Quality control analyst jobs in Harrisonburg, VA

Innovairre Communications - WE HELP PEOPLE WHO HELP PEOPLE We make great things happen for some of the world's most vibrant organizations. We are the worldwide leader in non-profit fundraising. The company serves more than 500 marketing agencies, non-profit organizations, and commercial clients, with 4000+ employees working across five different continents and 28 countries around the world. Our direct marketing services deliver results utilizing our in-house production, design capabilities, data and digital expertise, and fully integrated approach producing timely and cost-efficient direct mail packages for our worldwide clients. Shift - 2nd shift (4PM-12AM) Mon-Fri Job Summary The Quality Control Specialist is responsible for ensuring that products, processes, and services meet established quality standards. This role involves conducting inspections, tests, and audits, analyzing data, identifying defects or areas for improvement, and implementing corrective actions. The Quality Control Specialist collaborates with various departments to maintain and improve quality standards throughout the production process. Essential Duties and Responsibilities: Conducts thorough inspections and tests on products, components, and materials at various stages of production to ensure they meet specifications and quality requirements. Collects and analyzes data from inspections, tests, and audits to identify trends, patterns, and potential issues. Identifies and document any defects, non-conformances, or deviations from quality standards. Implements corrective and preventive actions to address identified quality issues and prevent recurrence. Contributes to the continuous improvement of quality processes and procedures by identifying and implementing enhancements. Collaborates with other departments, such as production, engineering, and customer service, to ensure that quality standards are met and maintained throughout the organization. Maintains accurate records of inspections, tests, audits, and corrective actions taken. Provides training and guidance to employees on quality standards, procedures, and best practices. Performs additional responsibilities as required to ensure the team's success. EEO Statement We are an equal opportunity employer. We recruit, employ, train, compensate, and promote regardless of race, religion, color, national origin, sex (including pregnancy and gender identity), sexual orientation, transgender status, disability, age, family or marital status, genetic information, military or veteran status, and other protected status as required by applicable law. At our Company, we have a clear vision: to foster and maintain a supportive and cooperative workplace that celebrates uniqueness and advances equity. We pride ourselves on helping people help people, and we know our company runs on the hard work and dedication of our passionate and creative employees. Diversity, Equity, and Inclusion is more than a commitment at our Company--it is in everything that we do. Benefits We are an equal opportunity employer. We recruit, employ, train, compensate, and promote regardless of race, religion, color, national origin, sex (including pregnancy and gender identity), sexual orientation, transgender status, disability, age, family or marital status, genetic information, military or veteran status, and other protected status as required by applicable law. At our Company, we have a clear vision: to foster and maintain a supportive and cooperative workplace that celebrates uniqueness and advances equity. We pride ourselves on helping people help people, and we know our company runs on the hard work and dedication of our passionate and creative employees. Diversity, Equity, and Inclusion is more than a commitment at our Company--it is in everything that we do.

Responsibilities Conduct quality inspections on incoming concrete deliveries to insure proper mix being used. Assist in concrete service issues. Assist with jobsite inspectors as well as testing companies. Maintain accurate records of any issues on jobsite. Collaborate with production teams to address quality issues. Skills Concrete construction experience Ability to interpret blueprints Familiarity with testing equipment and industry standards Excellent attention to detail with strong analytical skills. Ability to work collaboratively in a team environment while maintaining independent judgment

This position is for the Ocean City MD and surrounding area. Relocation is not offered for this position. We Deliver the Goods: Competitive pay and benefits, including Day 1 Health & Wellness Benefits, Employee Stock Purchase Plan, 401K Employer Matching, Education Assistance, Paid Time Off, and much more Growth opportunities performing essential work to support America's food distribution system Safe and inclusive working environment, including culture of rewards, recognition, and respect Position Summary: Responsible for managing accounts in geographical area providing assistance and training to such accounts by maintaining proper functioning of various beverage and chemical equipment. Installs and tests various equipment. Assists customers and sales people to determine best equipment or products for application. Communicates and interacts with customers, vendors and company personnel in a professional and courteous manner while providing accurate and timely information. Functions as a team member within the department and organization, as required, and perform any duty assigned to best serve the company. Position Responsibilities: Manage accounts in geographical area and provide assistance and training to such accounts. Maintain proper functioning of various beverage and chemical equipment. Install and test various equipment. Assist customers and sales people determine best equipment or products for application. Provide face-to-face customer service in various situations. Drive to customer sites to assist in correcting problems. Prepare schedules for service or installation. Performs other related duties as assigned. Qualifications: High School Diploma or Equivalent 6 - 12 months equipment sales and / or maintenance Company description Performance Foodservice, PFG's broadline distributor, maintains a unique relationship with a variety of local customers, including independent restaurants and hotels, healthcare facilities, schools, and quick-service eateries. A team of sales reps, chefs, consultants, and other experts builds close relationships with customers - providing advice on improving operations, menu development, product selection, and operational strategies. The Performance team delivers delicious food but also goes above and beyond to help independent restaurant owners achieve their dreams. Awards and Accolades Performance Food Group and/or its subsidiaries (individually or collectively, the "Company") provides equal employment opportunity (EEO) to all applicants and employees, regardless of race, color, national origin, sex, marital status, pregnancy, sexual orientation, gender identity, religion, age, disability, genetic information, veteran status, and any other characteristic protected by applicable local, state and federal laws and regulations. Please click on the following links to review: (1) our EEO Policy; (2) the "EEO is the Law" poster and supplement; and (3) the Pay Transparency Policy Statement.

