More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks. With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives. The Quality Specialist II position is a key role in meeting the quality policy through their management of the different quality systems, including production records and deviation system management. The ideal candidate will be responsible for managing the quality systems, including deviations, change control, corrective and preventive actions (CAPA), and document management. Additionally, this role involves making timely batch disposition decisions to ensure quality standards are met before product release, supporting the rapid processing times required by our product. You will have the unique opportunity to make a difference in the lives of many patients as Orca Bio develops next-generation cell therapies.
\n ResponsibilitiesQuality System Management:Oversee the management of quality systems including deviations, change controls, CAPAs, and document control.Ensure that all deviations are investigated thoroughly and timely, identifying root causes and implementing effective corrective actions.Review and approve change controls to ensure compliance with regulatory requirements and internal procedures.Maintain and improve CAPA processes to ensure effective resolution of quality issues.Batch Disposition:Evaluate batch records and associated documentation to make informed batch release decisions.Collaborate with manufacturing and quality control teams to ensure all products meet regulatory and quality standards before release.Monitor and document any quality issues related to batch production and implement corrective measures as necessary.Document Management:Maintain the document management system to ensure all quality-related documents are accurate, current, and compliant with regulatory standards.Conduct regular reviews of quality documentation to ensure adherence to established protocols and procedures.Regulatory Compliance:Stay informed of current regulations, industry trends, and best practices in pharmaceutical quality assurance.Assist in preparing for internal and external audits, ensuring that all quality systems and documentation are audit-ready.Training and Support:Provide training and guidance to staff on quality systems, processes, and compliance requirements.Serve as a point of contact for quality-related inquiries and issues, fostering a culture of quality within the organization.Continuous Improvement:Participate in continuous improvement initiatives to enhance the effectiveness and efficiency of quality systems and processes.Identify areas for improvement within quality operations and suggest appropriate solutions.Track completion of quality records and maintain metrics.Perform other duties as requested by supervisor/manager to support QualityWork collaboratively with cross-functional teams, including manufacturing, research and development, and quality assurance, to support the overall quality of cell therapy products. General RequirementsCommunicate effectively with team members and contribute to a positive and collaborative work environmentActively participate in group and project teamwork; project and process improvementsStrong organizational skills and the ability to manage multiple tasks concurrentlyWillingness to learn and adapt in a fast-paced, dynamic environmentAdhere to cGMP policies and procedures, including documentation activitiesAble to wear appropriate personal protective equipmentWillingness to work overtime as required Experienced RequiredBachelor's degree in a relevant scientific discipline (biology, biochemistry, immunology, etc.) with 5+ years of experience in quality control testing, analytical development, or GMP; OR a Master's degree in relevant scientific disciplines with 3+ years of experienceUnderstanding of FDA regulations, GMP compliance, and quality system processesExperience in quality control or GMP within a cell therapy or biopharmaceutical manufacturing environment is preferredAble to meet project and testing timelinesDetail-oriented with a commitment to data integrity and accuracy, and an ability to identify problems with data managementAble to work collaboratively to respond to changing priorities and challengesAbility to work both independently and collaboratively with a multi-disciplinary team in a fast-paced and regulated environmentPrior experience doing internal audits and document control management
\n$75,000 - $105,000 a year
\nThe anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. You will also be eligible to receive pre-IPO equity, in addition to medical, dental, and vision benefits, flexible PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include free daily lunches and snacks at our on-site locations.
Who we are We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them.
We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility.
We innovate on a path that hasn't been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren't afraid to ask "why not" and challenge the status quo.
We maintain a start-up culture of camaraderie and leadership by example, regardless of title.
We're proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers.
To learn more: https://orcabio.com/join-our-team/ **all official communication will be from @orcabio.com; please beware of scams**
Notice to staffing firms Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment.