Quality Systems Specialist (Food Manufacturing)
Actalent - st. louis, MO
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Job Title: Quality SpecialistJob Description If you are interested in a hands-on, continuous improvement-oriented, fast-paced role in a world-class manufacturing environment then our Quality Systems Business Process Manager (BPM) role is for you. This is a chance to be responsible for developing, implementing, and maintaining quality assurance programs. This role ensures compliance with all regulatory requirements and company standards, conducts audits, manages documentation, and provides training to staff on quality system practices. • Liaison directly with site FSQA Manager in support of the Quality System initiatives including Change Control, Corrective Actions (CA), CAPA, Complaints, Internal/External Audits. • Lead continuous improvement initiatives to ensure the Quality Management System (QMS) is implemented effectively by trending data and using metrics to analyze performance. • Develop, implement, and maintain quality assurance programs to ensure compliance with all regulatory requirements (e.g., FDA, USDA, EFSA, FSA) and industry standards (e.g., HACCP). • Collaborate cross-functionally to identify, develop, build, and implement QMS policies and procedures. • Manage and deliver projects to drive continuous quality excellence. • Participate, advise, and support FDA inspections, and customer audits, and support external audit response management. • Maintain knowledge of regulations and stay abreast of all regulatory changes relevant to the industry and organization. • Act as a SME supporting Quality/operations/R&D team members to ensure compliance requirements are being met during the management of change process. • Support a proactive approach toward investigation and resolving potential product compliance issues. • Develop and deliver training programs to educate staff on quality standards and procedures. Hard Skills Bachelor's degree in biological or STEM-related field 5-7 years of experience in food safety and quality assurance, preferably in a food or pharmaceutical manufacturing environment Strong expertise in deviation management processes including in-depth root cause analysis and CAPA implementation Thorough knowledge and application of Good Documentation Practices (GDP) Knowledge and understanding of cGMP regulations and FDA and EU requirements/guidance documents Proficiency in using quality management software and Microsoft Office Suite Soft Skills Self-motivated, organized, and proactive High degree of accuracy and attention to detail Ability to deliver results in a fast-paced, multi-tasking environment, and prioritize objectives effectively Effective communication and interpersonal skills Job Type This is a permanent position. Work Site This is a fully on-site position in St. Louis, Missouri. Work Environment Office About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email (%) for other accommodation options.
Created: 2024-10-16