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Specialist - Environmental Health and Safety

Employer
Novo Nordisk
Location
Boulder, CO
Start date
Aug 3, 2024
View more categoriesView less categories
Discipline
Administration, Clinical, Clinical Medicine
Required Education
Masters Degree/MBA
Position Type
Full time
Hotbed
Genetown, Best Places to Work

Job Details

About the Department                                                                                                                                               

The Boulder Site is home to the specialized technical operations/CMC team for oligonucleotides and RNAi therapeutics, continuing its legacy as the hub for all manufacturing-related activities for GalXC™ and GalXC-Plus™ investigational therapeutics developed from Novo Nordisk’s acquisition of Dicerna Pharmaceuticals, Inc. in December 2021. With a new laboratory completed in 2021 to support analytical and process development, the CMC team works alongside Quality, Regulatory, Technical Operations and RNAi Early Development professionals at our Boulder, Colorado facility and works closely with our teams in Lexington, Massachusetts. Ranked the No. 1 Place to Live for the second consecutive year by U.S. News & World Report, Boulder is experiencing a renaissance in biotech investment and is one of the world’s leading centers for oligonucleotide innovation and manufacturing. Together, we are driving change. Are you ready to make a difference?

 

The Position

The primary focus for this position is to ensure that the Boulder facility complies with all applicable environmental, health and safety regulations.

 

Relationships

Reports to the Associate Director, EHS. Internal relationships include working with Facility Personnel, Research Scientists, Research Associates and colleagues within Operations.  External relationships include those with business partners and valued vendors.

 

Essential Functions

  • Manage the maintenance and implementation of safety programs, compliance plans, and initiatives with primary focus on laboratories as well as office and support work areas
  • Lead the investigation of incidents, near misses and property damage incidents. Ensure follow-up is done to minimize future exposure and proper records/documents are maintained
  • Create, conduct, coordinate and track various training to support company programs
  • Coordinate and manage all PHAs
  • Chemical Hygiene officer and manage the chemical hygiene plan
  • Manage chemical and noise exposure plan. Create plan to mitigate
  • Review all chemical sds to determine compatibility and health issues
  • Coordinate and manage all permitting to include air ,water, waste
  • Manage the laboratory waste disposal
  • Perform risk assessments, job hazard analysis
  • Develop, maintain, and implement emergency procdure and evacuation plans
  • Implement and maintain LOTO plan
  • Lead on site emergency coordinators
  • Conduct routine safety observations to ensure compliance with regulatory agencies, company environmental, health, and safety policies, procedures and practices
  • Maintain internal and regulatory reporting including data collection and reporting including but not limited to waste management, air, storm water and waste water discharge
  • Ensure the company meets all its legislative compliance obligations with OSHA, WISHA, EPA, Colorado state, ADA, and fire codes
  • Serve as onsite contact for all regulatory agencies for inspections, permitting, reporting (e.g., flammable permits, water, waste)
  • Maintain compliance with permits, government regulations and other industry practices
  • Keep abreast of any safety and environmental law or regulation changes that impact the organization

 

Physical Requirements

0-10% overnight travel required.

 

Qualifications

 

  • Qualifications / Other Requirements
  • BS in Environmental Engineering, Chemistry, Occupational Health and Safety or related field, Master’s degree preferred  
  • 5+ years’ experience in a health sciences environment with responsibility for Environmental, Health and Safety or related field
  • Proficient PC skills including Microsoft Office applications
  • Ability to be on call or work off hours as needed
  • Demonstrated ability to work independently with attention to detail and organizational abilities
  • Superior analytical/ problem solving, written and verbal communications
  • Experience working with local regulatory agencies preferred
  • Familiarity with technologies to ensure compliance
  • Ability to take necessary steps to ensure a safe work environment for all employees
  • Participate in NNRC Seattle meetings to discuss workplace safety and regulatory concerns and opportunities
  • Actively role model all company environmental, health and safety standards
  • Establish and maintain effective relationships with Scientists, Managers, Supervisors and employees
  • Keep the Facilities Manager and Human Resources Manager up to date on matters relating to, environmental, health and safety
  • Assist in the oversight of the Workers Compensation program
  • Special projects as required
  • Critical Competencies
  • Safety Orientation
  • Active and Formal Communication
  • Functional/Technical Knowledge
  • Organizing and Planning
  • Problem Solving and Decision Making
  • Relationship Building
  • Initiative
  • Demonstrate resourcefulness

 

The base compensation range for this position is $85,000 to $115,000. 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. 

 

The job posting is anticipated to close on 08/22/2024. The Company may however extend this time-period, in which case the posting will remain available on our careers website at www.novonordisk-us/careers.com.

 

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.

Company

Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat diabetes and other serious chronic diseases such as obesity and rare blood and endocrine disorders. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 54,400 people in 80 countries and markets its products in around 170 countries. For more information visit novonordisk.com.

Our US Research & Development hub, located in the Greater Boston area, brings together the best talent to drive life science innovation. Located in Lexington, Watertown and Cambridge, our teams reflect the full scope of R&D, from early research through late-stage clinical development. We are building for the future by 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. By combining the speed and agility of biotech with the quality, resources, and stability of a large pharmaceutical company, our US R&D hub will benefit from the best of both worlds to develop new medicines that meet the needs of patients.

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Company info
Website
Phone
617-612-6200
Location
75 Hayden Avenue
Lexington
MA
02421
United States

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