Qa Batch Release Analyst

hace 1 mes


Barcelona, España Kymos Group A tiempo completo

.KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany and a Liaison office in South Korea, offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have been successfully inspected by EMA, FDA, and ANVISA.KYMOS GROUP is devoted to providing high quality and added value services to its partners and it is highly oriented to innovation, offering services of research, development and quality control in many different fields such as small molecules, proteins, antibodies, nucleic acids, and advanced therapies.KYMOS GROUP has a young and dynamic staff of more than 200 employees, and it is committed to promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion.Responsibilities:Be involved in the revision of manufacturing batch records and packaging batch records and other batch review documents of pharmaceutical products susceptible to be released.Support QA Release Scientists in the Review of Quality/Technical Agreements between the company and manufacturers and marketing authorisation holders, especially regarding batch certification activities.Review the documentation involved in the activity of the company: CoAs, COCs, SOPs, product specifications, in process controls, environmental controls, etc.Support QA Release Scientists involved in the evaluation of deviations, OOS/OOT, complaints, CAPA and Change Controls ensuring GMPs and MA or clinical trial authorisation.Participate in the implementation and improvement of the quality system of the company.Qualifications:The candidate should have Technical Superior Studies preferable with experience in Quality Assurance and Manufacturing. Experience on Biologicals will be highly valued.The candidate should have knowledge in Pharmaceutical Analysis, Quality Control, Manufacturing and/or Quality Assurance following the requirements of Good Manufacturing Practices.A good level of written English is required for this position.Benefits:Working in a dynamic company with a highly qualified growing team.Professional development and collaborative environment and a culture of empowerment.Flexible Working Hours and intensive schedule on Friday.Hybrid work, but mainly in the office.Access to the employee benefits flexibility platform.23 vacation days per year plus 24th and 31st of December.Fully stocked canteen and rooftop space (coffee, fruits, snacks, and beverages).Our headquarters located in Cerdanyola del Vallés, an amazing place at the foothill of Collserola Park, the green lung of Barcelona, with our Rooftop terrace.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



  • Barcelona, España Kymos Group A tiempo completo

    KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany and a Liaison office in South Korea, offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have...


  • Barcelona, España Kymos Group A tiempo completo

    KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany and a Liaison office in South Korea, offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have...


  • Barcelona, Barcelona, España Kymos Group A tiempo completo

    About the Role:The Kymos Group is seeking a highly skilled Quality Assurance Release Analyst to support our team in the revision of manufacturing batch records and packaging batch records. As a key member of our team, you will be involved in the review of quality/technical agreements between the company and manufacturers and marketing authorisation...


  • Barcelona, España Kymos Group A tiempo completo

    The QA Scientist will be assigned the following responsibilities: - 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 certification process of batches susceptible to be released to the market or for clinical trials. - Review...


  • Barcelona, España Kymos Group A tiempo completo

    .KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany and a Liasson office in South Korea, offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have...


  • Barcelona, España Kymos Group A tiempo completo

    .KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany and a Liasson office in South Korea, offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have...


  • Barcelona, España Kymos Group A tiempo completo

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  • Barcelona, España Kymos Group A tiempo completo

    The QA Scientist will be assigned the following responsibilities: 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...


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    The QA Scientist will be assigned the following responsibilities: 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...


  • Barcelona, España Kymos Group A tiempo completo

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  • Barcelona, España Kymos Group A tiempo completo

    The QA Scientist will be assigned the following responsibilities: 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...


  • Barcelona, España Kymos Group A tiempo completo

    KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany and a Liasson office in South Korea, offering comprehensive bioanalytical and CMC analytical services to the life sciences industry.Its laboratories are GMP and GLP certified and GCP compliant, and have...


  • Barcelona, España Kymos Group A tiempo completo

    KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany and a Liasson office in South Korea, offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have...


  • Barcelona, España Kymos Group A tiempo completo

    KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany and a Liasson office in South Korea, offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have...


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