmacovigilance as per local requirements
• Prompt and effective communication with local regulatory authorities
• Provision of local regulatory intelligence screening and expert advice
• Collection and reporting of locally suspected ADRs or ICSRs (FUs, translations)
• Local management / oversight of risk minimization measures related to urgent safety restrictions and emerging safety issues
• Preparation and collection of documentation for submissions to the regulatory authorities
• Review and linguistic input on local Product Information and Mock‑ups
• Development and implementation of local pharmacovigilance system in compliance with Global MAH’s system and local regulations
• Perform local non‑indexed literature screening and screening of regulatory authority website/s for potential Adverse Drug Reactions (ADRs) and safety information
• Maintain accurate records and documentation at local level
• Provide support to the RA & PV Global operations team
• Ensure compliance with MAH’s and PrimeVigilance’s procedures
• Support audits and Inspections
• Handle local QA tasks such as suspected falsified products, quality alerts received from health authorities and other quality‑related requirements received from the local market

Qualifications

• Bachelor’s Degree in Life Sciences or Chemistry, Nursing or equivalent professional experience
• Minimum 3 years within pharmaceutical or CRO industry or regulatory authority
• Minimum 2 years within LCPPV role, or relevant pharmacovigilance experience in safety‑related position
• Pharmacovigilance training and/or working experience and other educational or professional background as required by local regulations
• Prior experience in Regulatory Affairs is preferred but not mandatory
• Expert knowledge of ICH GVP and relevant local legislation/ regulatory requirements in territories of competency
• Proficiency in English and Portuguese, both written and verbal
• Strong skills in Microsoft Office applications, including Word, Excel, and PowerPoint

Additional Information

Why PrimeVigilance

We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human‑centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.

To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.

We offer:

• Training and career development opportunities internally
• Strong emphasis on personal and professional growth
• Friendly, supportive working environment
• Opportunity to work with colleagues based all over the world, with English as the company language

Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!

• Quality
• Integrity & Trust
• Drive & Passion
• Agility & Responsiveness
• Belonging
• Collaborative Partnerships

We look forward to welcoming your application.

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