Quality Control Microbilogy Manager

Job Title:

Quality Control Microbiology Manager Job Description This position will lead a small team of technicians in the Quality Control (QC) and Quality Assurance (QA) department, fostering a culture of excellence. You will ensure that quality and safety are integrated into day-to-day operations and long-term strategies. The role is accountable for ensuring that the company's products and services meet the required quality standards, from raw materials to finished products. You will collaborate with managers to develop quality standards, assess test results, and approve recommended changes. Additionally, you will review quality control documentation and report on its effectiveness, accuracy, and relevance. Responsibilities Develop Quality Control Plans for production and manufacturing unit operations. Monitor and manage the traceability of raw material quality and finished goods. Update facilities, policies, systems, and documentation to meet regulations set by federal, state, and local authorities, as well as all applicable certifying bodies. Represent the company to external stakeholders such as certifiers, customers, and authorities. Implement and renew the certifications required by customers. Provide leadership for developing and directing Quality Assurance, Inspection, Laboratory, and Quality improvement by scheduling and recording regular internal audits. Implement new Standard Operating Procedures (SOP) for Quality control and identify, write, and revise standard operating procedures, work instructions, and laboratory policies, procedures, and standard practices. Promote company-wide quality awareness and compliance. Manage the review and approval of complaints and non-conformances, and recommend corrective and preventative actions. Lead Root Cause Analysis and Corrective Action of nonconforming products (internally and externally). Ensure effective management of customer escalations, and timely and effective communication and resolution of issues that help drive customer satisfaction. Interact effectively with Fermentation, Production, and Maintenance teams to establish best practices, process control, discipline, and formulation of quality planning. Ensure the quality of finished goods based on legal and certification regulations, as well as customer needs. Conduct and record environmental analyses, storage suitability, and other controls and analyses specified in the quality control plan during certain stages of production, storage, and shipment operations. Provide information and guidance to relevant departments regarding the results of these analyses. Manage and monitor safety Key Performance Indicators (KPIs) for employee health and safety. Implement safety training programs and initiatives for workplace safety. Ensure the company complies with OSHA guidelines and other safety-related regulations. Conduct risk assessments and enforce preventative measures. Create and implement safety plans, ensuring they are followed daily. Maintain documentation of the company's safety procedures, accidents, and related events. Conduct monthly and new hire safety training as needed. Conduct contractor safety training as needed. Maintain OSHA log and submit periodic safety reports. Lead plant safety committee and conduct internal safety audits. Essential Skills Extensive experience in quality control operations in the food, biotech, high-tech, probiotics, or feed manufacturing industry. 10+ years of Microbiology quality experience with a minimum of 5 years of management experience. Proficiency in Quality control, Quality assurance, Microbiology, Fermentation, CAPA, Investigation, Root cause analysis, QC, QC testing, Bacteria, and Bacterial fermentation. Additional Skills & Qualifications Master of Science or bachelor's degree in Microbiology, Biotechnology, Quality Management, Food Science, or a relevant degree program; or a degree in an EHS-related field of study. Multiple years of health, safety, and environmental experience required, with manufacturing experience preferred. Work Environment The role operates in a manufacturing environment where safety and quality are prioritized. The manager will lead a dedicated team and interact with various departments to implement best practices and process controls. The position requires adherence to federal, state, and local safety and quality regulations. Job Type & Location This is a Permanent position based out of West Chester, PA. Pay and Benefits The pay range for this position is $90000.00 - $120000.00/yr. Benefits Overview Envera

LIC, LLC

provides a comprehensive benefits package for eligible employees.

Benefits include:

• Medical
• Dental
• Vision
• Short-Term Disability
• Long-Term Disability
• Life Insurance
• Accidental Death and Dismemberment
• Flexible Spending
• Retirement Savings Plan (401(K)) with match
• Tuition Reimbursement
• Bonus Program In addition, the Company provides provisions for family and medical leave, personal leave, and other types of paid and unpaid leave.

Benefits Eligibility Generally, fulltime employees are eligible to participate in the Company's employee benefits beginning the first day of employment, unless indicated otherwise. Eligible dependents would be legally married spouse, including legally married same-sex spouse; dependents who are physically or mentally disabled and dependent on you; your natural children, adopted children or children placed with you for adoption, your stepchildren, and children for whom you are the legal guardian. Dependent children remain eligible for coverage until the last day of the month when they attain the age of 26, regardless of student or marital status. Holidays The following paid holidays are offered each year to eligible employees:

• New Year's Day
• Good Friday
• Memorial Day
• Independence Day
• Labor Day
• Thanksgiving
• Day after Thanksgiving
• Christmas Eve
• Christmas Day
• New Year's Eve Sick Time Fulltime employees are eligible for 6 days of sick time annually.

Sick time is prorated in the calendar year employee is hired. Vacation Days Company policy is to provide vacation to fulltime employees based on their continuous service according to the following schedule. Years of Employment Vacation Less than a year 1.25 days per completed calendar 1 - 4 month 3 weeks (15 days) 5 - 9 4 weeks (20 days) 10+ 5 weeks (25 days) Workplace Type This is a fully onsite position in West Chester,PA. Application Deadline This position is anticipated to close on Mar 17, 2026. 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. 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.