PSC Biotech® Corporation
Overview
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 part of our team’s achievements. We employ a global team of skilled professionals across North America, Europe, Asia and the Middle East. At PSC Biotech®, our culture focuses on coaching and developing the next generation of industry leaders. You will be offered a compensation and benefits structure that rewards you and the tools to grow and learn. At PSC Biotech®, it’s about more than just a job—it’s about your career and your future. Your Role
We are hiring multiple QC Specialists to join our team. The QC Specialists will be responsible for ensuring the quality and compliance of pharmaceutical products through analytical testing, documentation, and collaboration with cross-functional teams. These roles play a key part in product release, regulatory compliance, and continuous improvement initiatives. Review changes to analytical methods. Review COA's and other required documentation to support batch release. Review stability program protocols and recommend changes as needed. Review reference standard documentation. Participate in meetings with CDMOs as needed. Assist with annual reports and answers to the FDA. Additional responsibilities as required. Requirements
Bachelor's degree in related discipline. 5+ years of experience in a quality control role within the pharmaceutical industry. Experience reviewing and approving documentation and data. Strong knowledge of quality documentation and regulatory compliance. Knowledge in OOX Triaging. Experience in testing support. Ability to recommend changes effectively and improvements. Strong analytical and problem solving skills. Excellent communication skills. Detail-oriented with a focus on maintaining high-quality standards. Willingness and ability to travel for project assignments and client engagements as needed. Must be authorized to work in the US. No C2C at this time. Benefits
W2 Temp positions include our medical and sick time benefits. The salary bracket for this role is set between $60,000 - $130,000 annually, and may be adjusted based on qualifications, skills, and experience, in compliance with New Jersey salary transparency requirements. Equal Opportunity Employment Statement
PSC is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. We comply with all applicable federal, state and local laws concerning employment discrimination. Employment decisions will be made without regard to 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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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 part of our team’s achievements. We employ a global team of skilled professionals across North America, Europe, Asia and the Middle East. At PSC Biotech®, our culture focuses on coaching and developing the next generation of industry leaders. You will be offered a compensation and benefits structure that rewards you and the tools to grow and learn. At PSC Biotech®, it’s about more than just a job—it’s about your career and your future. Your Role
We are hiring multiple QC Specialists to join our team. The QC Specialists will be responsible for ensuring the quality and compliance of pharmaceutical products through analytical testing, documentation, and collaboration with cross-functional teams. These roles play a key part in product release, regulatory compliance, and continuous improvement initiatives. Review changes to analytical methods. Review COA's and other required documentation to support batch release. Review stability program protocols and recommend changes as needed. Review reference standard documentation. Participate in meetings with CDMOs as needed. Assist with annual reports and answers to the FDA. Additional responsibilities as required. Requirements
Bachelor's degree in related discipline. 5+ years of experience in a quality control role within the pharmaceutical industry. Experience reviewing and approving documentation and data. Strong knowledge of quality documentation and regulatory compliance. Knowledge in OOX Triaging. Experience in testing support. Ability to recommend changes effectively and improvements. Strong analytical and problem solving skills. Excellent communication skills. Detail-oriented with a focus on maintaining high-quality standards. Willingness and ability to travel for project assignments and client engagements as needed. Must be authorized to work in the US. No C2C at this time. Benefits
W2 Temp positions include our medical and sick time benefits. The salary bracket for this role is set between $60,000 - $130,000 annually, and may be adjusted based on qualifications, skills, and experience, in compliance with New Jersey salary transparency requirements. Equal Opportunity Employment Statement
PSC is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. We comply with all applicable federal, state and local laws concerning employment discrimination. Employment decisions will be made without regard to 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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