Senior Manufacturing Engineer II

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well‑being for patients around the world.

As a Sr. Manufacturing Engineer II, you will play a critical role in driving manufacturing excellence through process optimisation, equipment innovation and cross‑functional collaboration. By leading initiatives that enhance productivity, quality and compliance, you will directly contribute to improved operational performance and product reliability. Your ability to develop and implement scalable manufacturing solutions, resolve complex technical challenges and partner with stakeholders will support continuous improvement and long‑term business success.

With a hands‑on, data‑driven approach, your expertise will help shape efficient, cost‑effective and compliant manufacturing processes that align with company goals and customer expectations.

• Lead efforts to monitor and optimise the performance of manufacturing equipment, ensuring compliance with CGMP standards.
• Troubleshoot and resolve complex issues to minimise production downtime.
• Identify and implement opportunities for continuous improvement through upgrades, process modification or alternative solutions. Lead the development and implementation of procedural or automation improvement changes.
• Lead lean manufacturing initiatives, Six Sigma projects and other process optimisation efforts to improve productivity, quality and cost efficiency.
• Assist with new product/equipment design reviews, process development and commercialisation activities, including training and development of manufacturing staff on operation and process.
• Serve as a technical point of contact for client and contract services.

• Develop and maintain measurement systems to visualise manufacturing key performance indicators (KPIs).
• Use data analytics tools and techniques to analyse equipment performance, identify trends and recommend corrective action and process improvement.

• Assist with manufacturing equipment‑related deviations and root‑cause analysis as the equipment SME.
• Support the development and execution of Corrective and Preventive Actions (CAPA) and Change Controls to address root causes of equipment failures and performance issues.
• Support equipment Installation, Operation and Performance Qualification (IOPQ) activities.
• Experience supporting client and regulatory audits as well as responding to action items.
• Provide SME input on equipment qualification processes, ensuring fit for commercial manufacturing use, compliance with FDA and other regulatory requirements.

• Bachelor’s degree in Engineering or related field and/or equivalent experience.
• 8+ years of relevant manufacturing experience in the pharmaceutical industry with a Bachelor’s degree; and 6+ years’ experience in the pharmaceutical industry and a Master’s degree or a PhD with 3 years in the pharmaceutical industry and a focus on equipment and process improvement.
• Proven track record of successfully implementing improvement initiatives in a pharmaceutical manufacturing environment.
• Strong analytical and problem‑solving skills with the ability to use data to drive decision‑making.
• Excellent communication and interpersonal skills, with the ability to influence and collaborate effectively across multiple departments.
• Ability to manage multiple projects and priorities in a fast‑paced environment.
• Technical writing experience, such as SOPs, maintenance PMs, user requirement specs, vendor requests for proposal.
• Experience with automation, nasal or related drug delivery device manufacture and packaging.

• Lean manufacturing or Six Sigma certifications.
• Proficiency in using Lean tools and software applications such as Smartsheet, Power BI, Power Apps, etc.
• Experience with site‑level automation systems, ex:
  • Serialization – Antares, Tracelink.
  • Data historian – Aveva OSI PI.
  • Reporting systems – OSI PI, MS Report Builder, SQL Development.
  • Kepware, Matrikon, AB Factory Talk.
  • Automated visual…