Project Farma
Project / Validation Engineer Chicago, Illinois, United States
Project Farma, Chicago, Illinois, United States, 60290
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 Project Engineer. 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
Project Engineer , you will provide hands-on support and troubleshooting for clients navigating the engineering life cycle of cutting-edge equipment and manufacturing processes. In your role, you will create alignment with cross-functional client departments including, but not limited to, Validation, Manufacturing, Quality, Supply Chain, and Engineering. You will proactively identify and elevate roadblocks and utilize critical thinking skills and knowledge of problem-solving skills to identify creative solutions to those problems and roadblocks.
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.
About You
You thrive in a fast-paced environment.
You are detail-oriented and exhibit natural leadership qualities.
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 involvement in professional development and philanthropic opportunities.
Day-to-Day Responsibilities
Provide support and troubleshooting to clients regarding equipment and manufacturing processes.
Perform due diligence on system and subject domains to generate high-quality project deliverables.
Author technical documents such as SOPs, requirements specifications, testing protocols, summary reports, etc.
Execute system and process validation protocols using GxP best practices.
Qualifications
Bachelor’s Degree in Life Science, Engineering, or related discipline (or a combination of equivalent work experience in CQV engineering, cGMP facility start-up, project management and/or comparable military experience).
Willingness to travel as required to support project and business needs.
Benefits
Competitive salary based on experience
Annual bonus (discretionary)
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
About Us 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 groundbreaking 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.
Compensation range: $50,000 - $240,000 USD.
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.
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As a
Project Engineer , you will provide hands-on support and troubleshooting for clients navigating the engineering life cycle of cutting-edge equipment and manufacturing processes. In your role, you will create alignment with cross-functional client departments including, but not limited to, Validation, Manufacturing, Quality, Supply Chain, and Engineering. You will proactively identify and elevate roadblocks and utilize critical thinking skills and knowledge of problem-solving skills to identify creative solutions to those problems and roadblocks.
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.
About You
You thrive in a fast-paced environment.
You are detail-oriented and exhibit natural leadership qualities.
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 involvement in professional development and philanthropic opportunities.
Day-to-Day Responsibilities
Provide support and troubleshooting to clients regarding equipment and manufacturing processes.
Perform due diligence on system and subject domains to generate high-quality project deliverables.
Author technical documents such as SOPs, requirements specifications, testing protocols, summary reports, etc.
Execute system and process validation protocols using GxP best practices.
Qualifications
Bachelor’s Degree in Life Science, Engineering, or related discipline (or a combination of equivalent work experience in CQV engineering, cGMP facility start-up, project management and/or comparable military experience).
Willingness to travel as required to support project and business needs.
Benefits
Competitive salary based on experience
Annual bonus (discretionary)
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
About Us 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 groundbreaking 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.
Compensation range: $50,000 - $240,000 USD.
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.
#J-18808-Ljbffr