Assoc Director, Quality Assurance GMP

Erascais a clinical-stage precision oncology company focused on discovering developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancersmost commonly mutated signaling cascades the RAS/MAPK pathway which affects approximately 5.5 million lives each year worldwide. The name Erasca has an important embedded meaning: it is a contraction of our audacious hope to erase cancer that drives our mission and everything that we do on behalf of patients with cancer.

PositionSummary:

Reporting to the Executive Director Quality Assurance GMP theAssociate Director Quality Assurance GMP supports GMP clinical manufacturing operations including product release analytical data review and approval of quality events. This person is a Quality point of contact for internal and external customers and ensures compliance with company policies and procedures and applicable domestic and international standards and regulations.

Essential Duties and Responsibilities:

• Support GMP CMC operations including review/approval of Manufacturer master and executed batch records Certificates of Analysis and associated analytical data of GMP products intended for human clinical use (Drug Substance Drug Product and Investigational Medicinal Product) to include biologic and small molecule products. Supports GMP/CMC Quality by Design (QbD) risk assessments and process performance qualification (PPQ)/process validation activities
• Works closely with Qualified Persons (QPs) for batch certification and release of drug product and final IMP for EU countries
• Assist with management and oversight of Erasca QA contractors supporting GMP QA operations.
• Perform final product disposition. Review and approve OOS deviations product complaints temperature excursions corrective and preventive actions and change controls prior to and/or after product release.
• Liaise with internal subject matter experts and 3rd party/contract vendors.
• Provide quality oversight for meeting clinical program supply demands both domestically and internationally.
• Develop review and support compliance to quality agreements and other customer contracts containing quality related information.
• May support both internal and external compliance audits. Assist with vendor management activities for GMP vendors including review and approval of audit agendas reports and corrective and preventive actions.
• Assist with selection and qualification of GMP vendors including representing Erasca Quality during Business Review Meetings (BRMs).
• May act as Quality Assurance Person-in-Plant representative at Contract Manufacturers during production of critical batches/campaigns.
• Evaluate author and/or review operating procedures (e.g. policies SOPs etc.) and perform other activities in support of an integrated cross-functional quality management system (QMS).
• Collaborate with key stakeholders and colleagues to establish metrics and report the state of the Quality Management System.
• Perform all duties in keeping with the Companys core values policies and all applicable regulations.

Required Education Experience and Attributes:

• Bachelor of Science in Biology Chemistry Physical Sciences or related degree and/or training or equivalent combination of education and experience in an FDA-regulated environment.
• Advanced degree in Pharmaceutics Chemistry or related field with 8 years of progressive industry experience in pharmaceutical small molecule drug product development.
• Minimum 8-10 years in GxP pharmaceutical environment in progressively responsible Quality roles. Highly desirable to have a minimum of 8 years of GMP QA experience. Quality Systems experience a plus.
• Previous Quality oversight/support experience in solid oral dosage and Biologics manufacturing is required.
• Experience with electronic document management systems and Quality Management System software platforms is a plus.
• Previous experience working with FDA and participating in regulatory agency inspections.
• Previous experience working with non-US regulatory agencies and/or international product supply is a plus.
• Strong interpersonal verbal and written communication skills.
• Ability to work well in a fast-paced team-oriented environment.
• Excellent organizational ability can easily multi-task and shift priorities as needed.
• Strong learning orientation curiosity and passion for science and patients.

The anticipated salary range for this position is $175000 to $210000.The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job type and length of experience within the industry education etcetera. In addition to base salary the hired applicant will be eligible to receive an annual bonus and an equity grant at hire and annually in the form of the option to purchase stock in the future for a specified price.

Along with our casual collaborative and fun work and the chance to make your mark in our mission to erase cancer Erasca offers a comprehensive and competitive benefits package that includes: Paid Time Off Holiday and Sick Leave Medical Dental and Vision Plans Short- and Long-Term Disability Basic and Voluntary Life/AD&D Coverage Flexible Spending Accounts (FSA HSA and Commute) Critical Illness and Accident Coverage Pet Insurance Employee Assistance Program 401(k) Plan with Erasca contribution and the opportunity to participate in an Employee Stock Purchase Program.

Erasca Inc. is an Equal Opportunity Employer and takes pride in maintaining a diverse and inclusive environment. We do not discriminate in recruitment hiring training promotion or other employment practices for reasons of sex race religion national origin ancestry physical or mental disability protected medical condition genetic information marital status registered domestic partner status age sexual orientation military and veteran status or any other basis protected by federal state or local law or ordinance or regulation.