Lab Analyst - 236289

**Support laboratory activities for both GMP and non-GMP testing of combination products and medical devices.Assist in managing quality system events, including deviations, CAPAs, and change controls.Handle materials management tasks such as receiving, labeling, storing raw materials and components, and ensuring documentation and compliance with inventory control procedures.Conduct inspections of incoming materials to confirm quality, specifications, and compliance with approved documentation.Perform tests per established protocols to support method validation and design verification.Analyze data and perform basic troubleshooting as needed.Maintain laboratory equipment and supplies to ensure operational efficiency.Prepare and manage laboratory records, ensuring accuracy and completeness.Communicate effectively with team members and other stakeholders.Adhere to all safety procedures.Work collaboratively within a matrixed team environment, supporting organization and attention to detail.Provide immediate project support as required.Author and review complex technical documentation to ensure compliance with applicable standards and regulations.Follow policies and standard operating procedures to support internal and client projects.Complete all assigned internal and external training requirements.Assist in planning and executing lab-related services and activities.Educational *Bachelor's degree in a science or engineering field, such as Chemistry, Biology, Biomedical Engineering, Mechanical Engineering, or Chemical Engineering.****At least 2 years of experience in the pharmaceutical or biopharmaceutical industry, including post-graduate experience.Strong understanding of the pharmaceutical, biotechnology, combination product, and/or medical device sectors.Preferred experience with pre-filled syringes, autoinjectors, co-packaged kits, other drug delivery platforms, and/or other combination product platforms.

Created: 2024-11-10