Senior Scientist, Analytical R&D

Job Description

Global Quality Large Molecule Analytical Sciences (GQ- LMAS) in our Manufacturing Division is accountable for the commercialization of large molecule vaccines and biologics analytical techniques from Phase III through launch and transfer to supply. This team is highly motivated fast-paced and focused on the rapid advancement of our Companys large molecule pipeline plus growth of existing products.

This position will involve oversight of late-stage method development validation and life-cycle management of methods with a focus on both global method transfer activities and external analytical.

From a Global Quality Large Molecule Analytical Sciences (GQ-LMAS) Analytical Transfer perspective this position includes activities such as interfacing with a global network of product manufacturing and testing sites collaborating with product development groups within our manufacturing division and our Research Laboratories division continuous improvement of analytical methodology assay validation analytical technical transfer and Biologics License Application preparation.

From a GQ-LMAS External Analytical perspective this position includes directing and managing the analytical activities within our commercial external manufacturing and testing network. This role involves developing and implementing site-related analytical strategies and site implementation of continuous improvement in analytical methods and techniques and driving successful analytical execution by the contract testing lab(s) to support on time batch release. Additionally this position will work directly with technical operations quality regulatory microbiology and analytical program leaders on a regular basis to review/approve critical documents relating to analytics and participate as a site representative for method life-cycle related tasks.

Responsibilities

Analytical Transfer:

• Lead method transfers and/or validations across vaccine and biologics programs including quality risk assessments/gap analysis.

• Provide sponsorship of both in-line and pipeline analytical methods. The candidate will interface across our Company network and external partners to ensure the successful commercialization of assays promoting our pipeline programs

• Involvement in development troubleshooting and optimization of analytical methods

• Continuous improvement using laboratory standardization lean laboratory and six sigmamethodology

• Assay Life Cycle activities across various large molecule franchises and analytical platforms

• Promote various vaccine and/or biologics registrations launches and troubleshooting activities external to the US including documentation preparation

• Direct strategic initiatives within departmental and cross-functional teams representing Global Quality Large Molecule Analytical Sciences (GQ- LMAS).

• Manage global registration and test on importation (TOI) activities

• Collaborating with commercial manufacturing teams to support facility start-up activities New Product Introduction and provide analytical support both within our Company network and at contract manufacturing organizations (CMOs) or contract testing laboratories

External Analytical:

• Analytical technical oversight working directly with the external provider(s) and internal cross-functional stakeholders to support analytical testing of large molecule (biologics and/or vaccine) products.

• Position includes significant on-site presence at external testing provider(s) to support direct engagement and technical oversight of critical analytical testing activities.

• Build and maintain strong relationship with External Entities as well as internal operations technology analytical and procurement organizations. Closely collaborates with appropriate business and functional areas to conduct Tier meetings and Joint Steering Committee meetings (as applicable) to achieve our objectives.

• Collaborate with departmental and cross-functional commercial manufacturing teams to support facility start-up and sustainability activities.

• Interface with Global Analytical Working Groups and Global Method Owners/SMEs

• Drive continuous improvement initiatives to enhance the quality and robustness of external /testing through implementation of proactive tools assay data trending corrective actions and best practices.

• Identify and resolve analytical issues deviations and out-of-specification results from external testing labs through technical support of investigating and troubleshooting analytical problems to ensure the accuracy and reliability of test results.

• Lead/support complex investigations and drive resolution of analytical technical issues

• Build and manage project plans timelines and schedules to effectively meet project timelines and deliverables.

• Ensure our external testing sites are prepared for inspections from multiple agencies (i.e. FDA EMA PMDA) from an analytical technical perspective

• Authoring and/or reviewing technical documents to support Process Performance Qualification (PPQ) licensure and regulatory technical questions.

Education

• Bachelors degree in biology chemistry biochemistry or related science with six (6) years of relevant industry knowledge in systematic development validation and/or quality control (QC) or

• Masters degree in biology chemistry biochemistry or related science with four ( 4) years of relevant industry knowledge in systematic development validation and/or quality control (QC) or

• PhD in biology chemistry biochemistry or related science with one (1) year of relevant industry knowledge in systematic development validation and/or quality control (QC)

Knowledge Skills

• Knowledge of ICH USP and other compendial chapters required for method transfer and validation.

• Knowledge with late-stage method development validation and transfer

• Experience with management of contract manufacturing organizations

• Minimum two (2) years working knowledge in a current Good Manufacturing Practices (cGMP) laboratory environment in large molecules (vaccines biologics)

• Experience in analytical product life cycle activities (development validation and /or transfer) across various large molecule analytical platforms (i.e. ELISA HPLC CE).

• Understanding biologics analytical technology such as bioassay (i.e. ELISA cell-based methods) chromatography (i.e. HPLC UPLC) and general biochemistry methods.

• Experience in the biopharmaceutical manufacturing industry such as in biologics or vaccines commercialization technical operations and/or Quality control.

• Development and management of project timelines and deliverables

• Participation in cross-functional project teams

• Authoring and review of technical documents

• Ability to work objectively and within a cross-functional team

• Ability to learn new techniques

• Technical verbal and written communications stakeholder management and teamwork skills

• Self-motivated with a positive attitude and proven performance record

• Knowledge with drug substance and drug product release stability and extended characterization testing for vaccines and biologics

• Strong organizational and project management skills

• Ability to effectively identify and express risks

Preferred

• Worked and interfaced with external partners (i.e. CMOs and CTLs).

• Deviation management and change control processes

• Authoring and/or reviewing technical documents to support Process Performance Qualification (PPQ)

• Ability to analyze interpret and troubleshoot analytical data.

• Global launch or supply experiences

• Supporting/writing regulatory filings (IND MAA BLA) and inspections with multiple agencies (FDA EMA JNDA)

• Continuous improvement or lean six sigma methodology

• Experience with laboratory data management systems (i.e. LIMS).

• Experience with software automation/digital systems (e.g. Veeva Vault MEDs IPI Spotfire).

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This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employees position within the salary range will be based on several factors including but not limited to relevant education qualifications certifications experience skills geographic location government requirements and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive if applicable.

We offer a comprehensive package of benefits. Available benefits include medical dental vision healthcare and other insurance benefits (for employee and family) retirement benefits including 401(k) paid holidays vacation and compassionate and sick days. More information about benefits is available at can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

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