Associate Scientist I & II

Core Responsibilities: Both LevelsReview laboratory data and scientific documentation for accuracy, completeness, and compliance with established quality standards. Verify data integrity before submitting R&D records to Quality Assurance (QA) for review and release. Organize, maintain, and upload R&D records into document management systems. Prepare and support technical reports, scientific summaries, and data visualizations. Follow established SOPs, cGMP requirements, and applicable quality procedures. Support documentation control activities related to R&D product development. Coordinate routine project activities, documentation, materials, and communications with internal teams and external partners. Participate in project meetings, maintain accurate records, and follow up on assigned action items. Collaborate with cross-functional teams to support project timelines and departmental objectives. Perform additional duties as assigned while maintaining compliance with established procedures. Associate Scientist I - Additional FocusAssist with initial reviews of analytical data and laboratory documentation. Support data verification and documentation preparation under supervision. Maintain accurate records and assist with document management activities. Identify and communicate discrepancies in laboratory records. Support routine laboratory documentation and project coordination tasks. Associate Scientist II - Additional FocusLead technical reviews of R&D documentation, analytical data, and laboratory records. Independently verify data integrity, accuracy, and completeness before QA submission. Prepare detailed technical reports, scientific data summaries, and visual presentations. Coordinate documentation activities and support project deliverables. Identify documentation inconsistencies and collaborate with appropriate teams to resolve issues. Contribute to improvements in documentation practices, data verification, and operational efficiency.

Associate Scientist I - Level Requirements: Foundational knowledge of laboratory practices and scientific documentation. Familiarity with cGMP principles and regulated laboratory environments. Ability to follow established procedures and perform documentation tasks with guidance. Previous exposure to R&D or laboratory operations is advantageous.

Associate Scientist II - Level Requirements: Minimum of 3 years of relevant professional experience in a cGMP-regulated environment. Experience reviewing analytical data, laboratory records, and technical documentation. Strong understanding of data integrity requirements and regulated documentation practices. Ability to independently manage technical documentation and data verification activities. Experience coordinating R&D activities and collaborating with Quality Assurance teams.