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Regulatory Affairs Specialist (M/F)

  • ... Posted on: Mar 19, 2026
  • ... Tecnimede Group
  • ... Sintra, null
  • ... Salary: Not Available
  • ... Full-time

Regulatory Affairs Specialist (M/F)   

Job Title :

Regulatory Affairs Specialist (M/F)

Job Type :

Full-time

Job Location :

Sintra null United States

Remote :

No

Jobcon Logo Job Description :

Tecnimede Group is a Portuguese multinational company, with more than 40 years of history in the life cycle of the drug product for human use - development, production, promotion and marketing - with the mission to improve and preserve the human life and the human health.Exporting to more than 100 countries worldwide, it is present in 6 countries (Portugal, Spain, Italy, Marocco, Columbia and Brazil) with strong focus in expanding internationally and building strategic partnerships.We are looking to reinforce our team with a Regulatory Affairs Specialist (M/F).Responsibilities:- Ensure the coordination of all activities related to the regulatory area, ensuring compliance with applicable regulations and guidelines;- Prepare and submit pharmaceutical product registration dossiers for approval by authorities;- Keep up to date with changes in regulations and guidelines and ensure the company is compliant;- Collaborate with internal teams in the pre-authorization phase (pharmaceutical, analytical and clinical development, and quality) and in the post-authorization phase (industrial production, pharmacovigilance, logistics, price and reimbursement and quality);- Participate in audits and inspections, providing support and necessary information;-Develop and update locally controlled regulatory documentation (SOP’s, training materials), ensuring they are updated and proactively identify procedural gaps to implement solutions in collaboration with all relevant stakeholders.Requirements:- Academic training in Pharmacy, Chemistry or a related field;- Proven experience in the pharmaceutical regulatory area;- In-depth knowledge of pharmaceutical legislation and regulations;- Analytical and problem-solving skills;- Excellent verbal and written communication skills;- Ability to work independently and in a team;- Fluency in English."In accordance with the provisions of the GDPR and other legislation in force on personal data protection, the contracting company guarantees that the processing of your personal data is lawful, fair, transparent, and limited to the purposes for which your data was collected."

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Jobcon Logo Position Details

Posted:

Mar 19, 2026

Reference Number:

25976_4328926366

Employment:

Full-time

Salary:

Not Available

City:

Sintra

Job Origin:

APPCAST_CPC

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Tecnimede Group is a Portuguese multinational company, with more than 40 years of history in the life cycle of the drug product for human use - development, production, promotion and marketing - with the mission to improve and preserve the human life and the human health.Exporting to more than 100 countries worldwide, it is present in 6 countries (Portugal, Spain, Italy, Marocco, Columbia and Brazil) with strong focus in expanding internationally and building strategic partnerships.We are looking to reinforce our team with a Regulatory Affairs Specialist (M/F).Responsibilities:- Ensure the coordination of all activities related to the regulatory area, ensuring compliance with applicable regulations and guidelines;- Prepare and submit pharmaceutical product registration dossiers for approval by authorities;- Keep up to date with changes in regulations and guidelines and ensure the company is compliant;- Collaborate with internal teams in the pre-authorization phase (pharmaceutical, analytical and clinical development, and quality) and in the post-authorization phase (industrial production, pharmacovigilance, logistics, price and reimbursement and quality);- Participate in audits and inspections, providing support and necessary information;-Develop and update locally controlled regulatory documentation (SOP’s, training materials), ensuring they are updated and proactively identify procedural gaps to implement solutions in collaboration with all relevant stakeholders.Requirements:- Academic training in Pharmacy, Chemistry or a related field;- Proven experience in the pharmaceutical regulatory area;- In-depth knowledge of pharmaceutical legislation and regulations;- Analytical and problem-solving skills;- Excellent verbal and written communication skills;- Ability to work independently and in a team;- Fluency in English."In accordance with the provisions of the GDPR and other legislation in force on personal data protection, the contracting company guarantees that the processing of your personal data is lawful, fair, transparent, and limited to the purposes for which your data was collected."

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