We are searching for an expert Validation Engineer to join our stellar team at PSC Biotech in Fort Worth, TX.
Growing your career as a Full Time Validation Engineer is an amazing opportunity to develop relevant skills.
If you are strong in project management, creativity and have the right experience for the job, then apply for the position of Validation Engineer at PSC Biotech today!
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 Responsible for validation of various equipment, SIP, CIP, Media Fill, Filter Validation, and Packaging Validation. Responsible for the Performance Qualification on processes, equipment, and manufacturing systems. Initiates, authors, revises, reviews, and completes all required validation documentation. Generate, prepare and execute protocols, analyze test results, and prepare technical reports with little supervision. Contribute directly to the completion of validation projects through the development of validation schedules, master plans, validation protocols and reports. Support the review and qualification of equipment for commissioning, qualification, and validation activities. Collaborate with multiple departments on assigned project activities and deliverables. Initiate and coordinate risk analyses, design reviews, execute FAT/SAT, IQ, OQ, and PQ. Additional duties and responsibilities as assigned.
Requirements Bachelor's Degree in Engineering or related. 3-5 years of applicable work experience in the pharmaceutical industry. Strong knowledge/experience of SIP, CIP, Media Fill, Filter Validation, and Packaging. Experience in authoring and executing validation documentation. Experience in developing SOPS, final reports, and validation/quality policies. Strong understanding of developing, executing, and maintaining CQV procedures and policies. Advanced understanding of cGMP guidelines. Ability to work independently with limited supervision. Excellent communication skills. Strong organization skills and attention to detail. Analytical and problem solving skills. Ability/willingness to travel is 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 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 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 related. 3-5 years of applicable work experience in the pharmaceutical industry. Strong knowledge/experience of SIP, CIP, Media Fill, Filter Validation, and Packaging. Experience in authoring and executing validation documentation. Experience in developing SOPS, final reports, and validation/quality policies. Strong understanding of developing, executing, and maintaining CQV procedures and policies. Advanced understanding of cGMP guidelines. Ability to work independently with limited supervision. Excellent communication skills. Strong organization skills and attention to detail. Analytical and problem solving skills. Ability/willingness to travel is preferred. B.S.
Benefits of working as a Validation Engineer in Fort Worth, TX:
? Excellent benefits
? Company offers career progression opportunities
? Advantageous package
