Emergent BioSolutions

Analyst

• Perform GMP compliant testing as required to support Raw Material testing, In-process, Finished Product Release & Stability, nonclinical / clinical studies, as well as assay or process validations.
• Maintain laboratory documentation and perform preventative maintenance and calibration on laboratory equipment per established procedures.
• Author and ownership of investigations, deviations, critical reagent and standard qualifications, validation/verification protocols and reports, supplier qualifications, CAPAs and change controls.
• Subject matter expert in defined areas of responsibility.
• Assist supervisor in lab scheduling and planning.
• Receive test samples, standards, chemicals, and reagents; maintain accurate laboratory records and inventory for all laboratory materials.
• Demonstrate a high degree of proficiency and independence when performing analytical test methods.
• Advanced proficiency in a wide variety of analytical/biological/Compendia methodologies and techniques with a clear understanding of regulatory requirements.
• Strong background in multiple analytical techniques chemical, physical, immunological, microbiological and viral. Examples include but are not limited to: • Spectroscopy (UV, IR, Ramen, etc) • Wet lab techniques (protein concentration, Particles HIAC, Extractable volume, osmolality, etc.) • Microbial counts, endotoxin, sterility • DNA extraction, Cell Culture, qPCR, ELISA, immunoglobulin assays, etc. • Report results and complete LIMS data entry in a timely manner. Perform peer review of QC data, review, and approval in LIMS.
• Adhere to all effective STM’s/SOPs and safety requirements and document laboratory work consistent with cGMP requirements.
• Perform preventative maintenance / calibration on laboratory equipment, demonstrate advanced proficiency, and perform training in their use and maintenance in accordance with established procedures.
• Execute critical reagent and standard qualification studies and independently write protocols/reports; review and provide feedback.
• Maintain a clean and sanitary work area in accordance with standard laboratory practice and procedures.
• Plan and execute experimental tasks, make detailed observations of experimental tasks and obtain and interpret experimental data with minimal guidance.
• Lead troubleshooting/laboratory investigation efforts. Identify patterns and trends, troubleshoot abnormalities, and investigate problems.
• Write clear and concise assay forms, TMDs, SOP’s, protocols, technical studies, and reports independently. Revise lab documentation including assay forms, test method documents, and standard operating procedures in accordance with document management procedures.
• Provide training and assistance to peers and junior staff in an effective manner.
• Execute development and validation studies and write protocols/reports; review and provide feedback.
• Identify opportunities for improvements within QC procedures and documentation.
• Perform tasks effectively and independently.
• Collaborate across functional areas to effectively resolve problems.
• Independently move projects forward; guide project progression through appropriate decision making.
• Other duties as assigned.

Analyst III, QC Laboratory Services

Director

• This person is responsible for assessing, developing and executing state-level strategies to expand access to the company’s naloxone portfolio. This individual will engage with key state level functions & personnel including procurement, state health departments, public health, correctional healthcare programs, and harm reduction organizations to ensure products and service offering are available, affordable, and aligned with the state’s goals related to opioid overdose prevention. This role drives high-level partnerships, ensuring fiscal stewardship and maximizing public health impact for state accounts.
• Engagement & Account Management: Develop and execute a state sales business strategy that meets or exceeds financial goals, aligning with broader organizational objectives.
• Identify trends and opportunities for sales optimization through data analytics and use insights to adapt sales strategies and maintain a competitive edge.
• Identify and interact with key decision makers and influencers within the region to gather insights, expand product visibility, and influence market strategies.
• Maintain compliance with all company policies, practices, and regulations in all aspects of regional sales operations.
• Serve as the primary liaison between the company and customer stakeholders involved in purchasing, distributing, or recommending naloxone.
• Develop and manage strategic relationships with: State public health departments and overdose prevention teams; Departments of Corrections and Behavioral Health; State Emergency Medical Services (EMS) coordinators; Harm reduction and syringe services programs (SSPs) funded by the state; Other key leaders as identified.
• Access, Contracting & Procurement: Lead or support the company’s participation in government-issued Requests for Proposals (RFPs), invitations to bid, and other public procurement processes.
• Coordinate cross-functional teams (legal, pricing, compliance, supply chain, market access) to develop high-quality, compliant RFP submissions that align with public health goals.
• Negotiate and manage state contracts and bulk purchasing arrangements.
• Public Health & Funding Strategy: Identify and support opportunities to leverage federal and state funding streams (e.g., SAMHSA block grants, opioid settlement funds, CDC cooperative agreements) to expand naloxone distribution.
• Partners with government and public health agencies on bulk purchasing programs and public access initiatives (e.g., vending machines, school-based access, first responder programs).
• Internal Collaboration: Provide real-time policy and regulatory insights to market access, government affairs, commercial, and compliance teams.
• Partner with Sr. Director National Sales Strategy & Innovations, Marketing, Analytics & Data, Medical Affairs, and State Government Affairs teams to identify and act on opportunities, share insights, and respond to market changes
• Partner with colleagues in training, analytics, and medical affairs to support appropriate product use and education.

Director, Key Accounts

Manager

• Lead the performance of all aspects of SEC reporting, including preparation of 10Ks and 10Qs, completion of disclosure checklists, data gathering and footnote preparation, discussing comments on various filing documents, and review of XBRL tagging
• Support effective preparation of the quarterly earnings releases and other investor relations presentations
• Ensure all non-GAAP disclosures are consistent and reported in accordance with SEC regulations
• Manage all equity plans alongside the Legal and HR teams, including monthly stock-based compensation journal entries, equity reconciliations, ESPP Purchases, personnel updates, grants, and exercises
• Keep business partners abreast of developments in accounting and financial reporting and related company policies and positions through review of various publications, training sessions, and other forums
• Provide support to external auditors during audits and interim reviews; coordinate requests and manage flow of information and documentation
• Assist with the maintenance and updating of Sarbanes-Oxley 404 processes and procedures
• Other special projects and duties as requested or assigned

Analyst III, QC Laboratory Services

Director, Key Accounts

Manager, SEC Reporting and Equity