Senior Engineer, Network Manufacturing (Orthopaedics)
for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). So we can include sections that have content.
We have:
- Job Function: Supply Chain Engineering, Sub Function Manufacturing Engineering, Category Scientific/Technology. Locations: Raynham, MA; Ringaskiddy, Cork, Ireland.
- Job Description: recruiting for Senior Engineer to join Network Tech Ops team in either Raynham, MA or Cork Ireland. Info about separation of Orthopaedics business to DePuy Synthes. Should accept position, after transaction you'd be employee of DePuy Synthes.
- About Orthopaedics: description.
- Job Purpose: As part of DePuy Synthes Network Edge strategy we are increasing global Manufacturing capacity within the DPS Orthopaedic franchise. Recruiting for Senior Engineer to execute capacity expansion projects. This role will execute engineering deliverables in support of large-scale manufacturing capacity projects that will yield stable, reliable and cost-effective manufacturing process meeting projects FPO’s of capacity, product cost, budget and timeline. The scope includes project delivery and ensuring knowledge transfer to developing manufacturing site staff and will work in collaboration with existing DPS functional organizations to ensure standardization and implementation of Best-in-Class practices.
- Key Responsibilities: bullet list (multiple sentences). We'll need to convert to - .
- Experience, Skills & Proficiencies Required: list.
- Education/Qualifications: bullet.
- Other: travel up to 25% domestic & international.
- Pay: anticipated base pay range: $79,000.00 - $127,650.00
- Benefits: detailed list.
- Additional Description For Pay Transparency: mention retirement plan etc. Might be part of Benefits.
- Required Skills Preferred Skills: list.
We need to decide sections.
Potential sections:
- About the role (could include job purpose, description, location, etc.)
- Responsibilities (Key Responsibilities)
- Requirements (Experience, Skills & Proficiencies Required)
- Qualifications (Education/Qualifications)
- Skills (maybe combine Required Skills Preferred Skills? Could be separate Skills section.)
- Benefits
- Pay
- Schedule (maybe travel? Not schedule. No explicit schedule info. Could omit Schedule if not present.)
We should not create empty sections.
We need to preserve all substantive info.
Let's extract content.
Company overview: Might be placed under About the role? Could be separate but not required. We could include a brief paragraph under About the role summarizing role purpose and company mission.
But we must not invent or summarize away detail. We can keep the original prose.
We need to avoid duplication.
Let's structure:
About the role
Johnson & Johnson is recruiting for a Senior Engineer to join our Network Tech Ops team in either Raynham, MA or Cork, Ireland. As part of DePuy Synthes Network Edge strategy we are increasing global Manufacturing capacity within the DPS Orthopaedic franchise. This role will execute engineering deliverables in support of large-scale manufacturing capacity projects that will yield stable, reliable and cost-effective manufacturing process meeting projects FPO’s of capacity, product cost, budget and timeline. The scope includes project delivery as well as ensuring knowledge transfer to developing manufacturing site staff and will work in collaboration with the existing DPS functional organizations to ensure standardization and the implementation of Best-in-Class practices.
That captures job purpose and description.
We could also include location info maybe in a within About the role.
Add: Locations: Raynham, Massachusetts, United States of America; Ringaskiddy, Cork, Ireland.
Now Responsibilities:
Take the bullet list from "Key Responsibilities". Let's extract each sentence:
- Supporting delivery of robust and fully developed and qualified orthopaedic implant manufacturing processes to Network Edge projects
- Ensure that all project activities are conducted in line with procedures and controls outlined in the QMS and that the quality and performance of the product conforms to specified standards and in compliance with the recognized Regulatory Standards for relevant markets.
- Collaborate with functional stakeholders to ensure that technical, validation and regulatory strategies are implemented in an efficient and compliant manner and at an appropriate risk level
- Partner with Regulatory to execute the strategy necessary for all filings, inspections, and registrations in multiple sites and countries.
- Communicates with internal and external partners to coordinate and execute project plans. Provides technical leadership and supports execution of EHS&S policies and procedures
- Supporting technical collaboration across functions
- Leads effective and timely communication processes and stakeholder management processes within the project scope and ensures project and program activities are consistently documented.
We need to ensure each is a
- .
Now Requirements (Experience, Skills & Proficiencies Required):
List:
- Experienced knowledge of medical device manufacturing and validation
- Minimum five (5) years of relevant professional work experience
- Statistical and problem-solving engineering expertise (Six Sigma, SE or A3)
- Strong interpersonal and communication skills & demonstrated ability to operate as part of a team.
- Track record of innovation and adaptability in project execution, with strong problem-solving skills.
- Proven competence to evaluate communicate and act upon significant risks, demonstrating leadership of the high standards of quality and compliance.
- Strong influencing skills - Excellent interpersonal skills (written and oral).
- Decision Making – Required to make decisions on technical and management issues.
