Project Engineer/Manager

Job Description

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 team’s 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 decide 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®, it is about more than just a job it is about your career and your future.

Your Role

We are hiring a Project Engineer / Manager to lead and coordinate activities related to a variety of projects within the pharmaceuticals and / or medical device manufacturing industry.

The ideal candidate will possess a technical background in engineering, validation processes, quality, and project management, coupled with excellent interpersonal and communication skills.

The Project Engineer / Project Manager will :

• Lead projects from initiation to completion, ensuring compliance with regulatory requirements and company standards.
• Develop project plans, schedules, and budgets, and track progress against milestones.
• Provide specific directions to project teams through written and verbal communication in order to execute work in a timely and efficient manner.
• Conceptualize solutions, define budgetary needs / scope, gain approval for funding, forecast spending, and accrue financials.
• Identify and proactively manage project risks. Develop mitigation plans and contingency strategies to address potential issues.
• Uphold project standards by ensuring compliance with relevant industry standards, regulations, and best practices.
• Track project performance and analyze the completion of key goals.
• Document and report project progress to stakeholders.
• Provide technical expertise and support to cross-functional teams overall.
• Provide expert-level project management for floating plant projects of high dollar value, of high complexity of extraordinary urgency, or having similar requirements.
• Foster a collaborative and positive team environment.

Requirements

At PSC Biotech, many of our projects and clients are in various regions around the country. Therefore, we value candidates who are willing and able to travel as needed for project assignments and client engagements.

The ability to adapt to various locations, cultures, and work environments is essential, as it allows our team members to collaborate effectively with clients and colleagues nationally.

• Bachelor’s degree or higher in a science, technology or engineering discipline.
• 5 years or more of experience in commissioning and qualifying pharmaceutical and / or medical device manufacturing facilities and equipment or in a GMP manufacturing environment.
• Experience with project management or engineering is preferred.
• PMP certification or Project Management Certification is highly preferred.
• Microsoft Excel, PowerPoint, Word, Project, and Access skills.
• Excellent verbal and written communication skills.
• Customer service driven.
• Problem solving and analytics aptitude.
• Experience in a pharmaceutical or medical device manufacturing environment is highly preferred.

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 happily and healthily.

• 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, 24-Hour Fitness & more
• Financial Perks and Discounts

Estimated annual salary (dependent on experience) $100,000 - $120,000

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 applicant’s, employee’s, or intern’s 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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Requirements

Bachelor's degree in related engineering discipline. 7 years or more of experience executing commissioning, qualification, and validation for a range of equipment within the pharmaceutical and / or medical device industries.

Knowledge of regulatory requirements (cGMP, FDA, etc.). Excellent problem-solving, analytical, and technical skills. Ability to problem-solve and troubleshoot effectively.

Strong time management and organizational abilities. Effective communication and interpersonal skills. Detail-oriented mindset with a commitment to maintaining high-quality standards.

Ability to work independently and as part of a team.