Quality Specialist Jobs Near Me

Datacenter People is a specialised recruitment company working with the leading data center commissioning and quality services firms in the world. Our client serves as an owner's representative, specialising in Data Center commissioning and QA/QC services. The Role Actively supports the Company's commitment to safety and its core values. Performs quality inspections in accordance with program quality control documentation. Participate and guide project quality control from kick-off until hand-off. Provides oversight of the implementation of the QA/QC management system at site. Coordinates the quality inspections with the site sub-contractors and vendors. Coordinates with the customers representative on all quality matters. Provides oversight in the distribution of relevant QA/QC documentation to site subcontractors while reviewing that completed documentation is stored appropriately upon completion. Verifies that the quality related site activities are in accordance with the design documents and program standards. Participates in the internal and external site audits. Coordinates all the quality site inspections through the Contractor QC team. Ensures all quality control documentation is compiled and competed for as-built hand over through the Contractor QC team. Provide review and reporting of all non-conformance reports and undertake remedial action. Monitors the implementation of the approved site QC Plan. Completes and coordinates the approval of the sites QC technical submittals to the customer. Coordinates with the Client and Contractor QA/QC team on all quality issues. Coordinate and chair the QA/QC site weekly meetings with the Contractor QC personnel. Assures all technical documents relative to site quality control are of current status. The Experience Profile Has data center commissioning/QA experience. Has a history and experience driving improved Quality at scale. Is able to work seamlessly across functional and department lines. Has experience with standard data center equipment to include: electrical distribution equipment from switchgear to panelboards, VFDs, low voltage power and moulded case circuit breakers, overhead IT busway, Diesel Generators, DX units, air handlers, water treatment equipment, BMS modules, and hot aisle containment accessories. Is able to travel domestically and internationally as needed. We regret that due to the high volume of applications we are unable to acknowledge each one. Please bear in mind that if you are selected for interview we will contact you within the next seven days.

Type: Full-Time (Direct Hire) Reports to: Quality Manager Salary Range: $85,000 to $110,000 Overview: In this role, you will have the opportunity to support the deployment of the quality strategy for a local organizational unit, including quality culture, systems, tools, and competent teams with the aim to achieve and exceed customer expectations, while ensuring sustainable operations. Each day, you will assist the organization in achieving the right mix of prevention, continuous improvement, robust root cause analysis, quick response, and sustainable solutions to problems. You will also showcase your expertise by collaborating with local functions that impact the quality results to reach the targets for the organizational unit and aim for world-class performance. Responsibilities: Supporting specific communication relevant to quality management in your area of responsibility. Assisting in continuously identifying and addressing risks and opportunities related to quality management in the local organization. Using quality data analytics from the organization to identify risks, failures, and non-conformances. Facilitating resolution of customer cases by following a robust root cause analysis and implementing preventive and corrective actions. Qualifications: Bachelor's degree in Electrical Engineering (or a related field). Minimum of 8 years of experience in a manufacturing or quality control environment. Hands-on experience with transformers, PDUs, STSs, and UPS products. Proficiency in testing, troubleshooting, evaluating, and servicing electrical distribution and control systems. Ability to read and interpret schematics of electrical equipment and printed circuit board assemblies (PCBAs); skilled in using electrical test equipment such as power supplies, multimeters, oscilloscopes, and power analyzers. Familiarity with Lean, Six Sigma, and other process improvement methodologies is highly desirable. Knowledge of industry standards such as UL1561, NEMA ST-20, IEEE C57.12.01, IEEE C57.12.91, DOE 2016, UL891, and CSA C22.2 preferred Able to travel up to 15% domestic

WITH CONSUMER CONNECTION*** Our client is seeking a Quality and Food Safety Manager for our food manufacturing client. Provides leadership to the company's Quality Food Safety department through coaching and development of front-line associates, driving a culture of safety, inclusion, engagement and accountability. Promotes a culture of Food Safety among all bakery associates through education and policy enforcement along with fellow department leaders. Ensures that our customer's receive the highest quality product in a food safe environment. Provides oversight of Quality and Food Safety programs, and evaluates for compliance through regular audits, inspections and risk assessments, ensuring that Corrective Actions are performed for any non-conformance. Ensures proper document control for all documentation within the food manufacturing facility. Leads all third-party audits .Example is SQF (Safe Quality Foods) Drives continuous improvement by ensuring that LEAN tools and 5S are practiced. Participates in and supports R&D efforts, through ingredient analysis and approval, and ensures that all regulatory guidelines are met. Qualifications Bachelor's degree in Food Science or related scientific major preferred. A combination of education, training and experience that results in demonstrated competency to perform the work may be substituted. GFSI (SQF, BRC, FSSC 22000, IFS, etc), PCQI, Food Defense and HACCP certifications strongly preferred. 5-7 years of experience leading Quality/Food Safety/Sanitation teams in a food production environment. Leadership skills with a focus on associate development and accountability. Excellent communication and interpersonal skills with the ability to work within cross-functional teams. Computer proficiency including MS Office products. Experience with 5S and LEAN tools highly preferred. Bilingual - Spanish and English highly preferred.