Quality Control (QC) Scientist Department: Quality Control / Quality Assurance Reports To: QC Manager / Chief Operating Officer The QC Scientist supports the development, manufacture, and release of In Vitro Diagnostic (IVD) products by performing quality control testing, method validation, and documentation in compliance with ISO 13485, FDA 21 CFR Part 820, IVDR, and other applicable regulatory requirements. This role ensures that all diagnostic products meet rigorous quality standards for accuracy, reliability, and safety prior to release. Key Responsibilities Perform QC testing on raw materials, intermediates, and finished IVD products, including reagents, controls, and kits, using established protocols (e.g., immunoassays, PCR, molecular diagnostic methods, spectrophotometry). Execute method validation, verification, and transfer for analytical and functional assays in compliance with CLSI and regulatory guidelines. Support stability studies, shelf-life testing, and lot-to-lot consistency evaluations for diagnostic products. Maintain accurate and compliant documentation in accordance with ISO 13485, IVDR, and GMP/GLP requirements. Investigate out-of-specification (OOS), out-of-trend (OOT), and nonconformance events; contribute to root cause analysis and CAPA implementation. Collaborate with R&D, Production, and QA to support new product introduction, technology transfer, and process improvements. Participate in internal audits, regulatory inspections (FDA, ISO, Notified Body), and quality system reviews. Provide technical training and guidance to QC Analysts and laboratory staff. Ensure laboratory equipment is calibrated, qualified, and maintained according to quality standards. Qualifications Bachelor's or Master's degree in Biology, Biochemistry, Molecular Biology, Biotechnology, or related life science discipline. 1-5+ years of quality control experience in an IVD, medical device, or regulated diagnostic manufacturing environment. Hands-on experience with relevant analytical methods (e.g., qPCR, spectrophotometry, electrophoresis). Strong knowledge of regulatory requirements: ISO 13485, FDA QSR (21 CFR Part 820), IVDR (EU 2017/746), CLSI guidelines. Familiarity with GMP, GLP, and good documentation practices (GDP). Proficiency in data analysis and use of laboratory software systems (LIMS, qPCR data analysis, chromatography software, etc.). Strong organizational, troubleshooting, and problem-solving skills. Effective written and verbal communication skills; ability to work collaboratively across functions. Preferred Skills Experience with diagnostic assay validation (sensitivity, specificity, accuracy, precision, robustness). Prior experience supporting regulatory submissions or audits (FDA, ISO, Notified Body). Knowledge of risk management principles (ISO 14971) and design control processes. Familiarity with statistical analysis tools for QC data trending. Working Conditions Laboratory-based position with regular handling of biological samples, reagents, and chemicals. May require occasional work outside normal business hours to support production timelines. Strict adherence to laboratory safety and biosafety protocols is required.

We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a **maker of possible** with us. **Summary** The ID/AST (Phoenix) QC Specialist II is a laboratory scientist, whose primary responsibility will be split between processing data generated from Quality Control testing of Phoenix disposable products and complaint investigations. The position will also be responsible for supporting the Phoenix Quality Control Lab by, but not limited to QC testing of Phoenix disposable products and all lab-related duties. **Responsibilities** + Upload and archive Phoenix instrument data. + Print Resident Panel Reports. + Copy, process, and import instrument data via queries. + Print reports, review data and analyze results for trends. + Completion of Phoenix Quality Control laboratory testing documentation and evaluation of test results against specifications to make pass / fail determinations. + Communicating results to the appropriate Plant personnel. + Generation of Quality Notifications upon testing failures. + Work closely with Product Support to evaluate and recommend proactive solutions. + Archive processed data and updating the MRB Database. + Review and release of drugs and substrates (frozen stocks) for the Solution Preparation department. + Perform routine Phoenix Quality Control testing, as well as any additional lab-related duties or special projects. + Coordination of complaint investigations including adhering to turnaround times and presenting findings during complaint meetings. + Additional duties and responsibilities as determined. + Able to handle a fast paced work environment + Able to adapt to rapid changes in prioritization + Able to take feedback and direction from the plant level Quality Engineers **Qualifications** Education + Bachelor Degree in Biology/Microbiology or other related Life Science. Certifications + ASQ Certification, Medical Laboratory Technician, or Medical Technologist Certification a plus. Experience + 3 years of relevant experience. Knowledge + Knowledge of IVD industry regulations (FDA, GMP/QSR, ISO, CE). + Knowledge of spreadsheet, word processing, and database applications. Abilities + Good verbal and written communication skills. + Team oriented. + Must demonstrate the ability to solve problems and make independent sound decisions. At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. **Why Join Us?** A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. \#CLOLI Required Skills Optional Skills . **Primary Work Location** USA MD - Sparks - 7 Loveton Circle **Additional Locations** **Work Shift** At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You (********************************************* . Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles. **Salary Range Information** 73 300,00 $ - 121 000,00 $ USD Annual Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

About Us: BlackSky is a real-time intelligence company. We own and operate the world's most advanced space-based intelligence platform and provide customers satellite imagery, automated analytics and high-frequency monitoring of strategic locations, economic assets and events from around the globe. BlackSky is trusted by the most demanding allied military and intelligence organizations and commercial companies to deliver foresight into critical matters that affect national security and the economy. BlackSky's data enables governments and businesses to see, understand and anticipate change as it happens, giving them the ultimate strategic advantage so they can act quickly. Our global team works with cutting-edge technology to make a difference around the world and prides itself on being people-first, customer-focused and fun. BlackSky is looking for a talented and creative Senior Image Annotation/Quality Control Analyst to support the development, operation, and capability evolution of Spectra AI, BlackSky's cutting edge AI/ML Platform. As part of the machine learning team, you are instrumental in shaping our computer vision products by managing the quality of data that trains AI/ML models. You will help manage and grow the entire labeling process that trains Spectra AI, overseeing remote data labeling teams and actively assessing the quality of trained models, which create critical timely insights for our customers. While the locations listed in the job posting are ideal, we would love candidates near either our Herndon, VA or Seattle, WA offices. We may also consider remote candidates in certain states. Responsibilities: Lead and manage data labeling teams, providing oversight for labeling campaigns. Research for AI product development, identifying geographic areas where objects exist, developing object ontologies, building annotation instructions, and identifying imagery for annotation. Collaborate with machine learning and product teams to define metrics, assess, and report on the quality of machine learning models in development and production using statistical and quality assurance approaches. Work with the machine learning and product teams to define and measure the performance of machine learning models against SLAs. Identify customer requirements and liaise with computer vision team to codify specifications for training datasets. Create processes, tools, and scripts to manage and track data quality and labeling performance. Take part in the entire project lifecycle from requirements development to deployment. Innovate and streamline data annotation processes. Other job-related duties as assigned. Required Qualifications: Minimum of five (5) years of hands-on experience as a data quality engineer, imagery analyst, GIS analyst, or quality assurance engineer in the space of satellites, computer vision, or machine learning. Bachelor's Degree or higher in one of the following fields: computer science, GIS, data science, mathematics, physics, statistics, or another scientific field. Experience interpreting satellite imagery to identify objects, behaviors, or activities and working with GIS datasets. Hands on experience with annotation platforms such as LabelBox, SuperAnnotate, AWS Sagemaker, or CVAT. Experience managing remote annotation workforces such as CloudFactory, Hive, or iMerit. Collaborates well with others and able to communicate ideas to those with other backgrounds. Experience with quality assurance practices, model testing & evaluation, and computing metrics & statistics from data. Attention to detail and ability to define, enforce, and follow rigorous process controls for managing data. The program this role will support requires Us-born citizenship. Preferred Qualifications: Experience with AI advancements in image annotation such as the Segment Anything Model (SAM). Embeddings and other AI Assistance tools. Experience writing code and scripts, especially for processing and evaluating large amounts of data. Proficiency with Python for automation and data manipulation tasks. Knowledge and experience working in an AWS Cloud environment. Demonstrated ability to lead and manage small teams. Ability to obtain and maintain a US security clearance. Life at BlackSky for full-time US benefits eligible employees includes: Medical, dental, vision, disability, group term life and AD&D, voluntary life and AD&D insurance BlackSky pays 100% of employee-only premiums for medical, dental and vision and contributes $100/month for out-of-pocket expenses! 15 days of PTO, 11 Company holidays, four Floating Holidays (pro-rated based on hire date), one day of paid volunteerism leave per year, parental leave and more 401(k) pre-tax and Roth deferral options with employer match Flexible Spending Accounts Employee Stock Purchase Program Employee Assistance and Travel Assistance Programs Employer matching donations Professional development Mac or PC? Your choice! Awesome swag The anticipated base salary range for candidates in Seattle, WA is $100,000-115,000 per year. The final compensation package offered to a successful candidate will be dependent on specific background and education. BlackSky is a multi-state employer, and this pay scale may not reflect salary ranges in other states or locations outside of Seattle, WA. BlackSky is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer All Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, sexual orientation, gender identity, disability, protected veteran status or any other characteristic protected by law. To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. #LI-Remote EEO/AAP/ Pay Transparency Statements: ***************************************************************** ************************************************************************************************

