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Job Description BEPC is actively looking for Automation and Validation Engineer, in San Angelo, TX area! W2 Contract – 1 year with possible extensions! Benefits include medical, dental, vision, and life insurance Pay Rate: $40.00 - $45.00/hour - Determined based on experience (Paid Weekly) Work Model: Onsite role Note: This is a W2 only role — C2C, C2H will not be considered Summary of the Role: BEPC is seeking a highly motivated Automation and Validation Engineer to join our client’s site in San Angelo, TX. This role will support the development, implementation, and maintenance of automated systems while ensuring validation processes comply with industry standards and regulatory requirements. The Automation and Validation Engineer will collaborate with cross-functional teams to support the development and testing of medical devices and ensure safety, quality, and performance criteria are met. Summary of Duties and Responsibilities: • Develop, validate, and maintain automated systems for medical device production and testing., • Lead and execute validation activities, including Software, Hardware, and Process Validation, for medical devices in compliance with FDA, ISO, and other regulatory requirements., • Generate equipment and fixture matrices for MVP, with qualification requirements defined by the medical device company., • Create detailed and specific IQ/OQ validation protocols for medical device manufacturing and laboratory settings in accordance with requirements and standards., • Author validation completion reports following successful completion of IQ/OQ validations., • Execute detailed and technical PQ validations in accordance with requirements and standards., • Author validation completion reports following successful completion of PQ validations., • Design, implement, and maintain automated test scripts, ensuring all validation protocols are met., • Perform risk assessments and provide corrective actions to improve the reliability of automated systems., • Collaborate with engineering, quality, and regulatory teams to ensure automation and validation activities meet industry standards., • Document validation processes, results, and reports in compliance with applicable regulatory standards., • Support new product development and process improvement efforts through automation and validation strategies., • Troubleshoot and resolve issues related to automated systems and ensure the reliability of validation equipment., • Maintain up-to-date knowledge of industry regulations and best practices in automation and validation within medical device development. Main Qualifications: • Education: Bachelor’s degree in Engineering, Electrical, or a related field., • Experience: Minimum of 4 years of experience in automation and validation engineering, specifically within the medical device or regulated industry., • Strong knowledge of regulatory requirements, including FDA 21 CFR Part 820 and ISO 13485., • Experience with automation tools and systems., • Familiarity with risk management processes, including FMEA, and statistical analysis., • Solid understanding of test methodologies and validation protocols, including IQ, OQ, and PQ., • Excellent problem-solving, troubleshooting, and analytical skills., • Strong attention to detail and excellent documentation practices., • Effective communication and interpersonal skills with the ability to work collaboratively with cross-functional teams. Preferred qualifications: • Master’s degree in Engineering, Electrical, or a related field. About BEPC BEPC Inc., founded in 2007, is a 100% employee-owned company providing top-tier consulting and staffing solutions across industries like technology, engineering, manufacturing, and project management. At BEPC, we are driven by innovation and a commitment to excellence. We take pride in fostering a collaborative and innovative environment where our team members thrive. With competitive benefits, including medical, dental, vision, and life insurance, BEPC is dedicated to supporting our employees' personal and professional growth. Apply Now! Qualified candidates are encouraged to apply by submitting an up-to-date resume that highlights how your experience aligns with the role. Please include specific examples that demonstrate your qualifications. We look forward to connecting with you! \nCompany Description About BEPC BEPC Inc., founded in 2007, is a 100% employee-owned company providing top-tier consulting and staffing solutions across industries like technology, engineering, manufacturing, and project management. At BEPC, we are driven by innovation and a commitment to excellence. We take pride in fostering a collaborative and innovative environment where our team members thrive. With competitive benefits, including medical, dental, vision, and life insurance, BEPC is dedicated to supporting our employees' personal and professional growth. About BEPC\n\nBEPC Inc., founded in 2007, is a 100% employee-owned company providing top-tier consulting and staffing solutions across industries like technology, engineering, manufacturing, and project management. At BEPC, we are driven by innovation and a commitment to excellence. We take pride in fostering a collaborative and innovative environment where our team members thrive.\n\nWith competitive benefits, including medical, dental, vision, and life insurance, BEPC is dedicated to supporting our employees' personal and professional growth.

