Quality Control Manager Omniwell labs Boise, ID Job Details Full-time $18 - $24 an hour 1 day ago Benefits Paid time off Qualifications Spreadsheets Manufacturing facility experience Manufacturing process inspections Compliance documentation Manufacturing company experience Quality control records management Full Job Description About Omniwell Labs Omniwell Labs is a U.S. based contract manufacturer specializing in pet supplements and cosmetic products. We manufacture a variety of products for established brands and are continuing to strengthen our quality systems, manufacturing processes, and GMP compliance. Position Summary Omniwell Labs is seeking a hands on Quality Control Manager to oversee and continue developing our manufacturing quality system. This is not an entry level quality position. Candidates must have previous professional Quality Control or Quality Assurance experience in a manufacturing environment. The Quality Control Manager will be responsible for maintaining quality procedures, performing and documenting inspections, maintaining batch and quality records, investigating quality issues, and helping ensure our manufacturing operation follows established procedures and quality standards. This person will work closely with Operations and Production and will play an important role in strengthening our GMP program and preparing the company for future customer and regulatory audits. Key ResponsibilitiesQuality Control and Quality Assurance Perform and document incoming material, in process, and finished product inspections. Verify products meet established specifications and quality requirements. Maintain quality inspection records and supporting documentation. Identify, document, and investigate quality issues and nonconformances. Work with Production and Operations to determine and implement corrective actions. Maintain and improve quality control procedures. Help establish consistent quality checkpoints throughout the manufacturing process. Maintain product specifications and quality requirements. Quality Systems and GMP Compliance Maintain, review, and improve Standard Operating Procedures. Help implement and maintain Good Manufacturing Practices throughout the facility. Support development of deviation, corrective action, preventive action, and other quality processes. Help ensure employees are following approved procedures and manufacturing documentation. Identify gaps in current quality systems and recommend practical improvements. Help prepare the facility and documentation for customer, regulatory, and certification audits. Assist with quality related training and documentation. Batch Records and Manufacturing Documentation Review production batch records for completeness and accuracy. Maintain organized batch and quality records. Verify required production and quality documentation is completed correctly. Maintain Certificates of Analysis, specifications, supplier quality documents, and related records. Assist with lot and material traceability. Support documentation requests from customers and management. Manufacturing Quality Support Work directly with Production and Operations to resolve quality issues. Verify raw materials and packaging meet requirements before use. Participate in receiving inspections when required. Help identify manufacturing processes that may create quality risks. Support continuous improvement of manufacturing processes. Assist with inventory and material verification when quality or traceability is involved. Required Qualifications Minimum 2 years of professional Quality Control or Quality Assurance experience in a manufacturing environment. Experience performing and documenting quality inspections. Experience working with manufacturing documentation and controlled records. Strong attention to detail and organizational skills. Ability to identify problems, investigate causes, and help implement solutions. Strong written and verbal communication skills. Comfortable working with spreadsheets, electronic records, and manufacturing software. Ability to work independently and take ownership of quality responsibilities. Preferred Qualifications Experience in dietary supplements, food manufacturing, cosmetics, personal care, pharmaceuticals, or pet products. Working knowledge of Good Manufacturing Practices. Experience with batch manufacturing and batch records. Experience with deviations, nonconformances, CAPA, or corrective action processes. Experience preparing for customer, regulatory, or certification audits. Experience with ERP or inventory management systems. Microsoft Excel proficiency. What Success Looks Like The successful candidate will help Omniwell build a quality system where: Quality inspections are performed consistently and documented properly. Batch records are accurate, complete, and traceable. Quality issues are identified and resolved promptly. SOPs and quality procedures reflect how work is actually performed. Manufacturing employees understand and follow established quality procedures. Materials and finished products can be traced by lot. Quality documentation is organized and audit ready. GMP practices become part of the company's everyday manufacturing culture.

Compensation and Benefits Pay:

$18.00 to $24.00 per hour

Benefits:

Paid time off

Work Location:

In person,

Boise, Idaho Pay:

$18.00 - $24.00 per hour

Benefits:

Paid time off Application Question(s): How many years of Quality Control or Quality Assurance experience do you have in a manufacturing environment?

Work Location:

In person