5,545 Engineering Consultant jobs in the United States

Engineering Consultant

Los Angeles, California Celerity Consulting Group, LLC

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Job Description

Job Description

Job Title: Engineering Consultant
Location: Los Angeles, CA
Company: Celerity Consulting Group

About Us:
Celerity  is a dynamic risk optimization firm that empowers public utilities to transform complex data into clear, actionable insights—helping reduce risk, enhance asset performance, and deliver superior project outcomes.
With a unique blend of client-side experience and vendor-side expertise, our employees deliver high-impact analytics, strategic consulting, and project management. We tackle the energy sector’s toughest challenges through deep listening, forward-thinking strategies, and unwavering determination.
Headquartered in Walnut Creek, CA, with a nationwide remote presence, our energy engineers serve as vital connectors—bridging data, infrastructure, and field teams to ensure seamless execution and measurable results.

Position Overview:
We are currently seeking motivated and detail-oriented individuals to join our team as an Engineering Consultant . This is an excellent opportunity for recent graduates or early-career engineers to launch their careers in the consulting industry. You’ll gain hands-on experience working with top-tier clients on impactful projects.

Responsibilities of this position include but are not limited to:

  • Review existing documentation for key information and specifications
  • Analyze data using appropriate quantitative methods
  • Review and verify tabular and spatial data against design or completion drawings for accuracy and consistency
  • Provide client with necessary documentation and reports
  • Update and inform project coordinator with all relevant project status and information
  • Perform engineering design and calculations, with minimal supervision
  • Review construction documents and report
  • Prepares cost estimates and construction plans for Utility infrastructure.
  • Estimates labor and material costs.
  • Obtains joint-pole agreements & initiates right-of-way procedures, licenses, permits, etc.
  • Provide project support duties as requested by the Project Manager.
  • Review and incorporate historical data into unit and man-hour figures.
  • Adheres to safety protocols as described in the safety manual and assigned checklists
  • Monitor and ensure maintenance of tracking logs and all project coordination tools to include project status, challenges, estimated project end date, and project completion
The ideal candidate will have the following qualifications:
  • Bachelor’s Degree in Engineering or related field and/or relevant work experience 
  • Ability to read and understand general engineering documents, including drawings and specifications
  • Able to work or travel to client sites
  • Proficient use of Microsoft Office Suite (Excel, Word, SharePoint, and Outlook)
  • Highly organized, deadline driven, and detail oriented
  • Flexible, analytical, and willing to tackle challenging work
  • Ability to work independently and collaboratively in an open environment
  • Excellent verbal and written communication skills (able to present technical matters in a clear and concise manner)
  • Experience in the Gas & Utility Industry is a plus
Physical requirements:
  • Must be able to remain in a stationary position 50% of the time
  • The person in this position frequently communicates with staff/clients who have inquiries. Must be able to exchange accurate information in these situations
  • Constantly operates a computer and other office productivity equipment, such as a mouse, keyboard, scanner, copier, and calculator

See full details and meet our leadership team on our website:   

The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.

We are proud to offer a comprehensive health and welfare benefit package that includes:
HEALTH & WELL-BEING

  • Medical Insurance
  • Dental Insurance
  • Vision Insurance

PEACE OF MIND

  • Disability Insurance (STD/LTD)
  • Flexible Spending Account
  • Health Savings Account
  • Basic Life/AD&D
  • 401(k) plan

WORK/LIFE BALANCE

  • Paid Time Off
  • Company Holidays
  • Leave of Absence
  • Flexible Work Schedules

ADDITIONAL PERKS

  • Employee Referral Program
  • Professional Development
  • Charitable Contribution Match

Employee welfare and development is important to us, and we sponsor many activities outside of work to promote team building as well as sponsor formal training and certification.

Based in Walnut Creek, CA with offices nationwide, Celerity energy engineers perform a critical, leadership role as strategic liaisons between data, assets and the teams that make projects happen in the field.
See full details and meet our leadership team on our website:

Celerity is an Equal Employment Opportunity (EEO) employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veterans’ status or other status protected by applicable law.
Pursuant to the Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records.