Job Description QA/QC Specialist San Angelo, TX Area The Company Our client is a high-growth startup in one of the most critical pockets within the defense industry: explosives production. They are further increasing our country's capacity to provide the energetic materials necessary for the numerous defense systems that keep us safe; both here at home and around the world. Now more than ever, explosives production is an extremely crucial component, while also being a major bottleneck, in the deployment and utilization of defense systems. Our client is leveraging decades of industry expertise to alleviate this concern and help the United States maintain its military excellence. The Job The QA/QC Specialist serves as the gatekeeper of product standards within an explosives manufacturing operation. Quality Assurance (QA) builds the systems and processes that prevent defects before they occur, including audits, Standard Operating Procedures (SOPs), certifications, and data packages. Quality Control (QC) performs hands-on testing, sampling, and inspection at defined stages of production to verify that materials, in-process product, and finished goods conform to specification. Together, QA and QC manage product release, ensure regulatory and contractual compliance, and drive continuous improvement using Lean Six Sigma (LSS) and related methodologies, all within the heightened safety and security context of energetic materials manufacturing. Functions Quality Assurance (Systems & Prevention) • Plan and conduct internal audits of production, laboratory, and storage/magazine areas; track findings through corrective and preventive action (CAPA) closure., • Support and host external/regulatory audits and customer quality surveillance visits., • Maintain the quality management system (QMS) documentation hierarchy and change-control/document-control processes., • Compile and issue certificates of analysis/conformance (CoA/CoC) and finished-goods data packages for product release and shipment., • Own and maintain calibration, preventive maintenance, and gauge R&R programs for inspection and test equipment., • Lead or support root-cause analysis for nonconformances, customer complaints, and process deviations., • Track quality metrics (yield, scrap/rework, first-pass yield, complaint rate, CAPA aging) and report trends to leadership., • Champion Lean Six Sigma and continuous-improvement projects; facilitate kaizen events and control-plan updates., • Support new product introduction, process validation (IQ/OQ/PQ), and first-article inspection activities., • Maintain training records and administer quality-related training and certification programs for production and lab personnel. Quality Control (Hands-On Testing & Inspection) • Perform incoming inspection and testing of raw materials and components against approved specifications., • Conduct in-process inspections and sampling at designated hold points throughout production per approved sampling plans (e.g., customer-specified plans)., • Execute physical, chemical, and functional testing per approved test methods, recording results in the ERP/MRP or paper batch record., • Perform final inspection, lot acceptance testing, and disposition (accept/reject/hold) of finished product prior to release., • Segregate, tag, and control nonconforming material per the material review board (MRB) process., • Maintain accurate, legible, and complete batch records, inspection logs, and chain-of-custody documentation., • Operate and maintain laboratory and inspection equipment; perform routine calibration checks and equipment verification., • Support environmental, safety, and process-safety monitoring tasks that intersect with quality (e.g., moisture content, density, sensitivity screening) as required by site procedures, without disclosing or handling classified or export-controlled formulation data outside authorized scope. Regulatory, Safety & Compliance • Support compliance with applicable federal, state, and local regulations governing explosives manufacturing (e.g., ATF licensing/recordkeeping, DOT/PHMSA transportation classification, OSHA Process Safety Management, and applicable military/customer specifications such as MIL-STD or AQAP where relevant)., • Maintain lot traceability and recordkeeping required for regulatory reporting and product recall/traceback capability., • Participate in process hazard analyses (PHA) and management-of-change (MOC) reviews from a quality/compliance perspective., • Adhere strictly to site security, access control, and handling procedures for regulated and hazardous materials. Qualifications Education & Experience • Bachelor's degree in Chemistry, Chemical Engineering, Materials Science, Industrial Engineering, or related field preferred; equivalent combination of education and experience considered., • 2–5+ years of experience in quality assurance/quality control, preferably within explosives, propellants, munitions, chemical processing, or another highly regulated manufacturing environment (years scale with level)., • Experience with ISO 9001 and/or AS9100 quality systems; energetics-specific standards (e.g., MIL-STD-1916, AQAP-2110/2130) a plus., • Lean Six Sigma certification (Yellow/Green/Black Belt) preferred. Knowledge, Skills & Abilities • Working knowledge of statistical process control (SPC), sampling plans, and measurement systems analysis., • Strong root-cause analysis and problem-solving skills., • Proficiency with quality/LIMS software, ERP/MES systems, and standard office software; data analysis tools (Minitab, Excel) a plus., • Excellent written communication for SOPs, audit reports, and data packages., • High attention to detail and unwavering commitment to data integrity, given the safety-critical nature of the product., • Ability to read and interpret engineering drawings, specifications, and test methods., • Ability to obtain and maintain any required background clearance/authorization for handling regulated materials. Certifications & Licensing (as applicable) • ASQ Certified Quality Technician/Engineer/Auditor (CQT/CQE/CQA) preferred., • Ability to pass background checks required for ATF-licensed explosives manufacturing facilities., • Site-specific hazardous materials handling and process safety training (provided post-hire).

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