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ADAPTED_NOW

Process Engineer

This role will be part of a Manufacturing Engineering team providing direct support to the manufacturing floor with: equipment troubleshooting and direct support to manufacturing teams, conduct deviation investigations, root cause analysis, validations for new equipment installs, and other tasks helping our manufacturing operations succeed day to day. The working environment includes a variety of physical conditions including noise, inside and outside conditions, working in narrow aisles, and temperature changes; atmospheric conditions including odors, fumes, and dust.

KBSkills

ACTIVE

About the Department     Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. It’s not your average production site – it’s a tight-knit, supportive community working together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything we do. We’re looking for individuals who are self-starters with a strong work ethic to join our team. At Novo Nordisk, you will find opportunities, resources and mentorship to grow and build your career. Are you ready to realize your potential? The PositionResponsible for the design and implementation of manufacturing processes, instrumentation, and equipment start-ups from the laboratory through manufacturing scale. This role will be part of a Manufacturing Engineering team providing direct support to the manufacturing floor with: equipment troubleshooting and direct support to manufacturing teams, conduct deviation investigations, root cause analysis, validations for new equipment installs, and other tasks helping our manufacturing operations succeed day to day. This role will work closely with different functional groups accross the site for projects including: Manufacturing, MSAT, QA, and other engineering teams.  This is an onsite based role 5 days a week Monday-Friday. Relocation assistance is available for eligible candidates. The specific level of this role will be commensurate with experience. RelationshipsReports to: Lead Engineer, Manufacturing Engineering (Supervisor) Essential Functions<ul><li>Leads process and equipment troubleshooting to support deviations, corrective actions and related issues</li><li>Coordinate fabrication, procurement, installation, engineering start-up, and validation activities of new equipment and systems, including documentation of IQ/OQ protocols, test executions, and summary reports</li><li>Participate in the development and implementation of procedural or automation improvement changes</li><li>Participate in design and hazard reviews of plant expansions or process changes and serving as the technical point of contact or user representative for contractor services including design, fabrication, installation, and validation</li><li>Point person for process improvement activities, including performing or authoring equipment specifications, user and functional requirements specifications, and necessary FAT and SAT protocols</li><li>Initiate and manage projects, tracking spending of budgets, creating scope of work, justification, risk assessments, cost estimates, implementing purchase order requisitions, and controlling payment schedules</li><li>Regular supervision of contractor or intern reports including mentoring, performance reviews, project and support advice as well as troubleshooting for the more complicated issues found in the manufacturing environment</li><li>Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes</li><li>Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others</li><li> Qualifications<ul><li>Education and Certifications</li><li>Bachelor’s degree in an engineering or technical discipline required; Master’s degree in engineering or related discipline preferred</li></ul></li><li>Work Experience</li><li>A minimum of seven (7) years’ experience in medium to large scale pharmaceutical or biotechnology process is required with a Bachelor’s degree. At least five (5) years’ is required with a Master’s degree</li><li>Knowledge, Skills, and Abilities</li><li>Normally receives no instructions on routine work, general instructions on new assignments</li><li>Knowledge of Automation, GMPs, Compliance, and Regulatory requirements is essential</li><li>Excellent communication skills and ability to work in a high-paced team-oriented environment</li><li> Physical RequirementsThe ability to climb. stoop, kneel, crouch, crawl, reach, stand, and walk. The ability to push, pull, lift, finger, feel, and grasp. The ability to speak, listen, and understand verbal and written communication. Repetition including substantial movement of wrists, hands, and or fingers. Lifting up to 33lbs/15kg of force occasionally, and/or up to 30 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects. Visual acuity to perform close activities such as: reading, writing, and analyzing; and visual inspection. The working environment includes a variety of physical conditions including noise, inside and outside conditions, working in narrow aisles, and temperature changes; atmospheric conditions including odors, fumes, and dust. Local and International Travel: 0-10%.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing. 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.</li></ul>

Novo Nordisk

Process Engineer III

Automation

Biotech and Pharmaceutical

Budget Management

Communication Skills

Community Support

Corrective Action

Cost Estimates

Customer Relations

Diversity

Documentation

Equipment Specification

Expense Tracking

GMP (Good Manufacturing Practices)

