Qa Scientist For Batch Release

buscojobs España; Barcelona; Presencial; EUR 35.000 - 50.000; Jornada completa

Descripción de la vacante

Una empresa en expansión busca un Científico de QA para liberación de lotes en Barcelona. El candidato ideal tendrá un título científico y experiencia en la industria farmacéutica. Se ofrece un entorno colaborativo, flexible y oportunidades de crecimiento profesional.

Servicios

Modelo de trabajo híbrido con horarios flexibles

23 días de vacaciones más festivos adicionales

Cocina totalmente equipada

Formación

• 2 años de experiencia en actividades de Control de Calidad o Aseguramiento de Calidad en la industria farmacéutica.
• Experiencia en productos biológicos es valorada.

Responsabilidades

• Revisión de documentos de lotes para liberar productos farmacéuticos.
• Evaluación de desviaciones y quejas en la producción.
• Participación en auditorías de calidad.

Conocimientos

Proactividad

Organización

Orientación al cliente

Inglés

Educación

Título científico en Biología, Química, Farmacia o Biotecnología

Descripción del empleo

Join to apply for the QA Scientist for Batch Release role at Kymos Group

Join to apply for the QA Scientist for Batch Release role at Kymos Group

Due to our business expansion and facility growth, we are looking for a QA Scientist for Batch release to join our dynamic team.

As QA Scietntist your responsibilities will include:

• Be involved in the revision of manufacturing batch records and packaging batch records and other batch review documents of pharmaceutical products to be released.
• Participate in the evaluation of deviations, OOS/OOT, complaints, CAPA and Change Controls of pharmaceutical products to be released ensuring the application of GMPs and according to the marketing authorisation or clinical trail authorisation.
• Participate in the certification process of batches susceptible to be released to the market or for clinical trials.
• Review of Quality/Technical Agreements between the company and manufacturers and marketing authorisatio holders, especially with regard to batch certification activities.
• Review and approve the documentation involved in the activity of the company: CoA, Site Master File, SOPs, product specifications.
• Collaborate and participate in the revision of audit reports carried out by third-parties to the manufacturers of pharmaceutical products to be released.
• Collaborate in audits carried out by our clients and give support in the Inspections of regulatory authorities.
• Participate in the implementation and improvement of the quality system of the company.
  
  
  

Join to apply for the QA Scientist for Batch Release role at Kymos Group

Join to apply for the QA Scientist for Batch Release role at Kymos Group

Due to our business expansion and facility growth, we are looking for a QA Scientist for Batch release to join our dynamic team.

As QA Scietntist your responsibilities will include:

• Be involved in the revision of manufacturing batch records and packaging batch records and other batch review documents of pharmaceutical products to be released.
• Participate in the evaluation of deviations, OOS/OOT, complaints, CAPA and Change Controls of pharmaceutical products to be released ensuring the application of GMPs and according to the marketing authorisation or clinical trail authorisation.
• Participate in the certification process of batches susceptible to be released to the market or for clinical trials.
• Review of Quality/Technical Agreements between the company and manufacturers and marketing authorisatio holders, especially with regard to batch certification activities.
• Review and approve the documentation involved in the activity of the company: CoA, Site Master File, SOPs, product specifications.
• Collaborate and participate in the revision of audit reports carried out by third-parties to the manufacturers of pharmaceutical products to be released.
• Collaborate in audits carried out by our clients and give support in the Inspections of regulatory authorities.
• Participate in the implementation and improvement of the quality system of the company.
  
  
  

If you join us, you will become part of an agile and growing company with a strong scientific culture.

Here's what you can expect:

• A collaborative, empowering environment focused on continuous learning and professional growth
• Hybrid work model with flexible Hours and intensive Fridays.
• A Flexible employee benefits platform.
• 23 vacation days per year + 24th and 31st of December as holidays.
• A Fully stocked kitchen (Coffee, fruits, snacks, and beverages).
• An inspiring workplace surrounded by nature- our headquarters located at the foot of Collserola Natural Park (Barcelona) with a Rooftop terrace an beautiful views
  
  
  

Requirements:

What we are looking for:

• Scientific degree in Biology, Chemistry, Pharmacy, Biotechnology or related disciplines.
• 2 years of experience in Quality Control or Manufacturing activities in Quality Assurance or Quality Control or Manufacturing in the Pharmaceutical Industry.
• Experience on Biologicals will be highly valued
• Proactive, organized, and client oriented mindset.
• A high level of English, both written and spoken is required for this position.
  
  
  

I

Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic.

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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