Project Farma
Senior Project/Validation Engineer
Project Farma, San Francisco, California, United States, 94199
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.
Hit Apply below to send your application for consideration Ensure that your CV is up to date, and that you have read the job specs first. Responsibilities
As a Senior Project Engineer, you will provide hands-on support and troubleshooting for clients navigating the engineering life cycle of cutting-edge equipment and manufacturing processes. 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 problem-solving to identify creative solutions. Requirements
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. 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 professional development and philanthropic opportunities. Daily activities
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, and summary reports. Execute system and process validation protocols using GxP best practices. Compensation and benefits
Competitive salary based on experience Annual discretionary bonus Medical, Dental, and Vision insurance from day one 401k Plan with company match Paid Time Off and company holidays Company paid maternity and parental leave Continuing Education Assistance About us We are a Patient Focused, People First delivery team committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. We provide project management, validation, engineering, quality/compliance, and consulting services to support partners across the life science space. Equal Employment Opportunity : 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 require a reasonable accommodation to participate in the application process, please contact us.
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Hit Apply below to send your application for consideration Ensure that your CV is up to date, and that you have read the job specs first. Responsibilities
As a Senior Project Engineer, you will provide hands-on support and troubleshooting for clients navigating the engineering life cycle of cutting-edge equipment and manufacturing processes. 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 problem-solving to identify creative solutions. Requirements
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. 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 professional development and philanthropic opportunities. Daily activities
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, and summary reports. Execute system and process validation protocols using GxP best practices. Compensation and benefits
Competitive salary based on experience Annual discretionary bonus Medical, Dental, and Vision insurance from day one 401k Plan with company match Paid Time Off and company holidays Company paid maternity and parental leave Continuing Education Assistance About us We are a Patient Focused, People First delivery team committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. We provide project management, validation, engineering, quality/compliance, and consulting services to support partners across the life science space. Equal Employment Opportunity : 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 require a reasonable accommodation to participate in the application process, please contact us.
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