Quality assurance specialist jobs in Portland, ME - 111 jobs

Vishay manufactures one of the world's largest portfolios of discrete semiconductors and passive electronic components that are essential to innovative designs in the automotive, industrial, computing, consumer, telecommunications, military, aerospace, and medical markets. We help the world's most in-demand technologies come to life. Every day our products touch your life and the lives of people across the world, though you likely do not know it. Come join us and help us build The DNA of tech.™ We are seeking great talent to help us build The DNA of tech. Vishay manufactures one of the world's largest portfolios of discrete semiconductors and passive electronic components that are essential to innovative designs in the automotive, industrial, computing, consumer, telecommunications, military, aerospace, and medical markets. We help the world's most in-demand technologies come to life. Every day our products touch your life and the lives of people across the world, though you likely do not know it. Come join us and help us build The DNA of tech.™ Vishay Intertechnology, Inc. is a Fortune 1,000 Company listed on the NYSE (VSH). Learn more at *************** Do you want to help us build the DNA of tech.? Vishay Dover is currently seeking applicants for a Quality Assurance Technician 1 position. Job Location: We're located southwest of downtown Dover which is the largest city in the New Hampshire Seacoast region, the oldest permanent settlement in New Hampshire, and the seventh oldest in the U.S.A. We're less than seven miles from the main campus of UNH, and another fun fact is that Dover even was the birthplace of the Teenage Mutant Ninja Turtles franchise. What you will be doing: Maintain Calibration System, including but not limited to instrument recall, vendor interaction, maintenance of records. Support Operations by responding to Production/Shop Floor requests, creating customer reports for shipment, maintaining traceability requirements, and assisting with inspections (Final, In-Process, 1st pc, or PPQ). Support FAI and APQP processes by completing inspections, measurements, gage studies, and related reports. Support Incoming/Receiving Inspection by developing/enhancing part specific protocols, creating automated inspection programs with Keyence inspection equipment, investigate and communicate issues, assist with inspections. Assist with troubleshooting product issues from customers or the production floor and completing related documentation. Support Customer Source Inspection and Self-Release. This may include becoming a designated agent for Self-Release and interacting with Customer Source Inspectors. Assist with executing NCR and MRB dispositions or coordinating completion. Conduct Production Floor and CAPA follow-up/verification audits. What you will bring along: Employee must be able to demonstrate the ability to develop a strong working knowledge of Vishay manufacturing processes, workmanship requirements, and documentation, and is expected to become proficient in reading of customer and Vishay specifications. Employee must have very strong communication skills as this role collaborates with several different departments. Ability to meet Vishay's attendance policy 2-year degree in a Science, Engineering, Business, or Technology track OR at least 1 year of related experience. Strong PC skills required. Specific on the job training and other training to be assigned by direct supervisor. Must become proficient in the requirements noted above within 1 year of date of hire. What can we offer you for your talent: Vishay offers a comprehensive suite of benefit programs including health care coverage, financial support programs and other resources designed to help you achieve your personal and professional goals. With us, you'll experience unique career paths, an open and collaborative culture, a stable business that will be there for you, and opportunities to work globally and locally. Do you have the skills we need? Are you ready to power your career as you power the world? If so, apply today. This position requires access to information subject to the International Traffic in Arms Regulations and/or the Export Administration Regulations. As such, this position is open only to applicants who qualify as “U.S. Persons” as defined by 22 C.F.R. §120.15 is required. “U.S. Person” includes U.S. Citizen, lawful permanent resident, refugee, or asylee.” It is the policy of Vishay to provide equal employment and advancement opportunities to all colleagues and applicants for employment without regard to sex, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. As an equal opportunity employer, Vishay is committed to a diverse workforce. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact ************************ for assistance. This position requires access to information subject to the International Traffic in Arms Regulations and/or the Export Administration Regulations. As such, this position is open only to applicants who qualify as “U.S. Persons” according to U.S. federal law. Vishay offers a comprehensive suite of benefit programs including health care coverage, financial support programs and other resources designed to help you achieve your personal and professional goals. With us, you'll experience unique career paths, an open and collaborative culture, a stable business that will be there for you, and opportunities to work globally and locally. Do you have the skills we need? Are you ready to power your career as you power the world? If so, apply today. Vishay is an AAP and Equal Opportunity Employer

Title: QA Specialist II Duration: 12 Months | 100% Onsite The Quality Assurance Specialist II position is part of the Infectious Disease Business Unit located in Scarborough, Maine. Under minimal supervision, this role performs a broad range of responsibilities to support the Quality Management System. Duties may evolve based on business needs, and this job description may be reviewed and updated periodically. Responsibilities Quality System Management Review production batch records (DHRs) for accuracy and completeness to approve intermediate products for production use; review finished goods batch records. Report any deviations and ensure they are resolved prior to approval. Perform spot-check inspections and audits of production operations. Participate in internal audit activities. Write, review, and approve Standard Operating Procedures (SOPs) as required. Assist with the development and review of validations and test protocols. Support testing of complaint and stability samples, reporting any results outside acceptance criteria. Provide backup support to other Quality Specialists. Initiate and author Deviations and Quality Incidents (QIs). Potentially administer programs such as calibration, document control, deviation/QI/CAPA, long-term stability, and sample retention. Maintain and administer Quality Records and support Document Control functions. Train new and existing Quality Assurance Technicians and Specialists as needed. Perform other duties as assigned. Change Control Management Maintain change management documentation, including assignment of Design History File (DHF) numbers. Compile and organize quality system records for design change projects (e.g., project definitions, first-lot-to-stock, qualification records), ensuring alignment with SOPs. Manage documentation storage, organization, and archival related to design changes and labeling. Provide proofreading and verification of product labeling prior to review and approval. Coordinate and implement labeling changes with internal teams and external partners. Assist with execution of product changes in collaboration with project leads. Manage assigned design change projects, typically related to product labeling. Perform other related duties as assigned. Basic Qualifications / Education Bachelor's degree in Chemistry, Biology, Life Sciences, or a related technical field; or an equivalent combination of education and experience. Minimum of three years of experience in a Quality Assurance role within manufacturing. Preferred Qualifications 3+ years of prior Quality Assurance or similar experience in the medical device industry. Competencies Strong adherence to procedures with accurate documentation skills. Knowledge of inventory management, document control, and quality incident tracking systems. Proficiency in Microsoft Excel and Word. Understanding of manufacturing processes and ability to identify deviations from documented procedures. Ability to read and interpret safety rules, operating instructions, and procedural documents. Strong written and verbal communication skills, including report writing and presenting to groups. Ability to interpret written, oral, diagrammatic, or schedule-based instructions. Ability to apply mathematical concepts such as fractions, percentages, ratios, and proportions. High attention to detail. Consultants Eligible Benefits Upon Waiting Period: Medical and Prescription Drug Plans Dental Plan Vision Plan Health Savings Account (for High Deductible Health Plans) Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit) Supplemental Life Insurance Short Term Disability (coverage varies by state) Long Term Disability Critical Illness, Hospital coverage, Accident Insurance MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance 401(k) Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines. Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.

