Title: Data Reviewer - Small Molecule (GMP) Location: Remote Wisconsin United States of America Full time This is a fully remote role supporting our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the US. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. Discover Impactful Work: The Data Reviewer performs review of a variety of routine and complex analytical analysis experiments that are conducted on pharmaceutical and biopharmaceutical compounds with various formulations and/or biological matrices. Ensures analyses are following validated or experimental analytical procedures, and compare results to methodology, protocol and product specifications, Standard Operating Procedures (SOPs) acceptance criteria, and Good Manufacturing Practices (GMP). Reviews data entered into databases and reports and monitors the quality of the laboratory data. Possesses a thorough understanding of laboratory procedures and can reliably conduct complex analysis review independently. A Day in the Life: - Evaluates laboratory data for compliance with analytical methods, client directives, and SOPs. - Reviews sample results for scientific soundness, completeness, accurate representation of the data, and final reported results. - Communicates with laboratory staff to proactively maintain the quality of laboratory documentation. - Delivers review findings noting deficiencies within the analytical data or reports in a clear and concise manner. - Escalate significant deficiencies to the project leader or supervisor for assessment. - Facilitates in conversations with lab staff on best documentation practices and addressing quality findings. - Advocates for quality and review process changes. - Identifies and supports process improvement initiatives. - Performs other duties as assigned. Keys to Success: Education - Bachelor's degree or equivalent and relevant formal academic / vocational qualification Experience - Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). - In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role Knowledge, Skills, Abilities - Demonstrated knowledge of PCR and sequencing strongly preferred - Previous experience with formal data review in GMP Lab strongly preferred - Previous experience with method validation or method validation data review strongly preferred - Previous experience with chromatographic review and Empower strongly preferred - Thorough knowledge of SOPs and Federal Regulations to include GLP and GMP - Thorough knowledge of chromatography may be required. - To demonstrate behaviors which align to the 4i Values of Thermo Fisher - Strong technical knowledge including an understanding of laboratory procedures, methodology, and standards - Strong verbal and written communication skills - Strong attention to detail - Ability to balance time and remain focused on work to meet goals - Ability to train staff on basic review techniques - Ability to independently review laboratory reports and analytical methods - Ability to deal with multiple and changing priorities - Ability to provide clear and concise feedback and/or documentation of results - Ability to work in a collaborative team environment - Ability to work efficiently in a remote capacity

• Design and run the global GTM readiness framework for new product introductions. • Partner with PM & PMM to understand new releases and translate them into "Seller-Speak." • Ensure that every new product launch reinforces our broader platform story. • You are responsible for the hands-on creation of GTM assets. • Partner with Sales Ops to track which releases are actually landing in the field.

• Manage logistical tracking and coordination to ensure Content Army creators receive timely assignments • Oversee payment coordination and track performance metrics • Identify opportunities to improve workflows and efficiency • Coordinate Product Marketing events including Town Halls, webinars, and partner sessions • Manage end-to-end event logistics including scheduling, presenter coordination, and follow-ups • Manage execution of marketing campaigns including events, drip campaigns, and landing pages • Build and maintain marketing automations and workflows within HighLevel • Manage project timelines, dependencies, and multiple initiatives simultaneously • Build high-quality, on-brand presentation decks • Develop and maintain product marketing collateral such as one-pagers, blogs, and comparison docs • Develop strong working knowledge of the HighLevel platform • Build in-app marketing experiences (Pendo) to drive adoption and engagement • Act as a reliable product knowledge resource for internal teams

• Support logistical tracking and coordination for Content Army video creators • Ensure assignments are distributed on time and tracked accurately • Assist with payment coordination and basic metrics tracking • Assist in coordinating Product Marketing events including Town Halls, webinars, and partner sessions • Support scheduling, presenter coordination, and run-of-show documentation • Help execute post-event follow-ups • Support execution of marketing campaigns including events, drip campaigns, and landing pages • Assist in building and maintaining workflows within HighLevel • Track project timelines and dependencies across initiatives • Create and format presentation decks for internal and external use • Support development of marketing collateral such as one-pagers and blogs • Build foundational knowledge of the HighLevel platform • Stay updated on feature releases and product updates • Support in-app marketing initiatives (e.g., Pendo)