A career at Resilience is more than just a job – it’s an opportunity to change the future.
Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.
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The Senior Manager, Quality Assurance within the Process Execution Team (PET) is accountable for all QA activities and decisions that directly support the execution of the PET mission. These activities and decisions include batch release, change control, and documentation, equipment and process validation, deviation investigations, SOPs, regulatory interactions and may also include incoming material inspection and release. This leadership role, reporting to the Director, QA and the Manufacturing Director (indirectly), is the primary point of contact for all QA matters related to PET execution (quality, supply, and cost) and the primary link between the PET and other QA/QC functions.
Develops and maintains a high level of understanding of the technical production process and quality systems being utilized within the Process Execution Team (PET)
Accountable for all QA decision-making in the PET; works with the PET leaders and other PET members to deliver all PET objectives
Provides direction, development, and performance management to the Quality professionals supporting the PET.
Accountable for the QA review and approval of the following GMP documentation that has a direct impact on the activities performed by, and the equipment and facilities utilized by the PET:
Change Management (OCM)
Batch Release decisions including Field Alert Assessments and Stop Shipments
Quality Investigations (Deviations, Product Complaints)
Validation Plans, Protocols and Reports
Standard Operating Procedures & Risk Assessments
May be accountable for release of incoming materials (bulk, APIs, excipients, packaging components and so on.)
Collaborates with Quality Managers and Quality professionals from other PETs (including other sites) to ensure consistent application of the key quality systems across all PETs
Interfaces with the Site Support Groups on improvement projects (capital and noncapital) that impact the PET, and proactively ensure GMP compliance during the planning, execution, and closeout phases of these projects.
Provides support to internal audits and regulatory agency inspections for queries relating to process execution activities
Ensures that PET complies with all GMP Compliance and Regulatory requirements by providing proper coaching, mentoring and consultation to the PET leader and PET members
Ensures that the QA processes including batch record review, product disposition and quality issues resolutions are executed to maintain the flow of products and documents to meet PET objectives
Serves as liaison in discussions and agreements with, and ensures timely communication to, other QA functions at the Site (Compliance and QC Labs)
Serves as the liaison to Resilience supply sites and quality organizations; may also serve as QA representative to U.S. product supply teams
Collaborates with other members of the PET to facilitate process improvements and risk assessments; benchmarks internal and external QA practices to identify innovative efficient and effective practices
Participates on internal task forces and external industry associations that evolve and transform the quality assurance discipline
Significant experience in a leadership capacity
Advanced knowledge of cGMP requirements, quality systems, and pharmaceutical manufacturing/packaging technologies
Advanced knowledge of regulatory agency interactions and compliance procedures, with ability to apply the knowledge in an operations environment
Demonstrated ability to influence leaders in a matrix environment and the personal conviction to make courageous decisions to ensure patient safety and to protect company reputation
Bachelor’s degree in a science/technical field such as Pharmacy, Biology, Chemistry or Engineering
Advanced degree, Masters or higher
Experience in supervisory/managerial roles within QA in the Pharmaceutical Industry
Multiple site or function experience
Ability to direct and participate in cross-functional teams
The items described here are representative of those that must be met successfully to perform the essential functions of this job.
Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.
Resilience offers employees a robust total rewards program including equity, an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $115,000.00 - $171,250.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.