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Senior Analytical Scientist - Synthetic API

$NVO →Høje-Taastrup, Capital Region of Denmark· posted Aug 16, 2026
R&D / DiscoverySeniorcontract

Department: Synthetic Analytical MSAT department

Location: Høje-Taastrup Your impact begins here

Are you an experienced analytical scientist who wants to help bring new medicines to market? Join Novo and take scientific ownership of analytical activities for synthetic APIs, working with Contract Manufacturing Organisations (CMOs) worldwide.

You will use your analytical and GMP expertise to support products from late-stage development through commercial supply. You will also help shape the processes and ways of working in our growing Synthetic Analytical MSAT department.

Submit your application today!

What you’ll bring

To succeed in this role, you have:

• A master’s degree or higher in Pharmacy, Chemistry, Biochemistry, Chemical Engineering or a related scientific discipline.

• At least five years of relevant experience in pharmaceutical analytical science.

• Practical experience working in a GMP-regulated environment, such as a QC laboratory.

• Strong knowledge of GMP, relevant ICH guidelines and pharmaceutical regulatory requirements.

• Experience with deviations, change control, out-of-specification investigations and analytical method validation.

• Full professional proficiency in written and spoken English.

You bring sound scientific judgement and communicate complex analytical topics clearly to different stakeholders. You enjoy working collaboratively, take ownership of your responsibilities and maintain a strong focus on quality. You are comfortable setting direction when processes are still developing and building effective relationships with colleagues and external partners.

Useful, but not essential:

• Experience with late-stage pharmaceutical development and synthetic APIs, including small molecules or peptides.

What you’ll do

As a Senior Analytical Scientist, you will provide scientific and GMP expertise to CMOs and internal stakeholders. You will help ensure that robust and efficient analytical methods and programmes are established at our manufacturing partners and maintained throughout the product lifecycle. You will also lead analytical contributions to regulatory submissions.

• Act as the scientific lead for analytical activities, providing expertise to CMOs and internal stakeholders.

• Lead analytical activities and contributions to regulatory submissions from late-stage development through the commercial lifecycle.

• Lead the transfer and implementation of analytical methods between Novo and external partners.

• Author and review analytical documentation, including SOPs, protocols, reports and method transfer plans.

• Develop and improve internal processes and SOPs to support consistent and efficient ways of working.

Who you’ll work with

You will work alongside analytical specialists and project managers in a team that encourages open discussion, knowledge sharing and collaborative problem-solving. As our manufacturing partners are based worldwide, the role includes some international travel ( What you can expect here

In this growing area, you will have the opportunity to shape analytical processes and ways of working. You will use your experience and scientific judgement to set direction, resolve analytical challenges and support the transition from development to commercial supply. A strong understanding of GMP will help you establish robust processes that support product approval and reliable commercial manufacturing.

Salary: For this role, the Annual Base Salary ranges from 651,000.00 to 956,900.00 DKK, corresponding to the level of the position.​ The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience.​ ​ Incentives and Benefits: The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.​ ​ Learn more about our Reward Philosophy here.

Start now

Your impact begins today. If you are ready to take scientific ownership of analytical work that helps new medicines reach people, apply for the Senior Analytical Scientist – Synthetic API role by 15th of October.

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

requirements

To succeed in this role, you: • Hold a minimum of a Master’s degree in Pharmacy, Chemistry, Biochemistry, Chemical Engineering, or other similar scientific disciplines • Have a minimum of 5 years of experience in a similar position within the pharmaceutical sector • You have hands-on experience working in a GMP regulated environment, e.g. QC laboratory • Possess strong knowledge within GMP, ICH guidelines, and pharmaceutical regulatory requirements • Working with deviations, change request, out of specifications and method validation is part of your experience • Showcase full professional proficiency in both spoken and written English Knowledge of late phase (phase 3 and ongoing) pharmaceutical development projects and previous experience working with chemical synthesis (e.g. small molecules or peptides) is an advantage. As a person, you thrive on a high level of flexibility and adaptation, enabling you to excel in a role where the quality of your work is paramount. You have “a firm hand” when it comes to science and possess good skills at communicating with all types of stakeholders both verbally and in writing, and you are motivated by the opportunity to expand your network within our field. About the Department External Analysis & QC is a department currently with teams based in USA and Denmark. We have a growing pipeline, many of which are based on new technology platforms coming through internal development projects or acquisitions. You will join a diverse team of Analytical Project Managers, Senior Analytical Professionals & Analytical Professionals. What we offer At Novo Nordisk, you’ll join a global healthcare company with a unique culture and strong results. We offer continuous learning, career development, and benefits tailored to your life and career stage. Salary: For this role, the Annual Base Salary ranges from 651,000.00 to 956,900.00 DKK, corresponding to the level of the position. The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience. Incentives and Benefits: The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks. Learn more about our Reward Philosophy here. 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 preventing 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.

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