Principal Manufacturing Engineer (Vision Systems)

Planet Pharma

San Diego (CA)

On-site

USD 117,000 - 145,000

Full time

6 days ago
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Job summary

Planet Pharma seeks a Vision Systems Specialist to lead design, validation, and optimization of vision inspection across manufacturing lines in a regulated environment. You will drive IQ/OQ/PQ programs and collaborate with R&D, Quality, and CM partners to define performance metrics and acceptance criteria.

The role requires expertise in vision systems, problem solving, and familiarity with MES, GD&T, and AI-based inspection concepts.

Qualifications

  • Serve as the primary technical expert for vision system design, implementation, validation, and optimization across manufacturing lines.
  • Lead the process development, qualification and validation of vision inspection systems (IQ/OQ/PQ) in compliance with FDA and ISO regulations.
  • Define vision system requirements, acceptance criteria, and performance metrics in collaboration with R&D, Quality, and Contract Manufacturing partners.
  • Troubleshoot and resolve complex vision system failures, driving root cause analysis and implementing sustainable corrective actions.
  • Evaluate and recommend new vision system technologies to improve inspection capability, yield, and throughput.

Responsibilities

  • Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.
  • Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.
  • Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.
  • Adapts machine or equipment design to factory and production conditions.
  • May incorporate inspection and test requirements into the production plan.
  • Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.
  • Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques.
  • Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques.
  • Ensures processes and procedures are in compliance with regulations.
  • TECHNICAL SPECIALIST CAREER STREAM: An individual contributor with responsibility in our technical functions to advance existing technology or introduce new technology and therapies. Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering R&D, systems or initiatives related to new technologies or therapies – from design to implementation – while adhering to policies, using specialized knowledge and skills.

Skills

Vision systems design
Root cause analysis
Quality compliance
Process optimization

Education

Six Sigma Green Belt or Black Belt certification

Tools

Minitab
AutoCAD
SolidWorks
SAP
Microsoft Office

Job description

Pay 85-105/h depending on experience


Vision Systems Expertise Required:


  • Serve as the primary technical expert for vision system design, implementation, validation, and optimization across manufacturing lines

  • Lead the process development, qualification and validation of vision inspection systems (IQ/OQ/PQ) in compliance with FDA and ISO regulations

  • Define vision system requirements, acceptance criteria, and performance metrics in collaboration with R&D, Quality, and Contract Manufacturing partners

  • Troubleshoot and resolve complex vision system failures, driving root cause analysis and implementing sustainable corrective actions

  • Evaluate and recommend new vision system technologies to improve inspection capability, yield, and throughput


Preferred Skills:


  • Experience with MES (Manufacturing Execution Systems) integration with vision systems o Familiarity with GD&T and optical measurement principles

  • Experience supporting Contract Manufacturers in a medical device environment

  • Knowledge of machine learning or AI-based vision inspection technologiesSix Sigma Green Belt or Black Belt certification.

  • Microsoft Office, Minitab, Document Management Systems, MES, AutoCAD, SolidWorks, SAP


Responsibilities may include the following and other duties may be assigned.



  • Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.

  • Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.

  • Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.

  • Adapts machine or equipment design to factory and production conditions.

  • May incorporate inspection and test requirements into the production plan.

  • Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.

  • Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques.

  • Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques.

  • Ensures processes and procedures are in compliance with regulations.


TECHNICAL SPECIALIST CAREER STREAM: An individual contributor with responsibility in our technical functions to advance existing technology or introduce new technology and therapies. Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering R&D, systems or initiatives related to new technologies or therapies – from design to implementation – while adhering to policies, using specialized knowledge and skills.


DIFFERENTIATING FACTORS

Autonomy: Recognized expert, managing large projects or processes. Exercises considerable latitude in determining deliverables of assignments, with limited oversight from manager. Coaches, reviews and delegates work to lower level specialists.


Organizational Impact: Contributes to defining the direction for new products, processes, standards, or operational plans based on business strategy with a significant impact on work group results. May manage large projects or processes that span outside of immediate job area.


Innovation and Complexity: Problems and issues faced are difficult, moderately complex and undefined, and require detailed information gathering, analysis and investigation. Develops solutions to moderately complex problems, and/or makes moderate to significant improvements of processes, systems or products independently to enhance performance of job area. Implements solutions to problems.


Communication and Influence: Represents organization as a primary contact for specific projects and initiatives; communicates with internal and external customers and vendors at various levels. May negotiate with others to reach understanding or agreement, and influence decision-making.


Leadership and Talent Management: Typically provides guidance, coaching and training to other employees within job area. Typically manages major / moderately complex projects, involving delegation of work and review of work products, at times acting as a team leader.


Required Knowledge and Experience: Requires mastery of a specialty area and full knowledge of industry practices, typically obtained through advanced education combined with experience. May have broad knowledge of project management. Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A) and minimum 7 years of relevant experience, or advanced degree with a minimum of 5 years of relevant experience.

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