QA Associate

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

• Create and establish processes and procedures to ensure compliance and adherence to regulated QA activities for Medical Device industries.
• Responsible for the execution of remediation/CAPA activities.
• Review and approve executed inspection and production related documentation.
• Perform QA document control activities including processing of change requests, manufacturing records.
• Determine root cause and potential preventative/corrective actions. Ensure support for the timely closure of investigations.
• Ensure adherence to SOPs, proper change controls, corrective action and preventative action plans, deviation management, impact assessments for changes to equipment and processes, risk management, and ensure documentation and investigations meet regulatory requirements.
• Additional duties as assigned.

Requirements

• Bachelor's degree in a related field.
• Minimum of 2 years of experience in quality assurance within the medical device industry.
• Experience with remediation plans with strong knowledge of CAPA activities.
• Excellent technical writing skills, and experience with standard operating procedures and additional industry regulated documentation.
• Document control experience.
• Knowledge of preventative/corrective actions and deviation management.
• Advanced knowledge of cGMP standards.
• Excellent communication skills both written and verbal.
• Strong organization skills with the ability to prioritize and multitask.
• Excellent analytical and problem solving skills.
• Ability and willingness to travel are 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) $61,300 - $72,800

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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