QC Officer
1 dag geleden
QC Officer
As a QC Officer in our Quality Control Operations, you'll play a pivotal role in maintaining the highest standards of product quality and compliance. Your expertise in Good Manufacturing Practice (GMP) and quality management will guide our teams, ensuring that every product meets our rigorous standards. You'll be actively involved in identifying and resolving quality issues, performing inspections, and driving continuous improvement initiatives. If you're detail-oriented and enjoy collaborative problem-solving in a complex organisation. As such, this role offers both challenge and fulfilment.
About the Role
As a QC Officer in our Quality Control Operations, you'll play a pivotal role in maintaining the highest standards of product quality and compliance. You will act as an SME in performing investigations, constantly looking for information: who, what, where, why and defining solutions to prevent from happening again. This role involves collaboration with different people within the organization and is therefore important to be a good listener, helper, thinker and sometimes persuasive to get colleagues on board with the necessary changes. It is also important to learn to deal with setbacks, as there can be times when decisions are made that you do not fully support. If you're detail-oriented and enjoy collaborative problem-solving in a complex organisation. As such, this role offers both challenge and fulfilment.
Responsibilities
- Demonstrates independent understanding and application of GMP fundamentals, including but not limited to: Good manufacturing practices, good documentation practice and data integrity.
- Perform investigations on non-conformances, deviations, and out-of-specification (OOS) results. Is acknowledgeable of root cause analysis tools.
- Conduct routine audits to ensure compliance with GMP and quality standards.
- Support and guide laboratory personnel in quality control practices and regulatory requirements.
- Collaborate with cross-functional teams to facilitate product release and resolve quality issues.
- Assist in identifying and implementing improvements Requirements
- Education: Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related field.
- Experience: Minimum of 3 years in a QC environment within the pharmaceutical or biotech industry. Experience in deviation management, on how to perform investigations, root cause analysis and define corrective and preventive actions is a must.
Skills:
- Strong understanding of GMP and regulatory requirements.
- Analytical thinking and problem-solving abilities.
- Excellent communication and interpersonal skills for cross-functional collaboration.
- Articulate written and oral communication, able to deliver effectively a message
- Proficiency in documentation practices and attention to detail.
- Ability to lead investigations and manage CAPA processes.
- Experience with measuring-equipment, qualification, and maintenance.
- Ability to work under stress, while being able to prioritize tasks.
- A true team player, you want your colleagues to be happy and successful too
- Strong grasp of English, both verbal and written. Dutch advantageous.
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