Food Quality Assurance / Supply Chain Specialist Department: Supply Chain Industry: Food Manufacturing Status: Full Time - Onsite (Monday - Friday from 8am to 4:30pm) Jones Networking is recruiting for a Food Quality Assurance Specialist to join the Supply Chain Department of a premium food manufacturing company in Sterling, VA. Our client offers the opportunity for a long term, rewarding career with excellent benefits and career growth potential. Benefits include medical, dental and vision insurance, 401(k) + 2% company match, life and disability insurance, paid vacation & holidays, bonus opportunities, employee assistance program, corporate discounts and much more! Food Quality Assurance / Supply Chain Specialist Position Summary: -Maintain supply chain procedures for the department within the corporate office. -Communicate with suppliers regarding initial approval, annual renewal process, as well as item-related documentation requests and follow ups. -Capture and organize food safety and ingredient documentation (electronically) from suppliers. -Work with the corporate Food QA Team and Supply QA Team to assess all suppliers. -Partner with the Procurement Team to ensure material risk assessment specifications are reviewed and agreed upon by the supplier. -Update supply chain QA databases, documenting the raw materials, food/non-food products, processes and regulatory requirements. -Create item information on Genesis R&D, ERPs, and supplier management software. -Assist sites with audits regarding supply chain programs. -Work with stakeholders and suppliers regarding export related documentation. -Partner with cross-functional teams regarding the on-boarding of new commodities and suppliers. -Effectively communicate scientific and technical information to both technical and non-technical personnel. Qualifications Summary: -Associate Degree and/or Bachelor's Degree in Biology, Microbiology, Food Science, Biochemistry or similar field required. -Prior experience within the food industry with knowledge of GMPs, Food Safety, Quality Systems, Quality Assurance and Quality Control. -Working knowledge of compliance expectations for the manufacture of food products. (FDA, USDA & Food Code regulations) -Strong analytical skills with excellent attention to detail. -Ability to successfully execute complex tasks simultaneously. Please visit jonesnet.com for a full list of career opportunities presented by Jones Networking!

We Create Products and Brands That People Trust to Clean, Sanitize, and Protect Their Homes and Pools When you join KIK Consumer Products, you're joining a team that cares about the work we do and also about each other. We bring exceptional brands and products to consumers that help them protect the health and wellness of their families and the cleanliness of their homes and pools. We are committed to building a culture of performance driven by accountability, collaboration, and agility that enables timely fact-based decision-making and exceptional execution with unwavering ethics. As one of North America's largest independent manufacturers of consumer products, KIK helps a large portfolio of brands and retailers bring their products to life. Your Role at KIK As the Quality Assurance Manager, you will report to the Plant Manager. In this role, you are responsible for overseeing the development, implementation, and maintenance of quality assurance systems and processes to ensure that products or services meet established standards and customer expectations. This role involves leading a team of QA professionals, collaborating with cross-functional teams, and driving continuous improvement initiatives. What You'll Be Doing Generate quality metric reports and graphs for the General Manager. Work with Processing Department to standardize the chemical batching process Familiar with quality systems and batching processes Manage, direct, and train Quality Laboratory Technician. Train on the use of KIK Quality Systems and all laboratory equipment. Provide supervision, coaching, and counseling. Train Tank Farm personnel on how to titrate samples for Sodium Hypochlorite and Caustic levels Conduct quality training for all plant personnel. Document all procedures. Lead on all external and regulatory quality audits Ability to take a formula card and develop a batching procedure with the Processing Department Work with vendors to resolve quality issues with raw materials or ingredients Review and approve all packaging changes Maintain the CoLOS database for bottle and case printing. Ability to make suggestions and informed decisions quickly. Ensure packaging operations adhere to all regulatory GMP and customer requirements for finished goods quality. Maintain a working knowledge of government and industry quality assurance codes and standards. Ensure all incoming testing of packaging and chemicals are completed according to GMP and customer requirements. Provide technical assistance to other departments, suppliers and customers as needed. Audit batch records to ensure compliance with applicable regulations. Investigate non-conformance batches and finished products. Interact with customers as required to support new product startups and development. Develop ways to improve component, on-line and finished product inspection methods to improve quality. Maintain formal quality improvement program, including supporting methodology, tools and training materials. Direct core processes and/or systems reviews. Assess critical-to-quality gaps, determine root cause, build business cases for improvement opportunities, and implement control procedures to measure and monitor results. What You'll Bring BS in Chemistry preferred Minimum 3 years of Quality experience in manufacturing or related field a plus Excellent organizational skills with the ability to prioritize workload Proficient computer skills, especially in Microsoft Office specializing in advanced Excel Ability to perform chemical concentration calculations Ability to work in a fast-paced, time-sensitive environment Strong communication skills at all levels What You Will Get KIK offers a competitive salary and comprehensive benefits including health, wellness, dental, vision, life, and disability insurance. You can plan for your future with KIK's retirement savings options including employer match. KIK also recognizes the importance of continuing education and offers Education Assistance to our employees to encourage continued personal development and growth. About KIK We create the products and brands that people trust to clean, sanitize, and protect their homes, pools, and cars. We are one of North America's largest independent consumer product manufacturers with 16 North American manufacturing facilities. We also operate globally in Canada, Europe, and Australia. We are known for our portfolio of notable brands including Spic and Span and Comet cleaning products, Clorox Pool&Spa™ (under license), BioGuard , and Natural Chemistry pool chemicals. We are also the #1 producer in North America of store-brand (“private label”) bleach and a leading private-label provider of laundry detergent and additives, dishwashing products, general-purpose cleaning, and other home care products. Our global team of over 2,300 employees drives our capabilities in product development, product formulation, strategic sourcing, manufacturing, packaging design, brand marketing, project management, quality assurance, compliance, distribution, and logistics. Our organization is constantly evolving and is driven by a set of “One KIK” values - a dedication to following through on commitments in a customer-focused, profit-motivated way; while never compromising on safety, ethics, or integrity. KIK is an Equal Employment Opportunity / Affirmative Action employer. KIK does not discriminate against qualified applicants or employees based on race, color, age, religion, sex, pregnancy, national origin, ancestry, age, physical or mental disability, veteran status, status in uniformed services, sexual orientation, gender identity, gender expression, marital status, genetic information or any other status protected by law. KIK is also committed to providing reasonable accommodations for applicants and employees with protected disabilities to the extent required by applicable laws. If you require a reasonable accommodation to participate in the job application, or interview process, or to perform the essential functions of the job, please contact Human Resources immediately. Privacy Policy: ************************************************