Description & Requirements Maximus is currently hiring for a Quality Assurance Manager to support our Missouri Enrollment Broker project. This is a full time remote opportunity. The Quality Manager is responsible for overseeing the daily operations for the Quality Assurance team, and for creating efficient business partnerships to meet business goals. The project will be a multi-channel contact center that will support multiple clients throughout the state of Missouri. *This job is contingent upon contract award.* At Maximus we offer a wide range of benefits to include: - • Competitive Compensation - Quarterly bonuses based on performance included! - • Comprehensive Insurance Coverage - Choose from various plans, including Medical, Dental, Vision, Prescription, and partially funded HSA. Additionally, enjoy Life insurance benefits and discounts on Auto, Home, Renter's, and Pet insurance. - • Future Planning - Prepare for retirement with our 401K Retirement Savings plan and Company Matching. - • Unlimited Time Off Package - Enjoy UTO, Holidays, and sick leave, - • Holistic Wellness Support - Access resources for physical, emotional, and financial wellness through our Employee Assistance Program (EAP). - • Recognition Platform - Acknowledge and appreciate outstanding employee contributions. - • Tuition Reimbursement - Invest in your ongoing education and development. - • Employee Perks and Discounts - Additional benefits and discounts exclusively for employees. - • Maximus Wellness Program and Resources - Access a range of wellness programs and resources tailored to your needs. - • Professional Development Opportunities- Participate in training programs, workshops, and conferences. Essential Duties and Responsibilities: - Oversee the day-to-day functions of the Quality Assurance (QA) department. - Manage an effective quality assurance program that monitors and resolves issues before they become problems. - Supervise the development and regular update of policies and procedures. - Evaluate the need for and ensure the provision of necessary training for project personnel, providing up-to-date information on relevant programs, community resources, and options for consumers. - Arrange staff training on a regular and ongoing basis. Ensure project training program meets all corporate requirements. - Provide project leadership with updates on all issues regarding quality, operations, training, and policy and procedures. - Provide leadership to all staff in the areas of quality improvement as it relates to process improvement, customer service and conflict resolution. - Prepare reports and briefings for project leadership and review monthly and quarterly project status reports provided to the Department. Minimum Requirements - Bachelor's degree in relevant field of study and 5+ years of relevant professional experience required, or equivalent combination of education and experience. - Must be willing and able to travel up to 25% of the time as business need dictates. - Lean Six Sigma experience with a minimum of Yellow Belt Certification required. - Experience managing direct reports remotely required. - Experience with designing, implementing and reporting customer satisfaction surveys required. - Experience with standardized quality tools required. - Experience with call and voice monitoring platforms required. - Experience with a large-scale telephony system required. - Experience with Client Relationship Management (CRM) platforms required. - Experience with contract compliance and quality platforms required. - Experience with statistical processes required. - Premium contact center billing experience required. - Financial experience with Oracle preferred. Home Office Requirements: - Internet speed of 20mbps or higher required (you can test this by going to ******************* - Connectivity to the internet via either Wi-Fi or Category 5 or 6 ethernet patch cable to the home router. - Must currently and permanently reside in the Continental US. #max Priority #LI-Remote EEO Statement Maximus is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information and other legally protected characteristics. Pay Transparency Maximus compensation is based on various factors including but not limited to job location, a candidate's education, training, experience, expected quality and quantity of work, required travel (if any), external market and internal value analysis including seniority and merit systems, as well as internal pay alignment. Annual salary is just one component of Maximus's total compensation package. Other rewards may include short- and long-term incentives as well as program-specific awards. Additionally, Maximus provides a variety of benefits to employees, including health insurance coverage, life and disability insurance, a retirement savings plan, paid holidays and paid time off. Compensation ranges may differ based on contract value but will be commensurate with job duties and relevant work experience. An applicant's salary history will not be used in determining compensation. Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances. Accommodations Maximus provides reasonable accommodations to individuals requiring assistance during any phase of the employment process due to a disability, medical condition, or physical or mental impairment. If you require assistance at any stage of the employment process-including accessing job postings, completing assessments, or participating in interviews,-please contact People Operations at **************************. Minimum Salary $ 80,000.00 Maximum Salary $ 95,000.00

Northpoint Mortgage, selected as one of the Boston Globe's Top Places to Work three years' running, is a growing New England-based mortgage lender seeking to add an entry-level, full-time employee to our South Portland, ME office. In addition to a great working atmosphere, we offer competitive pay, benefits, and a gateway into an exciting industry. We are seeking a candidate in the South Portland, Me area, as this is an in-office position. Responsibilities: Reception: Answer phones and greet clients with the highest level of customer service Communicate directly with operations staff and loan officers Sort and organize mortgage loan documents, adhering to compliance deadlines Review loan package documentation for discrepancies or omissions Verify loan information for accuracy at time of disclosure Ensure that all required regulatory, state and investor disclosures are included in disclosed packages Loan Opening-- provide administrative support through the loan application process Assist in special projects as needed by management Skills needed: Proficiency with Microsoft Office including Excel, Word, and Outlook Excellent phone manner Strong detail orientation with a solution-oriented demeanor Multitasking & a strong sense of responsibility for tasks assigned Ability to communicate comfortably with all levels of the organization Post- Secondary education preferred Compensation is commensurate with experience.

