Quality control Analyst

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.

Who you are :

Work with team members and collaborate across departments on assigned projects.

Cost-effective management of entrusted resources.

Support Operations and Quality Programs.

Generate QC data and certificate analysis for certified reference materials.

Your Role :

Undertake assigned projects, stability studies, writing of reports and batch records related to Certified Reference Material

Product & Application Development: process and evaluate analytical QC data generated- primarily by GC and HPLC

Follow regulatory, customer, and quality system requirements for product development.

Write reports on results of project work, document methods on project/product design, test specifications, etc.

Collaborate and work with other staff (Scientists and Technicians) remotely to complete QC data generation and analysis on Certified Reference Materials

Participate in training colleagues for technical transfer. Work with team and other departments to implement validation and tech transfer requirements

Contribute to project planning through communication with the manager, project manager, and team:

Identify and communicate resource requirements for specified projects

Provide timely updates and communicate project status to management and the project team

Communicate, in a timely manner, issues related to schedule, planning, and resources that may stall or prevent the execution of the project

Technical Expertise

Operation of chromatographic instrumentation including HPLC and GC

Operation of chromatographic detectors including UV-Vis, RI, MS, ELSD, ECD, FID, and others

Processing chromatographic data using chromatographic software

Utilizing Microsoft Excel to perform calculations

Develop and technical and subject matter expertise in assigned technical areas by seeking out training and knowledge-sharing

Technical project review of certificates for certified reference materials by mass balance techniques that may be traceable to primary pharmacopeias

Write reports on results of project work, document methods on project/product design, test specifications, write batch records, test specifications, etc. for transfer to QC.

Maintain batch records and other documentation.

Bachelor’s degree in chemistry, chemical engineering, or other related scientific disciplines. 1 year of relevant experience in a scientific laboratory

Demonstrated proficiency in basic analytical GC and HPLC techniques

Basic understanding of the relevant subject matter field (e.g., organic chemistry, analytical chemistry, process chemistry)

Demonstrated initiatives and critical thinking to learn new skills and technologies.

Strong verbal and technical writing skills

Ability to utilize a variety of software tools involving databases, spreadsheets, and project scheduling.

Ability to work independently and prioritize assigned work

Ability to collaborate and communicate well with peers

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!