Job Title: Research Chemist Reporting: Director of Innovation Ascent Industries Co. is seeking a Research Chemist to join our Research and Development team. This role will serve as the technical focal point for new custom and contract manufacturing projects and drive successful execution from proof of concept through commercial-scale production. This role will collaborate with cross-functional stakeholders in R&D, Sales, Marketing, Engineering, and Manufacturing to drive commercial success with a focus on speed to solution, commercial-scale viability, deep technical rigor, and a proactive safety mindset. The ideal candidate combines strong technical skills in experiment design, synthesis, process chemistry, commercial-scale unit operations, and scale up within the chemicals or materials industry. This role is expected to serve as the subject matter expert for all analytical testing related to the contract manufacturing projects, implementing customer specified tests and introducing new test methods that are critical for ensuring product quality. Duties and Responsibilities: Serve as the technical focal point for new contract manufacturing opportunities. Identify fastest and most efficient route to commercially viable solutions for new contract manufacturing and custom synthesis opportunities based on a deep understanding of process chemistry and plant unit operations. Establish R&D lab capabilities for synthesis, process development, sample preparation, and testing by evaluating current capabilities and additional needs to support project pipeline. Design experiments based on sound scientific principles and statistical methods to validate technical packages for proof of concept, optimize processes, and develop technical package for manufacturing to support First Time in Spec production. Rapidly produce samples for customer evaluation based on a thorough understanding of plant equipment capabilities and technical requirements Demonstrate expertise in a broad array of analytical instruments and drive new method development to align internal test methods and capabilities with customer methods and protocols. Leverage external labs for specialized test capabilities. Collaborate with key stakeholders in Sales, Engineering, Manufacturing, Procurement, and Product stewardship to drive successful commercialization. Engage with customers to gather process details, develop experimental plans, communicate project progress, present key findings, results, and support successful qualifications. Create Standard Operating Procedures and Work Instructions for core lab activities. Assure safe lab operations and compliance with site regulations while ensuring zero recordables. Skills, Qualifications, Experience, Special Physical Requirements: Bachelor's degree (advanced degree preferred) in Chemistry, Chemical Engineering, or Materials Science and Engineering Proven hands-on industrial scale-up and technical transfer experience (5+ years) in fine or specialty chemicals or materials industry with subject matter expertise in one or more product categories: Adhesives, Coatings, Surfactants, Dispersions, Specialty Additives, and Reactive Blends. Know-how of product requirements for one or more market segments: CASE, Oil and Gas Chemicals, Plastics/Engineered Polymers, Water Treatment Chemicals, Lubricants, and Personal Care. Strong lab scale synthesis skills, working knowledge of commercial-scale process equipment, and prior experience scaling a product from the laboratory scale through robust commercial scale production. Solid understanding of interplay between raw materials, formulations, manufacturing process variables, product specifications, and product performance. Prior experience with development of detailed technical packages for scale up. In depth analytical and method development experience with techniques such as GPC, GC, HPLC, FTIR, NMR, Rheology, Particle Size, and wet chemistry. Design of Experiments and Six Sigma Green Belt Experience Preferred. Ability to prioritize tasks, manage multiple projects simultaneously, and meet tight deadlines. Strong communication skills both written and verbal. US Citizenship or Green Card required Success Metrics On time execution of R&D work for new contract manufacturing projects per milestones established in NPD process Improve technology transfer from lab to plant with a focus on developing detailed technical packages for achieving target specifications in the first production run. Develop detailed understanding of customer technical protocols for testing and drive quick internal implementation Serve as a technical interface to provide outstanding customer engagement in all technical aspects and help position R&D as our unique value proposition to contract manufacturing customers

Job DescriptionWho we are REGENXBIO is an exceptional place to work. You'll have the opportunity to collaborate with some of the best and the brightest people, touch amazing science, and be a part of extraordinary plans. Our core values: Trust, Accountability, Perseverance, and Innovation drive everything we do. We aim to bring these values to life every day with all that we do, and we believe that what we do matters - to patients, to their families, and to their communities. As a member of our Bioanalytical Sciences team, you will be responsible for performing nonclinical and clinical sample testing (PK, Immunogenicity, PCR, etc.) following developed, qualified, and/or validated bioanalytical methods in support of REGENXBIO projects and programs. You will also be responsible for developing and validating bioanalytical methods for gene therapy products. You will also be responsible for performing QC review of documentation produced in the Bioanalytical laboratory, including assay runs, summary tables, reports, protocols and collaborate with various departments to ensure compliance with regulatory expectations.What you'll be doing Conduct assay operations and maintains accurate testing records. Review technical documents. Perform QC peer reviews and manages project-related activities. Troubleshoot analytical method issues and maintains lab inventories. Support Sample receipt/Accession, buffer preparation and lab maintenance Performs additional tasks or assist with special projects as assigned or needed. We set our employees up for success. To be successful in this role and help us achieve our goals, we are looking for someone with the following skills and qualifications: Bachelor's degree in a relevant scientific field with 2+ years of industry experience, or Master's with 1+ year. Hands-on experience with immunoassays (ELISA, MSD), cell-based assays, qPCR, and/or LC-MS. Analytical, problem-solving, and organizational skills with excellent attention to detail. Collaborative team player with strong written and verbal communication skills. Proficient in data analysis software (e.g., SoftMax) and Microsoft Office applications. By joining REGENXBIO, you will have the opportunity to be a part of a growing company and incredible team passionate about developing novel AAV gene therapy products to our patients. In addition, professional development is important to us. By joining our team, you'll have the opportunity to be exposed to challenging projects and development resources to help you grow personally and professionally. We are proud to offer a comprehensive rewards package which includes a market-competitive base salary, an annual performance-based bonus program, stock grants at all levels, and benefits such as health, dental, and vision insurance, retirement plan with 401(k) match, summer hours, and more! The estimated compensation range for this role is $66,000-$89,000 annually. The actual salary offered to the final candidate depends on a number of factors such as relevant work experience, skills, education, and years of experience.

