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
- Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards.
- Initiate/update GxP and Risk Assessments on system.
- Author, Review and or approve scheduled periodic reviews.
- Author, Initiate, and/or review and approve IT SOPs related to compliance
- Collaborate with project stakeholders and the information systems team to define needs and achievable solutions and/or justifications to system requirements
- Draft and execute computer system validation documentation such as:
o Validation Project Plan
o Requirement Specification (URS, DS, FS)
o IQ and OQ Test Scripts
o IQ/OQ/PQ Protocols, as necessary
o Traceability Matrix (TMX)
o System Release Memo
o Validation Summary Report
o Translate system requirement specifications into executable validation protocols - Provide support to executors of the protocols when needed
- Write reports summarizing system validation
Requirements
Bachelor’s Degree in Chemical Engineering, Biomedical Engineering, Computer Science or IT/IS from a 4 year University
- 4-5 years of CSV experience is required
- Previous experience in GxP / Life Science Industries is required
- Must have strong written and verbal communication skills
- Willingness to travel 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 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
Annual Salary Range (dependent on experience) $65,000 - $130,000
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: Bachelors Degree in Chemical Engineering or Biomedical Engineering from a 4 year University Must have strong written and verbal communication skills Previous experience in Life Sciences Industry is preferred Previous experience in GxP Industries are preferred Must be adaptable, customer service oriented, have a positive attitude This role requires additional hours worked. You must have a flexible schedule No C2C/ No Sponsorship
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