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Anna Rahmqvist is a Quality Systems Specialist at CCRM Nordic. She possess expertise in gmp, biotechnology, capa, pharmaceutical industry, change control and 13 more skills. She is proficient in German and English.
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Qa Implementation LeadCcrm Nordic Aug 2024 - PresentMölndal, Västra Götalands Län, Sverige -
Business OwnerAqipi Konsult Ab Oct 2018 - PresentSträngnäs, Sodermanland County, Sweden -
Validation SpecialistFujirebio Diagnostics Ab Sep 2021 - Mar 2024Göteborg, Västra Götaland, SverigeResponsibility for validation strategy during relocation of medical device research and production operations to new facility. Due to regulatory requirements the move was performed in stages over two years. Project manager for the implementation of an electronic documentation management system. This project included mapping of existing processes, system configuration, implementation, and user training. -
Interim Compliance Manager - Validation & QrmPfizer Feb 2021 - May 2021Strängnäs, Sodermanland County, SwedenResponsibility for maintaining and developing the site’s validation and quality risk management systems. The role included acting as SME for validation issues, risk assessment facilitator and trainer in validation and QRM procedures. -
Quality System SpecialistLantmännen May 2020 - May 2021Part of the core team leading the implementation of ISO28000 at three production sites. Development of security risk assessment model, templates and system documentation to support the implementation and integration with existing site procedures. Training, coordination and coaching of site representatives on the project. Participation and support in certification audits. -
Process And Development Engineer: Oat & BreakfastLantmännen Jun 2019 - Apr 2020Järna, SwedenPlanning, coordination and evaluation of production scale trial runs for new or updated products. Member of production management team and HACCP-team. Improvement and development of quality procedures and ways of working.
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Sme Validation & Quality SystemsAstrazeneca Oct 2018 - Jun 2019Sodertalje, SwedenPlanning and coordination of qualification activities in the site validation team. Key member of the site audit management team, preparing and organizing audits from global corporate quality and regulatory authorities. Developed training material for human error root cause analysis and delivered classroom training to investigators on site. -
Validation Manager, Sweden Biologics CentreAstrazeneca Oct 2017 - Oct 2018Södertälje, SverigeResponsible for establishing site specific validation procedures and site Validation Master Plan for the biomanufacturing site under construction. Planning and coordinating site validation activities with the qualification activities performed within the capital project.
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Quality Assurance ManagerNanologica Ab Sep 2016 - Sep 2017Sodertalje, SwedenResponsible for development of a quality system including production, quality control and administrative processes. Project manager for the implementation of an ERP system. Coordinator for work environment procedures. -
Quality And Validation EngineerÅf Jul 2015 - Sep 2016Stockholm, SwedenValidation lead, responsible for test activities in a project involving installation and automation of a new production line. The assignment involved planning and managing a group of ten validation engineers, as well as communicating and coordinating activities with the customer and other project groups. -
Quality Assurance OfficerPfizer Oct 2008 - Jul 2015Strangnas, SwedenDelegated Qualified Person from 2013. Responsible for the site’s deviation handling system. Quality assurance of GMP documentation as well as assessment and release of produced batches. Presentation and participation at regulatory inspections. Improvement work to reduce lead time for production and documentation review. Training of investigators and QA officers in investigative methodology, root cause analysis and CAPA. Responsible for the site's strategic work with Human Error Reduction.
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Production EngineerPfizer Feb 2005 - Sep 2008Working in a team of engineers supporting the manufacture of biotech pharmaceuticals my responsibilities included investigation of deviations, change control, continous improvements, validations and general production support.
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Laboratory Engineer In Bioprocess DevelopmentAffibody Ab Feb 2003 - Jan 2005Development and optimization of fermentation processes for production of recombinant proteins on a laboratory scale. Design of experiments and statistical analysis.
Anna Rahmqvist Skills
Anna Rahmqvist Education Details
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Engineering Biology -
Pedagogy, 20P
Frequently Asked Questions about Anna Rahmqvist
What company does Anna Rahmqvist work for?
Anna Rahmqvist works for Ccrm Nordic
What is Anna Rahmqvist's role at the current company?
Anna Rahmqvist's current role is Quality Systems Specialist.
What is Anna Rahmqvist's email address?
Anna Rahmqvist's email address is an****@****eca.com
What schools did Anna Rahmqvist attend?
Anna Rahmqvist attended Linköping University, Linköping University.
What skills is Anna Rahmqvist known for?
Anna Rahmqvist has skills like Gmp, Biotechnology, Capa, Pharmaceutical Industry, Change Control, Quality System, Human Error, Root Cause Analysis, Validation, Fermentation, Continuous Improvement, Design Of Experiments.
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Visual Merchandising Manager / Interior Design Manager På IkeaSundsvall Municipality1ikea.com
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