Healthcare

Hemophilia

Identify Issues

Instrumentation

Manufacturing

Manufacturing Engineering

Manufacturing Management

Manufacturing Operations

Manufacturing/Industrial Processes

Medications

Mentoring

Performance Reviews

Presentation/Verbal Skills

Procedure Development

Procedure Implementation

Process Engineering

Process Improvement

Process Validation

Project Tracking

Project/Program Management

Purchase Orders

Purchasing/Procurement

Quality Assurance

Regulations

Regulatory Compliance

Regulatory Requirements

Risk Analysis

Root Cause Analysis

Startup

System Start-Up

Team Player

Testing

Willing to Travel

BioSpace

Work Experience: Bachelor’s degree with 10 plus years’ experience in the pharmaceutical or biotechnology industry, or a Master’s degree with a minimum of eight (8) years’ experience in the pharmaceutical or biotechnology industry. Initiate and manage projects, tracking spending of budgets, creating scope of work, justification, risk assessments, cost estimates, implementing purchase order requisitions, and controlling payment schedules.

About the Department     Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. It’s not your average production site – it’s a tight-knit, supportive community working together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything we do. We’re looking for individuals who are self-starters with a strong work ethic to join our team. At Novo Nordisk, you will find opportunities, resources and mentorship to grow and build your career. Are you ready to realize your potential? The PositionThis position provides engineering and automation services with front line, on the floor support for the manufacture of our products for our patients. The engineer collaborates with all customers on site and facilitates the delivery of solutions based on customer needs. The engineering solutions provided need to be safe and effective using current and innovative technology. This position is responsible for the design and implementation of manufacturing processes, instrumentation and equipment start-ups from the laboratory through manufacturing scale of facilities, utilities, systems and equipment. This individual provides expertise in cell culture and purification process equipment and supporting utilities for biotechnology manufacturing. This individual is responsible for the creation, management and execution of engineering life cycle documentation and verification (i.e. commissioning through qualification) for manufacturing systems for the NNUSBPI site and manage projects as required. The position is expected to have a solid understanding of good engineering practice (GEP) industry standards, science and risk-based verification requirements and is required to supply support/technical knowledge for the development/refinement and implementation of the GEP program and validation standards based on risk-based practices as prescribed in ASTM E2500. Also, will work with NNUSBPI leadership to manage and create group strategy and systems, allocating resources to projects, managing timelines for projects and developing the talent within the department. RelationshipsReports to: Lead Engineer Number of subordinates with direct/indirect referral: none Essential Functions<ul><li>Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others</li><li>Leads process and equipment troubleshooting on the manufacturing floor to support product supply, deviations, corrective actions and related issues</li><li>System owner for manufacturing systems (i.e. facilities, utilities, systems and equipment) and associated life cycle documentation and procedures</li><li>Contribute to long-term strategic development of the engineering and verification program</li><li>Technically independent and maintains up-to-date knowledge of industry standards and regulatory compliance requirements and independently contributes to the development of the Engineering Team and contributes to the development of best practices</li><li>Coordinate fabrication, procurement, installation, engineering start-up, and validation activities of new equipment and systems</li><li>Lead the development and implementation of procedural or automation improvement changes</li><li>Participate in design and hazard reviews of plant expansions or process changes and serving as the technical point of contact or user representative for contractor services including design, fabrication, installation and validation</li><li>Point person for process improvement activities</li><li>Responsible for authoring equipment specifications, user and functional requirements specifications, and necessary verification documents (e.g.  