*W2 Only *Remote (Will work EST hours) *12 Month Contract Our client is seeking a Manager of Quality Assurance Operations to join their team. This role will support all GMP aspects of drug product (DP) manufacturing, CMC, and alliance management. The Manager will collaborate closely with internal teams and external partners to ensure clinical through commercial lifecycle activities comply with cGMP regulatory requirements and guidelines. This position reports to the Director of Quality Assurance. This is a remote position, with working hours aligned to the Eastern Time (EST) zone. Key Responsibilities: Provide quality oversight of external manufacturing for both clinical and commercial drug products, including lot disposition. Review and approve internal and external Deviations, Change Controls, and CAPAs. Support the review and data verification of clinical regulatory filings. Collaborate with alliance partners to ensure compliance with their quality systems and practices related to drug product manufacturing and disposition. Assist in establishing best practices with alliance partners to ensure consistent quality standards. Partner with internal teams and external vendors to address complex quality issues, ensuring compliant solutions that meet patient needs. Ensure timely and accurate reporting of key performance indicators (KPIs) and risk metrics. Drive continuous improvement initiatives to proactively mitigate risks and maintain effective operations to support business needs. Qualifications: Bachelor's degree in life sciences, engineering, or a related field. Minimum of 5 years of experience in a pharmaceutical or biopharmaceutical Quality Assurance role with increasing responsibility. Experience working with external Contract Manufacturing Organizations (CMOs) in a virtual environment. Strong knowledge of aseptic techniques and parenteral drug manufacturing operations. Hands-on GMP management experience, including exposure to regulatory authorities such as FDA, EMA, PMDA, or equivalent. Experience in Quality Operations roles for both investigational and commercial products is preferred. Proven experience collaborating with alliance partners to ensure compliance and drive best practices. Demonstrated ability to identify inefficiencies, improve processes, and enhance turnaround times.

Apex Systems is looking for a QA Test Manager to join one of our fortune 500 clients. Please see details below and apply if interested. Duration: 24 months Rate: $60-68hr on w2 dependent upon experience We are unable to work corp-to-corp or provide sponsorship for this role. Candidates must be able to work on Apex Systems W2 without sponsorship now or in the future. We are unable to accomodate fully remote requests. Candidates must be able to go into the office 3 days a week in Richmond, VA | Charlotte, NC Position Summary Test Manager to coordinate the functional testing of multiple applications. Testing will include functional, regression and End-to-End. Work to plan and implement the testing of project in a release. Required Skills Experience in coordinating functional, regression and End-to-End testing. Experience in reporting testing status and progress to LOB and technology teams. Experience in defect management and coordinate with the project team. Knowledge of ALM and/or JIRA Knowledge of SDLC : Waterfall, Agile methodologies Ability to work in fast paced and changing environment Ability to communicate with LOB and technology teams Ability to coordinate with multiple teams in diverse locations Knowledge of RTP or similar financial transactions protocols Desired Skills Knowledge of Jira Tool Knowledge of financial systems Work well with LOB and technology team

Senior QA QC & Commissioning Engineer DataX Connect are partnered with a global real estate company who are dedicated to making an impactful difference to the data center/ mission critical sector. Due to outstanding growth and further investments to the business, they are looking to hire an experienced of Senior QA/QC or Electrical Commissioning Engineer to take lead on multiple large data center projects. The position The position entails working with a diverse group of internal and external Stakeholders at all levels of the organization, and the individual will require the independent judgement to plan, prioritize, and organize a diverse workload in a fast-paced environment. This successful candidate will be detail oriented with strong organizational skills, and a team player attitude. Responsibilities Have fluency with all commissioning processes and deliverables covered in ASHRAE, CSA, and LEED commissioning requirements. Expertise in electrical equipment/systems installation (means & methods), system startup and pre-functional inspections, acceptance testing and associated commissioning activities. Work directly with General Contractors, trades, inspectors, AHJs, and others involved with the QA/QC program execution for large critical facility construction and commissioning. Monitor, review, and execute all facets of Commissioning related projects by providing exceptional technical and field activities. Perform Commissioning Design Drawing & Specification Reviews, as well as Submittal (shop drawing) reviews. Qualifications and previous experience A recognized university degree or equivalent, or at least 5 years of significant and applicable knowledge and experience in data center QA/QC. Engineering Degree is preferred. A minimum of 7 years of relevant electrical engineering and/or field-testing experience with minimum of 5 years in providing building commissioning and/or construction QA/QC field services for data centers Why Apply Join a fantastic group of experienced data center professionals. Continuous growth throughout the business. Competitive salary, benefits and bonus. Benefits 401(k) plan with matching company contributions Comprehensive Medical, Dental & Vision Care Paid parental leave at 100% of salary Paid Time Off and Company Holidays Flexible and Remote Work Arrangements may be available

Responsibilities of this position include, but are not limited to, Quality Operations review and approval of materials, bill of materials, batch records and GMP documentation to support the design, implementation, and maintenance of manufacturing processes that meets or exceed FDA requirements. Essential Duties and Responsibilities: Support operational compliance aspects of sterile fill-finish manufacturing of products including but not limited to material, bill of material and executed batch record review and approval. Partner with operations to develop manufacturing batch records to be compliant with regulatory and company requirements. Working cross-functionally to determine defect criticality, inspection methods, and training plans for both QA Operations and Manufacturing employees. Provide cross-functional support to MSAT and Operations in establishing process limits for manufacturing processes such as filling and packaging. Act as a resource for colleagues. Lead or participate in Quality Risk Management Processes as needed. Promote a safety and quality-first mindset in daily job functions. Consistently represent the Quality Unit as a proactive and GxP-compliant team player when working with Operations in daily job duties. Ensure that all aspects of the handling, and manufacturing of pharmaceutical products at the site comply with FDA and Drug Enforcement Administration (DEA) regulatory requirements. Support material receipt, quality control, chain of custody, disposition, and release of materials within the Enterprise Resource Planning system. Maintain current knowledge of FDA requirements to keep pace with evolving requirements for manufacturing. Support, lead, or approve documents, change controls, investigations and CAPAs to support the Quality Management System.

