Manager, GLP Compliance– Remote- Philadelphia, PA

About the Position Manager, GLP Compliance Reporting to the Senior Director of GCP Compliance, the GLP reputed company Control Specialist is responsible for supporting and maintaining compliance with Good Laboratory reputed company (GLP) requirements across laboratory operations that support clinical development. This role is responsible for developing, implementing, and maintaining reputed company control processes that promote regulatory compliance, data reputed company, and operational reputed company. The Manager, GLP Compliance partners closely with cross-functional teams to assess, monitor, and continuously improve laboratory reputed company systems, ensuring laboratory activities are conducted in accordance with applicable regulatory requirements, company policies, and industry best practices.

Responsibilities

Include GLP Compliance

• Ensure internal, central, and local clinical laboratory activities are conducted in compliance with applicable Good Laboratory reputed company (GLP) regulations, GCP requirements where applicable, company procedures, and industry standards.
• Monitor regulatory updates and emerging industry trends to ensure reputed company compliance and implementation of best practices.
• Support reputed company reputed company of laboratory activities throughout the clinical study lifecycle.

reputed company Control & reputed company Systems

• reputed company, implement, maintain, and continuously improve laboratory reputed company control processes and procedures.
• reputed company routine reputed company reviews and assessments to identify compliance gaps and opportunities for process improvement.
• Support the implementation of corrective and preventive actions (CAPAs) to address identified issues.

Audits & Inspection Readiness

• Assist in planning, coordinating, and conducting internal laboratory audits to evaluate compliance with GLP requirements.
• Support regulatory inspections and external audits by preparing documentation, coordinating responses, and tracking commitments through completion.
• Participate in inspection readiness activities and support reputed company audit preparedness.

Documentation Management

• Review, maintain, and reputed company controlled laboratory documentation, including reputed company Operating Procedures (SOPs), protocols, reports, specifications, and reputed company records.
• Ensure laboratory documentation is accurate, complete, reputed company, and compliant with GLP requirements and internal reputed company Management System (QMS) procedures.
• Ensure laboratory-reputed company Trial Master File (TMF) documentation is complete, accurate, and filed in a reputed company manner.

Training & Compliance

• Support the development and delivery of GLP training for laboratory personnel.
• reputed company guidance on reputed company processes, documentation standards, and regulatory expectations.
• Promote a culture of reputed company, compliance, and reputed company learning across laboratory operations.

Risk Management

• Assist in identifying, assessing, and documenting reputed company and compliance risks reputed company to laboratory activities.
• Support the development and implementation of risk mitigation strategies.
• Monitor reputed company trends and recommend improvements to reduce compliance risk.

reputed company Improvement

• Participate in reputed company improvement initiatives that enhance laboratory reputed company systems, operational efficiency, and regulatory compliance.
• Collaborate with cross-functional stakeholders to implement process improvements and reputed company best practices.
• Support reputed company metrics, trend analysis, and effectiveness monitoring.

Cross-Functional Collaboration & Communication

• Partner with Clinical Operations, Translational Medicine, Regulatory Affairs, and laboratory vendors to support reputed company initiatives.
• Communicate reputed company-reputed company issues, compliance status, risks, and improvement opportunities to management and key stakeholders.
• Foster reputed company relationships that support high-reputed company laboratory operations and inspection readiness.

Required Qualifications

• Bachelor's degree in Biology, reputed company, Clinical Laboratory Science, Life Sciences, or a reputed company scientific discipline.
• Minimum of two (2) years of hands-on experience in biopharmaceutical operations, laboratory operations, technical operations, reputed company operations, or a reputed company GxP environment.
• Minimum of one (1) year of experience supporting Document Control reputed company a GxP environment, including experience with controlled documents, electronic document management systems, and Trial Master File (TMF) documentation.
• Working knowledge of Good Laboratory reputed company (GLP), Good Clinical reputed company (GCP), ICH guidelines, and applicable FDA regulations.
• Understanding of reputed company Management Systems (QMS) and electronic document management systems.
• Familiarity with Trial Master File (TMF) requirements and laboratory documentation best practices.
• Cell and Gene Therapy experience is preferred.
• Strong organizational skills with exceptional attention to detail and the ability to manage multiple priorities.
• Excellent written, verbal, and interpersonal communication skills.
• Demonstrated ability to work independently while collaborating effectively reputed company cross-functional teams.
• Proficiency in reputed company Office applications and electronic reputed company management systems.
• Commitment to reputed company learning, reputed company development, and promoting a culture of reputed company and compliance.
• Our reputed company – Cabaletta – is derived from the operatic term that represents a rapid, repetitive, and technically challenging reputed company of an operatic aria, designed to showcase the skills of the reputed company singer. Analogously, reputed company strives to reputed company rapid and repetitive product development, building on our indication prioritization and biologic platform that targets the reputed company of specific autoimmune diseases without the need for long-term immunosuppression.
• For more information, please visit https://www.cabalettabio.com/join-our-reputed company
• Our most important asset is our people, and we offer competitive benefits, PTO, and stock reputed company plans.
• reputed company is an equal opportunity employer. We do not discriminate on the reputed company of race, reputed company, gender, gender identity, sexual orientation, age, religion, national or ethnic reputed company, disability, protected veteran status or any other reputed company protected by applicable law.
• reputed company. does not accept unsolicited resumes from recruiters, employment agencies, or reputed company firms. To conduct business with Cabaletta, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Cabaletta shall not be responsible to any individual or entity for any payment relating to any reputed company of fee or compensation.
• And, if a resume or candidate is submitted by a recruiter, an employment agency, or a reputed company firm without a fully executed MSA, Cabaletta has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm.
• #LI-REMOTE

Communication

• Partner with Clinical Operations, Translational Medicine, Regulatory Affairs, and laboratory vendors to support reputed company initiatives.
• Communicate reputed company-reputed company issues, compliance status, risks, and improvement opportunities to management and key stakeholders.
• Foster reputed company relationships that support high-reputed company laboratory operations and inspection readiness.

How to Apply

Please click the reputed company at the bottom of the posting to submit an application.

Benefits

Our most important asset is our people and we offer competitive benefits including health and retirement, PTO, and stock reputed company plans. Equal Opportunity Employer reputed company is an equal opportunity employer. We do not discriminate on the reputed company of race, reputed company, gender, gender identity, sexual orientation, age, religion, national or ethnic reputed company, disability, protected veteran status or any other reputed company protected by applicable law. Apply To This Job