QA Associate

Location: Breda, Noord-Brabant  |  Sector: Pharmaceuticals  |  Start Date: 2/12/2024  |  Job ref: 52260

The Company
Our client is known for its cutting-edge innovation and transforming discoveries. This company leads the way in biotechnology, driven by a commitment to progress an improving lives globally. Through relentless research and development efforts, it continually strives to address some of the most pressing medical challenges of our time. With a diverse portfolio spanning from innovative therapeutics to groundbreaking treatments, the company has earned a reputation for delivering life-changing solutions to patients worldwide. Its unwavering dedication to advancing science and improving patient outcomes underscores its position as a global leader in the biopharmaceutical industry. 

Role Description
As a Quality Assurance Specialist, you will have a crucial role within the company, leveraging in-depth knowledge of technical and scientific principles to initiate and manage product quality complaints, conduct safety quality investigations, and resolve product security issues. With a focus on problem-solving and adherence to regulatory standards, you will work under general direction to develop and approve procedures and work instructions, while also providing training to team members and external partners and actively participating in audits and inspections to ensure the quality of the complaints handling process.

Responsibilities
– As a part of your job, your reasonability includes as follows but is not limited to: 
– Initiating and managing product quality complaints.
– Conducting safety quality investigations.
– Resolving product security issues.
– Performing assessments to support complaint investigations.
– Collaborating with internal and external stakeholders to resolve complaints.
– Reviewing and approving procedures and work instructions.
– Providing training to team members and external partners.
– Actively participating in audits and inspections to ensure the quality of the complaints handling process.
– Performing batch record reviews as part of assessments to support complaint investigations.

Requirements
– MBO degree or equivalent with 3 or more years related professional
– Flexibility to work on-site as needed and willingness to changing schedules or requirements, including potential increases in office presence for audits or inspections.
– Ability to conduct research, gather information, analyze data, and interpret findings.
– Excellent problem-solving skills, with the ability to develop solutions to technical problems of moderate complexity.
– QA experience
– Fluency in English is required.

Other information
If you want to apply for this role, please fill out your applications via the apply button below.
 

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About us

Since 2012, SIRE Life Sciences is the most innovative and engaged consultancy company for the life sciences industries.

SIRE Life Sciences is proud of its ability to adapt to changing trends while always maintaining the highest level of quality for both our clients and our candidates.

Our team of knowledgeable professionals provides customized staffing services to clients and candidates, including secondment, direct hire, temporary-to-hire, temporary staffing, brokering, Statement of Work and we approach each type with the same degree of professional assessment. Our refined and collaborative style is unmatched in the staffing industry. We’re able to see beyond the surface to create matches that result in successful careers for our candidates and valuable talent for our clients.

Effective employment solutions need to put the right person in the relevant place every time, using advanced systems to streamline costs and time-frames for clients.