Are you ready to explore, break barriers, and discover more? We are seeking a talented Laboratory Analyst to join our team at Merck Millipore, where we use science and technology to enrich people's lives.
The role is part of the analytical laboratory project team and involves working on various activities including test method validation, equipment validation, training and development of laboratory processes and SOPs.
* You will be responsible for adhering to all company EHS guidelines and procedures with proactive involvement in laboratory safety initiatives.
* Development and validation of laboratory test methods.
* Collaboration on the preparation and execution of the Project Validation Master Plan ensuring it is compliant with relevant regulatory and quality standards.
* Preparation and execution of protocols and compilation of reports generated from validation activities identified in the validation master plan.
* Training on laboratory procedures and development of onboarding plans for future analysts within the area.
* Lead analytical method development/troubleshooting for the project laboratory groups.
* Review of laboratory data where required, ensuring accuracy for all relevant products within the project scope.
* Validation of laboratory equipment, software, spreadsheets and methods.
* Perform validation, release, and non-routine testing as required.
* Support site commercialization readiness.
* Maintenance of lab fitness for audits.
* Ensuring compliance of the laboratory projects to all applicable quality, regulatory and Pharmacopeia requirements as well as all relevant divisional and corporate requirements.
* Work within Filtration 2.0 laboratory calibration and preventative maintenance system.
* Provide technical support to all F2.0 functional groups as required.
* Ensure laboratory project timelines are adhered to, and timelines are communicated with the laboratory supervisor.
* Ensure protocols, reports, test methods, SOPs and all other relevant documentation are drafted and approved prior to use.
* Ensure all laboratory investigations are completed in a timely manner and in accordance with site procedures.
* Ensure laboratory colleagues have full support for laboratory investigations and that standard root cause analysis tools are utilised.
* Contribute to risk mitigation initiatives such as FEMAs and risk assessments.
* Identify and participate in Continuous Improvement initiatives.
* Control, issue and maintain laboratory documentation. Archive laboratory data, logbooks and samples in accordance with procedures.
* Order, receive and control laboratory chemicals, reagents and consumables.
* Thorough investigation of quality and safety issues using root cause analysis methodology and implementation of robust corrective and preventative actions.
To be successful in this role, you should have a B.Sc. in Analytical Chemistry, Microbiology or related discipline, a minimum of 2 years practical work experience in Medical Device/Pharmaceutical environment, and strong background in laboratory techniques. Experience in LIMS, Trackwise, MES and SAP, Lean Six Sigma Training (Yellow Belt, Blue Belt, etc.), good communication skills, good computer literacy, strong problem solving, organisational & time management skills are also an advantage.
This role may involve travel abroad, in some cases for extended periods. We celebrate diversity and believe it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. Our diverse businesses offer various career moves to seek new horizons.