We are currently recruiting for an Operations Administrator with a fantastic company bringing a unique level of expertise to the manufacturing process and serving their industry on a global scale. The person who will best fit this role is highly organized, detail-oriented, and comfortable multitasking. This is an excellent opportunity for anyone with administrative experience, so if you’re interested, submit your resume NOW because this position will fill quickly!
This is a full time, temp-to-hire position with a payrate of $22-$27/hr. (DOE). Hours from 7:30am to 4pm, Monday through Friday, or alternatively, 9 hour days Monday through Thursday and a 4 hour day on Fridays.
Duties & Responsibilities:
- Quality Assurance: Conduct in-process and final inspections of products to ensure they meet the company’s quality standards.
- Testing & Calibration: Perform and document routine tests, calibrations, and inspections using the appropriate equipment.
- Defect Identification: Identify and report any defects, deviations, or non-conformances in the product.
- Root Cause Analysis: Lead investigations of quality issues, determining root causes, and implementing corrective actions.
- Documenting Findings: Maintain accurate records of quality control activities, inspections, and results to support compliance with company policies and regulatory standards.
- Training: Provide guidance and training to junior QC technicians on quality standards, testing methods, and best practices.
- Regulatory Compliance: Ensure that all quality control activities comply with relevant regulations, such as GD&T, ISO, AS or other industry-specific standards.
- Internal Audits: Lead and/or participate in internal audits to ensure adherence to company procedures and regulatory requirements.
- Documentation Management: Prepare and review compliance documentation, such as SOPs, work instructions, and validation reports, ensuring they are up to date and accurately reflect regulatory requirements.
- Inspection Support: Assist in inspections by external regulatory bodies and ensure all necessary documentation is in order.
- Corrective Action Plans: Develop, implement, and monitor corrective and preventive action (CAPA) plans to address any quality or compliance issues.
Qualifications:
- Education: Bachelor’s degree in a related field or equivalent work experience.
- Certifications: Certifications in quality management (e.g., Six Sigma, ISO 9001, Quality Control certification) preferred.
Experience:
- 3+ years of experience in quality control and compliance roles within a manufacturing or laboratory setting.
- Experience with regulatory audits and quality systems in industries like pharmaceuticals, food and beverage, medical devices, or manufacturing is highly preferred.
- Experience with tight tolerances and small parts preferred.
- Must know how to proficiently use a CMM system and inspection and metrology equipment.
- Proficiency in using quality control tools, such as spectrometers, micrometers, and statistical software.
- Ability to analyze and interpret data to ensure quality standards are met.
- Experience with laboratory and testing methodologies is a plus.
- Ability to read and understand blue prints and drawings.
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Must understand FAIR, PPAP, Certificate of Conformance, NADCAP, Cp, Cpk, PFMEA.
We provide equal employment opportunities in hiring, promotion, transfer, compensation, benefits, and all other employment decisions. These opportunities and other conditions of employment are extended to qualified applicants and employees without regard to an individual’s ancestry, race, color, religious creed, sex, pregnancy, genetic information, sexual orientation, gender, gender identity (including transgender) or expression, age, marital status, medical condition, mental or physical disability, national origin, citizenship/immigration status, military or veteran status, or any other protected status under applicable laws.