Director, Quality Assurance Salary at Context Therapeutics Inc BETA

This position requires a hybrid working model, with expectations of being in office 2-3 days a week at an office in Princeton, New Jersey (preferred location) or Redmond, Washington. Company Overview: SystImmune Inc. is a dynamic clinical-stage bio-pharmaceutical company headquartered in Redmond, WA. Our mission is to revolutionize cancer treatment by developing breakthrough-therapeutic multi-specific antibodies and ADCs. With eight assets in ongoing clinical trials and a robust preclinical pipeline, we are committed to advancing innovative therapies from discovery through IND-enabling stages. Job Summary: We are seeking a meticulous and detail-oriented Quality Assurance candidate with expertise in Good Clinical Practice (GCP) to join our team. The ideal person will be responsible for ensuring that all clinical trials and research activities adhere to regulatory requirements, industry standards, and internal policies related to GCP. This role plays a crucial part in maintaining the int

Job Description Job Description Job Details Description Summary The Director of Quality Assurance is responsible for developing and directing robust quality processes and procedures to ensure the products manufactured meet customer requirements and specifications, including FDA, and AS compliance, as applicable. This position will develop and grow a capable team of quality assurance staff to achieve company goals and objectives. Primary Duties · Lead as the management representative for FDA 21 CFR 820 and AS certifications · Responsible for creation, implementation and maintenance of the Quality System processes, in compliance FDA 21 CFR, Part 820, Quality System Regulation o Systems include Corrective and Preventive Action, Non-conformance and Material Review Board, Validation and Qualification, Management Review, Document and Record Control, Risk Management Activities, Training and Resource Management, Supplier Management, Internal Audit System, Calibration, Inspection and Inspection

About Madrigal: Madrigal is a biopharmaceutical company pursuing novel therapeutics for non-alcoholic steatohepatitis (NASH), also known as metabolic dysfunction associated steatohepatitis (MASH). Our first therapy, Rezdiffra (resmetirom), was granted accelerated approval by the U.S. Food and Drug Administration (FDA) for the treatment of adults with NASH with moderate to advanced liver fibrosis (consistent with stages F2 to F3 fibrosis) and is being studied in a Phase 3 trial for the treatment of NASH with compensated cirrhosis. Role Overview: Director of Quality Assurance - Compliance and Batch Disposition We are seeking a highly experienced and motivated Director of Quality Assurance to lead the company's Quality compliance and batch disposition activities. Reporting to the Executive Director of GMP Quality Assurance, this role is critical in ensuring that all products meet regulatory and company standards for quality, safety, and efficacy. The Director will oversee the QA complianc

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Executive Director, Clinical Quality Assurance is a key lea

Job Description Title: Quality Assurance Specialist Department: Payroll Reports To: Director, Payroll Salary Range: $52,280 - $70,373 Job Summary Participates in the development, implementation and maintenance of quality assurance plans. Conducts quality assurance reviews to ensure that work plans are executed in accordance with the School District of Philadelphia policies and procedures. Studies processes to determine cause and effect. Documents and evaluates data gathered and makes recommendations to the Director, Payroll. Essential Functions Identifies, recommends and implements changes to enhance the effectiveness of quality assurance strategies; assists with the development of quality assurance initiatives . Verifies allocation and calculation of leave days in accordance with District policies. Researches information on current and former School District of Philadelphia employees using the payroll system. Prepares and analyzes basic reports and provides the Director, Payroll with

Over a decade of expertise in software quality assurance, including more than five years in leadership positions. Demonstrated proficiency in test automation, with practical experience using tools such as Selenium, NUnit, and MSTest. Skills and Competencies: In-depth understanding of the Software Development Life Cycle (SDLC) and agile methodologies. Proven leadership and team management abilities. Strong analytical and problem-solving capabilities. Outstanding communication and interpersonal skills. Adept at thriving in fast-paced settings and handling multiple projects concurrently. Technical Proficiencies: Expertise in the .NET framework and C# programming. Skilled in utilizing Azure DevOps Experience with Continuous Integration/Continuous Deployment (CI/CD) tools and methodologies. Knowledgeable in performance testing tools and techniques.

CONTRACT-TO-HIRE MUST HAVES: BA/BS degree in life sciences discipline or equivalent 2+ years of biopharmaceutical industry experience or similar regulated environment Good Aseptic gowning background/experience Manufacturing/GMP experience Overview The Quality Assurance Specialist II will report to the Director, Quality Assurance Operations. The position will support the quality and regulatory compliance of commercial and clinical products including manufacturing, testing, and release at contract service providers. Further, the position will be responsible for ensuring that these operational activities are maintained in accordance with GMPs, global health authorities’ requirements and expectations. Shift: Wednesday to Saturday from 7:00 AM - 6:00 PM. (4 days - 10 Hours Shift) Essential Functions and Responsibilities Represent QA by working on-site at the CMO for up to 5 days per week. Support CMO manufacturing, testing, and release activities on weekends, as needed. Establish and mainta

MUST HAVE DIRECT PRIME QUALITY EXPIERENCE FOR CONSIDERATION FOR THIS ROLE! Job Details Description Summary The Director of Quality Assurance is responsible for developing and directing robust quality processes and procedures to ensure the products manufactured meet customer requirements and specifications, including FDA, and AS compliance, as applicable. This position will develop and grow a capable team of quality assurance staff to achieve company goals and objectives. Primary Duties · Lead as the management representative for FDA 21 CFR 820 and AS certifications · Responsible for creation, implementation and maintenance of the Quality System processes, in compliance FDA 21 CFR, Part 820, Quality System Regulation o Systems include Corrective and Preventive Action, Non-conformance and Material Review Board, Validation and Qualification, Management Review, Document and Record Control, Risk Management Activities, Training and Resource Management, Supplier Management, Internal Audit Sys