FAT, SAT, commissioning, qualification protocols).  Leads the preparation and execution of protocols, data analysis and final reporting</li><li>Initiate and manage projects, tracking spending of budgets, creating scope of work, justification, risk assessments, cost estimates, implementing purchase order requisitions, and controlling payment schedules</li><li>Regular supervision of contractors for projects</li><li>Organizes and presents (either written or verbally) their work</li><li>Independently analyses and interprets data with limited consultation with supervisor, makes independent tactical decisions based on data, develops project strategies with consultation with supervisor</li><li>Contributes to mentoring activities for the development of the Engineering team</li><li>Represents the Engineering department on cross-functional teams</li><li>Independently initiates, designs, and evaluates plans for site projects, responsible for planning and execution of all tasks needed to meet goals. Executes priorities and begins to consider long range project planning with consultation with supervisor, good project and personnel management skills are required</li><li>No supervision for day-to-day activities required, meets regularly with supervisor to update on progress towards long-term goals</li><li>Provides input and direct support during regulatory inspections. Supports health authority and corporate audits</li><li>Implement department action plans based on the results from internal or external audits, CAPA and exception management processes</li><li>Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes</li><li>Other duties as assigned</li><li>#IND23 Qualifications<ul><li>Education and Certifications:</li><li>Requires a Bachelors/Master’s degree (or equivalent experience) in engineering or related life sciences discipline</li></ul></li><li>Work Experience:</li><li>Bachelor’s degree with 10 plus years’ experience in the pharmaceutical or biotechnology industry, or a Master’s degree with a minimum of eight (8) years’ experience in the pharmaceutical or biotechnology industry</li><li>Prefer medium to large scale pharmaceutical or biotechnology process experience</li><li>Knowledge, Skills, and Abilities:</li><li>A strong understanding of: GEP and Validation concepts, international cGMP regulations, GAMP and other industry standards pertaining to the technical and verification requirements for biopharmaceutical equipment, facilities, and/or instrumentation</li><li>A strong work ethic (self-motivated) honesty, excellent communication skills, and the ability to work in teams-displays initiative and commitment</li><li>Engineering and risk-based management within an FDA, EMEA, GMED or TGA regulated production facility</li><li>Knowledge of GMPs, Compliance and Regulatory requirements is essential</li><li>Excellent communication skills and ability to work in a high-paced team-oriented environment</li><li>Off Hours and Weekend Coverage expected for manufacturing support. May be called in on nights and weekends</li><li> Physical Requirements0-10% overnight travel required. The ability to climb. stoop, kneel, crouch, crawl, reach, stand, and walk. The ability to push, pull, lift, finger, feel, and grasp. The ability to speak, listen, and understand verbal and written communication. Repetition including substantial movement of wrists, hands, and or fingers. Lifting up to 33lbs/15kg of force occasionally, and/or up to 30 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects. Visual acuity to perform close activities such as: reading, writing, and analyzing; and visual inspection. The working environment includes a variety of physical conditions including: noise, inside and outside conditions, working in narrow aisles, and temperature changes; atmospheric conditions including: odors, fumes, and dust.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing. 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.</li></ul>

