Director of Quality (Pharmaceutical Manufacturing) at FIRST PRIORITY, INC

Elgin, Illinois, United States -

Full Time

Start Date

Immediate

Expiry Date

13 Jul, 26

Salary

145000.0

Posted On

14 Apr, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality assurance, Quality control, Pharmaceutical manufacturing, FDA regulatory compliance, cGMP, Regulatory affairs, Validation, Leadership, Strategic planning, Technical reporting, Problem solving, Critical thinking, Change management, Auditing, Personnel management, Risk assessment

Industry

Pharmaceutical Manufacturing

Description

Description First Priority, Inc. is the animal health industry's premier manufacturer and supplier of generic pharmaceutical products located in Elgin, IL. We are seeking a dynamic and experienced Director of Quality to lead our animal pharmaceutical manufacturing quality assurance and control operations. In this pivotal role, you will drive the development, implementation, and continuous improvement of robust quality systems that ensure our products meet the highest standards of safety, efficacy, and compliance. Your leadership will foster a culture of quality excellence across manufacturing processes, regulatory adherence, and inspection protocols, empowering the organization to deliver life-changing animal medicines with confidence. This is an exciting opportunity for a proactive leader passionate about advancing pharmaceutical quality standards on a large scale. GENERAL SUMMARY: Responsible for the organizational elements of First Priority’s Quality Control, Quality Assurance and R&D. This responsibility includes, but is not limited to, the effective planning and organization of personnel and workflow utilization in order to implement the timely submission, approval, validation, testing and release of products and processes in accordance with applicable internal quality system policies, procedures, and external regulations and standards that govern the products manufactured, labeled, tested, stored, promoted and/or distributed by or for First Priority Inc. PRIMARY RESPONSIBILITIES: Promoting quality achievement and performance improvement throughout the organization. Leads all regulatory inspections and responsible for all regulatory responses review and final review of all regulatory filings prior to submission. Setting QA compliance objectives and ensuring that targets are achieved. Assessing the product specifications of the company and its suppliers, and comparing with customer requirements. Working with purchasing staff to establish quality requirements from external suppliers. Ensuring compliance with national and international standards and legislation. Establishing standards and clearly defined quality methods for staff and all employees to apply. Defining quality procedures in conjunction with operating staff. Setting up and maintaining controls and documentation procedures. Identifying relevant quality-related training needs and delivering training. Ensuring tests and procedures are properly understood, carried out and evaluated and that product modifications are investigated if necessary. Supervising managerial staff ensuring that objectives are established and accomplished. Writing technical and management systems reports. Ability to use change intervention tools and techniques to gain acceptance of a quality culture. Liaising with customers' auditors and ensuring the execution of corrective action and compliance with customers' specifications. Participate in special projects when the business need arises. Requirements QUALIFICATIONS: Education and/or Experience: B.S. degree in Biology or Chemistry or related sciences Minimum of 10 years of pharmaceutical experience Must have FDA regulatory knowledge and experience. Minimum of 5 years’ experience leading a Quality function. Knowledge and/or experience in product formulation of liquids, ointments, powders, tablets and injectables. Knowledge of cGMP Knowledge of Regulatory Affairs required Compliance and Validation experience preferred Strong communications skills, ability to problem solve and use of critical thinking. Good level of computer literacy Change agent with the ability to influence all levels in the organization TRAINING: On the job training: SDS/Hazardous Awareness Good Manufacturing Practices (GMP) Laboratory Procedures Product knowledge Reasoning Ability: Teamwork/collaborative style of management Good business acumen, judgment and maturity with the ability to differentiate strategic vs. non-strategic opportunities Excellent organizational skills WORK ENVIRONMENT: Lab environment involving chemicals, solvents, gasses, and glassware Laboratory bench work and documentation Low to medium noise level Temperature controlled environment TOOLS AND EQUIPMENT: Computer and printer Phone Copy machine Appropriate personnel protective equipment (when necessary) Lab equipment Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. FLSA: Exempt Benefits: 401(k) Dental insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Paid time off Tuition reimbursement Vision insurance

Responsibilities

The Director of Quality leads quality assurance and control operations to ensure pharmaceutical products meet safety, efficacy, and regulatory standards. They are responsible for managing personnel, overseeing regulatory inspections, and driving continuous improvement across manufacturing processes.