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91,000+ live jobsPharmacovigilance and Registrations Specialist in Sant Just Desvern
On-site in Sant Just Desvern·Full-time·Added 4 days ago (last checked 22 Oct)
Our summary
- Work mode
- On-site, Sant Just Desvern
- Contract
- Permanent, full-time hours
- Education
- University degree
- Benefits
- Private health insurance, meal vouchers




Visa options
The ad rules out sponsorship
The advert says visa sponsorship isn’t available for this role.
STADA is hiring for this role in several places. This vacancy is in Sant Just Desvern.
This job advert was originally written in Spanish.
Requirements
What we're looking for
Requirements
- University degree in Health Sciences (Pharmacy, Biology, Biotechnology, Medicine, Nursing, or similar).
- Previous experience of approximately 1 year in pharmacovigilance or related drug safety areas.
- Basic knowledge of pharmacovigilance regulations and processes.
- Interest in professional development in the areas of pharmacovigilance and regulatory affairs.
- Ability to organize and manage multiple activities simultaneously.
- Analytical skills and attention to detail.
- Ability to work autonomously and proactively.
- Good communication and interpersonal skills.
- Ability to collaborate with multifunctional teams and in cross-functional environments.
- Proficiency in scientific literature and technical documentation related to medicinal products.
Pay & benefits
What you'll get
How we will take care of you
At STADA, we believe that caring for people's health starts with caring for those who are part of our team.
From your first day, you will have access to a wide range of benefits designed to boost your professional development and personal well-being. This includes a flexible working model, health insurance, meal vouchers and transport vouchers, physical and emotional well-being initiatives, as well as development programs that value your growth.
We want you to feel supported to give your best, both inside and outside of work. That is why we promote a culture based on trust, flexibility, inclusion, and work-life balance, where every person can develop authentically and find real opportunities to grow.
We drive a strong culture of growth that will allow you to learn continuously, take on new challenges, and build your own professional path. Through training and development programs, you will have access to opportunities to expand your knowledge, enhance your strengths, and advance your career in a company committed to the development of its talent.
You will be part of a team united by a common purpose: caring for people's health as a trusted ally. A company that bets on people recognizes their achievements and provides them with the necessary tools to continue growing.
STADA offers a competitive environment for personal and professional development in a growing company full of opportunities. Our future project requires dynamic and proactive professionals, capable of adding value in a changing environment.
The role
At STADA, we pursue the purpose of "Caring for people's health as a trusted partner." All our decisions and actions are driven by our purpose, vision, and values.
With our wide range of Generics, Consumer Healthcare, and Specialties, we offer patients, doctors, and pharmacists a wide range of therapeutic options.
Around 11,700 employees live our values of Integrity, Entrepreneurship, Agility, and One STADA, in order to achieve our ambitious goals and shape a successful future for our company. We continuously expand our goals in line with our ambition, and we achieve them with passion, commitment, and a growth mindset.
We continuously expand our goals in line with our ambition, and we achieve them with passion, commitment, and a growth mindset.
What you'll do
Responsibilities
- Manage and evaluate received suspected adverse reactions, ensuring their correct documentation and follow-up.
- Perform detection and evaluation activities for safety signals.
- Maintain and update the safety information of marketed medicinal products.
- Execute searches and reviews of scientific literature related to drug safety.
- Manage and follow up on the Risk Management Plans (RMP) of the products.
- Implement and monitor corrective and preventive actions (CAPAs) derived from audits and inspections.
- Prepare and follow up on regulatory communications with health authorities within the established deadlines.
- Manage and supervise product safety variations.
- Coordinate and follow up on risk minimization activities, especially for new launches.
- Review and manage Medical Enquiries.
- Maintain and update RSI (Reference Safety Information) documentation.
- Participate in internal training activities related to pharmacovigilance and safety.
- Collaborate on regulatory projects and provide support to the Regulatory Affairs department.
- Work cross-functionally with different areas of the company to ensure compliance with regulatory and pharmacovigilance requirements.
How you'll work
Barcelona| Full time | Permanent contract
About STADA
STADA Arzneimittel AG is a German pharmaceutical company headquartered in Bad Vilbel, Germany. The company develops, produces, and markets a wide range of pharmaceutical products, including generics, specialty pharmaceuticals, and consumer health products. With a global presence, STADA operates in multiple countries and has a significant workforce, making it a substantial player in the European and international pharmaceutical market.
In Spain, STADA has a notable presence with offices in Barcelona, which serves as a hub for its Iberian operations. The company is known for its international and multicultural work environment, offering opportunities for professionals from various backgrounds. For international hires, STADA provides a dynamic environment with roles in global supply chain management, regulatory affairs, and category management, making it a relevant employer for those looking to work in the pharmaceutical sector in Spain.
- Industry
- Pharma
- Founded
- 1895
- Employees
- 10,000–15,000
- Headquarters
- Bad Vilbel, Germany
- In Spain
- Barcelona
Good to know if you are moving
- STADA offers roles in global supply chain, regulatory affairs, and category management, which are relevant for international professionals with experience in the pharmaceutical industry.
- The company's Spanish operations are centered in Barcelona, providing a base for roles in the Iberian region.
- STADA is a publicly traded company (FSE: SAZ) with a global footprint, offering international career opportunities.
- The company's work environment is described as international and collaborative, with English often used as the working language in global roles.
- STADA provides opportunities for professional growth in a stable and established pharmaceutical company.
In their own words
Additional information
The STADA Group promotes a diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology, or sexual orientation.
We leverage the strength of this diversity to develop creative ideas, expand our expertise, and increase our capacity for innovation.
Our focus is centered on equal opportunities, respectful cooperation, and the promotion of an inclusive work environment.
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