What are the responsibilities and job description for the Process Engineer II position at Planet Pharma?
Additional Position Details From The Manager Below
Can you please confirm the 3 main responsibilities/day to day activities required for this role?
This role will be project focused, working with Program management and other engineers to perform root cause analysis and investigation tasks towards optimizing and implementing improvements within both production and pre-production environments. This role will be required to define optimization opportunities based on engineering findings, present to the team, and implement showing improvements within the manufacturing yield/process.
What products (if any) will this role support?
This role will have the opportunity to support products built for pharmaceutical operations (combination steroid/medical device products) and/or Cardiac Surgery.
What is your target years of experience?
Looking for E2 position equivalent. Target years of experience falls within 2-3 years within the medical device manufacturing or development engineering fields.
When do you plan to start interviewing? ASAP
Will you be looking to hire and start ASAP or will the start date be delayed? Hiring process will be focused on a start date of early to mid Q1 FY27.
Will the contingent worker be working remotely or onsite, or both (if both, please confirm possible schedule)? Full-time onsite (4 days)
_______________________________________________________________________________________________________________
Relevant experience in process development deliverables (IQ, OQ, PQ), process characterization work, and equipment development experience is preferred.
Responsibilities may include the following and other duties may be assigned:
Can you please confirm the 3 main responsibilities/day to day activities required for this role?
This role will be project focused, working with Program management and other engineers to perform root cause analysis and investigation tasks towards optimizing and implementing improvements within both production and pre-production environments. This role will be required to define optimization opportunities based on engineering findings, present to the team, and implement showing improvements within the manufacturing yield/process.
What products (if any) will this role support?
This role will have the opportunity to support products built for pharmaceutical operations (combination steroid/medical device products) and/or Cardiac Surgery.
What is your target years of experience?
Looking for E2 position equivalent. Target years of experience falls within 2-3 years within the medical device manufacturing or development engineering fields.
When do you plan to start interviewing? ASAP
Will you be looking to hire and start ASAP or will the start date be delayed? Hiring process will be focused on a start date of early to mid Q1 FY27.
Will the contingent worker be working remotely or onsite, or both (if both, please confirm possible schedule)? Full-time onsite (4 days)
_______________________________________________________________________________________________________________
Relevant experience in process development deliverables (IQ, OQ, PQ), process characterization work, and equipment development experience is preferred.
Responsibilities may include the following and other duties may be assigned:
- Provide technical and sustaining engineering support within a manufacturing environment.
- Recommend and implement equipment and process modifications to meet quality standards, improve production efficiencies, enhance manufacturing techniques, and increase yields for existing products.
- Integrate equipment and material capabilities to meet process module and technology target specifications.
- Review product development requirements for compatibility with processing methods and provide input on cost and schedule implications.
- Collaborate with product design and development teams to ensure processes and designs are aligned and manufacturable.
- Perform or support statistical analysis and contribute to documentation improvements when needed.
- Lead innovation, development, and optimization of new manufacturing concepts, processes, and procedures for transfer into manufacturing operations, including feasibility assessments, material selection, equipment selection, tooling and fixture development, and evaluation of process inputs and outputs.
- Develop manufacturing processes suitable for statistical process control and support development of measurement systems. Ensure all processes and procedures comply with regulatory requirements.