Novo Nordisk

Engineer

• Provide routine support & troubleshooting for the manufacturing facility.
• Primary tasks: provide input, review & approve design & requirement documents; provide input, review & approve technical specifications.
• Support development of design & requirement specifications documents
• Support quality of equipment & processes
• Support the creation of process tracks risk assessment documents, such as Requirement Risk Assessments (RRA’s)
• Participation in the creation of a project cGMP Statement
• Create & participate in Quality Risk Management (QRM) risk assessments, such as Closed-Process, Cross-Contamination, Contamination & Facility flows
• Own self development and partner with manager for clear understanding of development needs for desired career path
• Input & review to Process FMECA’s for the Process tracks
• Participation in design workshops with engineering suppliers
• Input & review of Process Module Diagrams, & Process Flow Diagrams
• Input & review of Process Scheduling & Capacity Calculations
• Support package in maintaining schedule adherence
• Ensure coordination & collaboration between project & other site stakeholders
• Gather & ensure knowledge transfer to project from DK sponsor site
• Follow all safety & environmental requirements in the performance of duties
• Other duties as assigned

Associate Process Engineer – API

Compliance

• Ensure evaluation, prioritisation, implementation, communication, and training in new Veeva RIM features across Regulatory Affairs
• Support and drive Veeva RIM process development and optimisation
• Engage with stakeholders and external vendors, providing technical guidance and regulatory input to ensure fit-for-purpose processes and solutions
• Guarantee alignment with external regulatory requirements

Regulatory Professional – Veeva RIM

Director

• formulate, negotiate & scale strategic eHealth partnerships
• lead end-to-end negotiation, customized commercial structuring, and deal closure with Tier 1 partners and digital disruptors
• design plug-and-play partnership frameworks to rapidly scale validated commercial models across growth markets
• deepen collaboration with existing eHealth and online‑selling partners
• serve as the primary regional connector across affiliates
• champion the integration of global clinical milestones into non-branded partner educational pathways
• lead advanced capability-building sessions, cross-market strategy workshops, and digital maturity standardizations
• secure deep-tier API and data-sharing agreements with platform partners
• leverage advanced analytics dashboards to actively audit consumer experiences
• conduct market assessments to understand digital maturity, platform dynamics, and competitive behaviours across APAC

Associate Director – e-Health Channel

• The purpose of this position is to maintain Utility systems for the API-US facility.
• Responsibilities include, but are not limited to: writing/reviewing specifications; design reviews; equipment installation; commissioning & qualifications; SOP development; maintenance development & training; management of cost, quality issues; schedule; establishing & maintaining positive working relationship with internal & external engineering team & stakeholders; re-validation, management of vendor & service contracts ensuring all activities are aligned with Environmental Health & Safety (EHS) program requirements.
• Train on systems, processes & related equipment
• Learn to create & maintain system specifications
• Support all design, installation, commissioning, qualification & training activities
• Provide additional technical support to team & project team as required
• Adhere to all Quality & Environmental regulations within area of responsibility
• Continuous process improvement on department owned systems using cLEAN® concepts
• Assist in developing & writing standards, procedures & maintenance plans
• All safety & environmental requirements in the performance of duties

Facilities Engineer – Utilities – Associate

Regulatory Professional

General Counsel

• Advise and support the Global Manufacturing & Supply organisation
• Assist and support on complex high-value matters
• Identify and assess critical legal issues
• Collaborate with senior stakeholders to guide decision-making
• Drive ad hoc projects focused on optimizing the way of working

Associate Process Engineer – API

Regulatory Professional – Veeva RIM

Associate Director – e-Health Channel

Facilities Engineer – Utilities – Associate

Regulatory Professional

Senior Corporate Counsel – GMS CMC & Supply Chain Legal