Applicants must be authorized to work for any US employer. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

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CQV Engineering Consultant

60086 North Chicago, Illinois Project Farma

Posted 3 days ago

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Job Description

3 weeks ago Be among the first 25 applicants

Welcome to the forefront of innovation in cutting edge patient centered treatments! We are seeking the best and the brightest to join our high performing organization as a CQV Engineering Consultant. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. Our dynamic team is composed of vibrant professionals who are passionate about delivering high quality work for our partners and changing the lives of patients across the globe. If you are looking for a career accelerator, are driven by innovation, thrive in a fast-paced environment, love to travel, and are ready to make a real impact, then Project Farma wants you to join our team.

  • As a CQV Engineering Consultant , you will coordinate with cross functional client departments providing hands-on support in navigating the engineering life cycle of cutting-edge equipment and manufacturing processes. In your role, you will lead, oversee, and execute client project initiatives, plans, or workstreams including ensuring team deliverables are completed in a timely and high-quality fashion.

About you:

  • You thrive in a fast-paced environment.
  • You are detail-oriented and exhibit natural leadership qualities.
  • You enjoy engaging teams and mentoring others.
  • You are currently or will live in the area where this job is posted.
  • You have a philanthropic drive and will embody our Patient Focused and People First Mission through the involvement in professional development and philanthropic opportunities.

How will you spend your days as a CQV Engineering Consultant?

  • Develop technical documentation such as SOPs, requirements specifications, testing protocols, summary reports, etc.
  • Build internal and external understanding, buy-in, and commitment to decisions through mutual understanding, collaboration, and effective presentations skills.
  • Mentor, coach and train internal Team Members on assigned duties, industry best practices, overall understanding of the business, and project driven technical skills.
  • Develop team members with foresight to support project succession plans as identified by leadership and provide feedback to Team Members along the way.
  • Support business development initiatives through building and maintaining professional networks as well as identifying and escalating client needs along with a proposed support plan.

Examples of our core services within the life science space, include: Capital Project Management (including Project Controls and Scheduling); Facility Management & Builds; Tech Transfers; Validation Life Cycle (including Commissioning and Qualification, Process Validation, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance.

Required:

  • Bachelors Degree in Life Science, Engineering, or related discipline and/or comparable military experience.
  • A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.
  • Willingness to travel as required to support project and business needs.
  • Covid Vaccine is required prior to the Team Members start date with exceptions for medical and religious accommodations when reasonable.

In return for your skills, knowledge, and passion, we offer a wide range of benefits including:

  • Competitive salary based on experience
  • Aggressive bonus structure
  • Medical, Dental, and Vision insurance effective your first day of employment
  • 401k Plan with company match
  • Paid Time Off and Company Paid Holidays
  • Company Paid Maternity and Parental Leave
  • Continuing Education Assistance

Who are we?

We areProject Farma , the leading advanced therapy technical operations consulting company in the life science industry. As a Patient Focused, People First delivery team, we are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. Our manufacturing playbook has led to the creation of the largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding ground-breaking treatments and solutions. We believe that our culture of philanthropy, teamwork, training and development and commitment to the patient is the foundation to our teams and partners long-term success.

Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range: $50,000 USD - $40,000 USD

Any data provided as a part of this application will be stored in accordance with ourPrivacy Policy.For CA applicants, please also refer to ourCA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Seniority level
  • Seniority level Mid-Senior level
Employment type
  • Employment type Full-time
Job function
  • Job function Engineering and Information Technology
  • Industries Technology, Information and Internet

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Data Engineering Consultant

78716 Austin, Texas eClercx

Posted 7 days ago

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Job Description

Job Description

Data Engineering Consultant

Location: Austin, TX, onsite

Type: Full-time

Department: Digital

Summary

As a Consultant, Data Engineering , you will be at the forefront of building robust and scalable data solutions for our banking and capital markets clients. You will be responsible for designing and implementing end-to-end data pipelines that transform raw data into valuable insights. This is a critical role for an experienced professional who can translate complex business problems into actionable data engineering solutions, while working with established data infrastructures and preparing for a future transition to cloud-based technologies.