PenFed is hiring a (Hybrid) Sr Analyst, Real Estate QC Underwriting at our Omaha, Nebraksa; San Antonio, Texas; Eugene, Oregon or Tysons, Virginia location. The primary purpose of this job is to perform quality control reviews for first trust conventional, VA, FHA and equity real estate loans. This role will evaluate the integrity and quality of the credit, compliance, and collateral aspects of the mortgage loan origination process through pre-funding and post-funding loan reviews designed to verify the accuracy and integrity of the information and loan documentation used to support the lending decision for conventional, VA, FHA, and Equity Line of Credit loans. It will validate adherence to PenFed's policies and procedures and secondary marketing investor guidelines. This role requires expertise in evaluating property valuations, including all types of appraisals, AVMs and property condition inspections, with knowledge of Interagency guidelines and Appraisal Independence Requirements. Responsibilities Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. This is not intended to be an all-inclusive list of job duties, and the position will perform other duties as assigned. + Conduct reviews of first trust conventional, VA, FHA and equity mortgage loans to ensure that loans were properly underwritten, and that sound judgment was used in the underwriting process. Complete a thorough analysis of loan files to determine member credit worthiness and collateral values were adequate. Review legal and compliance documentation as applicable. + Conduct reviews of mortgage loans to evaluate the accuracy and integrity of the information and loan documentation used to support the lending decision. + Conduct reviews of mortgage loans to ensure compliance with PenFed's policy and procedures, investor, agency, and secondary market requirements. + Analyze and determine accurate defect ratings based on investor's loan eligibility requirements. Evaluate the entire credit package and collateral for residential mortgage loans and ultimately ensure an investment quality loan product. + Follow up on previous deficiencies and examine samples of corrected files. + Ability to work collaboratively with Mortgage Operations, providing clarification of review results as needed. + Understand and interpret all credit underwriting documentation required to be reverified in each loan file and conduct further research as necessary. + Perform peer reviews and provide guidance to junior analysts as needed. + Assist with process testing as assigned and participate in special projects. + Maintain a working knowledge of internal policies, procedure, external regulations, secondary market underwriting guidelines, investor, and private mortgage insurance guidelines. + Maintain current knowledge of Fannie Mae, Veterans Administration (VA), Freddie Mac, FHA and external investors. Qualifications Equivalent combination of education and experience is considered. + Bachelor's degree in business, accounting, finance, or another related field required. + Minimum of three (3) years progressive experience in real estate lending with underwriting experience required, preferably in a bank or credit union environment. + Advanced knowledge of real estate loans (origination, processing, closing, funding) required. Broad knowledge of consumer real estate lending, including first trust mortgage loans, home equity loans and lines of credit. + Knowledge of lending compliance regulations and system definitions. + Active or recent VA SAR and/or FHA DE underwriting authority preferred. + Proficiency with Encompass is highly desirable. Supervisory Responsibility This position will not supervise employees. Licenses and Certifications There are no additional certifications required. Work Environment While performing the duties of this job, the employee is regularly exposed to an indoor office setting with moderate noise. *Most roles require working in an office setting with moderate noise and the ability to lift 25 pounds.* Travel The ability to travel to various worksites and be on-call may be required. #LI-Hybrid About Us Established in 1935, PenFed today is one of the country's strongest and most stable financial institutions with over 2.9 million members and over $31 billion in assets. We serve members in all 50 states and the District of Columbia, as well as in Guam and Puerto Rico. We are federally insured by NCUA and we are an Equal Housing Lender. We are available to members worldwide, via the web, seven days a week, twenty-four hours a day. We provide our employees with a lucrative benefits package including robust medical, dental and vision plan options, plenty of paid time off, 401k with employer match, on-site fitness facilities at our larger locations, and more. Equal Employment OpportunityPenFed management will maintain and observe personnel policies which will not discriminate or permit harassment or retaliation against a person because of race, color, creed, age, sex, gender, gender identity, gender expression, religion, national origin, ancestry, marital status, military or veteran status or obligation, the presence of a physical and/or mental disability or medical condition, genetic information, sexual orientation, and all statuses protected by applicable state or local law in all recruiting, hiring, training, compensation, overtime, position classifications, work assignments, facilities, promotions, transfers, employee treatment, and in all other terms and conditions of employment. PenFed will also prohibit retaliation against individuals for raising a complaint of discrimination or harassment or participating in an investigation of same. PenFed will also reasonably accommodate qualified individuals with a disability so that they can apply for a job or perform the essential functions of a job unless doing so causes a direct threat to these individuals or others in the workplace and the threat cannot be eliminated by reasonable accommodation or if the accommodation creates an undue hardship to PenFed. Contact human resources (HR) with any questions or requests for accommodation at ************.

Job Details Experienced Pocomoke City, MD Full Time $28.00 - $28.00 Hourly ManufacturingJob Posting Date(s) 07/02/2025 10/31/2025Description Responsible for performing quality control testing, creating technical reports on the specifications and outcomes of tests, products and processes. Responsible for all chemical manufacturing of Ricca's chemical inventory products. ESSENTIAL FUNCTIONS AND BASIC DUTIES: Act responsibly at all times to ensure the health, safety, and well-being of self, co-workers, visitors, neighbors, and property. This includes compliance with all RCC safety policies and procedures, and a working knowledge of government regulations, particularly hazardous material regulations. Schedule and assign daily testing based on the company's planning schedule to utilize available skills, knowledge and experience, labor hours, and lab equipment. Ensure that all assigned testing of finished products is conducted according to specified procedures and in a timely manner. Performing routine and non-routine analyses without supervision. Collect data and calculate Measurement Uncertainty Budgets for specified testing. Competently perform at least 95% of the types of analysis/testing. Make detailed observations, analyze data, and interpret results. Read and record data quickly and accurately and avoid perceptual errors in performing computations. Prepare Certificate of Analysis reports without errors. Review of data obtained for compliance with specifications and report abnormalities; including measurement uncertainty budgets for specified testing. Compile data for OOS investigations, documentation of test procedures, and abnormalities. Assist in technical complaint investigations and development of new methods and technologies. Participate and satisfy requirements for inter-laboratory round robin testing as well as ISO 17034 Proficiency Testing as required in order to maintain accreditation. Troubleshoot, calibrate and perform preventative maintenance on laboratory instruments and equipment and document events as required. Ensure inventory levels for laboratory supplies are kept current and are accurate. Stay abreast of ISO 17034 requirements and follow all RCC Standard Operating Procedures with special attention to those pertaining to the laboratory processes. Consistently meets/exceeds standards assigned within Functional Training Document (FTD) program. Any other tasks deemed necessary. Commitment to the organizations values; High Standards, Bias for Action, Teamwork, CustomerObsession, Trust, Accountability, Innovation and Growth & Learning. REQUIRED SKILLS: Good communication Critical thinking and problem-solving Time management Analytical Organizational skills Patience and determination Scientific and numerical skills EDUCATION AND EXPERIENCE: Bachelor's Degree in Chemistry or similar field, such as biology, engineering or physics. Three (3) to five (5) years of experience in quality control analytical laboratory or regulated manufacturing environment preferably in the chemical or pharmaceutical industry. Experience in handling and operating laboratory glassware and equipment for testing purposes. Working knowledge of ISO9001:2008 standards, cGMP/GLP regulation, and laboratory sample processes. Knowledge of ISO 17034 standard is a plus. This position requires a person to be able to speak, write and conduct business in English. This person shall also have sufficient eyesight to read business documents and properly fill out appropriate Quality System Records and Forms. This position should be able to understand and then follow written and verbal work instructions and quality system procedures without direct and constant supervision after the initial training period is successfully completed and documented. This position should have sufficient mental capacity to accommodate and successfully implement changes in work tasks and quality system changes when required. Strong organizational skills, meet deadlines, work independently and with the team with strong follow through, strong communication skills, both written and verbal and accuracy and attention to detail. WORK ENVIRONMENT: The physical environment may require the employee to work both inside and outside in heat/cold, wet/humid, and dry/arid conditions. This position may be working in the warehouse under various indoor environmental conditions, including supplemental heating in the winter months and without air-conditioning in the summer months. May be requested to work overtime and weekends. The position may occasionally be exposed to ruptured, leaking packages, some of which may contain Hazardous Materials. Where appropriate, proper safety equipment should be utilized and/or appropriate personnel notified. Frequently required to use personal protective equipment to prevent exposure to hazardous materials and chemicals. This job may require lifting of up to 50 pounds occasionally.

