Quality Control Project Manager

Requirements and QualificationsBachelor's degree in chemistry, biochemistry, biology, pharmaceutical sciences, or a related scientific discipline.5+ years of experience in pharmaceutical, biopharmaceutical, or other GMP-regulated environments, including Quality Control experience.3+ years of experience in QC project management, laboratory operations, stability management, or related project leadership. Responsibilities and DutiesLead end-to-end QC project management for complex pharmaceutical and biopharmaceutical programs, including project scope, timelines, milestones, resources, risks, deliverables, testing priorities, and customer commitments.

Corporate OverviewArgonaut Manufacturing Services Inc. is a leading contract development and manufacturing organization (CDMO) specializing in aseptic fill-finish services for pharmaceutical and biopharmaceutical products. Headquartered in Carlsbad, California, Argonaut supports clients from clinical development through commercial manufacturing, with a focus on product quality, yield optimization, and reliable delivery.Argonaut provides flexible drug product manufacturing solutions, including vial, syringe, and cartridge filling, as well as combination filling capabilities. The company also offers analytical services and short-term cGMP storage to support clients throughout the manufacturing process.With a commitment to quality standards and hands-on client support, Argonaut works closely with customers to help ensure consistent, compliant, and efficient manufacturing while meeting critical timelines and patient needs.Benefits and Pay RangeBenefits for this position, subject to applicable eligibility requirements.Medical Insurance Dental Insurance Vision InsuranceCompany Paid Life Insurance 1X annual SalaryVoluntary Life InsuranceLong-Term Disability Insurance and Short-Term Disability Insurance Flexible Spending Account and Health Saving Account 401(K) Retirement Plan 10 Days of Paid Time Off10 Paid Holidays Annually The pay range for this position is between $117K - $128K annually. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.Position and ScopeThe QC Project Manager leads and coordinates Quality Control projects and programs from initiation through completion, ensuring alignment with business objectives, customer expectations, regulatory requirements, timelines, and financial goals. The role serves as a key cross-functional liaison between QC, QA, Program Management, Finance, customers, and external partners, providing project leadership, risk and resource management, issue resolution, and performance oversight.This role is 100% On-Site, Monday – Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 6:00am and 9:00am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance.Responsibilities and DutiesLead end-to-end QC project management for complex pharmaceutical and biopharmaceutical programs, including project scope, timelines, milestones, resources, risks, deliverables, testing priorities, and customer commitments.Serve as the primary QC project lead, coordinating activities across QC, QA, Project Management, Finance, customers, and external laboratory partners to ensure timely, compliant, and efficient execution.Translate customer requirements into executable testing strategies, project plans, resource requirements, regulatory deliverables, and compliance objectives.Manage stability programs from study initiation through testing, data review, reporting, and completion, ensuring adherence to protocols, schedules, SOPs, quality requirements, and customer commitments.Ensure QC testing readiness across personnel, equipment, analytical methods, documentation, and laboratory systems, while proactively identifying and resolving operational risks and resource constraints.Participate in root cause investigations, CAPAs, change controls, remediation efforts, and continuous improvement initiatives to strengthen quality, compliance, and operational efficiency.Utilize project metrics to monitor performance, identify trends and resource gaps, and provide data-driven insights to support project and business decisions.Partner with Finance to track project activities and billable work, assign costs to appropriate customer and GL accounts, support accurate invoicing, and reconcile financial activity with approved project scope.Manage project governance and executive communications, including status reporting, risks, milestones, resource and financial updates, escalations, and key decisions.Participate in effective customer and stakeholder relationships through clear communication, alignment on requirements and deliverables, and timely resolution of project issues.Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs.Requirements and QualificationsBachelor's degree in chemistry, biochemistry, biology, pharmaceutical sciences, or a related scientific discipline.5+ years of experience in pharmaceutical, biopharmaceutical, or other GMP-regulated environments, including Quality Control experience.3+ years of experience in QC project management, laboratory operations, stability management, or related project leadership.Demonstrated experience managing multiple concurrent projects and cross-functional teams in a regulated environment.Strong working knowledge of GMP, QC laboratory operations, stability programs, analytical testing, data integrity, and quality systems.Experience with project planning, scheduling, risk management, resource coordination, and customer deliverables.Experience with deviations, investigations, CAPAs, change controls, and audit/inspection readiness.Proficiency with Microsoft Office; experience with Power BI or similar reporting tools preferred.Strong analytical, organizational, communication, and problem-solving skills, with the ability to work independently and effectively engage senior leadership and customers.Argonaut Manufacturing Services, Inc. is an equal opportunity employer committed to providing equal employment opportunities to all employees and applicants. We make employment decisions without regard to race, color, religion, sex, gender identity or expression, sexual orientation, pregnancy, national origin, ancestry, age, disability, genetic information, veteran or military status, marital status, or any other characteristic protected by applicable federal, state, or local law.Argonaut Manufacturing Services, Inc. complies with all applicable employment eligibility verification requirements. Candidates must be legally authorized to work in the United States. Employment eligibility will be verified in accordance with applicable federal law.As a condition of employment, employees are required to review and sign certain company agreements and policies, including a confidential information agreement and an arbitration agreement for the resolution of employment-related disputes, in accordance with applicable law.Background checks are conducted to support workplace productivity, safety, and security by ensuring applicant backgrounds and qualifications are suitable for the position being considered.It is the policy of Argonaut Manufacturing Services, Inc., as part of its hiring procedures, to conduct background checks on finalist(s) for all positions. These checks will be job-related, consistent with business necessity, and conducted pursuant to all applicable laws, rules, policies, and procedures. Background checks may include, but are not limited to, verification with educational institutions or licensing/credentialing boards; standard criminal checks; employment verification; and other pertinent information and resources.Employment offers will generally be made after successful completion of applicable background check(s). However, any offers of employment made prior to completion of the background check(s) shall be contingent upon successful completion of the check(s). Finalist(s) may be rejected if they provide inaccurate or untruthful information, do not fully participate in a required background check, or do not sign or complete a required form.