COMPANY MISSION
eGenesis is dedicated to giving patients with organ failure a second chance at life by harnessing the power of genome engineering to create safe, effective, and readily available solutions.
POSITION SUMMARY
The Manager of Quality Assurance (QA) is accountable for overseeing the GMP production operations to be conducted at Genesis. This will include supporting the manufacturing operations, facilities/utilities/systems/equipment lifecycle, and supporting all the records generated as part of the manufacturing operations to maintain the GMP facility.
This role will be responsible for ensuring compliance to GMP standards at eGenesis. This position reports to the Senior Manager of Quality and is a highly visible and impactful position that will require cross-functional interaction across the multiple teams in the organization.
PRIMARY RESPONSIBILITIES
Developing, implementing, and maintaining processes to support QA oversight for the manufacturing of drug product to be used in clinical studiesSupporting the development of policies, processes, procedures, and controls ensuring that facility operations conform to established cGMP standards and regulatory requirements and guidelinesSupporting the qualification activities associated with the implementation and release of systems, utilities, facility areas (i.e., manufacturing suites), and equipment onboarding/maintenance for the facilitySupporting day-to-day QA activities associated with manufacturing of drug productReleasing manufacturing suites and batch/product changeovers for continuation of manufacturing activitiesParticipating in cross-functional teams to resolve quality-related issues impacting manufacturing activitiesReviewing and approving documentation such as Manufacturing Batch Records (MBRs), product specifications, change controls, deviations and CAPAs associated with the operations at the manufacturing facilityEvaluating and approving proposed process changes and improvements in the manufacturing area, ensuring that appropriate risk assessments are conducted and proposed changes/improvements are consistent with applicable regulatory guidelinesSupporting investigations associated with critical or major manufacturing deviations and providing the necessary guidance to authorize manufacturing operations, as applicableAuthoring, reviewing, and approving internal quality documents (SOPs, investigations, etc.)Participating in supplier qualification audits and supporting internal audits and regulatory inspections, as neededDeveloping, trending, and reporting of relevant Quality Metrics associated with the area of responsibilityMaintaining the QA Operations function in a state of compliance and inspection readiness
BASIC QUALIFICATIONS
B.S./M.S. in Life Sciences or related field with 5+ years of experience, including leadership, in GMP Quality AssuranceExperience with QA and GMP compliance in clinical biologics productsExperience providing QA oversight to manufacturing operations in a pharmaceutical/ biotechnology environmentAbility to assess vendor quality core processes ensuring compliance with relevant guidelines and proceduresExperience with implementation of electronic system(s) to ensure compliance in 21CFR Part 11 and other applicable regulationsAbility to organize and prioritize workload to meet deadlines and company objectives.Ability to work independently and within cross-functional teamsKnowledge of FDA/EMA/ICH regulations and guidelines regarding clinical production and supply of biopharmaceutics
LEADERSHIP QUALIFICATIONS
Organizational, staff mentorship, and time management skills with attention to detailsHandling multiple assignments in a fast-paced environment with changing prioritiesIndependent development and execution of work plans with minimal supervisionStrong analytical problem-solving, and critical thinking skillsExcellent written and verbal communication skills with the ability to communicate effectively
