Associate Director - Drug Product Manufacturing & Development

Associate Director Of Drug Product Manufacturing

Our Research & Development organization brings together the best minds in life science innovation. The teams located in facilities in Lexington, Watertown, Cambridge and Seattle reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct R&D community based on collaboration, partnerships, and cutting-edge research across multiple modalities and therapeutic areas. We recognize that improving human health starts here and that patients rely on us. Our R&D hub merges biotech speed and agility with large pharmaceutical company quality, resources, and stability, uniting the best of both worlds to develop new medicines for patients.

The Associate Director of Drug Product Manufacturing is accountable for all clinical drug product manufacturing including process characterization activities to support commercialization for nucleic acid programs and will have thorough knowledge of cGMP's for aseptic pharmaceutical products. Frequent cross-functional interaction with multiple departments will be required while supporting multiple projects. The position will manage CMO's to ensure the continuous supply of product and apply risk mitigation strategies, as well as perform formulation studies in a laboratory setting as needed. This position will lead a team of Drug Product Managers and manage their own projects.

This position reports to the Executive Director, Manufacturing.

Lead, manage, and advise all aspects of drug product manufacturing operations at CMOs to manufacture clinical parenteral medicines according to approved protocols, master batch records, regulations, and timelines.

Lead and be an example for a drug product team that is responsible for ensuring clinical supply using aseptic manufacturing.

Identify and work with formulation development CROs to implement new production processes at CMOs and NDA-enabling work. Processes may include but are not limited to formulation, sterilization, filling, and lyophilization.

Responsible for key manufacturing metrics / goals, support critical program milestones, and drive continuous improvement initiatives that are essential to meeting patient and business needs.

Rapidly and accurately communicate issues to Senior Leadership. Resolve manufacturing and facility issues to mitigate any supply disruptions to our patients.

Work effectively across all departments, such as Quality Assurance / Control, Chemical Development, Program Management, Regulatory, Analytical Development, Materials Management, and Clinical Supply.

Write, review, and / or approve Standard Operating Procedures, specifications, regulatory filings, Master / Executed Batch Records, or other controlled documents as needed.

Responsible for managing timelines, production plans, and material requirements.

Manage DP team resource loading and personnel development.

Ensure the effective use of material, equipment, and personnel in producing quality products.

Optimize and investigate formulation, sterilization, and filling processes and parameters through experiments in a laboratory setting.

Approximately 15 - 20% overnight travel. Ability to lift 0 - 10lbs.

Supervisory. Ensure that reporting personnel have individual development plans (IDP), with annual goals and measurements that are consistent with the priorities of the business, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process. Ensure that the IDP forms include completed learning and aspiration plans and are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility. Manage the application and communication of all Novo Nordisk policies, procedures, and Novo Nordisk Way.

Bachelor's degree with 9+ years of experience, Master's degree with 7+ years of experience, or PhD with 5+ years of experience in a cGMP setting required. Degree in Biochemistry / Chemistry / Engineering or related discipline required.

In-depth experience in pharmaceutical operations associated with aseptic processing required.

Proven leadership of technical teams required.

Experience working to standards required for regulatory compliance of Aseptic Processing facilities required.

Understanding of engineering and process knowledge associated with various sterilization technologies, GMP utilities, and associated pharmaceutical processes required.

Experience with the drug product formulation development process and optimization preferred.

Understanding of equipment, instrumentation, and materials of construction to design, specify, procure, start-up, fully commission and troubleshoot equipment and systems required.

Ability to perform risk assessments required.

Experience in problem solving and continuous improvement techniques required.

Excellent verbal and written communication skills required.

Ability to work effectively managing CMOs required.

Strong planning & organizational skills (and an ability to work to targets, deadlines, and prioritize) required.

Proficient in MS Word, Excel, MS Project & PowerPoint required.

Understanding of national and international regulatory requirements as it relates to Aseptic Manufacturing required.

Proficient in generating and executing protocols and reports required.

Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.

The base compensation range for this position is $ 148,290 to $ 259,510. Base compensation is determined based on a number of factors. This position is also eligible for a company bonus based on individual and company performance.

Novo Nordisk offers long-term incentive compensation and or company vehicles depending on the position's level or other company factors.

Employees are also eligible to participate in Company employee benefit programs including medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; employee assistance program; tuition reimbursement program; and voluntary benefits such as group legal, critical illness, identity theft protection, pet insurance and auto / home insurance. The Company also offers time off pursuant to its sick time policy, flex-able vacation policy, and parental leave policy.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.