Responsibilities
  • Problem-Solving & Solution Design: Work closely with business stakeholders to understand complex business challenges and translate them into a clear, technical data engineering plan.
  • Data Pipeline Development: Design, build, and maintain efficient and reliable ETL/ELT pipelines to ingest, transform, and load large datasets from various sources.
  • Process Engineering: Design new data workflows or analyze existing ones to identify bottlenecks, then design and implement more efficient, repeatable, and scalable data processes.
  • Data Modeling: Translate technical requirements into logical and physical data models, designing relational data structures that support client analytics and reporting needs.
  • Automation and Optimization: Develop scripts and procedures to automate data delivery, reporting, and analysis, continuously optimizing these processes for performance and scalability.
  • Knowledge Transfer & Mentorship: Act as a key liaison between the on-site client team and a larger, off-shore team. You will be responsible for assimilating knowledge, creating documentation, and conducting training to ensure the wider team understands the project's architecture and can effectively contribute.
  • Client Communication: Communicate complex technical concepts clearly to both technical and non-technical audiences, acting as a trusted advisor to our clients.
Eligibility Requirements
  • A bachelor's degree in Computer Science, Engineering, or a related field.
  • 5+ years of professional experience in data engineering, building and managing large-scale data solutions.
  • Proven ability to understand business problems and translate them into actionable data engineering solutions. This requires strong analytical and problem-solving skills.
  • Deep expertise in designing and implementing ETL/ELT processes and working with very large datasets.
  • Strong experience with data modeling and relational database design.
  • Excellent communication and presentation skills, with a knack for translating technical challenges into business solutions.
  • Demonstrated experience in mentoring and teaching technical concepts to other team members.
  • Programming & Databases: Proficiency in programming languages like Python or Scala, and experience with SQL and NoSQL databases.
  • Data Platforms: Experience with data integration tools like SSIS or similar technologies.
  • Cloud & Data Platforms: While this project involves established infrastructure, familiarity with cloud platforms like AWS, GCP, or Azure, and data engineering tools such as Databricks, Snowflake, or Apache Spark is highly valued for future projects.
  • Business Intelligence: Exposure to data visualization and BI tools like Tableau, PowerBI, or QlikView.
  • Adaptability: A proven ability to quickly learn and apply new technologies and methodologies to solve complex problems. We're looking for someone who has a solid understanding of data engineering fundamentals and can adapt to different client tech stacks.


In the US, the target base salary for this role is $150,000-$180,000. Compensation is based on a range of factors that include relevant experience, knowledge, skills, other job-related qualifications, and geography. We expect the majority of candidates who are offered roles at our company to fall throughout the range based on these factors.

About eClerx

eClerx is a leading provider of productized services, bringing together people, technology and domain expertise to amplify business results.

The firm provides business process management, automation, and analytics services to a number of Fortune 2000 enterprises, including some of the world's leading financial services, communications, retail, fashion, media & entertainment, manufacturing, travel & leisure, and technology companies. Incorporated in 2000, eClerx is traded on both the Bombay and National Stock Exchanges of India. The firm employs more than 19,000 people across Australia, Canada, France, Germany, Switzerland, Eqypt. India, Italy, Netherlands, Peru, Philippines, Singapore, Thailand, the UK, and the USA.

eClerx is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law. We are also committed to protecting and safeguarding your personal data. Please find our policy here.
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CQV Engineering Consultant

20022 Washington, District Of Columbia Project Farma

Posted 9 days ago

Job Viewed

Tap Again To Close

Job Description

Welcome to the forefront of innovation in cutting edge patient centered treatments! We are seeking the best and the brightest to join our high performing organization as a CQV Engineering Consultant. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. Our dynamic team is composed of vibrant professionals who are passionate about delivering high quality work for our partners and changing the lives of patients across the globe. If you are looking for a career accelerator, are driven by innovation, thrive in a fast-paced environment, love to travel, and are ready to make a real impact, then Project Farma wants you to join our team.

  • As a CQV Engineering Consultant , you will coordinate with cross functional client departments providing hands-on support in navigating the engineering life cycle of cutting-edge equipment and manufacturing processes. In your role, you will lead, oversee, and execute client project initiatives, plans, or workstreams including ensuring team deliverables are completed in a timely and high-quality fashion.
About you:
  • You thrive in a fast-paced environment.
  • You are detail-oriented and exhibit natural leadership qualities.
  • You enjoy engaging teams and mentoring others.
  • You are currently or will live in the area where this job is posted.
  • You have a philanthropic drive and will embody our Patient Focused and People First Mission through the involvement in professional development and philanthropic opportunities.
How will you spend your days as a CQV Engineering Consultant?
  • Develop technical documentation such as SOPs, requirements specifications, testing protocols, summary reports, etc.
  • Build internal and external understanding, buy-in, and commitment to decisions through mutual understanding, collaboration, and effective presentations skills.
  • Mentor, coach and train internal Team Members on assigned duties, industry best practices, overall understanding of the business, and project driven technical skills.
  • Develop team members with foresight to support project succession plans as identified by leadership and provide feedback to Team Members along the way.
  • Support business development initiatives through building and maintaining professional networks as well as identifying and escalating client needs along with a proposed support plan.
Examples of our core services within the life science space, include: Capital Project Management (including Project Controls and Scheduling); Facility Management & Builds; Tech Transfers; Validation Life Cycle (including Commissioning and Qualification, Process Validation, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance.