Join our Quality Assurance team and help us deliver life-changing medicines. In this role, you will ensure compliance with global regulations and maintain inspection readiness across our operations. Your expertise will drive continuous improvement and support our mission to improve millions of lives. What you will get: An agile career and dynamic working culture An inclusive and ethical workplace Competitive compensation programs that recognize high performance Medical, dental, and vision insurance Opportunities for professional growth and development Our full list of global benefits can be found here: ************************************** What you will do: Review and approve quality records to ensure compliance Support audits and inspections, maintaining inspection readiness Lead compliance initiatives and continuous improvement projects Collaborate with cross-functional teams to strengthen quality culture Develop and update standard operating procedures (SOPs) Monitor key performance indicators and identify trends Provide guidance and training to team members What we are looking for: Bachelor's degree in a scientific field or equivalent experience 5-10 years in GMP environments and quality assurance Strong knowledge of compliance and regulatory requirements Excellent organizational and analytical skills Ability to prioritize tasks and work in a dynamic environment Effective communication and collaboration skills A proactive, detail-oriented mindset with a focus on quality About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

**Title:** QA Specialist II **Duration:** 12 Months | 100% Onsite **Pay Range:** $30-$33 per hour (W2) We are seeking a **QA Specialist II** to join one of our leading healthcare clients. The **Quality Assurance Specialist II** position is part of the Infectious Disease Business Unit located in Scarborough, Maine. Under minimal supervision, this role performs a broad range of responsibilities to support the Quality Management System. Duties may evolve based on business needs, and this job description may be reviewed and updated periodically. **Responsibilities** **Quality System Management** + Review production batch records (DHRs) for accuracy and completeness to approve intermediate products for production use; review finished goods batch records. Report any deviations and ensure they are resolved prior to approval. + Perform spot-check inspections and audits of production operations. + Participate in internal audit activities. + Write, review, and approve Standard Operating Procedures (SOPs) as required. + Assist with the development and review of validations and test protocols. + Support testing of complaint and stability samples, reporting any results outside acceptance criteria. + Provide backup support to other Quality Specialists. + Initiate and author Deviations and Quality Incidents (QIs). + Potentially administer programs such as calibration, document control, deviation/QI/CAPA, long-term stability, and sample retention. + Maintain and administer Quality Records and support Document Control functions. + Train new and existing Quality Assurance Technicians and Specialists as needed. + Perform other duties as assigned. **Change Control Management** + Maintain change management documentation, including assignment of Design History File (DHF) numbers. + Compile and organize quality system records for design change projects (e.g., project definitions, first-lot-to-stock, qualification records), ensuring alignment with SOPs. + Manage documentation storage, organization, and archival related to design changes and labeling. + Provide proofreading and verification of product labeling prior to review and approval. + Coordinate and implement labeling changes with internal teams and external partners. + Assist with execution of product changes in collaboration with project leads. + Manage assigned design change projects, typically related to product labeling. + Perform other related duties as assigned. **Basic Qualifications / Education** + Bachelor's degree in Chemistry, Biology, Life Sciences, or a related technical field; or an equivalent combination of education and experience. + Minimum of three years of experience in a Quality Assurance role within manufacturing. **Preferred Qualifications** + 3+ years of prior Quality Assurance or similar experience in the medical device industry. **Competencies** + Strong adherence to procedures with accurate documentation skills. + Knowledge of inventory management, document control, and quality incident tracking systems. + Proficiency in Microsoft Excel and Word. + Understanding of manufacturing processes and ability to identify deviations from documented procedures. + Ability to read and interpret safety rules, operating instructions, and procedural documents. + Strong written and verbal communication skills, including report writing and presenting to groups. + Ability to interpret written, oral, diagrammatic, or schedule-based instructions. + Ability to apply mathematical concepts such as fractions, percentages, ratios, and proportions. + High attention to detail. **We are looking for the candidate who are eligible to work with any employers without sponsorship** . If you're interested, please click **"Apply"** button. ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.

