What are the responsibilities and job description for the Associate Director, Analytical Development position at BioSpace?
About The Department
The Boulder Site is home to the specialized technical operations/CMC team for oligonucleotides and RNAi therapeutics. 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. Together, we are driving change. Are you ready to make a difference.
The Position
The Associate Director, Analytical Development oversees personnel and the daily operations of the analytical development team and experimental design at the Boulder, CO laboratory, including internal non-GMP production support and oversight of analytical actvities at CMOs. This role is a people manager and may manage up to ten scientists, locally.
Relationships
This position reports to the Senior Director, Analytical Development.
Essential Functions
Direct daily analytical lab operations, including experimental design and execution, for analytical development activities for both the analytical development and development pilot plant analytical laboratories in the Boulder, CO
Lead and direct a team of up to 10 analytical development scientists, fostering effective collaboration, productivity, and professional growth
Plan laboratory activities, including budget management, equipment procurement, resource allocation, and space planning
Ensure that all analytical lab equipment is maintained and qualified in compliance with internal requirements
Responsible for the development of robust HPLC methods for the analysis of highly modified oligonucleotides, design of unique experiments for their characterization, including identification of drug substance impurities using LC-MS and forced degradation studies
Provide scientific support for the development, transfer, and validation of analytical methods for custom phosphoramidite raw materials, drug substances, and drug products both in-house and at contract manufacturing organizations (CMOs)
Responsible for supporting analytical needs throughout internal departments including facilities, chemical development, amidites, bioconjugation activities and others as necessary
Contribute to raw material and drug substance specification limits in accordance with regulatory requirements and in alignment with IND or IMPD filings
Troubleshoot analytical methods both in-house and at CMO’s to resolve issues effectively
Conduct laboratory work efficiently while ensuring a safe work environment
Physical Requirements
0-10% overnight travel required.
Development of People
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.
Qualifications
PhD in Chemistry, Biochemistry or related field with a minimum of 5 years, MS with a minimum of 7 years, or a BS with a minimum of 9 years of industrial experience required
Minimum of 5 years leadership/management experience in an analytical laboratory required
Strong background in the analytical development of methods for the analysis of oligonucleotide therapeutics
Experience with IP-RP-UHPLC and AX-HPLC analytical techniques using Agilent, Waters and/or Thermo UHPLC’s and associated software
In depth knowledge of GLP/GMP’s in a pharmaceutical environment
The successful candidate must possess excellent writing and communication skills and a demonstrated ability to work independently and with cross-functional teams
The base compensation range for this position is $170,000 to $205,000. 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 April 21, 2026. 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're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
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.
The Boulder Site is home to the specialized technical operations/CMC team for oligonucleotides and RNAi therapeutics. 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. Together, we are driving change. Are you ready to make a difference.
The Position
The Associate Director, Analytical Development oversees personnel and the daily operations of the analytical development team and experimental design at the Boulder, CO laboratory, including internal non-GMP production support and oversight of analytical actvities at CMOs. This role is a people manager and may manage up to ten scientists, locally.
Relationships
This position reports to the Senior Director, Analytical Development.
Essential Functions
Direct daily analytical lab operations, including experimental design and execution, for analytical development activities for both the analytical development and development pilot plant analytical laboratories in the Boulder, CO
Lead and direct a team of up to 10 analytical development scientists, fostering effective collaboration, productivity, and professional growth
Plan laboratory activities, including budget management, equipment procurement, resource allocation, and space planning
Ensure that all analytical lab equipment is maintained and qualified in compliance with internal requirements
Responsible for the development of robust HPLC methods for the analysis of highly modified oligonucleotides, design of unique experiments for their characterization, including identification of drug substance impurities using LC-MS and forced degradation studies
Provide scientific support for the development, transfer, and validation of analytical methods for custom phosphoramidite raw materials, drug substances, and drug products both in-house and at contract manufacturing organizations (CMOs)
Responsible for supporting analytical needs throughout internal departments including facilities, chemical development, amidites, bioconjugation activities and others as necessary
Contribute to raw material and drug substance specification limits in accordance with regulatory requirements and in alignment with IND or IMPD filings
Troubleshoot analytical methods both in-house and at CMO’s to resolve issues effectively
Conduct laboratory work efficiently while ensuring a safe work environment
Physical Requirements
0-10% overnight travel required.
Development of People
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.
Qualifications
PhD in Chemistry, Biochemistry or related field with a minimum of 5 years, MS with a minimum of 7 years, or a BS with a minimum of 9 years of industrial experience required
Minimum of 5 years leadership/management experience in an analytical laboratory required
Strong background in the analytical development of methods for the analysis of oligonucleotide therapeutics
Experience with IP-RP-UHPLC and AX-HPLC analytical techniques using Agilent, Waters and/or Thermo UHPLC’s and associated software
In depth knowledge of GLP/GMP’s in a pharmaceutical environment
The successful candidate must possess excellent writing and communication skills and a demonstrated ability to work independently and with cross-functional teams
The base compensation range for this position is $170,000 to $205,000. 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 April 21, 2026. 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're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
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.
Salary : $170,000 - $205,000