Under minimal supervision of QC management, the QC Chemist performs physical and chemical testing on raw materials, in-process and finished products, as well as stability samples. Utilizes established methods and standard operating procedures and laboratory equipment to perform testing of materials. Prepares high quality written documentation, such as notebooks, logbooks, standard operating procedures (SOPs) and LIMS reports. Trouble shoots analytical equipment. Provides training on analytical methods and new technologies. Responsibilities: Performs analytical testing of raw materials, in-process materials, finished products and stability samples. Operates laboratory equipment such as balances, pH meters, hardness testers, particle size analysis, LOD, Karl Fischer, Melting Point, etc. in accordance with laboratory SOPs and test methods. Effectively performs routine testing using HPLCs, GCs, UV-VIS, FT-IR and ICP-MS equipment in accordance with SOPs and test methods. Performs data analysis and evaluation of test results. Prepares reports and reviews data. Maintains accurate records of test data, maintains laboratory notebooks and logbooks in accordance with company guidelines and GDPs. Assists in writing and revising SOPs and tests methods as needed. Follows documented procedures: SOPs, test methods, and transfer protocols. Performs routine maintenance, calibration, and performance verification on applicable instruments. Performs investigation activities and writes deviation and investigation reports. Suggests and writes CAPAs. Follows lab safety procedures. Perform other duties as assigned. Qualifications: Bachelors in chemistry or related physical/biological science, or equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities. Minimum of 3 years' experience in Pharmaceutical Analysis Must understand analytical chemistry. Demonstrated knowledge of cGMP regulations and ICH guidelines Computer literacy and ability to use data acquisition and processing software, such as EMPOWER 3 Demonstrate the ability to read, analyze, and interpret USP/NF methods, SOPs and technical procedures manuals, and batch records. Demonstrate the ability to define problems, collect data, establish facts, and draw valid conclusions; interpret an extensive variety of technical instruction in mathematical or diagram form. Knowledge of basic laboratory practices, methods, and techniques Demonstrate the ability to carry out work assignments communicated orally or in writing. Demonstrate familiarity with Lean Six Sigma Methodologies and proven analytical/ problem solving capabilities. Demonstrates the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates. Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision. Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as required. Must be able to comprehend and follow all applicable SOPs. Demonstrate ability to acquire the appropriate knowledge from resources on with electronic Quality Management Systems such as MasterControl and Trackwise. Demonstrate understanding of the current federal, local, and international regulations regarding the production, testing, and release of drug substances and products. Good understanding of cGMPs, industry, and regulatory standards and guidelines. Demonstrate familiarity with Microsoft programs like Word, Excel, PowerPoint, Project, Teams, Outlook, etc. Demonstrate the ability to portray the appropriate level of integrity and professionalism. Demonstrate the ability to communicate effectively with management, staff, regulators, and client representatives in written and verbal formats. Demonstrate the ability to complete tasks accurately and according to established and shifting timelines. Demonstrate the ability to make quality scheduling, resource allocation, and priorities decisions. Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment. Results-oriented and efficient. Creative and open-minded who fosters an environment in which sharing of ideas is encouraged. Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally). Demonstrate the ability to work well in a cross-functional team environment. Must communicate fluently in English and have legible handwriting. Physical Demands: Ability to travel between and within facilities to visit staff, operations, and projects, as needed. Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary). Ability to lift up to 40 pounds on occasion. Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).

Science you can trust from concept to consumer. Since 1967, Deibel Laboratories has operated several private food testing facilities providing services in both Microbiology and Chemistry testing. We play an integral role in food and product safety for industry-leading producers, as well as family-run operations much like our own. Our lab location in Chester, VA is hiring a full-time Food Laboratory Technician. (40 hours/week plus benefits included). We offer a competitive salary based on knowledge and experience. This position includes full health benefits for self and family (employer pays for 90% of employee premiums and 50% of dependents on our base plan). Deibel also offers a self-funded dental plan, vision plan, and 401K option along with profit sharing. Check out our website to learn more about what we do at ******************* Compensation : Starting hourly rates $21 - $22.50 D.O.E. plus a competitive benefits package. Shift Available: Wednesday - Saturday 11:30am - 9pm Required Skills/Abilities: Entry Level Position: We Are Happy to Train Must have an interest in learning basic knowledge of microbiology and to accurately perform testing procedures and obtain accurate results. A basic knowledge of personal computers is useful to accurately enter testing data and results. Planning skills are useful to maintain supplies of analysis materials and ensure analysis is completed within a specified time. Basic math skills are essential to complete analysis. Physical dexterity is required for manipulating samples. We'd Love to Hear from People With: Previous experience in manufacturing, production, warehouse, food industry, food service, baking, baristas, or retail. Strong problem-solving skills, ability to multitask, and work in a fast-paced environment. Skills to communicate effectively and develop good working relationships with all employees. A professional workplace appearance, ethical conduct, honesty, and integrity in all communications. A thirst to seek out and participate in appropriate training and professional development. Fluency in written and spoken English is required. Physical Requirements: Safety equipment of gloves, laboratory coat, and eyeglasses may need to be worn depending on the testing process. Extended time spent in a standing position. Ability to lift up to 50lbs occasionally and 10 - 15lbs repeatedly.All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Deibel is committed to fostering a diverse and welcoming workplace with people of all types of backgrounds and experiences.SERVICE - QUALITY - TRANSPARENCY - PARTNERSHIP - EDUCATION - PROFESSIONALISM

