Sr.Product Engineer ,R&D
West Pharmaceutical Services · Bengaluru, Karnataka, India
Full-time · Senior · Posted 15 days ago
Job Summary
In this role, you will support design and development activities within West's Product Development Process demonstrating leadership and strategic thinking within a goal-oriented organization. The incumbent will demonstrate accountability for the successful and timely achievement of goals, work independently only with strategic guidance in the most complex situations, interpret internal and external business issues and unmet needs, and take a broad perspective to define/plan/lead/develop solutions. You may collaborate with local and global functional groups, stakeholders, and management to deliver project goals and meet project milestones.Essential Duties and Responsibilities
Plan and execute projects through all phases with a focus on design and qualification through verification and validation.Create and edit product models/drawings.Write engineering test protocols, reports, and work instructions. Plan, execute, and analyze design of experiments (DOE).Lead technical and design reviews. Drive innovation and process efficiency of integrated systems by applying innovative and logical risk-based approach to product development challenges with the capacity for original thinking.Apply engineering principles for design/analysis of complex technical problems and develop solutions using sound principles, and utilizing experimental, computational, and analytical methods. Examine solutions based on functionality, quality and cost. Write, implement, and leads bench studies, tolerance stack up analysis, design verification, validation, materials specifications, and component specifications.Generate, record and analyze data, and present results to peers and business leadership.Point of contact for technical product related discussions with the team. May provide technical expertise and communication for internal and external partners.Integrate planning activities between West and development/manufacturing partners, and work closely with Procurement to identify and qualify vendors ensuring appropriate components are procured and delivered as needed throughout the phased development process.May characterize system and/or sub-system inputs, outputs and functionality, utilize analytical skills and develop simulation tools to define appropriate product specifications, and system reliability.May implement best practices for methodology, and attend and conduct necessary training for staff as methodology is established. Mentor and guide system engineers.Additional Responsibilities
Education
Bachelor's Degree in Mechanical or Biomedical Engineering required; or equivelant experience
Master's Degree Mechanical or Biomedical Engineering preferred; or equivelant experience
Work Experience Minimum 5 years Experience in the medical device or combination product industry required Experience in high-volume, automated manufacturing processes, and glass forming preferred Experience in Human Factors for Medical Devices preferred Expertise with test method development, validation strategy, and execution required Preferred Knowledge, Skills and Abilities Expertise with risk management, design verification and validation strategy development and executionExpertise in medical device design control and change managementExperience with combination products requirements and regulationProficiency in solid modeling/draftingProficiency in solid mechanics/mechanics of materialsProficiency in statistical methods/toolsProficiency in project managementKnowledge of Six Sigma (DMAIC) practices, and Design for Six Sigma (DFSS) methodologiesAbility to lead and teach others to assess project/program needs, formulate strategies, build support, and execute initiativesStrong interpersonal and decision-making skills and the ability to effectively manage change and uncertaintyKnowledge of applicable ISO, and USP standards for drug deliveryKnowledge of applicable health authority regulations including FDA, MDRAbility to comply with the company's safety and quality policies at all timesLicense and Certifications Travel Requirements 20%: Up to 52 business days per yearPhysical Requirements Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.Additional Requirements Able to routinely use standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Position operates in a professional office environment. May stand or sit for extended periods of timeMust be able to communicate effectively with written and oral skills, make quick decisions, interpret data, read and write, speak in front of groups, express and exchange ideas, understand direction and adhere to proceduresOrganizational skills will enable planning, prioritization and achievement of goals especially of importance for the successful execution of related activitiesRead and interpret data, information and documentsMust maintain the ability to work well with others in a variety of situationsMust be able to multi-task, work under time constraints, problem solve, and prioritizeAbility to make independent and sound judgmentsObserve and interpret situations, analyze and solve problemsAble to perform Research and Development lab activities Must be able to deal with ambiguity, use timely decision making, understand sensitivity for IP protection, deliver concise presentations to high-profile conferences, understand strategic direction, make contributions to strategy formation, be reliable and have predictable attendanceWhat We Offer Shift