Job Title: Construction Quality Control Manager (CQCM) Overview: The Construction Quality Control Manager (CQCM) is a vital position overseeing quality control activities throughout the project life cycle. The CQCM will be on site from NTP (Construction) through Final Acceptance, ensuring adherence to quality plans and procedures. With a focus on safety, compliance, and quality, the CQCM plays a critical role in achieving project success. Qualifications: • Bachelor's degree in construction management, construction science, engineering, or related field (preferred). • Minimum of 15 years of experience in quality control activities on design-build projects of a comparable size and scope. • Current OSHA 30, First Aid/CPR, and Construction Quality Control Management certifications, or ability to obtain within 30 days of hire. Responsibilities: • Develop and implement project-specific quality control plans. • Inspect and evaluate work areas, reporting deficiencies and ensuring safe work practices. • Coordinate with subcontractors to enforce project quality control standards. • Conduct a three-phase inspection program, including preparatory meetings, initial phase inspections, follow-up inspections, and final phase inspections. • Lead and document quality control meetings with the project team and/or customers. • Provide daily quality control reports, addressing non-conformance promptly. • Verify materials/equipment conformity, handle and store them appropriately. • Schedule, coordinate, and document code and independent inspections. • Review as-built drawings and ensure they align with the contract drawings. • Review and verify the Job Site Safety Plan, conducting safety inspections during the follow-up phase of control. • Exercise the authority to stop work, reject materials, and direct removal and replacement of non-compliant work. Minimum Requirements: • Bachelor's degree in a relevant field (preferred). • Minimum of 15 years of experience in programs of comparable size and scope. • Current OSHA 30, First Aid/CPR, and Construction Quality Control Management certifications. • Exceptional communication skills (written and verbal). • Proficiency in Microsoft Office (Outlook, Excel, Word, PowerPoint) and Procore. • Experience in planning, scheduling, and project control functions. • Knowledge of engineering, procurement, contracts, construction, and startup work processes. • Experience on major lump sum projects with a direct-hire construction strategy. • Experience in PANYNJ Projects. • Proven ability to work independently and efficiently. • Must pass PANYNJ background check and badging. • Must be able to commute to EWR Airport. If you possess these qualifications and are ready for a challenging role ensuring top-notch construction quality, we encourage you to apply. Join a dynamic team shaping the future of construction and infrastructure! JGM offers a comprehensive benefits package designed to support employee well-being and financial security. Our benefits include: Medical, Dental, and Vision Insurance Comprehensive health coverage to ensure employees and their families receive quality healthcare protection. 401(k) Retirement Plan Competitive retirement savings program with up to 4% company matching, helping employees build long-term financial stability. Flexible Work Schedule Empowering employees with the ability to balance work and personal life through adaptable working hours and potential remote work options. Additional Insurance Benefits Life insurance to provide financial protection for employees' loved ones Pet insurance to support employees' furry family members Paid Time Off Flexible time off to promote work-life balance and employee wellness

About the Company: Propedix is a biopharma and consumer health company dedicated to advancing innovative treatments in healthcare. Our flagship product, featuring our breakthrough anti-fungal and drying agent technology, launches in Q2 2025, with a pipeline of advanced OTC and Rx treatments in dermatology and health. Driven by strong research and development, we're delivering the next generation of health solutions. Position: Consultant Quality Assurance Manager/Assoc Dir Position Overview: The Quality Assurance Manager/Director will be responsible for ensuring the highest standards of quality throughout the product development lifecycle. This role is pivotal in preparing for the commercial launch in 2025 of an Over-The-Counter (OTC) athlete's foot treatment by working closely with our Contract Manufacturing Organization (CMO) to develop and finalize critical quality documentation. The ideal candidate will have a solid background in biopharmaceuticals, experience with regulatory compliance, and the ability to manage complex QA activities that support the manufacturing and launch of new products. Key QA Manager Responsibilities Quality Documentation Preparation & Review: Lead the preparation, review, and finalization of essential quality assurance documentation to meet the regulatory requirements for commercial launch. This includes Vendor Qualification and Audits, Standard Operating Procedures (SOPs), and release protocols. CMO Management and Oversight: Serve as the primary point of contact between internal teams and CMOs for all quality-related matters. Coordinate with external partners to ensure that manufacturing processes align with the company's quality standards and regulatory requirements, including cGMP (current Good Manufacturing Practices). Regulatory Compliance: Ensure that the company's products and processes are compliant with global regulatory standards, including FDA and other relevant health authorities. Support the preparation and submission of quality-related documents for any OTC level regulatory filings. Risk Management: Identify potential quality risks early in the development process, especially related to manufacturing and supply chain, and collaborate with relevant teams to mitigate these risks before the commercial launch. Product Release & Commercial Launch: Oversee the release of products for clinical trials and the commercial market, ensuring that all batch release documentation and certifications are accurate and complete for the timely launch of the product in April 2025. Internal Quality Audits & Inspections: Manage internal OTC standard quality audits and regulatory inspections, ensuring compliance with all internal and external quality requirements. Support preparation for inspections by regulatory authorities and third-party audits. Cross-Functional Collaboration: Collaborate closely with Product Development, Regulatory Affairs, Manufacturing, and Supply Chain teams to ensure quality requirements are met at each stage of the product lifecycle, from development through to commercial launch. Location: Virtual, but MUST reside in Southern California. Work can be performed remotely with attendance required for live meetings once a month. Travel out of region (in U.S.) expected 3 to 4 times a year. Experience/ Necessary Skills Education: Bachelor's or Master's degree in Life Sciences, Chemistry, Engineering, or a related field. Advanced degree or certifications (e.g., ASQ, Six Sigma) is a plus. Experience: Experience with OTC biopharma and consumer system and quality standards required. 5+ years of experience in quality assurance within the biopharmaceutical or biotechnology industry, with a focus on cGMP-compliant manufacturing. Proven experience working with CMOs in preparing for commercial product launches, including development of quality-related documentation (BPRs, SOPs, Master Batch Records, etc.). Strong understanding of regulatory guidelines (FDA, OTC) and quality systems. Hands-on experience with risk management, CAPA (Corrective and Preventive Actions), and change control processes. Skills & Competencies: In-depth knowledge of biopharmaceutical manufacturing processes and quality systems. Strong project management skills and the ability to prioritize and manage multiple tasks in a fast-paced environment. Knowledge and experience with OTC quality standards. Proficiency in quality management software, document control systems, and MS Office Suite. Hours: Approx 10 hours a week for first 10 weeks, then 6 hours a week thereafter. Candidates must be available for live meetings and email correspondence on average 1 hours a day during normal business hours. Attendance at a once a week management meeting (usually scheduled for Tuesday) a requirement. Compensation. $5,000 per month for first 10 weeks than $3,500/mo thereafter . This is an independent contractor 1099 position. Potential LTI stock options awarded after 3 months. Support and Supervisor: Position will report to the CEO who will be their administrative supervisor. This position is expected to work closely on a daily basis with the CTO/VP of Product Development, Sr. Director of Manuf, Chair of Scientific Advisory Board, CCO, and all 3rd party production and component vendors. Application: Interested parties should send their resume, brief cover note, and their LinkedIn profile to Nicole Lewis, at ******************.