Managing quality and Food Safety in the facility while promoting continuous improvement through personnel, processes, procedures, and specifications. Manages plant QA team (QA Technicians, QA Supervisor) as well as, the plant Sanitation Function. This position supports the Production Plant, Procurement, Marketing, Sales, Research and Development and Corporate Quality and Food Safety. Fosters a strong quality and food safety culture throughout the organization and leading by example. Identifies Quality and Food Safety opportunities and risks across the operation and partners with appropriate stakeholders to drive improvement initiatives. Is a strong leader, partnering with fellow plant leadership on the implementation and execution of the High Liner Operating system; consistently producing products that meet or exceed customer and consumer expectations. Assuring the manufacturing and processing of quality, food safe and compliant products. * Relocation support available for the successful candidate* Essential Duties and responsibilities Corporate: Managing the plant QA team and assuring the objectives of HLFs are supported and achieved. Day-to-day responsibilities: * Lead the day-to-day operations of the Quality and Sanitation Departments, which includes the management of a Quality Supervisors, Sanitation Supervisors, Sanitation Hourly employees, and Quality Technicians. * Ensures the implementation and execution of quality and food safety programs and procedures to lead and support all stakeholders in the production of safe, quality and compliant products. * Local HACCP Team coordinator. Partnering with Corporate Quality and Food Safety for the launch, maintenance and improvement of corporate policies, procedures and guidelines. * Responsible to host and lead all customer, regulatory and third party quality and food safety audits and corrective action process. * Investigate, review and respond to consumer and customer complaints. * Manage the non-conformance process ensuring the completion of robust investigations, timely disposition and the execution of a strong corrective and preventative actions. * Serve as the lead for validation of all changes in manufacturing process * Support new product and process trials and new product launches, collaborating with corporate R&D. * Member of the Plant Leadership Team * Budget owner for lab supplies, labor, general supplies, lab services, and pest control. * Ensure superior performance and compliance with GMP's, SOPs, Corporate Programs & Training etc. * Ensures the plant sanitation processes are followed and are effective. * Provides oversight to sanitation employees and inspects completed work for conformance to standards. * Oversees the ordering/maintaining of all cleaning chemicals and maintaining all cleaning equipment. Additionally, the incumbent will oversee the requisition or purchased of cleaning supplies and equipment. * Oversees special cleaning projects as assigned. * Ensures the master cleaning schedules are maintained and addressed. * May provide oversight to be a liaison between the 3rd party pest control vendors. Continuous Improvement: * Analyzes key performance metrics and leads the plant in the establishment of a quality improvement plan and the execution of data driven quality improvement initiatives. * Continuously reviews core competencies and department processes for cycles of improvement. Identifies, leads and implements process and cost improvement opportunities while maintaining quality and food safety standards as well as agreed upon service levels. * Ensures the creation and implementation of a robust corrective/preventative action program utilizing customer/consumer complaint data, audit findings, and internal non-conformance feedback as examples, in order to drive improvements and reduction of observations. Leadership: * Ability to lead the Quality and Sanitation team to provide exceptional service to internal and external stakeholders, upholding High Liner's quality and food safety standards * Coach, develops and mentors team members to achieve personal growth and success while making meaningful contributions to the success of the Quality and Sanitation teams and High Liner Foods. * Manages performance expectations including daily accountabilities, annual goals and annual performance reviews. * Accountable for supporting annual budget process and complying with final approved budget expectations. * Ensures the allocation and maintenance of department headcount; seamlessly manages vacation times and gaps in plant coverage and support. Code of Business Conduct: * To foster a positive working environment ensuring that Policies of the Company and the Company's Code of Conduct are respected in your area and the Company's responsibilities to employees are fulfilled. This would include being familiar with and implementing, according to your role within the Company, Company policies as published from time to time. In particular, as a leader with accountability for fostering our vision and values, the incumbent must review and communicate on a regular basis the High Liner Code of Conduct. The incumbent must at all times demonstrate behavior and actions consistent with the Code and ensure that employees in his or her area do the same, and are knowledgeable about the Code and all policies referred to in the Code. Qualifications * Minimum: BS Degree/ Food Science or Nutrition preferred and/or five years of direct experience in food manufacturing environment. * Technical / specification writing experience, knowledge of USDC, USFDA, and USDA * Understanding of food technology, quality management philosophy and quality tools. * HACCP certified with knowledge & experience of the Global Food Safety Initiative and FSMA * Strong leadership skills * Ability to manage and resolve conflict in a positive way * Absolute accuracy and attention to detail are essential. * Ability to work independently and in a team environment. * Excellent verbal and written communication skills (an ability to express complicated concepts accurately in clear and simple language). * Excellent organizational, time management skills. * Excellent computer skills (i.e. JDE, BOSS, GSM, ISD (?), Lotus notes, Adobe Acrobat Standard, Adobe Illustrator, all Microsoft Applications and basic in Genesis SQL). What's in it for you? Join High Liner Foods for a career where you shape your path, backed by great benefits, flexible work, and a culture of diversity, innovation, and sustainability. Immerse yourself in opportunities to make a real impact and grow with us in our mission to nourish lives. Start your adventure where endless possibilities to thrive together await. * Competitive Salary * Heath, dental & vision coverage * Pay for performance incentives * Employee & Family assistance programs * Wellness Programs * Retirement Planning * Supplemental Parental Leaves * Disability Support * Family friendly Flex policies & Summer hours * Volunteer hours * Learning and mentorship opportunities * Safety focused work environment To learn more please visit our career/LinkedIn/Indeed page #HLSJ

Join our Quality Assurance team and play a key role in ensuring GMP compliance and operational excellence. You'll be part of a collaborative environment where your expertise helps deliver life-changing therapies. What you will get: * An agile career and dynamic working culture. * An inclusive and ethical workplace. * Competitive compensation programs that recognize high performance. * Medical, dental, and vision insurance. * Access to our global benefits: *************************************** What you will do: * Provide real-time Quality Assurance support on the manufacturing floor. * Review GMP documentation and observe operational practices. * Offer guidance on routine and non-routine GMP issues. * Respond to QA hotline calls and escalate complex issues. * Authorize equipment release and manage quality tag-outs. * Apply data integrity principles in all aspects of work. * Represent QA in meetings and project teams. What we are looking for: * Bachelor's degree in a science-related field or equivalent experience. * 5-10 years of cGMP experience in a regulated environment. * Strong understanding of GMP and ICH guidelines. * Familiarity with systems such as TrackWise, SAP, LIMS, and Microsoft Office. * Ability to identify and escalate quality issues promptly. * Collaborative mindset and commitment to continuous improvement. * Excellent communication and problem-solving skills. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

Today, Lonza is a global leader in life sciences operating across five continents. While we work to deliver new therapies, we also support our employees in building rewarding careers. Join us and help shape the future of life sciences. The actual location of this job is on site in Portsmouth, NH. As a QA Specialist III - Raw Materials Compliance, you will provide operational support and ensure compliance throughout the raw material lifecycle, including receipt, storage, handling, testing, dispensing, and disposition. You will also support final product storage and shipping logistics. This role serves as a Subject Matter Expert (SME) for cGMP documentation review and approval, working independently and guiding team members to resolve complex issues. You will collaborate with Supply Chain, Quality Control, and Manufacturing to maintain quality standards and deliver superior customer service. What you will get: An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. Medical, dental, and vision insurance. Our full list of global benefits can be found here: *************************************** What you will do: Perform SAP transactions and other quality functions to support raw material lifecycle. Provide on-the-floor support for raw material requests and guide team members. Review material documents for disposition to ensure timely release independently. Review and approve SOPs, work instructions, and validation documents in DMS. Review and approve records in QMS (e.g., investigations, change controls, CAPAs). Collaborate with Supply Chain, Quality Control, and Manufacturing for raw material support. Lead meetings, participate in projects, and drive process improvements. What we are looking for: Bachelor's degree in science required; equivalent experience considered. 3-7 years of experience in Quality Assurance and GMP environments. Strong knowledge of GMP regulations and raw material compliance. Familiarity with SAP, TrackWise, and Microsoft Office Suite preferred. Excellent communication skills and ability to manage priorities independently. Attention to detail and ability to work collaboratively and lead initiatives. Business-fluent English required. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