Now Qualifications (Education/Qualifications):
- Minimum of a Bachelor’s degree or University degree required; focused degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering or in a supply-chain related field preferred.
Now Skills (maybe combine Required Skills Preferred Skills list). The list includes many items: Accelerating, Analytical Reasoning, Coaching, Communication, Facility Management, Good Manufacturing Practices (GMP), Lean Manufacturing Principles, Lean Supply Chain Management, Manufacturing Engineering, Manufacturing Science and Technology (MSAT), Problem Management, Project Engineering, Project Schedule, Report Writing, Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Technologically Savvy
We could put them under Skills section as a
.
Now Benefits: we have a detailed list. We'll put under Benefits.
Now Pay: we have anticipated base pay range.
Now Schedule: Not present; we have travel up to 25% domestic & international. That's not schedule but maybe we could put under Other? But we have no Schedule section; we should not create it if no content. So omit Schedule.
We also have "Other" travel info; we could include under About the role or a separate "Other" but not required heading. Could add a paragraph under About the role about travel.
We must not include boilerplate like EEO, legal, application instructions, etc.
Now ensure we don't repeat content.
Let's craft HTML.
We'll start with About the role
then ...
.
Include location and travel maybe.
Let's write:
About the role
Johnson & Johnson is recruiting for a Senior Engineer to join our Network Tech Ops team in either Raynham, MA or Cork, Ireland. As part of DePuy Synthes Network Edge strategy we are increasing global Manufacturing capacity within the DPS Orthopaedic franchise. This role will execute engineering deliverables in support of large-scale manufacturing capacity projects that will yield stable, reliable and cost-effective manufacturing process meeting projects FPO’s of capacity, product cost, budget and timeline. The scope includes project delivery as well as ensuring knowledge transfer to developing manufacturing site staff and will work in collaboration with the existing DPS functional organizations to ensure standardization and the implementation of Best-in-Class practices. The position may require up to 25% domestic and international travel.
Now Responsibilities:
Responsibilities
- Supporting delivery of robust and fully developed and qualified orthopaedic implant manufacturing processes to Network Edge projects
- Ensure that all project activities are conducted in line with procedures and controls outlined in the QMS and that the quality and performance of the product conforms to specified standards and in compliance with the recognized Regulatory Standards for relevant markets.
- Collaborate with functional stakeholders to ensure that technical, validation and regulatory strategies are implemented in an efficient and compliant manner and at an appropriate risk level
- Partner with Regulatory to execute the strategy necessary for all filings, inspections, and registrations in multiple sites and countries.
- Communicates with internal and external partners to coordinate and execute project plans. Provides technical leadership and supports execution of EHS&S policies and procedures
- Supporting technical collaboration across functions
- Leads effective and timely communication processes and stakeholder management processes within the project scope and ensures project and program activities are consistently documented.
Now Requirements:
Requirements
- Experienced knowledge of medical device manufacturing and validation
- Minimum five (5) years of relevant professional work experience
- Statistical and problem-solving engineering expertise (Six Sigma, SE or A3)
- Strong interpersonal and communication skills & demonstrated ability to operate as part of a team.
- Track record of innovation and adaptability in project execution, with strong problem-solving skills.
- Proven competence to evaluate communicate and act upon significant risks, demonstrating leadership of the high standards of quality and compliance.
- Strong influencing skills - Excellent interpersonal skills (written and oral).
- Decision Making – Required to make decisions on technical and management issues.
Now Qualifications:
Qualifications
- Minimum of a Bachelor’s degree or University degree required; focused degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering or in a supply-chain related field preferred.
Now Skills:
Skills
- Accelerating
- Analytical Reasoning
- Coaching
- Communication
- Facility Management
- Good Manufacturing Practices (GMP)
- Lean Manufacturing Principles
- Lean Supply Chain Management
- Manufacturing Engineering
- Manufacturing Science and Technology (MSAT)
- Problem Management
- Project Engineering
- Project Schedule
- Report Writing
- Safety-Oriented
- Science, Technology, Engineering, and Math (STEM) Application
- Technologically Savvy
Now Benefits:
We need to capture the benefits list exactly as given.
Let's extract:
- Vacation –120 hours per calendar year
- Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
- Holiday pay, including Floating Holidays –13 days per calendar year
- Work, Personal and Family Time - up to 40 hours per calendar year
- Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
- Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
- Caregiver Leave – 80 hours in a 52-week rolling period
- Volunteer Leave – 32 hours per calendar year
- Military Spouse Time-Off – 80 hours per calendar year
- Additionally: "Subject to
About the role
Johnson & Johnson is recruiting for a Senior Engineer to join our Network Tech Ops team in either Raynham, MA or Cork, Ireland. As part of DePuy Synthes Network Edge strategy we are increasing global Manufacturing capacity within the DPS Orthopaedic franchise. This role will execute engineering deliverables in support of large-scale manufacturing capacity projects that will yield stable, reliable and cost-effective manufacturing process meeting projects FPO’s of capacity, product cost, budget and timeline. The scope includes project delivery as well as ensuring knowledge transfer to developing manufacturing site staff and will work in collaboration with the existing DPS functional organizations to ensure standardization and the implementation of Best-in-Class practices.