We are looking for a Quality Assurance/Quality Control Associate to write or revise quality documentation, assist with raw material qualifications, perform process and final quality inspections and lab testing. You will assist in conducting product extensions. As the Quality Associate, you will be expected to work under general supervision or as part of a multifunctional team on assignments of varying degrees of complexity to ensure products and processes comply with the Company's quality system and applicable regulatory requirements. Responsibilities: Write/revise SOP's, work instructions, forms, component specifications, etc. related to QA/QC processes Write and/or revise raw material component specifications Write and at times execute product extension and other various studies. Review and record test data for consistency and accuracy. Conduct laboratory testing on incoming, in process and finished materials using laboratory equipment, as required. Record and maintain temperature data for various equipment. Learn the applicable QC functions as related to the new ERP system. Interface with operations, R&D and Marcom as a team member to accomplish goals. Work as an ambassador and liaison for QA and other departments. Cross train in the value assignment process, as to data entry and review. learn the coordination with outside value assignment laboratories. Complying with cGMP and laboratory safety practices Perform special projects as assigned by department head or other duties as assigned Employee will contribute to a positive work environment Assist in maintaining Quantimetrix Corporation quality system Qualifications: Bachelor of Science degree in clinical, biological, or chemical sciences 2+ years' experience working in a clinical or medical device/IVD laboratory or an FDA regulated quality assurance medical device or pharmaceutical manufacturing environment Ability to write technical reports and/or studies Ability to analyze and present data in a coherent and scientific manner Excellent communication skills (both verbal and written) Basic use of Excel spreadsheets and statistics Detail oriented Experience working under FDA/ISO regulations Best-in-Class Benefits and Perks: We value our employees' time and efforts. Our commitment to your success is enhanced by competitive compensation of $30-35/hour, depending on experience, and an extensive benefits package including: Comprehensive health coverage: Medical, dental, and vision insurance provided Robust retirement planning: 401(k) plan available with employer matching Financial security: Life and disability insurance for added protection Flexible financial options: Health savings and flexible spending accounts offered Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture. Join us on the journey of excellence and innovation. Apply now and be a part of something extraordinary! Ready to take the lead in our manufacturing revolution? If you're excited to drive change, inspire a team, and make a lasting impact, we want to hear from you! We are committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law.

About Us Desi Fresh Foods is a leading "cultured" dairy manufacturer with over 23 years of experience. We produce high-quality and consistent products, which include yogurt (Dahi or Indian, Greek and traditional), smoothies / yogurt drinks, sour cream, and dips from single serve options to food service side. We are currently seeking a skilled Facility Porter to join our team and contribute to the ongoing success of our facility in Frederick Country, Virginia! About the Role Hours: Monday - Friday 6 am - 4 pm plus possible weekends Pay: $60k annually The Quality Assurance (QA) Supervisor is responsible for maintaining Food Safety and Quality Assurance Management Systems to support manufacturing of wholesome and quality food. QA Supervisor serves as SQF Practitioner, maintains, and implements Policies and Procedures in accordance with SQF code. Responsibilities Implement corrective actions and preventative measures related to food safety and food non-conformities Supervise QA Technicians Implement developed policies and procedures Conduct documentation and records daily verification Implement cleaning, housekeeping activities, and master sanitation schedule Responsible for investigating food safety and quality related incidents discovered through customer complaints and reported by Production personnel Responsible for Pest Control Program Implement Microbiological Program Conducts Internal Monthly Audit Responsible for Foreign Material Program Manage Product Specification & compliance with labeling Maintains Company Food Safety and Quality Training in new hires Conduct pro-op inspections and operational inspections Collects Finished product weights to make sure they are complaint Monitor Coolers Temperature Conduct Verification throughout the day to make sure GMP's are being followed Responsible for implementation of Maintenance documents Leads Customers Audits/ and any other 3rd party Audits Respond to customers' requests in a promptly matter Lead inspections from the Agriculture Department Responsible for sampling product to the State of Agriculture Responsible for approving new ingredients and packaging Support product development and launch Qualifications Must have at least 3 years quality experience in food manufacturing environment (dairy preferred), knowledge of FDA, and Experience with 3rd party food safety audits Food Safety Certificates: HACCP, SQF Practitioner, PCQI Proficiency in quality management systems and tools (e.g., ISO 9001, Six Sigma) Maintain a positive work environment Understanding of regulatory guidelines Bilingual English/Spanish preferred Availability to work 1st or 2nd shift as needed by the business Willingness and ability to travel for training in Farmingdale, NY which may be required for up to 4 - 6 weeks. Our competitive compensation package includes: Medical health insurance Dental insurance Vision insurance Vacation time off Sick leave Holiday time off Short-term disability Long-term disability PandoLogic. Keywords: Quality Control / Quality Assurance Technician, Location: Stephenson, VA - 22656RequiredPreferredJob Industries Customer Service