Support updates to formal Corporate QA/QC Program Standard Operating Procedure (SOP); Support updates of project specific QA/QC Project templates to facilitate program development for specific types of projects; Develop the project specific QA/QC program in accordance with the designated project requirements and industry accepted best-practices; Confirm that the designated project representatives are providing the proper QA/QC inspections, creating the required mock-ups, utilizing the appropriate third-party consultants, inspections and verification that the proper documentation is be executed to formally document the QA/QC program requirements; Audit the project teams to ensure they are tracking and managing the preparation and process through resolution of all Non-Conformance Reports (NCR's) and Corrective Action Reporting (CAR) to ensure appropriate and timely resolution; Organize Quality Assurance reports for submission to the designated project representative as required; Verify 3rd party independent testing services through assigned project management staff for all applicable requirements; Overall quality control management of all construction and maintenance disciplines within the organization; Reviews and approves records of worker qualifications (i.e. Certified Welder, Licensed Electrician, Etc.), as required for Authorities Having Jurisdiction (AHJ); Responsible for reviewing and approving all subcontractor related quality assurance programs with project management team; Support specialty vendor Factory Acceptance Tests (FAT's) and field material utilization compliance; Responsible for providing weekly and monthly reporting regarding quality assurance program status; Maintain a corporate Quality Assurance Manual / database for all CSI divisions and ensure it is up to date with all recognized industry best-practices; Supports scheduling with respect to deliveries and required quality related inspections in coordination with the individual project teams; Initiate continuous improvement objectives and embrace technology enhancements; Promote, foster and maintain open communication among all project team members, consultants inspectors, applicable agencies, and the supporting subcontractors and trade participants; Qualifications Participation in lessons learned sessions, operational development initiatives, and best practice training to support a continuous improvement working philosophy; Maintain a willingness to reinvest in yourself with continuing education and professional development initiatives (i.e. LEED Certification, 30 Hour OSHA Certification, etc.) as recommended by the Company; Support the development and formalization of the corporate Project Engineering / Manager Training Program; Support additional intermittent corporate needs which may include project management and construction administration responsibilities; Other duties as assigned by management. A/Z Corporation is an AA/EOE Employer

Quality Improvement Analyst - Certified Professional in Healthcare Quality (CPHQ) Job Title: Quality Improvement Analyst Coordinates complex assignments involving cross functional teams in the fulfillment of contract deliverables, regulatory and accreditation requirements with focus on data analytics and performance improvement. Models and promotes the core values of the Collaborative and Our Client. Provides data analytics assistance to all levels within Quality Improvement at both a market and corporate level. RESPONSIBILITIES: · Defines analysis methodology and provides analytic support to QI staff · Maintains databases and reports specific to QI functions and regulatory and accreditation requirements · Collaborates with other teammates to deliver solid, effective solutions · Provides data for select performance measures to regional offices · Communicates with external data sources as needed to gather data necessary to measure identified outcomes · Prepares ad hoc reports as needed for QI management · Identifies, evaluates and implements new data-driven strategies and processes for the organization · Develops tools and reports that lend valuable insights that capitalize on a combination of internal and external data · Recommends enhancements to existing systems in accordance to business needs by creating ad hoc and standard reports as well as new information delivery technologies · Acts as point of contact for business users providing both tool support and data expertise · Develops and provides insights into streamlining analytic QI processes · Assists in the HEDIS data collection process, analyzing trends and identifying areas of improvement · Prepares reports and quality improvement studies in an accurate, concise and timely fashion · Coordinates centralized and market work plans and actions with team members assuring project timeliness and expectations are met · Manages key project initiatives associated with delegated vendor functions, monitoring and summarizing vendor oversight project progress · Participates in cross functional internal and external quality teams to improve overall organization performance · Performs data collection, analysis, reporting and presentation of quality improvement activities · Performs other duties as assigned QUALIFICATIONS: · A Bachelor's Degree in Public Health, Epidemiology, Information Management or other related health field (required) · A Master's Degree in a related field (preferred) · Or equivalent work experience (preferred) REQUIREMENTS: · 3+ years of experience in collecting, analyzing and presenting data and recommendations to management (required) Licenses and Certifications: · Certified Professional in HealthCare Quality (preferred) Skills: · Demonstrated written communication skills - intermediate · Demonstrated interpersonal/verbal communication skills - intermediate · Ability to identify basic problems and procedural irregularities, collect data, establish facts and draw valid conclusions - intermediate · Ability to multi-task - intermediate · Ability to work in a fast paced environment with changing priorities - intermediate · Knowledge of quality improvement philosophy and techniques - intermediate · Ability to utilize other data management systems to pull and analyze information to draw conclusions and recommendations - intermediate Technology: · Microsoft Word - advanced (required) · Microsoft Excel - advanced (required) · Microsoft PowerPoint - advanced (required) · Microsoft Access - advanced (required) · Microsoft Outlook - advanced (required) · Ability to utilize other data management systems to pull and analyze information to draw conclusions and recommendations · Mainframe applications and/or statistical applications - advanced (required) Qualifications A Bachelor's Degree in Public Health, Epidemiology, Information Management or other related health field (required) A Master's Degree in a related field (preferred) Certified Professional in HealthCare Quality (CPHQ) Additional Information Certified Professional in HealthCare Quality

