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Quality Assurance Specialist & Qualified Person Deputy

On-site in Barcelona·Added 14 days ago (last checked 2 Nov)

Insud Pharma

61 open roles

Our summary

Work mode
On-site, Barcelona
Contract
Permanent
English
Required
Experience
2+ years
Education
University degree

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    The advert says visa sponsorship isn’t available for this role.

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Skills

This job advert was originally written in Spanish.

Requirements

What we're looking for

  • Bachelor's Degree in Pharmacy.
  • At least 2 years of experience in a Quality Assurance Department, a necessary requirement to be able to assume functions as a Deputy Technical Director.
  • High level of English.
  • Knowledge of regulations and quality systems in a pharmaceutical environment.
  • Knowledge of GMP / GDP.
  • Experience in document management, certifications, licenses, and relationship with regulatory authorities.
  • SAP proficiency.

Nice to have

  • Training in animal nutrition will be valued.

Pay & benefits

What you'll get

📜 Permanent contract

🎯 Professional development in an international environment

🍏 Subsidized canteen

🅿️ Parking available

🎓 Continuous training

The role

Position: QA Specialist / Deputy QP

Location: Barcelona

Experience: At least 2 years in Quality Assurance within a pharmaceutical environment

What you'll do

  • Guarantee the implementation and maintenance of a quality management system in accordance with current regulations.
  • Manage communication with the different Regulatory Authorities, including annual declarations of antimicrobial sales.
  • Prepare and review PQRs.
  • Provide technical support to internal departments and customers.
  • Manage the release of batches to the market.
  • Manage complaints, incidents, and associated deviations.
  • Obtain and maintain certifications and permits, including GDP, GMP+, pesticides, and other Vetpharma authorizations.
  • Manage Change Controls.
  • Manage returns and destructions.
  • Request import licenses for active pharmaceutical ingredients (APIs).
  • Request export licenses for veterinary medicines (CEXGAN).
  • Request NOC licenses for non-controlled substances.
  • Coordinate supplier qualification, including questionnaires, agreements, certificates, and ASL.
  • Prepare Quality Technical Agreements (QTAs).
  • Participate in new product launches and technology transfers.
  • Create material codes in SAP.

What are we looking for? 🔎

We are looking for a QAQP Deputy to support the Quality area, guaranteeing the correct implementation and maintenance of the quality management system in accordance with current regulations, as well as ensuring compliance with the regulatory and quality requirements applicable to Vetpharma's activities.

The selected person will actively participate in quality activities, technical support, certifications, document management, relationship with regulatory authorities, and key processes linked to veterinary products, raw materials, and licenses.

Skills that will make a difference

  • Rigor and attention to detail
  • Organizational and follow-up skills
  • Orientation towards quality and regulatory compliance
  • Good communication skills
  • Ability to provide technical support and coordinate with different areas

🔷Do you think this offer is not for you?🔷

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Hiring process

  • Initial contact by telephone or email.
  • 1 or 2 in-person interviews in Barcelona.
  • Constant communication regarding the status of the process.

About Insud Pharma

Industry
Pharmaceuticals

In their own words

About the company & team

Vetpharma, a company of the Insud Pharma group, specializes in the development, manufacture, and commercialization of animal health products, working with the highest standards of quality, safety, and regulatory compliance.

At Vetpharma, we bet on excellence, continuous improvement, and the development of professionals who want to grow in a technical, demanding, and international environment.

Additional information

At Vetpharma, we are committed to equal opportunities and to creating a diverse and inclusive work environment. All applications will be valued without discrimination based on gender, age, ethnic origin, nationality, religion, sexual orientation, gender identity, disability, or any other personal or social condition.

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