A leader in the natural and cultural resource services is looking for a NEPA Regulatory and Permitting Specialist to join the team in Virginia Beach, VA. The firm: Leader in the natural and cultural resources space Offer the resources of a large firm while maintaining the culture and lack of red tape that a small firm can offer Invest in their employees with technology, benefits, and learning opportunities Clear paths for growth Working with residential, utility, commercial, and environmental partners Position Overview: An environmental consulting firm is seeking a Regulatory and Permitting Specialist with expertise in Wetlands and Waters Permitting, and NEPA. This role involves serving as a liaison between clients and regulatory agencies, focusing on technical writing, regulatory expertise, and permit application and NEPA document preparation. Job Duties Prepare and manage permit applications for state and federal agencies. Write and manage NEPA documents. Research current state and federal regulations and project design needs for clients. Coordinate large-scale projects with multiple staff members and consultants. Prepare scopes of work, fee proposals, and Design-Build bid materials. Build practice with private development clients, localities, state and federal agencies. Mentor junior staff and help grow the team. Coordinate with regulatory team members at other offices. Collaborate with team members and Project Manager to ensure project objectives are met. Minimum Qualifications: Bachelor's degree in environmental planning, science, or policy. 5+ years of experience in permitting/NEPA. Thorough understanding of environmental regulations related to the Clean Water Act, Virginia Water Protection permit program, NEPA, and Chesapeake Bay Preservation Act. Ability to handle multiple tasks/projects and deadlines under limited supervision. Demonstrated ability to organize and manage multiple priorities. Excellent customer service skills. Excellent written and verbal communication skills. Experience preparing scopes of work and fee proposals. Strong organizational, time management, attention to detail, and analytical skills. Ability to work independently and in a team environment. Proficient with Microsoft Office suite. Preferred Qualifications: Experience with NEPA concerning various federal and state programs. Experience with wetland delineations, hazardous materials investigations, fisheries, air and noise regulations, and/or grant writing and planning related to coastal resiliency. Experience using GIS and GPS; working knowledge of AutoCAD. Knowledge and experience with land development, utilities, transportation, stormwater, flood mitigation, and/or resilience practices. Benefits Paid time off and paid holidays. Opportunities for advancement. All job-specific equipment and safety gear provided. 401(k) retirement savings plan with a company match. Employee-owned company with discounted stock purchase options. Group Health Plan. Employee Referral Bonus Program. Locations throughout the United States in major cities and desirable areas. Career Development Program supported by industry expert safety specialists and skilled trainers. Scholarship program for children of employees. Charitable matching gift program. If you are passionate about environmental consulting and meet the qualifications listed above, we encourage you to apply for this exciting opportunity. Join our team and contribute to meaningful projects that make a difference. Apply now to become a part of our dynamic and growing team!

At Vertosoft, the Contracts team plays a vital role in the structure and success of the organization, making a significant impact across a wide range of functions. As a full-time Federal Contract Specialist, you will support our Contracts team in ensuring compliance with contractual requirements and managing Vertosoft's rapidly expanding government contract portfolio. This role offers comprehensive insight into the contract landscape across both Federal and State & Local Government markets. This role will be based in Leesburg, VA. Responsibilities: Federal Market Expertise: Stay informed on trends and developments in Federal procurement, identifying strategic opportunities to grow our Federal business. End-to-End Contract Management: Manage the full lifecycle of Federal contracts, from proposal development to contract closeout, ensuring compliance with regulations such as FAR and DFARS. Contract Marketing and Outreach: Develop and execute strategies to promote Vertosoft's Federal contracts and capabilities to potential government customers, suppliers, and teaming partners. Proactively identify and pursue opportunities to increase awareness, utilization, and sales of our Federal contract portfolio through targeted outreach, presentations, and participation in government-focused events. Proposal Development: Partner with various members of team to craft compliant, compelling responses to Federal solicitations (RFPs, RFQs, RFIs). Performance Reporting: Collaborate with internal teams to gather data, prepare detailed reports, and maintain transparency with Federal contracting offices. Risk Mitigation: Analyze contract terms to identify potential risks, develop mitigation strategies, and ensure favorable outcomes for Vertosoft. Partnership Coordination: Serve as a Federal liaison between Vertosoft, suppliers, and teaming partners, aligning their contributions with Federal requirements. Audit and Compliance Support: Ensure readiness for audits and reviews, maintaining clear and organized records for Federal agencies. Data Accuracy: Conduct data audits to reinforce compliance, improve system accuracy, and support informed decision-making. Process Innovation: Continuously enhance internal contract management processes to improve efficiency and align with evolving Federal standards. Other Duties: In addition to the responsibilities outlined above, you may be required to perform additional tasks and duties as assigned. These may include supporting other departments, participating in specialized projects, and contributing to the overall success of the organization. Qualifications: Experience: 2-5 years of hands-on Federal government contracting experience, with a strong understanding of FAR/DFARS, GSA Schedules, and Federal contracting vehicles. Skills: Exceptional attention to detail, critical thinking, and problem-solving abilities. Strong written and verbal communication skills are essential. Tools Knowledge: Familiarity with Federal systems such as Army CHESS, SAM.gov, eBuy, GSA Advantage, and more. Education: Bachelor's degree in a relevant field such as Business Administration, Public Administration, or Management. *Desirable Requirements: Industry certifications such as CFCM, CPCM, or DAWIA. Advanced knowledge of Federal acquisition strategies and contract structures. Experience leveraging Salesforce or similar CRM tool for contract management and streamlining business development processes. To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status. About Vertosoft At Vertosoft, we are a small business focused on accelerating the adoption of innovative and emerging technology in the Government. Consistent with our dedication to government customers, Vertosoft has deep knowledge and experience supporting all phases of the government acquisition life cycle. Strategic sourcing is our forte, streamlining the time required to provide critical technology and services to government end users at reduced prices. We provide the flexibility, agility, and responsiveness of a small company with the experience of a large organization. Vertosoft's staff is widely respected and relied upon for its professional, ethical business approach. Our success is based upon the leadership of a highly experienced management team. Our current staff has deep expertise in both meeting each agency's specific requirements and the technology to satisfy those needs. Vertosoft is an Equal Employment Opportunity Employer. Vertosoft will consider all qualified applicants for employment without regard to race, color, religion, sex, age, national origin, sexual orientation, gender identity, marital status, disability, veteran status, or any other characteristic protected by law.

