CQV Engineer

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 hiring a motivated CQV Engineer responsible for the commissioning qualification and validation for facilities utilities and equipment in the pharmaceutical and biotech industries. Our engineers play a critical role in driving project success while supporting validation planning development documentation and execution and ensuring regulatory standards and quality requirements are met.

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 effective mitigation strategies.

Troubleshoot and resolve issues related to equipment and process performance.

Collaborative with cross-functional teams to ensure alignment on CQV activities and project timelines.

Ensure compliance with regulatory requirements (FDA EMA etc.) and industry standards (GMP GAMP etc.).

• Additional responsibilities as required to drive successful validation project deliverables.

Requirements

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.

Insurance options for Employee Assistance Programs Basic Life Insurance Short / Long Term Disability and more.

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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Key Skills

ASP.NET,Health Education,Fashion Designing,Fiber,Investigation

Employment Type : Full Time

Experience : years

Vacancy : 1