Technical Project Manager - W-2 Full-Time HybridRemote
Technical Project Manager - W-2 Full-Time HybridRemote
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Job Description
Intrepid:Technical Project Manager
We are proud to be aGreat Place To Work US Certified company!
Check out what our employees say makes working here so great: Technical Project Manager W2 FullTime Hybrid (Remote) with Limited Travel 10 or Less)
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.
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.
What does it mean to be a Technical Project Manager with GMP Pros
The Essential Duties:
Apply bestinclass governance and deployment lifecyclefor client MES project across multiple Unit Ops.
Develop and maintain detailed project plans timelines and budgets for the deployment of MBRs and ESPs.
Coordinate and manage crossfunctional teams and client resources through the development and deployment of MBRs and ESPs for operational use.
Coordinate subcontractors and vendors as required for infrastructure and manufacturing/packaging retrofits.
Allocate and deploy resources as required to accomplish project deliverables and maintain timelines.
Manage project scope risks and changes while maintaining adherence to quality and compliance standards.
Set clear expectations assign actions and drive accountability across the project team to ensure timely completion of deliverables.
Ensure technical deliverables such as product specifications manufacturing processes and validations meet project objectives and regulatory requirements.
Develop appropriate understanding of the projectspecific lifecycle.
Ensure compliance with GMP FDA EMA and other relevant regulatory guidelines.
Act as the primary point of contact for project stakeholders including internal teams external partners and clients.
Communicate project progress risks and issues to senior leadership and stakeholders.
Define and execute project communication standards facilitate regular steering and action / status meetings and manage task list.
Define project success metrics and monitor performance against goals.
Develop manage and utilize project management tools and supplemental resources across the project lifecycle to ensure ontime onbudget delivery.
Implement lessons learned and continuous improvement strategies for future projects.
Maintenance of project risk register and management of identified project risks according to risk management plan.
Communicate clearly and definitively building a sense of confidence.
Here are the requirements we are looking for:
Bachelors degree in an engineering field (Mechanical Chemical Biomedical preferred)
At least 10 years in project management role plus 3 years prior technical experience within an FDA regulated production facility.
Proven experience and expert knowledge in the use of project management tools and methodologies.
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 $1MM.
Proven ability to operate under highpressure in a timeline constrained environment.
Some other things that would help you stand out to us:
Direct experience with deploying MES in an FDA regulated environment such as MasterControl Siemens or Tulip but especially PASX.
Experience managing projects in a Pharma or BioTech production facility.
PMP Certification a plus.
Program management experience.
Experience with validation lifecycle in a production environment.
Experience with managing and leading software development in a regulated space.
Direct supervisory and management experience a plus.
Management of capital projects in excess of $10MM.
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.
Key Words: Pharma BioTech Biologics eBR MES Technical Project Manager Project Manager PMP
GMP Pros is an Equal 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 apply. It is the policy of GMP Pros to 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 GMO 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 you have 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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This company participates in the United States Department of Homeland Security EVerify program. The EVerify program is an internetbased employment eligibility verification system operated by the U.S. Citizenship and Immigration Services. Please use the links provided for important information when applying for work with this company:Everify English / Spanish
Required Experience:
Senior IC
Employment Type
Full-Time