Senior Process Engineer (Manufacturing Support)

Best Practices

Biology

Cell Cultures

Commissioning

Corrective and Preventative Action (CAPA) Systems

Cross-Functional

Current Good Manufacturing Practice (cGMP)

Data Analysis

External Audit

FDA (Food and Drug Administration)

GEP (Good Engineering Practices)

Industry Standards

Internal Audit

Leadership

Manufacturing Systems

People Management

Process Manufacturing

Product Support

Project Development

Project Planning

Protocol Analysis

Requirements Validation/Verification

Resource Management

Risk

Risk Management

Site Evaluation

Strategic Planning

Talent Management

Team Lead/Manager

Technical Support

Time Management

Verification Engineering

Validation Engineer

The working environment includes a variety of physical conditions including noise, inside and outside conditions, working in narrow aisles, and temperature changes; atmospheric conditions including: odors, fumes, and dust. Support facility certification for new Manufacturing (process equipment & facility-support equipment) and Quality Control facilities as needed as well as the continued operation of such facilities.

About the Department       Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. What we offer you:<ul><li>Leading pay and annual performance bonus for all positions</li><li>36 Paid days off including vacation, sick days & company holidays</li><li>Health Insurance, Dental Insurance, Vision Insurance</li><li>Guaranteed 8% 401K contribution plus individual company match option</li><li>14 weeks Paid Parental Leave</li><li>Free access to Novo Nordisk-marketed pharmaceutical products</li></ul> At Novo Nordisk, you will find opportunities, resources and mentorship to grow and build your career. Are you ready to realize your potential?   The PositionThe person in this role will also be responsible for validation activities in several areas of pharmaceutical manufacturing including, but not limited to, DQ, IQ, OQ, PQ, requalifications, cleaning, sterilization and utilities. This position will support the day to day execution of validation activities, and related documentation/technical writing overseen by support of more senior Validation Engineers.  This is an onsite based role Monday-Friday at our West Lebanon, NH bio-production facility. Relocation assistance may be available for elgibile candidates. RelationshipsReports to: Lead Engineer, Validation (Supervisor) Essential Functions<ul><li>Primary responsibilities include validation protocol execution (IQ, OQ, PQ & PV), data analysis and final report preparation for utilities, equipment and instrumentation</li><li>Maintain effective communication and ensure alignment in coordination with appropriate teams</li><li>Support facility certification for new Manufacturing (process equipment & facility-support equipment) and Quality Control facilities as needed as well as the continued operation of such facilities</li><li>Ensures systems and processes are validated in a compliant manner in accordance with FDA, EU and NN requirements</li><li>Actively participate on cross functional teams to determine the root cause and corrective actions for problems associated with investigations</li><li>Completes accurate and timely assessments associated with change control activities</li><li>Ensures change control activities for systems are completed in a manner in compliance with FDA, EU and NN regulations</li><li>Support validation of new and existing equipment, processes and instrumentation as needed</li><li>Write and review protocols, summary reports and other documentation associated with validations</li><li>Coordinate Validation activities within Novo Nordisk US Bio Production, Inc. as well as with outside vendors as needed</li><li>Represent the Validation department on cross-functional teams (Manufacturing, Engineering, Technical Support and Quality groups)</li><li>Assist in the training of and/or direct the efforts of less experienced Validation Engineers and Validation Technicians</li><li>Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes</li><li>Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others</li><li> Qualifications<ul><li>Education and Certifications</li><li>Bachelor’s degree or equivalent experience in life sciences or engineering</li></ul></li><li>Work Experience</li><li>A minimum of three (3) years validation experience in the pharmaceutical or biotechnology industry</li><li>Experience preparing protocols, executing data analysis, and report writing</li><li>Experience preparing protocols, executing data analysis, and report writing</li><li>Knowledge, Skills, and Abilities</li><li>Ability to demonstrate broad understanding of</li><li>Concepts of Validation</li><li>Change control processes</li><li>Root cause analysis techniques and cGMP documentation practices</li><li>cGMP regulations, GMP and other industry standards pertaining to validation</li><li>Technical requirements for Validation and of biopharmaceutical equipment, facilities and/or instrumentation</li><li>Excellent written and verbal communication skills a must</li><li>A strong work ethic (self-motivated) and demonstrated ability to work in teams</li><li> Physical RequirementsThe ability to climb. stoop, kneel, crouch, crawl, reach, stand, and walk. The ability to push, pull, lift, finger, feel, and grasp. The ability to speak, listen, and understand verbal and written communication. Repetition including substantial movement of wrists, hands, and or fingers. Lifting up to 33lbs/15kg of force occasionally, and/or up to 30 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects. Visual acuity to perform close activities such as: reading, writing, and analysing; and visual inspection. The working environment includes a variety of physical conditions including noise, inside and outside conditions, working in narrow aisles, and temperature changes; atmospheric conditions including: odors, fumes, and dust. Local and International Travel: 0-10%.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing. 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.</li></ul>

