Microbiology Programs Lead
Solomon Page - Orangeburg, NY
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Our client is now hiring a Microbiology Programs Lead for a consumer forward, health and beauty manufacturer. This is an onsite role with a growing, fast-paced company. This role is balanced between laboratory and manufacturing environments, with approximately 50% of the time spent in each setting The Microbiology Programs Lead is accountable for leading the laboratory and environmental excellence programs. The incumbent will be responsible for leading all laboratory compliance and validation activities, ensuring that all microbiological testing and processes adhere to regulatory standards and internal quality requirements. This role encompasses the duties of Plant Hygienist, overseeing and managing environmental monitoring programs to maintain sanitary conditions and compliance within the facility. The ideal candidate will bring expertise in microbiology, a strong understanding of quality assurance principles, and a proactive approach to maintaining a high standard of plant hygiene and compliance.Salary:$85-$100kResponsibilities:Responsible to lead the development, implementation, and maintenance of microbiological validation protocols, ensuring laboratory compliance with the industry regulations and company standards.Write or update Standard Operating Procedures in accordance with company and regulatory standardsDevelop and write validation protocols related to method suitability, equipment validations, environmental monitoring validations and or IQOQPQ protocolsConduct regular audits of laboratory practices and documentation, identifying areas for improvement and implementing corrective actions as necessary.Interface with R&D, external partners or contract labs on projects and business initiatives.Support validation activities and testing for special assigned microbiology projects.Collaborate with the Microbiology, Manufacturing, Quality & Engineering department to support activities for environmental and laboratory programsAble to write scientifically sound investigations, regarding laboratory investigations, non- conformances, and corrective action preventative actions (CAPA's)Support inspection audits by outside agencies as necessaryServe as the Plant Hygienist, overseeing all environmental monitoring programs, including but not limited to air, water, cleaning & sanitization activities, and surface testing to ensure compliance with hygiene standards.Lead laboratory and/or manufacturing investigations of microbiological contamination incidents, determining root causes and implementing corrective and preventive actionsTrend, review and write environmental monitoring data reports. Identify opportunities for improvement or revalidation opportunitiesProvide training and guidance to plant personnel on best practices for maintaining a clean and safe production environment.Lead and conduct daily manufacturing cGMP assessments with cross functional teams to ensure manufacturing practices are adhering to quality and compliance standards. Track and follow up on observations to ensure timely closure and monitor improvementsSupport manufacturing with scheduling maintenance service and ordering suppliesvalidation activities and testing for special assigned microbiology projectsCollaborate with the Microbiology, Manufacturing, Quality & Engineering department to support activities for environmental and laboratory programsAble to write scientifically sound investigations, regarding laboratory investigations, non- conformances, and corrective action preventative actions (CAPA's)Support inspection audits by outside agencies as necessarySupport laboratory and/or manufacturing investigations of microbiological contamination incidents, determining root causes and implementing corrective and preventive actionsTrend, review and write environmental monitoring data reports. Identify opportunities for improvement or revalidation opportunitiesProvide training and guidance to plant personnel on best practices for maintaining a clean and safe production environment.Lead and conduct daily manufacturing cGMP assessments with cross functional teams to ensure manufacturing practices are adhering to quality and compliance standards. Track and follow up on observations to ensure timely closure and monitor improvementsRequired Qualifications:Bachelor's Degree in biology, microbiology, or related fieldMinimum of five years of proven experience in pharmaceutical or cosmetic manufacturing environment, manufacturing processes, with a deep understanding of the role of microbiology and hygiene in maintaining product quality and safety.Experience in microbiology laboratory testing and operations with a strong focus on compliance, validation, and protocol writing.Excellent investigation and technical writing skills, particularly in the context of microbiology, manufacturing, and environmental quality.Demonstrates a strong understanding of microbiological procedures, laboratory processes and regulatory guidanceExperience and understanding with USP, FDA, AAMI, and ISO guidelines regarding Microbiology, Validation, Good Manufacturing PracticesIf you meet the required qualifications and are interested in this role, please apply today.The Solomon Page DistinctionOur teams, comprised of subject matter experts, develop an interest in your preferences and goals and we act as an advisor for your career advancement. Solomon Page has an extensive network of established clients which allows us to present opportunities that are well-suited to your respective goals and needs - this specialized approach sets us apart in the industries we serve.About Solomon PageFounded in 1990, Solomon Page is a specialty niche provider of staffing and executive search solutions across a wide array of functions and industries. The success of Solomon Page reflects an organic growth strategy supported by a highly entrepreneurial culture. Acting as a strategic partner to our clients and candidates, we focus on providing customized solutions and building long-term relationships based on trust, respect, and the consistent delivery of excellent results. For more information and additional opportunities, visit: and connect with us on Facebook, and LinkedInOpportunity Awaits.
Created: 2025-02-07