Senior Project / Validation Engineer

Project Farma (PF); Houston (TX); On-site; Full time

Benefits offered by this job

Competitive salary

Annual discretionary bonus

Medical, Dental, and Vision insurance

401k Plan with company match

Paid Time Off and Company Paid Holidays

Company Paid Maternity and Parental Leave

Continuing Education Assistance

Job summary

A leading consulting firm in healthcare is seeking a Project Engineer to deliver hands-on support and troubleshoot engineering life cycles for clients. This role requires a Bachelor's degree in Life Science or Engineering and a willingness to travel. You'll be part of a dynamic team focused on providing innovative solutions and improving client outcomes. Competitive salary, annual bonus, and comprehensive benefits are offered.

Qualifications

• Experience in CQV engineering, cGMP facility start-up, and project management.
• Willingness to travel as required.

Responsibilities

• Provide hands-on support and troubleshooting for clients.
• Create alignment with cross-functional client departments.
• Proactively identify and escalate roadblocks.

Skills

Detail-oriented

Problem-solving skills

Leadership qualities

Education

Bachelor’s Degree in Life Science, Engineering, or related discipline

Job description

Overview

Welcome to the forefront of innovation in cutting edge patient centered treatments. We are seeking a Project Engineer to join our high performing organization. Our dynamic team is composed of professionals who are passionate about delivering high quality work and changing the lives of patients across the globe. If you thrive in a fast-paced environment and are ready to make a real impact, Project Farma invites you to join our team.

Responsibilities

• Provide hands-on support and troubleshooting for clients navigating the engineering life cycle of cutting-edge equipment and manufacturing processes.
• Create alignment with cross-functional client departments including, but not limited to, Validation, Manufacturing, Quality, Supply Chain, and Engineering.
• Proactively identify and escalate roadblocks and apply problem-solving skills to develop creative solutions.
• 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 and Qualifications

• Bachelor’s Degree in Life Science, Engineering, or related discipline (or an equivalent combination of 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.

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.

Compensation and Benefits

• Competitive salary based on experience.
• Annual discretionary bonus.
• Medical, Dental, and Vision insurance effective on 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 and 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. We are 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.

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. The disclosed range is a general guide and may be adjusted based on experience and location. This role may be 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.

If you have a disability and require a reasonable accommodation to complete any part of the application process, please contact us at [e-mail].

For CA applicants, please refer to our CA Privacy Notice. It has come to our attention that some individuals or organizations are posing as potential employers offering enticing employment offers. These offers are not associated with our company. We will not extend a job offer without prior communication with our recruiting team, hiring managers, and a formal interview process.