QA Specialist & QP / Permanent / Pharma / Region Ghent / Broad, dynamic role
Location: BelgiumSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Oost-Vlaanderen Belgium.
- Provide input to key quality systems: change control, customer complaints, PQRs, product investigations, RA strategies, supplier management and technical transfers
- Participate in meetings and advisor to the site, ensuring compliance requirements
- Assist in supporting operational compliance
- Responsible for compliance standards on site, working with stakeholders to ensure that quality standards are maintained and opportunities for improvement
- Manage department-level projects/ initiatives
- Provide guidance and mentorship to other QA department members
- Audits
- The candidate must be eligible for being named on a manufacturing license as a Qualified Person.
- Experience in Quality position and multiple QA activities.
- Hand-on mentality and motivated, positive personality
- Willing to both lead and participate in group activities in order to achieve company successes.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
The Company
They are dedicated to making lives better by bringing high quality and affordable healthcare products to consumers. They are an international company and a leading global healthcare supplier.Role Description
Main purpose of the role is to support compliance activities on site, working within the QA department. The successful candidate will work within the Quality team to support in different activities and ensure GMP compliancy. Moreover you will be involved with supplier management and the internal audit program are key components to the role.Responsibilities
- Perform duties of a Qualified Person as defined by Directive 2001/83/EC- Provide input to key quality systems: change control, customer complaints, PQRs, product investigations, RA strategies, supplier management and technical transfers
- Participate in meetings and advisor to the site, ensuring compliance requirements
- Assist in supporting operational compliance
- Responsible for compliance standards on site, working with stakeholders to ensure that quality standards are maintained and opportunities for improvement
- Manage department-level projects/ initiatives
- Provide guidance and mentorship to other QA department members
- Audits
Requirements
- Pharmacy degree qualification with several years of experience in the pharmaceutical industry.- The candidate must be eligible for being named on a manufacturing license as a Qualified Person.
- Experience in Quality position and multiple QA activities.
- Hand-on mentality and motivated, positive personality
- Willing to both lead and participate in group activities in order to achieve company successes.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
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