Required:
  • Bachelor's Degree in Life Science, Engineering, or related discipline and/or comparable military experience.
  • A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.
  • Full-time on-site client presence.
  • Willingness to travel as required to support project and business needs.
In return for your skills, knowledge, and passion, we offer a wide range of benefits including:
  • Competitive salary based on experience
  • Aggressive bonus structure
  • Medical, Dental, and Vision insurance effective your first day of employment
  • 401k Plan with company match
  • Paid Time Off and Company Paid Holidays
  • Company Paid Maternity and Parental Leave
  • Continuing Education Assistance

Who are we?

We are Project Farma , the leading advanced therapy technical operations consulting company in the life science industry. As a Patient Focused, People First delivery team, we are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. Our manufacturing playbook has led to the creation of the largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding ground-breaking treatments and solutions. We believe that our culture of philanthropy, teamwork, training and development and commitment to the patient is the foundation to our teams' and partners' long-term success.

Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$50,000-$240,000 USD

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
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CQV Engineering Consultant

60290 Chicago, Illinois Project Farma

Posted 17 days ago

Job Viewed

Tap Again To Close

Job Description

Welcome to the forefront of innovation in cutting edge patient centered treatments! We are seeking the best and the brightest to join our high performing organization as a CQV Engineering Consultant. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. Our dynamic team is composed of vibrant professionals who are passionate about delivering high quality work for our partners and changing the lives of patients across the globe. If you are looking for a career accelerator, are driven by innovation, thrive in a fast-paced environment, love to travel, and are ready to make a real impact, then Project Farma wants you to join our team.

  • As a CQV Engineering Consultant , you will coordinate with cross functional client departments providing hands-on support in navigating the engineering life cycle of cutting-edge equipment and manufacturing processes. In your role, you will lead, oversee, and execute client project initiatives, plans, or workstreams including ensuring team deliverables are completed in a timely and high-quality fashion.
About you:
  • You thrive in a fast-paced environment.
  • You are detail-oriented and exhibit natural leadership qualities.
  • You enjoy engaging teams and mentoring others.
  • You are currently or will live in the area where this job is posted.
  • You have a philanthropic drive and will embody our Patient Focused and People First Mission through the involvement in professional development and philanthropic opportunities.
How will you spend your days as a CQV Engineering Consultant?
  • Develop technical documentation such as SOPs, requirements specifications, testing protocols, summary reports, etc.
  • Build internal and external understanding, buy-in, and commitment to decisions through mutual understanding, collaboration, and effective presentations skills.
  • Mentor, coach and train internal Team Members on assigned duties, industry best practices, overall understanding of the business, and project driven technical skills.
  • Develop team members with foresight to support project succession plans as identified by leadership and provide feedback to Team Members along the way.
  • Support business development initiatives through building and maintaining professional networks as well as identifying and escalating client needs along with a proposed support plan.
Examples of our core services within the life science space, include: Capital Project Management (including Project Controls and Scheduling); Facility Management & Builds; Tech Transfers; Validation Life Cycle (including Commissioning and Qualification, Process Validation, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance.

Required:
  • Bachelor's Degree in Life Science, Engineering, or related discipline and/or comparable military experience.
  • A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.
  • Full-time on-site client presence.
  • Willingness to travel as required to support project and business needs.
In return for your skills, knowledge, and passion, we offer a wide range of benefits including:
  • Competitive salary based on experience
  • Aggressive bonus structure
  • Medical, Dental, and Vision insurance effective your first day of employment
  • 401k Plan with company match
  • Paid Time Off and Company Paid Holidays
  • Company Paid Maternity and Parental Leave
  • Continuing Education Assistance

Who are we?

We are Project Farma , the leading advanced therapy technical operations consulting company in the life science industry. As a Patient Focused, People First delivery team, we are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. Our manufacturing playbook has led to the creation of the largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding ground-breaking treatments and solutions. We believe that our culture of philanthropy, teamwork, training and development and commitment to the patient is the foundation to our teams' and partners' long-term success.

Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$50,000-$240,000 USD

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
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CQV Engineering Consultant

46262 Indianapolis, Indiana Project Farma

Posted 17 days ago

Job Viewed

Tap Again To Close

Job Description

Welcome to the forefront of innovation in cutting edge patient centered treatments! We are seeking the best and the brightest to join our high performing organization as a CQV Engineering Consultant. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. Our dynamic team is composed of vibrant professionals who are passionate about delivering high quality work for our partners and changing the lives of patients across the globe. If you are looking for a career accelerator, are driven by innovation, thrive in a fast-paced environment, love to travel, and are ready to make a real impact, then Project Farma wants you to join our team.

  • As a CQV Engineering Consultant , you will coordinate with cross functional client departments providing hands-on support in navigating the engineering life cycle of cutting-edge equipment and manufacturing processes. In your role, you will lead, oversee, and execute client project initiatives, plans, or workstreams including ensuring team deliverables are completed in a timely and high-quality fashion.
About you:
  • You thrive in a fast-paced environment.
  • You are detail-oriented and exhibit natural leadership qualities.
  • You enjoy engaging teams and mentoring others.
  • You are currently or will live in the area where this job is posted.
  • You have a philanthropic drive and will embody our Patient Focused and People First Mission through the involvement in professional development and philanthropic opportunities.
How will you spend your days as a CQV Engineering Consultant?
  • Develop technical documentation such as SOPs, requirements specifications, testing protocols, summary reports, etc.
  • Build internal and external understanding, buy-in, and commitment to decisions through mutual understanding, collaboration, and effective presentations skills.
  • Mentor, coach and train internal Team Members on assigned duties, industry best practices, overall understanding of the business, and project driven technical skills.
  • Develop team members with foresight to support project succession plans as identified by leadership and provide feedback to Team Members along the way.
  • Support business development initiatives through building and maintaining professional networks as well as identifying and escalating client needs along with a proposed support plan.
Examples of our core services within the life science space, include: Capital Project Management (including Project Controls and Scheduling); Facility Management & Builds; Tech Transfers; Validation Life Cycle (including Commissioning and Qualification, Process Validation, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance.

Required:
  • Bachelor's Degree in Life Science, Engineering, or related discipline and/or comparable military experience.
  • A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.
  • Full-time on-site client presence.
  • Willingness to travel as required to support project and business needs.
In return for your skills, knowledge, and passion, we offer a wide range of benefits including:
  • Competitive salary based on experience
  • Aggressive bonus structure
  • Medical, Dental, and Vision insurance effective your first day of employment
  • 401k Plan with company match
  • Paid Time Off and Company Paid Holidays
  • Company Paid Maternity and Parental Leave
  • Continuing Education Assistance

Who are we?

We are Project Farma , the leading advanced therapy technical operations consulting company in the life science industry. As a Patient Focused, People First delivery team, we are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. Our manufacturing playbook has led to the creation of the largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding ground-breaking treatments and solutions. We believe that our culture of philanthropy, teamwork, training and development and commitment to the patient is the foundation to our teams' and partners' long-term success.

Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$50,000-$240,000 USD

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
View Now

CQV Engineering Consultant

92189 San Diego Country Estates, California Project Farma

Posted 17 days ago

Job Viewed

Tap Again To Close

Job Description

Welcome to the forefront of innovation in cutting edge patient centered treatments! We are seeking the best and the brightest to join our high performing organization as a CQV Engineering Consultant. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. Our dynamic team is composed of vibrant professionals who are passionate about delivering high quality work for our partners and changing the lives of patients across the globe. If you are looking for a career accelerator, are driven by innovation, thrive in a fast-paced environment, love to travel, and are ready to make a real impact, then Project Farma wants you to join our team.