We're looking for a Senior Software QA Engineer to lead the charge in designing, developing, and executing software test plans for embedded products. If you love hunting down bugs, automating everything in sight, and making engineers sigh with your extremely thorough reviews, this one's for you. What You'll Do + Build and execute test plans for new software. + Create and maintain manual and automated tests (yes, both - we checked). + Track down defects, document them, and make sure they never return. Ever. + Help shape internal standards, processes, and test automation frameworks. + Keep test environments configured and behaving (mostly) nicely. + Review software throughout the dev cycle and ask the important question: "But... can we verify it?" What You Bring + Top‑tier collaboration skills - you play well with engineers of all kinds. + Excellent technical writing skills for crafting plans others can follow without crying. + Strong scripting/programming chops for tests, tools, and reporting. + Hands-on experience with embedded software development. + Confidence in testing methodologies, metrics, and design/implementation reviews. + Ability to read C/C++ without flinching. Tools You Know + Version control + defect tracking systems + Build systems + CI/CD pipelines + Testing tools and frameworks + Bonus points for JIRA workflow design and test management. Your Background + Bachelor's degree in CS, Software Engineering, or a related STEM field + 3+ years of SQA experience in embedded systems Requirements - Proven experience in software quality assurance for embedded systems, with a minimum of 3 years. - Strong programming skills, including scripting for test automation and tool integration. - Proficiency in C/C++ and the ability to review software designs for verifiability. - Expertise in testing methodologies, quality metrics, and defect tracking systems. - Familiarity with building systems and CI/CD pipelines. - Bachelor's degree in Computer Science, Software Engineering, or a related field. - Ability to produce technical documentation and protocols for execution by others. - Knowledge of test management tools and frameworks. Technology Doesn't Change the World, People Do. Robert Half is the world's first and largest specialized talent solutions firm that connects highly qualified job seekers to opportunities at great companies. We offer contract, temporary and permanent placement solutions for finance and accounting, technology, marketing and creative, legal, and administrative and customer support roles. Robert Half works to put you in the best position to succeed. We provide access to top jobs, competitive compensation and benefits, and free online training. Stay on top of every opportunity - whenever you choose - even on the go. Download the Robert Half app (https://www.roberthalf.com/us/en/mobile-app) and get 1-tap apply, notifications of AI-matched jobs, and much more. All applicants applying for U.S. job openings must be legally authorized to work in the United States. Benefits are available to contract/temporary professionals, including medical, vision, dental, and life and disability insurance. Hired contract/temporary professionals are also eligible to enroll in our company 401(k) plan. Visit roberthalf.gobenefits.net for more information. © 2025 Robert Half. An Equal Opportunity Employer. M/F/Disability/Veterans. By clicking "Apply Now," you're agreeing to Robert Half's Terms of Use (https://www.roberthalf.com/us/en/terms) and Privacy Notice (https://www.roberthalf.com/us/en/privacy) .

Managing quality and Food Safety in the facility while promoting continuous improvement through personnel, processes, procedures, and specifications. Manages plant QA team (QA Technicians, QA Supervisor) as well as, the plant Sanitation Function. This position supports the Production Plant, Procurement, Marketing, Sales, Research and Development and Corporate Quality and Food Safety. Fosters a strong quality and food safety culture throughout the organization and leading by example. Identifies Quality and Food Safety opportunities and risks across the operation and partners with appropriate stakeholders to drive improvement initiatives. Is a strong leader, partnering with fellow plant leadership on the implementation and execution of the High Liner Operating system; consistently producing products that meet or exceed customer and consumer expectations. Assuring the manufacturing and processing of quality, food safe and compliant products. *Relocation support available for the successful candidate* Essential Duties and responsibilities Corporate: Managing the plant QA team and assuring the objectives of HLFs are supported and achieved. Day-to-day responsibilities: Lead the day-to-day operations of the Quality and Sanitation Departments, which includes the management of a Quality Supervisors, Sanitation Supervisors, Sanitation Hourly employees, and Quality Technicians. Ensures the implementation and execution of quality and food safety programs and procedures to lead and support all stakeholders in the production of safe, quality and compliant products. Local HACCP Team coordinator. Partnering with Corporate Quality and Food Safety for the launch, maintenance and improvement of corporate policies, procedures and guidelines. Responsible to host and lead all customer, regulatory and third party quality and food safety audits and corrective action process. Investigate, review and respond to consumer and customer complaints. Manage the non-conformance process ensuring the completion of robust investigations, timely disposition and the execution of a strong corrective and preventative actions. Serve as the lead for validation of all changes in manufacturing process Support new product and process trials and new product launches, collaborating with corporate R&D. Member of the Plant Leadership Team Budget owner for lab supplies, labor, general supplies, lab services, and pest control. Ensure superior performance and compliance with GMP's, SOPs, Corporate Programs & Training etc. Ensures the plant sanitation processes are followed and are effective. Provides oversight to sanitation employees and inspects completed work for conformance to standards. Oversees the ordering/maintaining of all cleaning chemicals and maintaining all cleaning equipment. Additionally, the incumbent will oversee the requisition or purchased of cleaning supplies and equipment. Oversees special cleaning projects as assigned. Ensures the master cleaning schedules are maintained and addressed. May provide oversight to be a liaison between the 3rd party pest control vendors. Continuous Improvement: Analyzes key performance metrics and leads the plant in the establishment of a quality improvement plan and the execution of data driven quality improvement initiatives. Continuously reviews core competencies and department processes for cycles of improvement. Identifies, leads and implements process and cost improvement opportunities while maintaining quality and food safety standards as well as agreed upon service levels. Ensures the creation and implementation of a robust corrective/preventative action program utilizing customer/consumer complaint data, audit findings, and internal non-conformance feedback as examples, in order to drive improvements and reduction of observations. Leadership: Ability to lead the Quality and Sanitation team to provide exceptional service to internal and external stakeholders, upholding High Liner's quality and food safety standards Coach, develops and mentors team members to achieve personal growth and success while making meaningful contributions to the success of the Quality and Sanitation teams and High Liner Foods. Manages performance expectations including daily accountabilities, annual goals and annual performance reviews. Accountable for supporting annual budget process and complying with final approved budget expectations. Ensures the allocation and maintenance of department headcount; seamlessly manages vacation times and gaps in plant coverage and support. Code of Business Conduct: To foster a positive working environment ensuring that Policies of the Company and the Company's Code of Conduct are respected in your area and the Company's responsibilities to employees are fulfilled. This would include being familiar with and implementing, according to your role within the Company, Company policies as published from time to time. In particular, as a leader with accountability for fostering our vision and values, the incumbent must review and communicate on a regular basis the High Liner Code of Conduct. The incumbent must at all times demonstrate behavior and actions consistent with the Code and ensure that employees in his or her area do the same, and are knowledgeable about the Code and all policies referred to in the Code. Qualifications Minimum: BS Degree/ Food Science or Nutrition preferred and/or five years of direct experience in food manufacturing environment. Technical / specification writing experience, knowledge of USDC, USFDA, and USDA Understanding of food technology, quality management philosophy and quality tools. HACCP certified with knowledge & experience of the Global Food Safety Initiative and FSMA Strong leadership skills Ability to manage and resolve conflict in a positive way Absolute accuracy and attention to detail are essential. Ability to work independently and in a team environment. Excellent verbal and written communication skills (an ability to express complicated concepts accurately in clear and simple language). Excellent organizational, time management skills. Excellent computer skills (i.e. JDE, BOSS, GSM, ISD (?), Lotus notes, Adobe Acrobat Standard, Adobe Illustrator, all Microsoft Applications and basic in Genesis SQL). What's in it for you? Join High Liner Foods for a career where you shape your path, backed by great benefits, flexible work, and a culture of diversity, innovation, and sustainability. Immerse yourself in opportunities to make a real impact and grow with us in our mission to nourish lives. Start your adventure where endless possibilities to thrive together await. Competitive Salary Heath, dental & vision coverage Pay for performance incentives Employee & Family assistance programs Wellness Programs Retirement Planning Supplemental Parental Leaves Disability Support Family friendly Flex policies & Summer hours Volunteer hours Learning and mentorship opportunities Safety focused work environment To learn more please visit our career/LinkedIn/Indeed page #HLSJ

