Project Engineer - W-2 Full-time On-site
Project Engineer - W-2 Full-time On-site
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Job Description
Intrepid: Project Engineer
We are proud to be aGreat Place To Work US Certified company!Check out what our employees say makes working here so great: Pros seeks an experienced Project Engineer W2 Fulltime Onsite
Benefits: #ValuePeople
Includes a highquality benefit package: 401(k) with a 5 company match with no requirement to match and immediate vesting flex time off group healthcare plans dental vision life AD&D HSA/FSA/DCA EAP competitive compensation Stock Appreciation Rights (SAR) Plan paid floating holidays and paid time off.
What You Can Expect:
- Hard work relentless challenges and the pressure of high expectations.
- Generous recognition in times of success yet unwavering support during setbacks.
- A journey that will test your limits and push you to new heights.
- The opportunity to make a significant impact and leave a legacy.
- The camaraderie of a dedicated and passionate team.
This role requires a minimum of 3 years of experience in the Food Pharmaceutical Animal Health Medical Device or BioPharmaceutical manufacturing industries.
Be part of an exciting startup that supports the worlds leading pharmaceutical medical device food and animal health companies. Attain the best of both worlds. Gain experience at a company that leads projects for global pharmaceutical companies while enjoying the flexibility energy and personal attention that can only be found working in a small closeknit company.
What You Can Expect:
- Hard work relentless challenges and the pressure of high expectations.
- Generous recognition in times of success yet unwavering support during setbacks.
- A journey that will test your limits and push you to new heights.
- The opportunity to make a significant impact and leave a legacy.
- The camaraderie of a dedicated and passionate team.
What does it mean to be a Project Engineer with GMP Pros
The Essential Duties:
- Develop a detailed business case and project justification to support the capital expenditure for a large $20MM$25MM) biotech construction project.
- Develop comprehensive project plans including scope schedule WBS and budget.
- Identify and deploy resource and project needs across the project lifecycle.
- Coordinate with internal teams external stakeholders and vendors to ensure project objectives are met.
- Support conceptual and feasibility assessments and requirements.
- Oversee the design and construction of office space gowning rooms and Grade D rooms/corridors to include Personnel and Material Air Locks.
- Prepare technical documentation such as drawings specifications and reports.
- Identify and support permitting requirements as needed.
- Monitor project progress identify and escalate potential risks and recommend solutions to mitigate issues.
- Support procurement activities including sourcing materials and negotiating with suppliers/vendors.
- Ensure compliance with CFR USP requirements industry standards EHS and Client company policies.
- Maintain clear communication with team members contractors and clients.
- Prepare regular status updates and progress reports for project stakeholders.
- Assist in commissioning and qualification phases to verify system performance and compliance.
Here are the requirements we are looking for:
- Bachelors degree in an engineering field (Mechanical Chemical Biomedical preferred).
- At least10 years in a project engineering or project management role within an FDA regulated production facility.
- Proven experience and expert knowledge in the use of project management tools and methodologies.
- Proven understanding of the project lifecycle.
- Proven ability to influence decision making with executive level stakeholders.
- Proven exceptional social and diplomacy skills.
- Proven ability to lead and manage a team across a multidepartmental project with direct and indirect management of functional resources.
- Fully leveraging the power of Microsoft platforms to support team collaboration and communication.
- Excellent communication and organization skills with an analytical and problemsolving mindset.
- Documented success with leading capital projects in excess of $10MM.
- Proven ability to operate under highpressure in a timeline constrained environment.
Key Words:Pharma BioTech Biologics eBR MES Project Management Project Engineering
Preferred Qualities and Traits:
- Must be driven to seek out new opportunities ask questions and keep pursuing things when information is limited or not given at all.
- Must be able to quickly turn information received into concise verbiage on paper. Complete stories must be told of events that occurred and actions to be taken but should not use fluff.
- Must be capable of leading and championing change in a highstress environment.
- Must advocate for and endorse changes required for successful outcomes and subsequently influence others when change has negative perceptions or connotations.
- Must be an ambassador of GMP Pros and reflect company Core Values through excellence of .
- Must be capable of learning and understanding new or foreign processes.
- Must be able to adapt to changes and continue making progress.
- Must be patient and focused while also having a continuous sense of urgency.
- Must be able to perform work under rigid timelines in support of client success.
PreEmployment Requirements:
- Pass and maintain preemployment/contract background check and safety certification including but not limited to outstanding professional references.
- Subject to motor vehicle report review.
- Maintain valid drivers license and endorsements as required per position.
- Pass preemployment/contract physical medical evaluation and drug screen due to the safety sensitive nature of this position.
- Successfully complete and maintain any required safety certification and testing on an annual basis.
GMP Pros is an Equal Employment Opportunity / Affirmative Employer (EEO/AA) and actively seeks to diversify its work force. Therefore all qualified applicants regardless of race color national origin religion gender gender identity sexual orientation age disability or veteran status are strongly encouraged to is the policy ofGMP Prosto provide equal opportunity in employment for all qualified individuals regardless of race color religion ethnicity national origin ancestry disability medical condition age citizenship sex sexual orientation gender gender identity gender expression marital status pregnancy genetic information military status veteran status and any other characteristic protected by law.
By submitting material for consideration for this position you are attesting that no material or interaction with GMP Pros Team Members establishes any obligation for GMP Pros to hire you. If you are hired you understand that either GMP Pros or you can terminate your employment at any time and for any reason with or without cause and without prior notice. Further you understand that no representative of GMP Pros has the authority to make any assurance to the contrary.
By submitting your application for this position you attest that you have given GMP Pros true and complete information on this application. No requested information has been concealed. You are authorizing GMP Pros to contact references provided for employment reference checks. If any information youhave provided is untrue or if you have concealed material information you understand this will constitute cause for the denial of employment or immediate dismissal.
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Required Experience:
Senior IC
Employment Type
Full-Time
