CMC QA Associate - Bedford, MA

CMC QA Associate - Bedford, MA CMC QA Associate Location: Bedford, MA Contract: Up until the end of the year Orbis Clinical is seeking a CMC QA Associate located in Bedford, MA for up until the end of the year. Summary The CMC QA Consultant will report to the Director of CMC QA and be responsible for supporting cross functional team (i.e. PD, MSAT, CMC, Manufacturing, Regulatory Affairs etc) to confirm the appropriate quality as well as compliant controls are in place for assigned Gene Therapy programs, and working with colleagues to improve processes utilized to ensure product quality. In this role, in collaboration with key stakeholders in Technical Operations, Regulatory Affairs and extended Quality (ie. QC, Supplier Quality), you will provide Quality oversight and support to ensure clinical through commercial development lifecycle activities for drug substance and drug product meet cGMP regulatory requirements and guidelines at GTMF and/or contract manufacturing organizations (CMO). Responsibilities Review and approve batch records, CC, deviations, and other quality systems Support review and approval of process characterization studies and associated report Provide quality oversight of process performance qualifications and associated studies Review and approve process validation protocols and reports (i.e., Mixing validation, hold studies, extractable and leachable, impurity, column storage etc..) Review and approve tech transfer plan, report, and associated deliverables Author/Review of regulatory submissions and responses Review and approve batch records, Change Controls, Deviations, and other quality systems Support batch disposition and release Ensure GMP processes are implemented in the Quality Management System (QMS) for clinical and commercial product process lifecycle (e.g. control strategy, technology transfer, process validation lifecycle, continuous process verification) Provide oversight to ensure the creation of product specifications, method validation, stability, and comparability assessments for technology transfers are in accordance with global regulatory requirements and internal procedures/policies Provide quality support for Quality System records (i.e. Deviations/CAPA/Change Controls) Author/review CMC sections of relevant regulatory dossiers and strategize responses to regulatory agency queries and Qualified Person (QP) queries throughout the product lifecycle Communicate and promote a culture of quality and operational excellence Requirements BS degree preferably in an Engineering, Biotechnology, Biological/Physical sciences or equivalent. Minimum of 9 years experience in a GMP biopharmaceutical manufacturing environment in Technical Operations and/or Quality. Strong working knowledge and interpretation of FDA, EMA, local regulations and guidelines, Good Distribution Practices, ICH guidelines and industry best practice. Experience supporting authoring/reviewing/approving technical studies Experience leading and participating in investigations into manufacturing and analytical deviations and determination of product impact, root cause, and corrective and preventive actions. Experience supporting manufacturing operations in a Quality Assurance role Experience with performing technical assessment of changes for potential impact to qualification/validation of processes, equipment, utilities, facilities, and systems. Capability of collaboratively engaging with CMO's. Experienced in all phases of biologics, gene therapy, and/or cell therapy drug development. Demonstrated high personal and professional ethical standards. Possesses excellent judgement with the ability to think and act quickly. Must be able to identify creative solutions to complex technical problems. Ability to interpret and relate Quality standards for implementation and review. Ability to communicate clearly and professionally both in writing and verbally. Strong organizational and project management skills with a track record fo meeting goals/objectives. Strong experience with regulatory authority inspections, including FDA and EMA. Travel may be required when appropriate (approximately 10%). Expert knowledge of cGMP compliance regulations and industry practices for US/Ex-US Compensation Details: Orbis Clinical is an equal opportunity employer that provides a reasonable range of compensation for our positions. Actual compensation is influenced by a wide array of factors including, but not limited to, skill set, level of experience and specific office location. The Pay Range for this position is $101.55 per hour, can vary depending on employment status. Orbis Clinical offers eligible employees health benefits (medical, dental, and vision), employer-paid basic life and AD&D insurance, and a partial employer match on a 401(k). EEO and Reasonable Accommodation Statement: Stone Harbor Staffing Group is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, genetic information, veteran status, or any other characteristic protected by law. We also consider qualified applicants with criminal histories, consistent with applicable law. If you need assistance or an accommodation during the application process, please contact us. By applying for this position, you agree that any calls from Orbis Clinical and its subsidiaries may be monitored or recorded for training and quality assurance purposes. Stone Harbor Staffing