Come Join Us! From apartments in New York to hospitals and stadiums in Dallas, libraries at prestigious universities to creating modern retail experiences, our teams contribute architectural glass and building products to projects that shape the way people live, work, heal, learn, and play. At OBE, the work of our employees truly matters. With over 6,500 employees, we operate more than 80 manufacturing and distribution facilities in five countries. You can see some of our favorite projects here. Start your journey with OBE and help us build the future. What You'll Get to Do The Quality Specialist is focused on the quality program and ensure that required product, manufacturing testing, and reporting are completed to meet external industry and safety standards. and reports to the OpEx Manager. This role is perfect for an individual who drives quality standards, a problem solver and able to understand the customer. A vital member of the Operations Team, this is an opportunity to build a career with an industry leader. Job responsibilities include: Develop and administer quality standards and set the strategic direction Train, mentor, and coach each team consisting of managers, engineers, supervisors, and technicians and extended team members involving new techniques or quality related procedures. Evaluate all department capabilities and protocols to ensure that they will produce product that meet world class performance levels for the industry Ensure the execution of corrective actions when existing supplier quality issues arise and specifications are not being met. Drive corrective actions with operations and design when production issues result in service calls or specifications not being met. What We Are Looking For Minimum of a Bachelor's degree in a technical field and 3+ years of relevant quality experience is required. Leadership / management experience in a relevant technical field. Has worked with suppliers in a Quality Organization and is familiar with Quality and Reliability Management Systems. ASQ certification in Quality Engineering desirable. What OBE Offers You Benefits that benefit you - industry competitive benefits at the lowest cost to the employee Work-life balance - PTO and holidays, including floating holidays you can choose Compensation that rewards your hard work - A pay-for-performance culture with potential for annual raises and bonuses Training - We will equip you with the knowledge and skills you need to succeed OBE Privacy Policy OBE will not discharge or discriminate against employees or applicants for discussing, disclosing, or inquiring about their own or others' pay.

TD Bank is a member of TD Bank Group and a subsidiary of The Toronto-Dominion Bank of Toronto, Canada, a top 10 financial services company in North America. The Toronto-Dominion Bank trades on the New York and Toronto stock exchanges under the ticker symbol "TD". For more information visit ********** Job Description Mobile Application Software QA Tester Summary On behalf of our client Procom Services is searching for a Mobile Application Software QA Tester to test mobile applications running on iOS or Android devices. The Quality Assurance Tester (QA.T) role is to read, review, run test cases and capture screenshots of successful or unsuccessful test activity within the HP QC tool for in-house software application development, information system launches, and operations systems enhancements. This individual will inform the QA analyst associated with the project of the variances/ defects found, re-test the functionality once the variances / defects have been addressed and also inform the QA analyst of any updates to the test steps, as required. Mobile Application Software QA Tester Job Details A vacancy exists for a QA Tester to join the team and be responsible for MOBILE application testing. As part of this team, prime responsibility will be to: - Test mobile banking applications across cellular phones and tablets - test updates to mobile operating systems - Review scenarios and HP QC content to understand test requirements. - Participate in data requisitioning - Run identified test cases for identified functionality - Inform QA analyst of actual results that defer from the expected results - Identify and document variances/defects in User Experience, Usability, process flows, identified functionalities and communicate them to the team. - Participate in variance / defect reviews - Engage with development team to resolve identified variances; - Assist in the preparation of test result walkthroughs / presentations to the project team and business representatives. -Under supervision the QA Tester will participate in data requests, report generation, defect reviews and specified project status meetings. Mobile Application Software QA Tester Start Date ASAP Mobile Application Software QA Tester Assignment Length 3 months+ extensions up to two years Qualifications Mobile Application Software QA Tester Mandatory Skills - Very familiar with smartphones and tablets: at least 1 year mobile application test experience on iOS, or Android devices - Previous engagement on projects using Rapid Application Development process - Agile / Scrum - Familiarity with online banking applications: Web or mobile platform based - Solid understanding of QA methodology and practices, within SDLC - Intrigued by technology and new applications - Familiar with HPQC - Strong MS Office skills - Effective communicator - Team player Additional InformationAll your information will be kept confidential according to EEO guidelines.

WHO WE ARE: Harvey Performance Company is a fun, dynamic, and fast-growing company of people who care about community, celebrating our successes, and creating opportunities for personal and professional advancement. THE OPPORTUNITY: Our Quality Associates play a collaborative role to the many different daily quality control department needs. Hands-on training is provided on all metrology equipment, and in all Inspection Department processes. Our newly built facility is located in Gorham ME, less than a twenty-minute drive to Portland ME. The Gorham area offers easy access to great outdoor activities, safe communities, and quality schooling both K through 12 and Colleges. IN THIS ROLE, YOU WILL: Perform mechanical, physical, and visual inspection of tools to ensure conformance to specified requirements and become proficient in the inspection of customer RMAs and sample tools. Properly use optical comparator, vision systems, Helicheck and hand-held inspection tools to identify tool dimensions and characteristics. Comprehend tool dimensions and specifications in relation to their associated print. Work with Fulfillment, Receiving and Production staff to ensure the accuracy of routers, packing slips and tooling descriptions. Assist the Technical Sales Department in troubleshooting customer quality issues and fulfilling special request. Assist the Inspection Department Manager in data collection and non-conformance reporting. Identify manufacturing failures and accurately document failures through Nonconforming Product Documentation. Cross train with other departments to grow knowledge of company product and processes. YOU'LL BRING: High School Degree or equivalent. Ability to read and interpret mechanical drawings, along with a mathematical aptitude desired. Familiarity with Geometric Dimensioning and Tolerancing fundamentals desired. Prior knowledge of proper use and calibration of metrology tools desired. Excellent communication skills, both verbal and written. WHERE YOU'LL WORK: Our state-of-the-art facility is located in the charming town of Gorham, ME, known for its natural beauty and friendly community. While also being just 14 miles outside of Portland, ME. Being part of Harvey means you can experience the fulfilling professional life and the leisurely small-town living that Gorham offers. WHAT HARVEY PROVIDES: A fun, rapid-growing environment where new opportunities are regularly made available. A comprehensive benefits package, including PTO, paid holidays, health, dental, vision insurance, employee equity program, and a 401k match program, along with profit sharing. 79,000 Sq Ft. state of the art manufacturing facility. Generous Shift Differential for Second and Weekend Shifts. Opportunities for tuition reimbursement and a robust tiered training program. Exceptional Employee Referral Program.

