Project Engineer
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Job Location:
San Mateo County, CA - USA
Monthly Salary:
USD 140000 - 140000
Experience Required:
4-5years
Posted on:
2 hours ago
Vacancies:
1 Vacancy
Job Summary
PSC Biotech provides the life sciences with essential services to ensure that health care products are developed manufactured and distributed to the highest standards in compliance with all applicable regulatory requirements.
Our goal is to skyrocket our clients success and you can be a part of our teams achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America Europe Asia and the Middle East we are proud of the roles we have fulfilled to help our clients achieve success.
The Experience
With operations spanning the globe and featuring a multi-cultural team PSC Biotech is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team you will be offered the ability to feel inspired in your career explore your professional passions and work alongside a group of people who will value and nurture your talents.
We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such you will not only be offered compensation and benefits structure that rewards you but also be provided with the tools that will help you grow and learn.
At PSC Biotech its about more than just a jobits about your career and your future.
Your Role
We are seeking a technically strong and highly organized Project Engineer with a background in construction tenant improvements and facilities engineering to support capital projects within a regulated biotech/GMP environment. This role ensures that facility modifications buildouts and engineering activities are executed efficiently safely and in compliance with industry standards.
- Manage and support facility and constructionrelated projects including tenant improvements utility modifications equipment installations and facility upgrades.
- Coordinate design reviews scheduling contractor activities and walkthroughs to maintain alignment with project scope and timelines.
- Lead or support project meetings including preparing agendas documenting minutes tracking action items and ensuring followthrough.
- Handle critical project administration tasks such as budget tracking timeline management procurement coordination and document control.
- Ensure all project work complies with GMP safety and company engineering standards.
- Support risk assessments change controls impact assessments and deviation documentation where applicable.
- Interface with crossfunctional partners (Engineering QA Validation Operations) and external vendors to ensure seamless execution.
- Assist in developing or reviewing technical documentation (URS drawings specifications commissioning plans).
- Monitor construction and installation activities to ensure adherence to design quality expectations and regulatory requirements.
Requirements
- Bachelors degree in Engineering Construction Management or a related technical field preferred.
- 27 years of experience in construction facilities engineering or capital project delivery preferably in biotech pharmaceutical or other regulated industries.
- Previous experience with tenant improvement projects.
- Experience in GMP environments preferred.
- Demonstrated ability to run meetings coordinate stakeholders and manage project administrative tasks.
- Strong communication skills and ability to collaborate with crossfunctional teams.
- Ability to manage multiple projects simultaneously in a fastpaced environment.
- Proficiency with project management tools construction documentation drawings and MS Office/SharePoint.
Benefits
Offering a full suite of benefits PSC Biotech is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance so you not only enjoy your work but also have the time and resources to live your life happy and healthy.
- Medical Dental and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents
- Insurance options for Employee Assistance Programs Basic Life Insurance Short/Long Term Disability and more.
- 401(k) and 401(k) matching
- PTO Sick Time and Paid Holidays
- Education Assistance
- Pet Insurance
- Discounted rate at Anytime Fitness
- Financial Perks and Discounts
Adhering to the requirements of Californias law on salary transparency the salary bracket for this role is set between $100000 - $120000 annually. The salary offered may be adjusted based on various factors such as the applicants qualifications skills and professional experience.
Equal Opportunity Employment Statement
PSC is committed to is committed to a policy of Equal Employment Opportunity with respect to all employees interns and applicants for employment. Consistent with this commitment our policy is to comply with all applicable federal state and local laws concerning employment discrimination. Accordingly the Company prohibits discrimination against qualified employees interns and applicants in all aspects of employment including but not limited to: recruitment interviewing hiring (or failure or refusal to hire) evaluation compensation promotion job assignment transfer demotion training leaves of absence layoff benefits use of facilities working conditions termination and employer-sponsored activities and programs including wellness social and recreational programs. Employment decisions will be made without regard to an applicants employees or interns actual or perceived: race color religion sex (including pregnancy gender identity and sexual orientation) national origin age (40 or older) disability genetic information or any other status protected by law.
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Required Skills:
Bachelors degree in Engineering or a related scientific discipline. Minimum 10 years of hands-on validation experience in GMP environments including equipment utilities and process validation. Minimum 5 years of project management experience leading large-scale CQV capital projects. Demonstrated experience serving as an Owners Representative or leading multi-disciplinary CQV programs. Strong technical background in sterile injectable or combination product manufacturing. Expertise in industry regulations validation standards and risk-based CQV methodologies. Proven ability to manage project schedules budgets and cross-functional teams. Exceptional analytical problem-solving and technical communication skills. Experience with ATEC systems preferred. Willingness to travel as required for project execution and client engagement. Must be authorized to work in the US. No C2C at this time.
Company Industry
IT Services and IT Consulting
Key Skills
- Primavera
- Microstation
- Bluebeam
- Construction Estimating
- Construction Experience
- ProCore
- Mechanical Engineering
- Project Engineering
- Project Management
- Autocad
- Project Management Software
- Microsoft Project