  • As a CQV Engineering Consultant , you will coordinate with cross functional client departments providing hands-on support in navigating the engineering life cycle of cutting-edge equipment and manufacturing processes. In your role, you will lead, oversee, and execute client project initiatives, plans, or workstreams including ensuring team deliverables are completed in a timely and high-quality fashion.
About you:
  • You thrive in a fast-paced environment.
  • You are detail-oriented and exhibit natural leadership qualities.
  • You enjoy engaging teams and mentoring others.
  • You are currently or will live in the area where this job is posted.
  • You have a philanthropic drive and will embody our Patient Focused and People First Mission through the involvement in professional development and philanthropic opportunities.
How will you spend your days as a CQV Engineering Consultant?
  • Develop technical documentation such as SOPs, requirements specifications, testing protocols, summary reports, etc.
  • Build internal and external understanding, buy-in, and commitment to decisions through mutual understanding, collaboration, and effective presentations skills.
  • Mentor, coach and train internal Team Members on assigned duties, industry best practices, overall understanding of the business, and project driven technical skills.
  • Develop team members with foresight to support project succession plans as identified by leadership and provide feedback to Team Members along the way.
  • Support business development initiatives through building and maintaining professional networks as well as identifying and escalating client needs along with a proposed support plan.
Examples of our core services within the life science space, include: Capital Project Management (including Project Controls and Scheduling); Facility Management & Builds; Tech Transfers; Validation Life Cycle (including Commissioning and Qualification, Process Validation, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance.

Required:
  • Bachelor's Degree in Life Science, Engineering, or related discipline and/or comparable military experience.
  • A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.
  • Full-time on-site client presence.
  • Willingness to travel as required to support project and business needs.
In return for your skills, knowledge, and passion, we offer a wide range of benefits including:
  • Competitive salary based on experience
  • Aggressive bonus structure
  • Medical, Dental, and Vision insurance effective your first day of employment
  • 401k Plan with company match
  • Paid Time Off and Company Paid Holidays
  • Company Paid Maternity and Parental Leave
  • Continuing Education Assistance

Who are we?

We are Project Farma , the leading advanced therapy technical operations consulting company in the life science industry. As a Patient Focused, People First delivery team, we are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. Our manufacturing playbook has led to the creation of the largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding ground-breaking treatments and solutions. We believe that our culture of philanthropy, teamwork, training and development and commitment to the patient is the foundation to our teams' and partners' long-term success.

Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$50,000-$240,000 USD

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
View Now
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About the latest Engineering consultant Jobs in United States !

CQV Engineering Consultant

19117 Philadelphia, Pennsylvania Project Farma

Posted 17 days ago

Job Viewed

Tap Again To Close

Job Description

Welcome to the forefront of innovation in cutting edge patient centered treatments! We are seeking the best and the brightest to join our high performing organization as a CQV Engineering Consultant. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. Our dynamic team is composed of vibrant professionals who are passionate about delivering high quality work for our partners and changing the lives of patients across the globe. If you are looking for a career accelerator, are driven by innovation, thrive in a fast-paced environment, love to travel, and are ready to make a real impact, then Project Farma wants you to join our team.

  • As a CQV Engineering Consultant , you will coordinate with cross functional client departments providing hands-on support in navigating the engineering life cycle of cutting-edge equipment and manufacturing processes. In your role, you will lead, oversee, and execute client project initiatives, plans, or workstreams including ensuring team deliverables are completed in a timely and high-quality fashion.
About you:
  • You thrive in a fast-paced environment.
  • You are detail-oriented and exhibit natural leadership qualities.
  • You enjoy engaging teams and mentoring others.
  • You are currently or will live in the area where this job is posted.
  • You have a philanthropic drive and will embody our Patient Focused and People First Mission through the involvement in professional development and philanthropic opportunities.
How will you spend your days as a CQV Engineering Consultant?
  • Develop technical documentation such as SOPs, requirements specifications, testing protocols, summary reports, etc.
  • Build internal and external understanding, buy-in, and commitment to decisions through mutual understanding, collaboration, and effective presentations skills.
  • Mentor, coach and train internal Team Members on assigned duties, industry best practices, overall understanding of the business, and project driven technical skills.
  • Develop team members with foresight to support project succession plans as identified by leadership and provide feedback to Team Members along the way.
  • Support business development initiatives through building and maintaining professional networks as well as identifying and escalating client needs along with a proposed support plan.
Examples of our core services within the life science space, include: Capital Project Management (including Project Controls and Scheduling); Facility Management & Builds; Tech Transfers; Validation Life Cycle (including Commissioning and Qualification, Process Validation, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance.

Required:
  • Bachelor's Degree in Life Science, Engineering, or related discipline and/or comparable military experience.
  • A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.
  • Full-time on-site client presence.
  • Willingness to travel as required to support project and business needs.
In return for your skills, knowledge, and passion, we offer a wide range of benefits including:
  • Competitive salary based on experience
  • Aggressive bonus structure
  • Medical, Dental, and Vision insurance effective your first day of employment
  • 401k Plan with company match
  • Paid Time Off and Company Paid Holidays
  • Company Paid Maternity and Parental Leave
  • Continuing Education Assistance

Who are we?

We are Project Farma , the leading advanced therapy technical operations consulting company in the life science industry. As a Patient Focused, People First delivery team, we are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. Our manufacturing playbook has led to the creation of the largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding ground-breaking treatments and solutions. We believe that our culture of philanthropy, teamwork, training and development and commitment to the patient is the foundation to our teams' and partners' long-term success.

Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$50,000-$240,000 USD

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
View Now

CQV Engineering Consultant

07175 Newark, New Jersey Project Farma

Posted 17 days ago

Job Viewed

Tap Again To Close

Job Description

Welcome to the forefront of innovation in cutting edge patient centered treatments! We are seeking the best and the brightest to join our high performing organization as a CQV Engineering Consultant. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. Our dynamic team is composed of vibrant professionals who are passionate about delivering high quality work for our partners and changing the lives of patients across the globe. If you are looking for a career accelerator, are driven by innovation, thrive in a fast-paced environment, love to travel, and are ready to make a real impact, then Project Farma wants you to join our team.

  • As a CQV Engineering Consultant , you will coordinate with cross functional client departments providing hands-on support in navigating the engineering life cycle of cutting-edge equipment and manufacturing processes. In your role, you will lead, oversee, and execute client project initiatives, plans, or workstreams including ensuring team deliverables are completed in a timely and high-quality fashion.
About you:
  • You thrive in a fast-paced environment.
  • You are detail-oriented and exhibit natural leadership qualities.
  • You enjoy engaging teams and mentoring others.
  • You are currently or will live in the area where this job is posted.
  • You have a philanthropic drive and will embody our Patient Focused and People First Mission through the involvement in professional development and philanthropic opportunities.
How will you spend your days as a CQV Engineering Consultant?
  • Develop technical documentation such as SOPs, requirements specifications, testing protocols, summary reports, etc.
  • Build internal and external understanding, buy-in, and commitment to decisions through mutual understanding, collaboration, and effective presentations skills.
  • Mentor, coach and train internal Team Members on assigned duties, industry best practices, overall understanding of the business, and project driven technical skills.
  • Develop team members with foresight to support project succession plans as identified by leadership and provide feedback to Team Members along the way.
  • Support business development initiatives through building and maintaining professional networks as well as identifying and escalating client needs along with a proposed support plan.
Examples of our core services within the life science space, include: Capital Project Management (including Project Controls and Scheduling); Facility Management & Builds; Tech Transfers; Validation Life Cycle (including Commissioning and Qualification, Process Validation, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance.

Required:
  • Bachelor's Degree in Life Science, Engineering, or related discipline and/or comparable military experience.
  • A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.
  • Full-time on-site client presence.
  • Willingness to travel as required to support project and business needs.
In return for your skills, knowledge, and passion, we offer a wide range of benefits including:
  • Competitive salary based on experience
  • Aggressive bonus structure
  • Medical, Dental, and Vision insurance effective your first day of employment
  • 401k Plan with company match
  • Paid Time Off and Company Paid Holidays
  • Company Paid Maternity and Parental Leave
  • Continuing Education Assistance

Who are we?

We are Project Farma , the leading advanced therapy technical operations consulting company in the life science industry. As a Patient Focused, People First delivery team, we are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. Our manufacturing playbook has led to the creation of the largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding ground-breaking treatments and solutions. We believe that our culture of philanthropy, teamwork, training and development and commitment to the patient is the foundation to our teams' and partners' long-term success.

Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$50,000-$240,000 USD

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
View Now

Software Engineering Consultant

99302 Pasco, Washington Ippon Technologies

Posted 21 days ago

Job Viewed

Tap Again To Close

Job Description

We're hiring a Software Engineering Consultant

Employment type: Full Time/Direct Hire (No Agencies)

Location: Atlanta, GA Metro, Washington DC Metro, Charlotte Metro, NYC, or Richmond, VA

Location Type: Hybrid - Home Office/Local Ippon Office (1-2 days per week onsite)

About Ippon:

The Ippon story started in 2002 in Paris, France - cue in the accordion. Our founder and CEO Stéphane Nomis used his unique experience as an international Judo champion to create a culture based on the sports values of ambition and excellence. Our USA Headquarters office is located in Richmond, VA, with additional offices in New York, NY, Washington DC, and Atlanta, GA. We are a technology consulting firm that specializes in helping accelerate our client's digital roadmap in the areas of Product Management, Cloud, Data, and Software Engineering.

