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Quality Assurance specialist Oversight

Quality Assurance specialist Oversight

Hipramadrid, España
Hace 20 días
Descripción del trabajo

HIPRA is a pharmaceutical and biotechnological company focused on prevention and diagnosis for animal and human health, with a broad range of highly innovative vaccines and an advanced diagnostic service.

HIPRA has a solid international presence in more than 40 countries, with its own subsidiaries, 11 diagnostic centres, and 6 production plants strategically located in Europe (Spain) and America (Brazil).

Research and Development constitute the core of its knowledge. HIPRA dedicates 15% of its annual turnover to R&D activities that concentrate on the creation and application of the latest scientific advances to develop high-quality innovative vaccines. The company also develops medical devices and traceability services to add value to its vaccination experience.

We are currently looking for a motivated Quality Assurance Specialist - Oversight for our offices in Amer, Girona, to join our team and support FDA Inspection for Human Health projects .

Main Responsibilities :

  • Actively participate in plant QA oversight regarding aseptic behavior and contamination risk control, ensuring activities comply with cGMP, corporate policy, local procedures, and regulatory expectations.
  • Address gaps and implement improvements identified across the organization for FDA inspections.

Qualifications :

  • Bachelor's degree in biology, biotechnology, chemistry, pharmacy, or veterinary sciences.
  • Minimum of 2 years of experience in Quality Assurance within the pharmaceutical or biotechnological sector.
  • Proactive, flexible, and eager to contribute in a fast-paced, evolving environment. Team player and able to work under pressure.
  • Proficient in written and spoken English.
  • Experience with FDA processes and inspections is a plus.
  • Willingness to work on rotating morning and afternoon shifts and in aseptic conditions.
  • Functions :

  • Supervise on-site processes related to products in the Human Health area to ensure compliance with GMP and HIPRA's Quality System.
  • Analyze processes and work methods to identify improvements and prevent deviations.
  • Implement corrective and preventive actions to resolve non-compliances and improve processes.
  • Ensure proper investigation and documentation of deviations, with root cause analysis and corrective actions.
  • Monitor critical data and process indicators to ensure process robustness and effectiveness of measures.
  • Ensure staff training on GMP and participate in training delivery as needed.
  • Propose and implement ideas for improvement and innovation.
  • Contribute to departmental projects with ideas and proposals.
  • Reasons to Join HIPRA :

  • Involvement in relevant, long-term projects to expand knowledge and experience.
  • Growing multinational company with 40 subsidiaries worldwide.
  • Multicultural environment fostering teamwork.
  • Opportunities for training and professional development.
  • Equal opportunity employment policy, considering all qualified applicants without discrimination.
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