ISI Professional Services is seeking a Contract Management Specialist (CMS). The contractor provides acquisition support to the Directorate Management Division (DMD), Administration and Contract Liaison Branch (ACLB) at the Pentagon, including directorates and subordinate branches in support of the facility's overall objectives. The successful candidate will have experience in contract-related administration with Federal construction contracts. They will play a key role in supporting construction projects within a secured facility, coordinating with multiple stakeholders, and ensuring the success of highly technical and sensitive projects. This position will support multiple construction trades on projects valued at a minimum of $1 million each while ensuring close coordination with the Government/Owner on daily construction issues. Essential Job Functions: Provide general direction, establish overall objectives, and plans and carry out analysis of assigned projects as directed. Assist in the formation of Excel spreadsheets, which may include but not limited to: graphs, statistical analysis, and other data that may not be readily available. Assist in the formation of executive presentations. Advise leadership and contracting personnel on matters of contracting policies and procedures. Assist in developing guidance material and/or conducting training for FSD personnel. Maintain various databases that are used to capture contractual data. Assist in creating and maintaining monthly reports for leadership personnel, including ad hoc reports as directed. Prepare special and one-time reports, summaries, or replies to inquiries selecting relevant information from a variety of sources such as reports, documents, correspondence, or other offices. Arrange meetings and take meeting minutes. Organize and maintain a centralized digital filing system. Create, enter, save, retrieve, edit, file, and present text, spreadsheets, and/or charts. Review written correspondence for grammar and punctuation and provide recommendations as needed. The CMS shall be able to work independently, with little to no supervision. Required Education and Experience: Education: Bachelor's Degree Experience: Five (5) years of Acquisition experience, with contract-related administrative/analytic experience of Federal construction contracts Technical Expertise: Proficiency in Microsoft Office products with emphasis on: Outlook, Teams, Excel, Word, and PowerPoint (SharePoint experience is a plus) Good written and oral communication skills Secure Facility Experience: Previous experience a plus Stakeholder Management: Demonstrated experience in communication and coordination among multiple stakeholders, including government agencies, contractors, and other third parties Organizational Support: Experience in creating comprehensive summary reports and organizing and maintaining document retrieval that complies with standards Physical Requirements: This job operates in a professional office environment. The physical demands described here are representative of those that an employee must meet to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Flexibility related to work hours as project demands arise. Occasionally required to move 5 - 15 pounds. Must remain in a stationary computer position for extended periods. Must be able to walk and stand for extended periods. Work Setting/Environment/Travel Requirements: Monday through Friday, Normal business hours 8:00 am - 5:00 pm

Seeking an ENERGETIC Networker to TALK to decision makers & hiring managers to E X P A N D our contacts to capture new business! SPARKS is honored to be selected continuously as one of the TOP WORK PLACES by the Washington Post and consistently the BEST OF STAFFING awards voted by our own clients & our talent! Our CHARISMATIC staff fosters a FUN & HIGH ENERGY culture working as a team for a meaningful purpose to partner with organizations to fulfill their talent needs. If you are confident yet COACHABLE, independent, innovative, and have an insatiable desire to win, then this could be your chance to be recognized for your successes and earn great compensation! We're looking for talented Networker who can establish new customer relationships, and then continue to maintain and grow the business. We want someone to help innovate, strategize, energize and contribute to the company's growth. What you'd be doing... Use SOCIAL MEDIA, your network, and our CRM system to acquire, maintain, and increase staffing business within the greater DC area. Work on a professional and personal level to deepen relationships - increasing business commitments, attending networking at events, Social Outings, and introducing our service by visiting companies and cold calling in your territory. Leverage our world class quality control program to manage customer feedback and follow through on any issues resolution