That captures job purpose and description. We could also include location info maybe in awithin About the role. Add: Locations: Raynham, Massachusetts, United States of America; Ringaskiddy, Cork, Ireland. Now Responsibilities: Take the bullet list from "Key Responsibilities". Let's extract each sentence: - Supporting delivery of robust and fully developed and qualified orthopaedic implant manufacturing processes to Network Edge projects - Ensure that all project activities are conducted in line with procedures and controls outlined in the QMS and that the quality and performance of the product conforms to specified standards and in compliance with the recognized Regulatory Standards for relevant markets. - Collaborate with functional stakeholders to ensure that technical, validation and regulatory strategies are implemented in an efficient and compliant manner and at an appropriate risk level - Partner with Regulatory to execute the strategy necessary for all filings, inspections, and registrations in multiple sites and countries. - Communicates with internal and external partners to coordinate and execute project plans. Provides technical leadership and supports execution of EHS&S policies and procedures - Supporting technical collaboration across functions - Leads effective and timely communication processes and stakeholder management processes within the project scope and ensures project and program activities are consistently documented. We need to ensure each is a
- .
Now Benefits: we have a detailed list. We'll put under Benefits.
Now Pay: we have anticipated base pay range.
Now Schedule: Not present; we have travel up to 25% domestic & international. That's not schedule but maybe we could put under Other? But we have no Schedule section; we should not create it if no content. So omit Schedule.
We also have "Other" travel info; we could include under About the role or a separate "Other" but not required heading. Could add a paragraph under About the role about travel.
We must not include boilerplate like EEO, legal, application instructions, etc.
Now ensure we don't repeat content.
Let's craft HTML.
We'll start with
- Supporting delivery of robust and fully developed and qualified orthopaedic implant manufacturing processes to Network Edge projects
- Ensure that all project activities are conducted in line with procedures and controls outlined in the QMS and that the quality and performance of the product conforms to specified standards and in compliance with the recognized Regulatory Standards for relevant markets.
- Collaborate with functional stakeholders to ensure that technical, validation and regulatory strategies are implemented in an efficient and compliant manner and at an appropriate risk level
- Partner with Regulatory to execute the strategy necessary for all filings, inspections, and registrations in multiple sites and countries.
- Communicates with internal and external partners to coordinate and execute project plans. Provides technical leadership and supports execution of EHS&S policies and procedures
- Supporting technical collaboration across functions
- Leads effective and timely communication processes and stakeholder management processes within the project scope and ensures project and program activities are consistently documented.
- Experienced knowledge of medical device manufacturing and validation
- Minimum five (5) years of relevant professional work experience
- Statistical and problem-solving engineering expertise (Six Sigma, SE or A3)
- Strong interpersonal and communication skills & demonstrated ability to operate as part of a team.
- Track record of innovation and adaptability in project execution, with strong problem-solving skills.
- Proven competence to evaluate communicate and act upon significant risks, demonstrating leadership of the high standards of quality and compliance.
- Strong influencing skills - Excellent interpersonal skills (written and oral).
- Decision Making – Required to make decisions on technical and management issues.
- Minimum of a Bachelor’s degree or University degree required; focused degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering or in a supply-chain related field preferred.
- Accelerating
- Analytical Reasoning
- Coaching
- Communication
- Facility Management
- Good Manufacturing Practices (GMP)
- Lean Manufacturing Principles
- Lean Supply Chain Management
- Manufacturing Engineering
- Manufacturing Science and Technology (MSAT)
- Problem Management
- Project Engineering
- Project Schedule
- Report Writing
- Safety-Oriented
- Science, Technology, Engineering, and Math (STEM) Application
- Technologically Savvy
About the role
then...
. Include location and travel maybe. Let's write:About the role
Johnson & Johnson is recruiting for a Senior Engineer to join our Network Tech Ops team in either Raynham, MA or Cork, Ireland. As part of DePuy Synthes Network Edge strategy we are increasing global Manufacturing capacity within the DPS Orthopaedic franchise. This role will execute engineering deliverables in support of large-scale manufacturing capacity projects that will yield stable, reliable and cost-effective manufacturing process meeting projects FPO’s of capacity, product cost, budget and timeline. The scope includes project delivery as well as ensuring knowledge transfer to developing manufacturing site staff and will work in collaboration with the existing DPS functional organizations to ensure standardization and the implementation of Best-in-Class practices. The position may require up to 25% domestic and international travel.
Now Responsibilities: