Job Details

Join to apply for the Project Engineer / Senior Project Engineer role at Project Farma (PF)

Overview

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.

Responsibilities

• 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 escalate roadblocks and utilize critical thinking skills and knowledge of problem-solving skills to identify creative solutions to those problems and roadblocks.

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 the involvement in professional development and philanthropic opportunities.

Day-to-day

• 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.

Required 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).


• Full-time on-site client presence.


• Willingness to travel as required to support project and business needs.

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.

Compensation and Benefits

• 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

About the Company / Equal Opportunity

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.

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.

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.