Validation Engineer I

Change Control

Drug Manufacturing

Product Marketing

Quality Control

Reporting Skills

Sterilization

Technical Writing

Validation Plan

Writing Skills

Leads process and equipment troubleshooting to support deviations, corrective actions and related issuesCoordinate fabrication, procurement, installation, engineering start-up, and validation activities of new equipment and systems, including documentation of IQ/OQ protocols, test executions, and summary reportsParticipate in the development and implementation of procedural or automation improvement changesParticipate in design and hazard reviews of plant expansions or process changes and serving as the technical point of contact or user representative for contractor services including design, fabrication, installation and validationPoint person for process improvement activities, including performing or authoring equipment specifications, user and functional requirements specifications, and necessary FAT and SAT protocolsInitiate and manage projects, tracking spending of budgets, creating scope of work, justification, risk assessments, cost estimates, implementing purchase order requisitions, and controlling payment schedulesRegular supervision of contractor or intern reports including mentoring, performance reviews, project and support advice as well as troubleshooting for the more complicated issues found in the manufacturing environmentPerforms all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codesIncorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others . Prefer medium to large scale pharmaceutical or biotechnology process experienceKnowledge, Skills, and AbilitiesNormally receives no instructions on routine work, general instructions on new assignmentsKnowledge of Automation, GMPs, Compliance, and Regulatory requirements is essentialExcellent communication skills and ability to work in a high-paced team-oriented environment .

About the Department     Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. It’s not your average production site – it’s a tight-knit, supportive community working together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything we do. We’re looking for individuals who are self-starters with a strong work ethic to join our team. At Novo Nordisk, you will find opportunities, resources and mentorship to grow and build your career. Are you ready to realize your potential? The PositionResponsible for the design and implementation of manufacturing processes, instrumentation and equipment start-ups from bench top scale through commercial manufacturing scale. This individual provides expertise in support of manufacturing capacity expansions projects at our cGMP commercial manufacturing facility. This role will work within our Process Engineering team focused on brownfield projects including: equipment upgrades, new equipment installations, capital projects, and validation/commissioning support for new equipment installed onsite. This role will work cross functionally with other functional groups including: Manufacturing, Facilities Engineering, QA, MSAT, and external vendors. This role is onsite based 5 days a week Monday-Friday at our West Lebanon, NH bio-production facility. Relocation assistance may be available for selected candidate if they are eligible. The specific level and pay grade of this role will be commensurate with candidate experience and qualifications.  RelationshipsReporting to: Lead Engineer, Manufacturing Engineering (Supervisor) Essential FunctionsLeads process and equipment troubleshooting to support deviations, corrective actions and related issuesCoordinate fabrication, procurement, installation, engineering start-up, and validation activities of new equipment and systems, including documentation of IQ/OQ protocols, test executions, and summary reportsParticipate in the development and implementation of procedural or automation improvement changesParticipate in design and hazard reviews of plant expansions or process changes and serving as the technical point of contact or user representative for contractor services including design, fabrication, installation and validationPoint person for process improvement activities, including performing or authoring equipment specifications, user and functional requirements specifications, and necessary FAT and SAT protocolsInitiate and manage projects, tracking spending of budgets, creating scope of work, justification, risk assessments, cost estimates, implementing purchase order requisitions, and controlling payment schedulesRegular supervision of contractor or intern reports including mentoring, performance reviews, project and support advice as well as troubleshooting for the more complicated issues found in the manufacturing environmentPerforms all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codesIncorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others Qualifications<ul><li>Education and CertificationsRequires a Bachelors/Masters/PhD degree (or equivalent experience) in engineering or related discipline</li></ul>Work ExperienceA minimum of five (5) years related experience with a Bachelor’s or three (3) years related experience with a Master’s or higher. Prefer medium to large scale pharmaceutical or biotechnology process experienceKnowledge, Skills, and AbilitiesNormally receives no instructions on routine work, general instructions on new assignmentsKnowledge of Automation, GMPs, Compliance, and Regulatory requirements is essentialExcellent communication skills and ability to work in a high-paced team-oriented environment Physical RequirementsThe ability to climb. stoop, kneel, crouch, crawl, reach, stand, and walk. The ability to push, pull, lift, finger, feel, and grasp. The ability to speak, listen, and understand verbal and written communication. Repetition including substantial movement of wrists, hands, and or fingers. Lifting up to 33lbs/15kg of force occasionally, and/or up to 30 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects. Visual acuity to perform close activities such as: reading, writing, and analysing; and visual inspection. The working environment includes a variety of physical conditions including noise, inside and outside conditions, working in narrow aisles, and temperature changes; atmospheric conditions including: odors, fumes, and dust. Local and International Travel: 0-10%.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing. 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.

Process Engineer (Equipment Installation & Upgrades)

Brownfield Redevelopment

Capital Equipment

Capital Project

Facilities Engineering

Physical Demands

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