About Us: Here at Thermo Fisher Scientific, our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research, clinical to commercial production means you can have a broad and significant impact. All while working in an environment where you will be supported, valued and rewarded for your performance. Join our Sales & Marketing team with an unmatched depth of capabilities and help our customers solve some of the world's toughest challenges. As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. DESCRIPTION: Join our team at Thermo Fisher Scientific as a Quality Control Scientist II, where you'll contribute to global health through innovative process development and optimization. You'll provide technical leadership in technology transfer, process validation, and manufacturing support across our facilities. Working at the intersection of R&D and manufacturing, you'll collaborate with cross-functional teams to ensure successful execution of manufacturing processes while driving continuous improvement initiatives. Your expertise will be vital in resolving complex technical challenges, conducting investigations, and implementing solutions that maintain our high standards of quality and efficiency. REQUIREMENTS: • Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 3 years of experience in GMP-regulated pharmaceutical/biotech manufacturing preferred. • Experience in LabVantage LIMS configuration, customization, and scripting preferred • Strong technical expertise in process development, scale-up, and technology transfer • Proven ability to lead complex investigations and implement effective solutions • Experience with process validation and qualification activities • Expert knowledge of cGMP regulations and quality systems • Configure, maintain, and enhance LIMS functionality, including master data, workflows, test methods, specifications, stability protocols, and user roles. • Strong analytical and statistical analysis capabilities • Excellent verbal and written communication skills • Ability to work collaboratively in a matrix environment • Proficiency with statistical analysis software and Microsoft Office suite • Create and maintain QC dashboards, reports, and KPIs to support decision-making. • Ability to support manufacturing operations as needed, including some weekend/off-hours coverage Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. A one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! **************************** Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Accessibility/Disability Access Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at ***************. Please include your contact information and specific details about your required accommodation to support you during the job application process. *This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

Job Title: Quality Control Microbiology Technician FLSA Exemption Status: Nonexempt Status: Hourly Department: Quality Control Reports To: Quality Control Supervisor Job Summary: The Quality Control Microbiology Technician is responsible for all in-house raw material and finished goods microbiological testing at Bowman Andros Products. Essential Functions and Responsibilities: Perform microbiology testing on raw material and finished product, shelf stability studies, and any other samples as requested. Report results in a timely manner. Complete Day 21+ testing for all required products. Ensure all supplies for the micro laboratory are available in adequate amounts, as needed and organize first in first out to avoid expired reagents. Review and save results to shared drive for all plated samples to ensure quick release off positive hold. Assists with training team members on microbiology subjects and procedures to help ensure knowledge is shared amongst the team. Help troubleshoot microbiology failures within area of responsibility. Perform gluten and allergen testing as needed. Understand and perform all duties of Quality Control Sanitation Technician as needed when absence occurs. Notifies appropriate management of out of specification microbiology results on any testing so action can be taken. Ensures that all documentation filled out is complete and accurate. Assist and support the functions and responsibilities of the Quality Control Supervisor and Quality Manager. Understands the production process flow and is actively engaged with the operational lines and teammates on the lines. Sets up, adjusts and operates all lab equipment and instruments to conduct lab testing. When requested, tests samples of products and raw materials (sauces, ingredients, and packaging) to verify conformity to specifications. Maintains clean and orderly work areas, to include general housekeeping, workstations, overall appearance of the lab, retain rooms, equipment, re-stocking of the supplies and maintaining calibration of lab instruments. Troubleshoots lab equipment if issues occur. Review quality documentation for product release from positive hold. Release product from positive hold for orders. Initiate quality hold when product does not meet specification and/or requirements during review of quality documentation. Role model, promote and assist with enforcing all Bowman Andros Products Food Safety policies, Good Manufacturing Practices (GMP's) and Quality standards for all teammates. Other duties as required. Required Knowledge, Skills and Abilities: Preferred: Associates degree or equivalent of: Two years related experience and/ or training Combination of education and experience Basic algebra: reliably add, subtract, multiply, divide, take averages, etc. Proficient written and verbal communication: Detailed technical writing skills- documenting, emailing, note taking Excellent public speaking skills- relaying information, discussing issues with co-workers, presenting information. Previous work experience in a food manufacturing setting. Ability to work effectively with various lab equipment including but not limited to: scales, torque meter, refractometer, pH meter, ATP Meter, Bostwick meter, manual titrator, colorimeter, etc. Regular and reliable attendance required. Has the ability to become proficient in the BAP WMS (warehouse management system). Knowledge of Food Safety regulations and manufacturing processes. Teamwork- ability to work well with others to solve problems, complete tasks and achieve company goals. Proficient in Microsoft Office. Ability to work in a fast-paced environment where priorities change frequently. Capable of reading and interpreting data. Ability to work with minimal supervision and take initiative to resolve issues independently when discovered. Self-motivated and task driven. Able to communicate constructively and professionally, firmly focused on a quality mentality, when faced with crucial decision making across departments. Must be able to work overtime and weekends as necessary. Working Environment: The work environment characteristics described here are representative of those a teammate encounter while performing the essential functions of this job. The QC Tech is required to work in an office environment, on the production floor, and in a lab. While performing the duties of this job, the teammate frequently will be exposed to wet and/or humid conditions, extreme heat and/or cold, and will involve exposure to chemicals in lab settings during testing. The teammate occasionally works near moving mechanical parts. The incumbent will be exposed to loud noises from production equipment and thus will be required to wear PPE. The noise level in the work environment is usually moderate but may be high at times due to production and mechanical equipment noise. Physical Demands: The physical demands described here are representative of those that must be performed by a teammate to successfully perform the essential functions of this job. While performing the duties of this job, the teammate is regularly required to stand, walk, use hands to handle, or feel objects, equipment, or controls; reach with hands and arms; see, talk and /or hear. The QC Tech must be able to spend almost all their time standing or walking for up to 10 hours daily. The teammate frequently is required to climb or balance and stoop, kneel, sit, crouch, or crawl, frequently traveling up and down stairs and other uneven work surfaces. The teammate is occasionally required to taste, touch or smell. Teammates must be able to lift, carry, push and/or pull, and balance up to 25 pounds. This description is intended to indicate the kinds of tasks and levels of work difficulty that will be required of positions that will be given this title and shall not be construed as declaring what the specific duties and responsibilities of any position shall be. It is not intended to limit or in any way modify the right of any supervisor to assign, direct, and control the work of teammates under his/her supervision. The use of a particular expression or illustration describing duties shall not be held to exclude other duties not mentioned that are of similar kind or level of difficulty.

