LIMS Specialist
SIRE® Life Sciences
LIMS Specialist
Samenvatting
Wat krijg je?
Wat ga je doen?
- Lead digitalisation of laboratory methods
- Maintain LIMS templates and master data
- Support validation and change control activities
- Manage updates to digital methods
- Support LIMS-to-instrument interface validation
Wat verwachten wij?
- Degree in Chemical Sciences or Life Sciences
- 5 years experience in regulated QC environment
- Experience working with LIMS and LabVantage
- Knowledge of GMP requirements and validation processes
Volledige vacaturetekst
At this global biopharmaceutical leader, you will drive the digital evolution of laboratory processes within a regulated QC environment. By transforming paper-based methods into advanced digital workflows and managing LIMS templates, you ensure innovation reaches the patient. The company offers a vibrant international setting where your expertise in harmonisation directly impacts global healthcare quality. Ready to redefine digital standards in the lab? Jump into this pivotal role today.
The company
Our client is a global biopharmaceutical organisation committed to advancing innovative medicines that improve patients' lives worldwide. Through advanced research, biologics manufacturing, and a strong focus on quality and innovation, the organisation delivers life-changing therapies across a wide range of therapeutic areas.
Role Description
As a LIMS Specialist, you will play a key role in the implementation, maintenance, and digitalisation of laboratory methods within a regulated Quality Control environment. You will focus on LIMS method templates, master data, validation, and the harmonisation of paper-based laboratory methods into digital workflows. You will also support laboratory teams with digital processes, instrument interfaces, and LIMS-related activities.
Responsibilities
- Lead the harmonisation and digitalisation of paper-based laboratory methods within a regulated QC environment.
- Create, configure, and maintain method execution templates, master data, and digital laboratory methods in LIMS.
- Support validation activities, change controls, and technical documentation related to digital laboratory processes.
- Manage updates and improvements to existing digital methods in collaboration with laboratory SMEs and other sites.
- Support the setup, testing, and validation of LIMS-to-instrument interfaces and related digital laboratory workflows.
- Act as a key point of contact for laboratory users regarding LIMS, digital methods, and laboratory workflows.
- Provide training and guidance to laboratory teams on digital methods and LIMS functionality.
- Collaborate with laboratory, Quality, IT, and technical stakeholders to ensure effective implementation and maintenance of digital laboratory solutions.
Requirement
- Bachelor's degree or equivalent qualification in Chemical Sciences, Life Sciences, or a related field.
- Minimum 5 years of experience in Quality Control, Quality Assurance, analytical testing, laboratory systems, or IT within a regulated environment.
- Hands-on experience working with LIMS; experience with LabVantage is highly desirable.
- Experience as a LIMS Key User, Business Administrator, Subject Matter Expert, or in a similar role is preferred.
- Good knowledge of GMP/GxP requirements, laboratory testing, validation, and change-control processes.
- Strong communication and stakeholder-management skills.
- Ability to work effectively with both laboratory and technical teams in a regulated environment.
- Structured and analytical approach with strong attention to detail.
Other information
Looking for a new opportunity? Well, it's right here! If you're interested, please click the below button to apply for the job.
59033
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