Duration: 9++ months Visa copy mandatory and looking for 10+yrs exp We need a general QA Lead to run and oversee the QA for ongoing internal projects, a number of which and the primary will be for Java based work. Prior QA for Java development is a strong plus and some standard testing tools/Suites is required. Such as the Rational suite, Mercury and other automation tools. · Quality Control functions · Ensure that all current applications have unit test cases that map to signed off requirements · Train development teams as needed on how to create unit tests (and/or create unit tests) · Determine staffing for QA analysts Qualifications BS Degree Additional Information All your information will be kept confidential according to EEO guidelines.

WHO WE ARE: Harvey Performance Company is a fun, dynamic, and fast-growing company of people who care about community, celebrating our successes, and creating opportunities for personal and professional advancement. THE OPPORTUNITY: Our Quality Associates play a collaborative role to the many different daily quality control department needs. Hands-on training is provided on all metrology equipment, and in all Inspection Department processes. Our newly built facility is located in Gorham ME, less than a twenty-minute drive to Portland ME. The Gorham area offers easy access to great outdoor activities, safe communities, and quality schooling both K through 12 and Colleges. IN THIS ROLE, YOU WILL: * Perform mechanical, physical, and visual inspection of tools to ensure conformance to specified requirements and become proficient in the inspection of customer RMAs and sample tools. * Properly use optical comparator, vision systems, Helicheck and hand-held inspection tools to identify tool dimensions and characteristics. * Comprehend tool dimensions and specifications in relation to their associated print. * Work with Fulfillment, Receiving and Production staff to ensure the accuracy of routers, packing slips and tooling descriptions. * Assist the Technical Sales Department in troubleshooting customer quality issues and fulfilling special request. * Assist the Inspection Department Manager in data collection and non-conformance reporting. * Identify manufacturing failures and accurately document failures through Nonconforming Product Documentation. * Cross train with other departments to grow knowledge of company product and processes. YOU'LL BRING: * High School Degree or equivalent. * Ability to read and interpret mechanical drawings, along with a mathematical aptitude desired. * Familiarity with Geometric Dimensioning and Tolerancing fundamentals desired. * Prior knowledge of proper use and calibration of metrology tools desired. * Excellent communication skills, both verbal and written. WHERE YOU'LL WORK: * Our state-of-the-art facility is located in the charming town of Gorham, ME, known for its natural beauty and friendly community. While also being just 14 miles outside of Portland, ME. Being part of Harvey means you can experience the fulfilling professional life and the leisurely small-town living that Gorham offers. WHAT HARVEY PROVIDES: * A fun, rapid-growing environment where new opportunities are regularly made available. * A comprehensive benefits package, including PTO, paid holidays, health, dental, vision insurance, employee equity program, and a 401k match program, along with profit sharing. * 79,000 Sq Ft. state of the art manufacturing facility. * Generous Shift Differential for Second and Weekend Shifts. * Opportunities for tuition reimbursement and a robust tiered training program. * Exceptional Employee Referral Program.

Job DescriptionAbout the role: As a Quality Specialist you will work toward ensuring services, processes, and facilities comply with our Quality Assurance (QA) standards, international standards, and government regulations. Establish quantitative measurements and techniques for measuring quality and guide improvements. Conduct process quality audit and documents inspection records. You will report to the Quality Assurance Manager and be located at Newington, NH. You will support this role 100% onsite. Key Responsibilities: Support Quality Materials effort by: Ensuring contract and code requirements are maintained throughout manufacture. This will include industry standards such as:- ASME NQA-1 ISO-9001-2015 AWS ASTM Be a supplier quality interface Develop and implement surveillance program for supplier activities Provide quality surveillance of supplier activities Coordinate supplier inspections. Review of procurement documents (Purchase Requisitions; Job related Materials and Services, and Calibration). Provide support for the control of purchased items and services (Purchase Orders, CMTRs, GRS). Create and approve non-conforming material documentation (QNs and SDCRs). Develop and comply with instructions and procedures (Technical Procedures, Suppliers Submittals). Review processes documentation (Heat Treat Charts, in-house and OSV). Help with ASME Code reconciliation. Resolve contractual conflicts regarding procurement and supply of material. Conduct internal audits. Provide Process improvement in QME area. Coordinate with project engineering to determine/communicate customer and regulatory requirements Evaluate non-conforming products for acceptance Determine and organize inspection efforts for non-destructive testing and dimensional inspection Produce and revise technical procedures which support the QA program Compile lifetime records which represent the manufactured product for archival and end-user need Provide quality oversight at vendors and other Westinghouse sites Provide auditing and audit support Evaluate quality assurance program effectiveness Review supplier documentation for compliance with purchase order and standard requirements Assist manufacturing and inspection with job instruction interpretation Provide guidance to the quality inspection department Guide corrective action Participate in causal analysis Analyze customer feedback, making changes Determine quality metrics which support continuous improvement Qualifications: High School Diploma Bachelor's Degree or pursuing a degree program applicable to the position preferred 2+ years of manufacturing QA experience Previous qualifications in non-destructive testing with potential to pursue Level III qualifications or dimensional inspection skills.