Apply for this opportunity as a Microbiology MT/MLT in Southeastern Virginia for permanent hire. Opportunities on the day and night shift! Job Title: Microbiology Medical Technologist / Technician Job Description: We are looking for a dedicated Microbiology Medical Technologist to join our laboratory team. You will be responsible for performing microbiological tests, analyzing samples, and ensuring accurate and timely results. Key Responsibilities: Conduct microbiological testing on various specimens. Identify and characterize microorganisms. Maintain laboratory equipment and ensure compliance with safety standards. Collaborate with healthcare professionals to interpret results. Qualifications: Minimum Associate's degree in Medical Technology or related field. ASCP or equivalent certification preferred. Strong analytical and problem-solving skills. Benefits: Competitive salary Health insurance Professional development opportunities Click to apply or send a resume to marissak@ka-recruiting.com for immediate consideration. (Reference Code: MK1024)

Job Title: Quality Control Microbiology Technician FLSA Exemption Status: Nonexempt Status: Hourly Department: Quality Control Reports To: Quality Control Supervisor Job Summary: The Quality Control Microbiology Technician is responsible for all in-house raw material and finished goods microbiological testing at Bowman Andros Products. Essential Functions and Responsibilities: Perform microbiology testing on raw material and finished product, shelf stability studies, and any other samples as requested. Report results in a timely manner. Complete Day 21+ testing for all required products. Ensure all supplies for the micro laboratory are available in adequate amounts, as needed and organize first in first out to avoid expired reagents. Review and save results to shared drive for all plated samples to ensure quick release off positive hold. Assists with training team members on microbiology subjects and procedures to help ensure knowledge is shared amongst the team. Help troubleshoot microbiology failures within area of responsibility. Perform gluten and allergen testing as needed. Understand and perform all duties of Quality Control Sanitation Technician as needed when absence occurs. Notifies appropriate management of out of specification microbiology results on any testing so action can be taken. Ensures that all documentation filled out is complete and accurate. Assist and support the functions and responsibilities of the Quality Control Supervisor and Quality Manager. Understands the production process flow and is actively engaged with the operational lines and teammates on the lines. Sets up, adjusts and operates all lab equipment and instruments to conduct lab testing. When requested, tests samples of products and raw materials (sauces, ingredients, and packaging) to verify conformity to specifications. Maintains clean and orderly work areas, to include general housekeeping, workstations, overall appearance of the lab, retain rooms, equipment, re-stocking of the supplies and maintaining calibration of lab instruments. Troubleshoots lab equipment if issues occur. Review quality documentation for product release from positive hold. Release product from positive hold for orders. Initiate quality hold when product does not meet specification and/or requirements during review of quality documentation. Role model, promote and assist with enforcing all Bowman Andros Products Food Safety policies, Good Manufacturing Practices (GMP's) and Quality standards for all teammates. Other duties as required. Required Knowledge, Skills and Abilities: Preferred: Associates degree or equivalent of: Two years related experience and/ or training Combination of education and experience Basic algebra: reliably add, subtract, multiply, divide, take averages, etc. Proficient written and verbal communication: Detailed technical writing skills- documenting, emailing, note taking Excellent public speaking skills- relaying information, discussing issues with co-workers, presenting information. Previous work experience in a food manufacturing setting. Ability to work effectively with various lab equipment including but not limited to: scales, torque meter, refractometer, pH meter, ATP Meter, Bostwick meter, manual titrator, colorimeter, etc. Regular and reliable attendance required. Has the ability to become proficient in the BAP WMS (warehouse management system). Knowledge of Food Safety regulations and manufacturing processes. Teamwork- ability to work well with others to solve problems, complete tasks and achieve company goals. Proficient in Microsoft Office. Ability to work in a fast-paced environment where priorities change frequently. Capable of reading and interpreting data. Ability to work with minimal supervision and take initiative to resolve issues independently when discovered. Self-motivated and task driven. Able to communicate constructively and professionally, firmly focused on a quality mentality, when faced with crucial decision making across departments. Must be able to work overtime and weekends as necessary. Working Environment: The work environment characteristics described here are representative of those a teammate encounter while performing the essential functions of this job. The QC Tech is required to work in an office environment, on the production floor, and in a lab. While performing the duties of this job, the teammate frequently will be exposed to wet and/or humid conditions, extreme heat and/or cold, and will involve exposure to chemicals in lab settings during testing. The teammate occasionally works near moving mechanical parts. The incumbent will be exposed to loud noises from production equipment and thus will be required to wear PPE. The noise level in the work environment is usually moderate but may be high at times due to production and mechanical equipment noise. Physical Demands: The physical demands described here are representative of those that must be performed by a teammate to successfully perform the essential functions of this job. While performing the duties of this job, the teammate is regularly required to stand, walk, use hands to handle, or feel objects, equipment, or controls; reach with hands and arms; see, talk and /or hear. The QC Tech must be able to spend almost all their time standing or walking for up to 10 hours daily. The teammate frequently is required to climb or balance and stoop, kneel, sit, crouch, or crawl, frequently traveling up and down stairs and other uneven work surfaces. The teammate is occasionally required to taste, touch or smell. Teammates must be able to lift, carry, push and/or pull, and balance up to 25 pounds. This description is intended to indicate the kinds of tasks and levels of work difficulty that will be required of positions that will be given this title and shall not be construed as declaring what the specific duties and responsibilities of any position shall be. It is not intended to limit or in any way modify the right of any supervisor to assign, direct, and control the work of teammates under his/her supervision. The use of a particular expression or illustration describing duties shall not be held to exclude other duties not mentioned that are of similar kind or level of difficulty.