Lewisville, TX 75067 Salary: 62-67K Status: Full-time, Exempt, Hybrid for training with a remote option after 60 days Reports To: Human Resources Manager PRIMARY FUNCTION: The Compliance Specialist is an integral function of the US Compliance Team in its efforts to promote overall regulatory compliance throughout the JAFRA US market, specifically US Beauty Consultant Compliance with JAFRA Policies & Procedures and US business compliance with laws and regulations, including but not limited to FTC regulations related to marketing communications, direct sales, and multi-level marketing. Generally, the Compliance Specialist will intake, create records of, investigate, review, and report on compliance issues, as well as conduct training and education and support the US Compliance Team. This person will communicate with JAFRA Consultants, employees, and third parties on compliance-related issues, manage compliance software programs and vendors, maintain compliance files and logs, and engage in compliance strategy planning, project planning, and training initiatives ESSENTIAL DUTIES AND RESPONSIBILITIES: Search for and investigate US Field Compliance incidents as issues are reported, communicate with Jafra management about such issues, and prepare reports and documentation regarding those incidents Carry out the main functions of the US Market Income Claims Policy by investigating potential compliance issues, reviewing marketing materials, and working with US Market management to resolve issues Manage US Field Compliance email account and respond to emails, delegate issues back to CRT, elevate issues to Compliance Counsel, and/or log incidents into Compliance Log Prepare US Field Compliance communications and communicate via mail, electronically, or over the phone in both English and Spanish. Such communications will include formal compliance letters, emails, direct messages on social media, and phone calls to US Consultants and third parties Serve as an expert resource regarding the US Consultant Policies & Procedures and respond to questions regarding the policies from CRT members, other JAFRA employees, and JAFRA Consultants, and elevate questions to the Compliance Counsel or Committee as needed As necessary, prepare agenda for US Field Compliance Committee meetings, report on US Field Compliance Log and other compliance incidents to Compliance Committee Maintain all documents on the SharePoint US Compliance website, including meeting notes, agendas, Compliance Log, enforcement letter templates, and any other documents as needed Support the US Market by investigating and addressing financial fraud issues. Create, maintain, and execute fraud policy Liaise with and manage compliance vendors and software programs Collect, analyze, and report metrics and data on compliance efforts and issues, including enforcement, training, processes, events, and policy Maintain current and historical files and documentation for all enforcement incidents, investigations, and matters Update job knowledge by participating in educational opportunities; reading professional publications; and attending industry webinars, calls, and meetings Support Compliance Counsel as needed with general compliance-related tasks, including in preparing and presenting training, communications, documents, reports, and other materials QUALIFICATIONS: Education: Bachelor's Degree is highly desirable but not required Experience: Highly desirable but not required - Experience in compliance, either within direct sales, financial, banking, or other relevant area Skills: Bilingual (Professional Spanish and English, oral and written) We are an equal opportunity employer, and we are an organization that values diversity. We welcome applications from all qualified candidates, including minorities and persons with disabilities. req25-00051

Develops, modifies, applies and maintains quality evaluation systems and procedures for processing materials into finished product. Collaborates with engineering and manufacturing functions to ensure quality standards are in place. Devises and implements methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment. Areas of specialization include design, validation, root cause analysis, statistical risk management, production control or product evaluation and reliability as they apply to product or process quality. May be certified in lean and six-sigma quality engineering methodologies. May also be responsible for PEx project portfolio assuring the effective use of different improvement methodologies (DMAIC, Lean, DESGN, etc.) toward the achievement of plant strategic goals. Exercises judgment within defined procedures and practices to determine appropriate action. Key Responsibilities: Lead and participate in project teams to quickly and effectively implement improvement initiatives or manufacturing process improvements. Provide manufacturing support activities to include validation projects, equipment validation projects, and or involvement in improvement projects related to products or services consistent with FDA requirements for medical device products. Participate in continuous improvement and Performance Excellence activities to include leading, participating, or coaching project teams, facilitating events, or providing training. Provide technical support and guidance to other staff and/or project team members in Quality Systems improvement efforts. Apply quality engineering practices and guidance to support project teams and manufacturing operations using Six Sigma tools, FMEA, CE Diagram, CE Matrix, DOE, MSA, Validation Protocol development, review, approval and Control Plans. May lead execution of validation protocols. Develop/Revise Quality Plans including incoming, in-process and final inspection, and provide training to those affected by the plans. Perform technical reviews and interprets data for accuracy of equipment/process performance. Write Technical Reports and Protocols, as needed, and write, revise, and review SOPs. Frequently interacts with colleagues, team members, supervisors, and other teams/departments. Oversees the change management program to assure there is a proper technical review of requested changes and that there is a risk assessment of requested changes. Manages CAPAs assigned to the QE department to closure and assures corrective actions are effective. Participates in MRB, reviews and/or completes nonconformance reports, FIRs, and CAPA documents to assure root cause analysis is reached and corrections are appropriate to prevent further nonconformances. Reviews QS metrics and makes recommendations for corrective actions. Performance Metrics: Quality Customer: Satisfaction (Product Quality), Continuous improvement Culture: Training compliance, cGMP compliance Cost: Reduce cost of quality through product and process improvements PEOPLE Competencies: Learning on the Fly Approachability Listening Interpersonal Savvy Patience Perseverance Influencing BUSINESS Competencies: Action Oriented Customer Focus LEADERSHIP Competencies: Drive Deployment Pursue and Apply Learning Required Experiences/Education: Minimum of a 4-year degree in relevant fields of study such as microbiology, chemistry, biology, or engineering with 4-7 years of work experience Can balance team and individual responsibilities Can apply basic mathematical concepts such as percentages, ratios, and proportions to practical situations Basic computer knowledge in Microsoft Word and Excel Must be detail oriented Able to work well both independently and in a group setting Demonstrated technical writing skills Desired: Advanced degree Familiarity with cGMP, IS9001, IS13485, QSR 21 CFR 820,210,211 is highly desirable Capable of Certified Quality Engineer recognition by ASQ Track record of delivering results Six-Sigma I Lean experience Proficiency in Minitab, MS Project.