About the position:

We are looking to add a motivated and experienced Full-stack Product Engineering Consultant, with some experience in data engineering to our tech consulting team. Whether it is a migration or a new client assessment, this role will be responsible for designing, developing, and maintaining software applications that meet the needs of our clients. You will collaborate with cross-functional teams to define project requirements and ensure the successful delivery of high-quality software solutions. As a member of our team, you will have the opportunity to work on a diverse range of projects in a dynamic and fast-paced environment. You will use your technical expertise to solve complex problems and contribute to the improvement of our clients' software development processes.

Roles and Responsibilities:
    • Technical:
    • Design, code, and debug software applications utilizing industry best practices in various languages and frameworks
    • Develop robust backend systems, emphasizing RESTful services, ORM, CRUD operations, and OAuth 2.0, with a keen understanding of DDD, Hexagonal Architecture, and API design
    • Develop and deploy applications on AWS utilizing services like AWS Lambda, AWS Fargate, and AWS ECS
    • Collaborate with cross-functional teams to define, design, and implement new features, ensuring alignment with project requirements and specifications
    • Develop and maintain comprehensive software documentation, including specifications, user manuals, and maintain high standards in code quality through regular code reviews and adherence to coding standards
    • Troubleshoot and resolve software defects and issues, contributing to the reliability and robustness of our applications
    • Consulting:
    • Participate actively in meetings and discussions, offering technical guidance and insights to support Ippon's commitment to top-notch delivery and consulting engagements
    • Ensure excellent consulting engagement experiences for clients, fostering relationships, managing external dependencies, and driving projects to successful outcomes
    • Contribute effectively to projects within a short onboarding period
    • Build and maintain strong relationships with the client's peer engineers, effectively driving work and managing work's dependencies within the client ecosystem
    • Proactively pull work to accomplish project goals, with a continuous drive to expand the scope of influence and delivery
    • Personal Development:
    • Contribute to thought leadership through participation in conferences, events, blogging, and white-paper drafting, promoting the brand, and fostering sales leads
    • Stay abreast of the latest technologies, frameworks, and best practices in the field, continuously improving technical skills
Competencies we are looking for:
    • Minimum:
    • 3+ years of production software development experience using Go and/or Java.
    • 3+ years of experience with JavaScript, TypeScript, or Python is a plus.
    • 2+ years of experience in cloud-based solutions, familiar with container-based architectures and serverless technologies
    • 2+ years of experience with SQL and NoSQL databases, capable of complex querying and modeling
    • 2+ years of proven experience working collaboratively on a team to develop applications that read and write data from a data store in the cloud
    • Proficiency in testing methodologies, including unit testing with JUnit/ Jest and E2E testing with tools like Godog, Cucumber, Cypress, or Gatling
    • Strong knowledge of software engineering principles and methodologies
    • Experience in Agile project environments and cloud-based solution development
    • Preferred:
    • Bachelor's degree in Computer Science or a related field, or equivalent work experience
    • Skilled in DevOps practices, effectively using pipelines to contribute to projects and ensure quality deliverables
    • Experience with infrastructure as code (IaC) tools like Terraform or CloudFormation for managing AWS resources is desirable.
    • Strong understanding and experience with containerization technologies, such as Docker
    • Demonstrated ability to learn quickly and contribute significantly within a short period
What we offer:
    • Competitive salary - Great starting salaries for well-qualified candidates
    • Generous Paid Time Off policy - Ippon offers flexible time off to help you be your best
    • Health, dental, and vision insurance - We are dedicated to helping our employees live healthier lives through comprehensive health programs
    • 401k with company match - Ippon offers an industry-leading 401(k) matching plan
    • Family Leave - We support the importance of family and offer maternity, paternity, and family medical leave plans
    • A fun, smart, and healthy work environment, focused on our values and teamwork


$115,000 - $130,000 a year

We value the diversity and different perspectives each of our employees bring to Ippon Technologies.

Ippon Technologies is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, age, national origin, veteran, or disability status.

Visit us on LinkedIn or at to learn more.

So, do YOU speak Ippon?
View Now
 

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