Senior CQV Engineer
Senior CQV Engineer
Posted on :
25-06-2025
Employer Active
1 Vacancy
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Jobs by Experience
7years
Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
25-06-2025
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 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 it s about more than just a job it s about your career and your future.
Your Role
Senior CQV Engineers are responsible for leading commissioning qualification and validation projects for pharmaceutical facilities utilities equipment and systems. Our Senior CQV Engineers play a critical role in overseeing project planning CQV execution and ensuring the operational readiness of capital projects in order to support our clients success.
- Drive project success by assessing priorities and project plans schedule and budget and ensure timely and effective resolution of potential risks and issues.
- Develop and execute commissioning qualification and validation protocols for required equipment and systems.
- Prepare and maintain comprehensive documentation including validation protocols plans reports and standard operating procedures.
- Identify and assess risks associated with CQV activities and develop mitigation strategies.
- Troubleshoot and resolve issues related to equipment and process performance.
- Collaborative with cross-functional teams to ensure alignment of CQV activities and project timelines.
- Serve as liaison between vendors and contractors coordinating required hand-offs.
- Ensure compliance with regulatory requirements (FDA EMA etc.) and industry standards (GMP GAMP etc.).
- Provide ongoing support and technical expertise through validation execution and qualification activities.
- Additional responsibilities as required.
Requirements
- Bachelor s degree in engineering or a related field.
- 7 years of commissioning qualification and validation engineering experience in the pharmaceutical and/or biotech industries.
- Well-rounded versatile equipment and systems experience.
- Proven success in leading CQV projects and experience with project management methods and tools.
- Advanced knowledge of regulatory requirements and industry standards.
- Experience with validation lifecycle management and risk-based approaches.
- Excellent analytical and technical problem-solving skills. Ability to analyze project risks effectively and implement resolutions.
- Strong technical writing skills and understanding of full lifecycle documentation (protocols reports procedures risk assessments specifications and requirements etc.)
- Effective communication and interpersonal skills. Ability to manage stakeholder communication and cross-functional team collaboration.
- Proactive with strong organization and time management skills.
- Excellent attention to detail with commitment to quality and compliance.
- Travel is required. At PSC Biotech many of our projects and clients are located 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 different locations cultures and work environments is essential as it allows our team members to collaborate effectively with clients and colleagues nationally.
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
Estimated annual salary (dependent on experience) $100000 $130000
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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Bachelor s degree in engineering or a related field. 7+ years of commissioning, qualification, and validation engineering experience in the pharmaceutical and/or biotech industries. Well-rounded, versatile equipment and systems experience. Proven success in leading CQV projects and experience with project management methods and tools. Advanced knowledge of regulatory requirements and industry standards. Experience with validation lifecycle management and risk-based approaches. Excellent analytical and technical problem-solving skills. Ability to analyze project risks effectively and implement resolutions. Strong technical writing skills and understanding of full lifecycle documentation (protocols, reports, procedures, risk assessments, specifications and requirements, etc.) Effective communication and interpersonal skills. Ability to manage stakeholder communication and cross-functional team collaboration. Proactive with strong organization and time management skills. Excellent attention to detail with commitment to quality and compliance. Travel is required. At PSC Biotech, many of our projects and clients are located 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 different locations, cultures, and work environments is essential, as it allows our team members to collaborate effectively with clients and colleagues nationally.
Employment Type
Full Time
Key Skills
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