QUALITY CONTROLLER The Quality Controller reports to the Quality Control Leader. The Quality Controller is responsible for ensuring that products meet the established quality standards set by Serioplast and the regulatory bodies. This role involves inspecting raw materials and finished products, identifying defects, suggesting improvements, and maintaining detailed records to ensure continuous compliance and customer satisfaction. The role of Quality Controller is based on the following activities: HSE STANDARDS: Follows the application of safety rules according to company policies and regulations. Maintains order, organization and cleanliness in all assigned areas, working in line with correct workplace hygiene practices, with the aim to be an example to others. QUALITY CHECKS: Performs controls according to the quality control plan for each product and during technical interventions and product industrializations using lab instruments (scale, caliper, thickness gage, top load tester, torque meter, etc.). Sorts defected bottles, contributes to decisions on discarding or keeping batches and provides support in the evaluation of quality problems. PRODUCTION MATERIALS CHECKS: Checks incoming material against quality specifications and verifies documentation compliance. QUALITY DOCUMENTS AND REPORT WRITING: Fills in and verifies quality measurement information in the proper sheets and systems, and timely signals any issues. Creates production stock labels. Supports the Quality Manager in ensuring that all Quality Control standard methods and procedures are constantly updated in terms of efficiency and compliance to customer requirements. QUALITY CONTROL INSTRUMENTS: Performs calibrations and cleaning of measuring instruments within the production or Lab. Is able to run a program on the CMM Machine. COMMUNICATION and COOPERATION: Guarantees proper information sharing, reports relevant issues to the Quality Manager. Supports the Quality Manager in organizing and performing periodic training for new and existing staff on quality standards, in managing and archiving quality documentation. Participates in internal and external quality audits. Communicates and cooperates with Quality team to ensure quality and hygiene of the final product. Promotes effective communication between team and Manager. Interacts with different business functions to drive high performance culture. Ability to oversee all quality aspects of production during shift. Comfortable in addressing other employees to ensure adherence to all GMP standards and to help promote a strong quality culture within the facility. Technical Skills: Excellent applied knowledge of measuring instruments and techniques High level of attention to details Good knowledge of plastic molding technologies (EBM and/or SBM and/or IM) Good knowledge of ISO standards Basic knowledge of Health, Safety and Environment rules and practices Basic knowledge of Statistical Process Control and statistical analysis Basic knowledge of English Personal Skills: Accountability. Accept responsibility for your actions. Be accountable for your results. Take ownership for your mistakes. Problem solving. Be analytic. Be frugal and avoid sophistication to get the job done without compromising on quality. Resilience and put passion in what you do. Patience, tenacity and hard work allow you to reach your goals and positively respond to challenges. Never give up. Team Play. Build trust in your relationships and contribute to making the work environment positive and stable. Education and Experience: Minimum 3 years' experience working in a BRCGS certified Quality Lab of a manufacturing company, preferably in the FMCG sector This indicates in general terms the type and level of work performed as well as the typical responsibilities of employees in this position. The duties described are not to be interpreted as being all-inclusive. Management reserves the rights to add, modify, change or rescind the work assignments and to make reasonable accommodations in order to comply to country specific laws and/or corporate needs. Job descriptions are periodically revised to include any changes in the organization and/or aspects of the position. Powered by JazzHR td OPmxo5Jo

Summary/Objective Responsible for reviewing consumer pre-closing and post-closing loan packages to ensure accurate documentation, compliance with regulations, identification of legal issues and adherence to bank policies and department procedures. Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Conducts pre-funding review of consumer loans to ensure accuracy and completeness of closing packages. Conducts post-closing review of completed consumer loan documents to ensure compliance with all Federal, State, and local regulations. Acts as an independent reviewer to conduct compliance and post-closing audits on consumer loans, including conventional and government (agency) type mortgage loan files, to ensure compliance and investor guidelines have been met. Identify areas of deficiency and maintain records, responses, and results of all audits. Verify that the terms included in loan documentation match terms approved in the loan request and/or loan presentation. Ensure loan closers correct outstanding errors prior to closing. Establish and maintain production standards and quality requirements. Responsible for the quality control reporting of pre-funding and post-funding files in addition to denied loan files and early payment defaults. Work independently with auditors to resolve exceptions, questions, and concerns about underwriting, documentation, and data integrity errors. Assign, manage, and report Quality Control monthly review of production to Director of Loan Operations. Work with other department managers in complying with responses and action plans for Quality Control exceptions. Determine if internal/external parties involved in all aspects of the loan have successfully met the guidelines and responsibility for particular loan programs. Other Duties Other duties as assigned. Skills/Abilities Strong data entry skills. Detail-oriented and well-organized. Highly professional in all written and verbal communications. Advanced computer skills with working knowledge of Microsoft Office (Word, Excel, Outlook). Able to manage time efficiently and prioritize workloads to meet strict deadlines while handling multiple tasks. Thorough knowledge of various types of secured and unsecured consumer transactions, loan products, and legal and regulatory issues related to lending. Supervisory Responsibility This position does not have supervisory responsibilities. Work Environment This job operates in an office setting, the opportunity to telework is not available. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Office environment with job duties conducted via telephone, face to face meetings, and on the computer. Physical Demands This position requires manual dexterity, the ability to lift files and open cabinets. This position requires bending, stooping or standing as necessary. Travel Limited local travel may be required for this position. Education and Experience 2 years experience in conventional and government compliance, loan file reviews, or associated processes in the lending industry required. 4-year college degree or equivalent additional related work experience preferred. In-depth knowledge of all federal, state, and local compliance regulations to include: Truth in Lending; Equal Credit Opportunity laws, Reg Z, Reg B, and Reg X. Advanced knowledge of total closing function to include: underwriting condition to closing, closing instructions, closing procedures, and TRID. Equal Employment Opportunity/M/F/disability/protected veteran status Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Wallace Montgomery is currently hiring for a full-time Quality Control Inspector to inspect job sites and ensure work is performed according to plan in the Culpeper, VA area. This inspection position earns a competitive wage, based on skills and experience. In addition to competitive pay and our exceptional culture, we offer our Quality Control Inspectors the following benefits: Medical Dental Vision So, now that you've learned the who, what, where, and why, you may be wondering HOW? It's easy! Just fill out our initial mobile-friendly online application. We hope to meet you soon! DAY-TO-DAY As a Quality Control Inspector, you enjoy getting out of the office and out in the field. You provide daily site inspections to ensure compliance with approved plans, specifications, and codes. Once you arrive at job sites, you assess general progress, quality of workmanship, and conformity of the work with the contract documents. You feel good about the part you play in our success and know that you are always valued at our company. ABOUT WALLACE MONTGOMERY Since 1975, our multi-disciplined engineering organization has grown to become a recognized leader in planning, engineering, and construction management. As an Engineering News-Record (ENR) Top 500 design firm, our staff of professional engineers, planners, surveyors, technicians, construction inspectors, and support personnel work on a diverse portfolio of projects involving highways, bridges, mass transit facilities, water resources, utilities, as well as water and wastewater facilities. Our mission is to provide quality professional engineering and technical services to develop innovative solutions that meet the needs of our clients and help build sustainable, resilient projects within our communities. We strive to be the best public infrastructure firm in the Mid-Atlantic region. Our growth and reputation are a result of our incredible team of highly respected and well-trained professionals. We value integrity, quality, teamwork, and respect. Those values are integral to our positive culture. Join our innovative team and enjoy competitive pay, an excellent benefits package, and the chance to make a difference. OUR IDEAL QUALITY CONTROL INSPECTOR Career-minded - Looking for more than just a job Dependable - Reliable, shows up on time and prepared Takes pride in your work - Pays close attention to detail and goes above and beyond Team player - Works well with others Respectful - Treats others with kindness and dignity If this sounds like you, keep reading about this inspection position! REQUIREMENTS FOR A QUALITY CONTROL INSPECTOR High school diploma or equivalent Valid driver's license Reliable transportation If you meet the above requirements, we need you. Apply today to join our team as a Quality Control Inspector! Location: 22701