Senior Process Engineer

About the Department

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 Position

The Senior Process Engineer position will support the design build and operation of research and manufacturing facilities located in Boulder CO. The role is expected to be a key technical resource supporting Novo Nordisks investigational products pipeline.

Relationships

This position reports to the Manager of Engineering. This position interacts with manufacturing chemical development QC facilities QA and external contractors.

Essential Functions

• Independently lead and support small to large sized capital engineering projects from concept design start-up and operation. Responsible for all phases of the project lifecycle including the development of user requirement specifications process design equipment and instrumentation specification/selection equipment procurement installation commissioning qualification and turn-over
• Support Chemical Development and Manufacturing with activities such as technical transfer and scale-up of manufacturing process operation and equipment optimization equipment trouble-shooting and continuous improvement goals
• Support EHS activities including chemical and hazardous assessments relating to building codes and waste management regulatory assessments for federal state and local regulatory requirements for air emissions hazardous waste generation wastewater discharge and stormwater runoff PHAs PSSRs etc.
• Work with internal and external resources to develop and review engineering documentation technical standards SOPs protocols risk assessments and reports
• Provide technical engineering support for quality activities including investigations deviations CAPA change controls and gap analysis
• Develop evaluate and implement cost effective engineering solutions for equipment facility and utility systems
• Support process and automation system designs and project lifecycle activities
• Support equipment calibration and maintenance programs
• Promote a culture of safe and compliant design and operation

Physical Requirements

0-10% overnight travel required. Lifting up to 50lbs/23kg of force occasionally and/or up to 30 pounds of force frequently and/or up to 10 pounds of force constantly to move objects.

Qualifications

• Bachelors or more advanced degree in Chemical Engineering or related technical field required
• Minimum of five (5) years of relevant experience in the pharmaceutical biotechnology or related industry focused on drug development and manufacturing required
• Knowledge of pharmaceutical unit operations and equipment including chemical / API synthesis chromatography ultrafiltration and lyophilization is preferred
• Knowledge of process utility systems including; high purity water process waste process solvent inert gas and glycol
• Knowledge of process and equipment design controls hardware/software and strong understanding of GMPs and good engineering guidelines
• Knowledge with the execution of commissioning and validation activities including FAT SAT TOP and IQ/OQ/PQ
• Ability to start-up and trouble-shoot equipment
• Strong technical leadership and communication skills (written and verbal) including experience presenting in front of multidisciplinary teams
• Experience leading projects that include managing external vendors with development design and testing activities
• Ability to provide technical leadership on multiple projects operating in parallel
• Experience in the transfer and scale-up of development processes to the manufacturing scale is preferred
• Experience with new plant startup and operations is preferred
• Possess excellent written and verbal communication skills
• Thorough understanding of cGXP and applicable regulations ability to interpret and apply regulations to complex issues to make risk management recommendations
• Ability to manage people and competing priorities and timelines in a fast-paced rapid-growth environment

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 $96670 to $178840. 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 positions 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.

Were not your typical healthcare a modern world of quick fixes we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science make healthcare more accessible and treat prevent and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real lasting change in health.

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-. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.