Jobs Available at Novo Nordisk

The Position

• As a Demand Planning Manager, you will be responsible for maintaining and updating the rolling forecast in the planning system, ensuring accuracy, timeliness, and that adequate stock is planned in line with demand.
• You will play a key role in facilitating the Sales and Operations Execution (S&OE) & planning (S&OP) Processes, leading the short- and long-term forecasting process across the entire portfolio.

Your main accountabilities will be:

• Short- and long-term Demand Planning and forecast
• Inventory planning and projections, ensuring a balance between incoming orders and projected sales
• Working closely and collaboratively with key customers to ensure a balanced distribution of stock nationally and adequate inventory to meet the demand, and facilitating the S&OP and S&OE process with key functions
• Processing purchase orders with suppliers in line with the demand
• Identifying, proposing, and implementing improvements for distributor/wholesaler management to ensure adequate and timely sharing of data

Qualifications

• As a Demand Planning Manager, you need to have a minimum of a Bachelor’s degree in Supply chain or Logistics with 5-8 years of experience in Demand Planning or Logistics in the pharmaceutical industry, including working cross-functionally with commercial teams.

To be successful in this role:

• Strong working knowledge of SAP and Excel
• Excellent analytical and problem-solving skills
• Ability to work effectively and in cross functionally in a fast-paced and dynamic environment.
• Very good English knowledge, both written and spoken

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The Position

• As a Quality Analyst, you will be ensuring quality assurance of outsourced and License Manufacturing of semi-finished and finished drug products. In addition, you will be conducting audits, monitoring processes, and determining the quality of outputs against defined internal or regulatory standards.
• Moreover, you will ensure that retention samples received from the manufacturer meet regulatory requirements for each locally manufactured batch and that the retention samples are retained at the affiliate for the regulated time frame.

Your main accountabilities will be:

• Developing and maintaining an accurate filing system for local product batch release information, reporting on process deviations and defects, and providing recommendations for improvements
• Collaborating with suppliers and vendors to negotiate service-level agreements and ensure contractual obligations are met
• Assessing potential risks for patients and products and offering advice and recommendations
• Perform due diligence check on relevant Batch Manufacturing and Packaging Records for locally manufactured Products, according to regulatory requirements
• Manage the handling of counterfeit processes for the affiliate which include logging of new cases, follow-up, and reporting of cases to the Health Authority and Global Security

Qualifications

• As a Quality Analyst, you need to have continuous further education in quality assurance, Good Manufacturing Practice (GMP), and Good Distribution Practice (GDP). Nevertheless, you need to have experience in handling deviations and change requests.

To be successful in this role:

• A degree in pharmacy or a relevant technical/scientific field.
• A minimum of 2 years’ experience in quality assurance and production.
• Experience in handling deviations and change requests.
• Strong attention to detail and a quality mindset.
• Proficient in prioritization and execution of activities.
• Excellent communication and stakeholder management skills.
• Strong inter-cultural understanding.