Quality assurance specialist jobs in Gorham, ME - 90 jobs

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 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

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

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 II - Raw Materials Compliance, you will support the operational compliance of the raw material lifecycle, including receipt, storage, handling, testing, dispensing, and disposition. You will also assist with final product storage and shipping logistics. This role is a developing Subject Matter Expert (SME) in cGMP documentation review and approval for raw materials, working closely with Supply Chain, Quality Control, and Manufacturing teams. 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, including inspection and labeling. Review material documents for disposition to ensure timely release. 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. Participate in projects and routine meetings with minimal guidance. What we are looking for: Associate's degree in life sciences required; equivalent experience considered. 0-4 years of experience in Quality Assurance or GMP environments. Knowledge of GMP regulations and raw material compliance preferred. Familiarity with SAP, TrackWise, and Microsoft Office Suite preferred. Strong communication skills and ability to manage changing priorities. Attention to detail and ability to work independently and in teams. 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.

**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.

QA Specialist III - Lot Review Join our Quality Assurance team in Portsmouth, NH, where you'll play a critical role in ensuring the integrity and compliance of our manufacturing processes. This is an exciting opportunity to contribute to the release of life-changing therapies while developing your skills in a collaborative environment. 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 * Opportunities for professional growth and leadership development * Our full list of global benefits can be found here: ************************************** What you will do: * Review and close manufacturing batch records and related documentation for API release * Resolve issues and escalate complex cases when needed * Participate in daily lot release meetings and routine QA activities * Train junior staff on record review processes * Apply data integrity principles in all aspects of work * Support process improvement projects and quality initiatives * Collaborate with QA, QC, and Manufacturing teams to maintain compliance What we are looking for: * Bachelor's degree in Science or related field * 5-10 years of experience in cGMP environments * Strong knowledge of quality systems and good documentation practices * Excellent attention to detail and critical thinking skills * Effective written and verbal communication skills * Ability to work independently and within a team environment * Proficiency in Microsoft Office; experience with Trackwise and SAP preferred 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.

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.

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

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

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.

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.

Hours: 40 Pay Details: $86,840 - $139,360 USD TD is committed to providing fair and equitable compensation opportunities to all colleagues. Growth opportunities and skill development are defining features of the colleague experience at TD. Our compensation policies and practices have been designed to allow colleagues to progress through the salary range over time as they progress in their role. The base pay actually offered may vary based upon the candidate's skills and experience, job-related knowledge, geographic location, and other specific business and organizational needs. As a candidate, you are encouraged to ask compensation related questions and have an open dialogue with your recruiter who can provide you more specific details for this role. Line of Business: Compliance : Why Work with Us? At TD Bank US Compliance, we're on a mission to build a more resilient and scalable compliance risk management function. As part of our team, you'll play a key role in reshaping compliance structures and processes, driving innovation at every level. Here, each team member has a chance to make a tangible impact - both in day-to-day operations and in the design of a future-focused compliance program. This not just about implementing a new program - it's about creating a culture of compliance that will cascade throughout the organization. Department Overview The Compliance Quality Assurance (US) team is responsible for providing independent quality assurance of compliance risk through the execution of reviews. These reviews assess whether Risk Owners and Oversight functions are complying with established policies, standards and procedures. The Compliance Quality Assurance Manager (US) will execute these reviews and/or perform peer reviews. This role will play a key role in providing strategic guidance that reshapes Compliance's structures and processes. We're counted on to provide recommendations to enhance operational performance, foster meaningful process improvements and ensure adherence to internal policies, standards and procedures. Here, each team member has a chance to make a tangible impact - both in day-to-day operations and in the design of a future-focused Compliance Quality Assurance function. This is not just about implementing a new program - it's about creating a culture of compliance that will cascade throughout the organization. The above details are specific to the role which is outlined in the general description below. Please review Desired Skills & Experience below as you consider this opportunity. Our team currently operates under a hybrid work model, with employees expected to work in the office two days per week. Starting in November 2025, this expectation will increase to four days per week. Please note that, due to limited office space, the exact timing of this transition may vary depending on availability and individual circumstances Job Description Summary: The Compliance Testing Manager is responsible for planning and overseeing independent Compliance testing completed by specialists. May execute some independent testing as applicable. This role provides subject matter expertise on Compliance controls/processes and is responsible for leading all phases of the assigned testing engagement. Depth & Scope: * Works independently and be accountable for acting as a lead in executing engagements and provides work direction to others on those engagements * Considered subject matter expert in Compliance testing methodologies * Provides subject matter expertise and/or guidance to various stakeholders and team members * Advanced knowledge of external competition, industry and/or market trends in relation to own function/business * Scope of role may have enterprise impact * Undertakes and completes a variety of complex projects and initiatives requiring specialist knowledge and/or the integration of cross functional processes within own area of expertise * Independently performs concurrent multiple reviews and related tasks from end to end * May act as highest point of team escalation for resolution and provides direction to resolve issues or escalates Education & Experience: * Undergraduate degree or equivalent work experience * 7+ years of experience Desired Skills & Experience: * CPA, CIA, CFE, CRCM or equivalent a plus * 8+ years of internal audit, testing and/or quality assurance experience * Knowledge of financial institution laws/regulations, strategies and risk management/compliance programs * Possesses and demonstrates expertise in the advisory of policy, change management, project management and operations * Skilled in using computer applications including MS Office suite, with a focus on Excel and PowerPoint * High personal and professional integrity and standards to advance TD's vision and protect the brand * Strategic critical thinker: has excellent judgment, achieves the right risk/reward balance * Delivers on objectives, focuses on what matters and can work across silos to build effective working relationships * Clear and concise verbal and written communication skills Customer Accountabilities: * Executes and manages testing activities in accordance with established standards and strategic direction to achieve completion within target timelines * Executes follow-up on findings raised from testing engagements in accordance with established standards * Conducts skilled analytical research and analysis as part of testing engagement and initiatives * Understands risk identification, risk analysis, and risk mitigation according to regulatory requirements and best business practices * Develops strong relationships and works collaboratively with key partners * Oversees/leads the testing engagement, including communications and the reporting processes * Provides subject matter expertise and/or input to projects/initiatives as a representative for area of specialization * Proactively identifies matters which require additional attention, further escalation, or review, and liaises with the appropriate staff to resolve Shareholder Accountabilities: * Prioritizes and manages workload to deliver quality results and meet testing timelines * Contributes to the review of internal processes and activities and assists in identifying potential opportunities to improve operational efficiencies for area of responsibility * Adheres to internal policies/procedures, enterprise frameworks and methodologies and applicable regulatory guidelines * Clearly and concisely documents research as required to understand requirements specific to an engagement * Protects the interests of the organization - identifies and manages risks, and escalates non-standard, high risk transactions/activities as necessary * Applies subject matter expertise in the discipline, provides guidance, assistance, and direction to others * Actively manages relationships within and across various business lines, corporate and/or control functions, and drives alignment with enterprise and/or regulatory requirements * Assesses/identifies key issues and escalates to appropriate levels and relevant stakeholders where required * Participates in cross-functional/enterprise initiatives as a subject matter expert helping to identify risk/provide guidance for complex situations * Keeps abreast of emerging issues, trends, and evolving regulatory requirements and assesses potential impacts to the Bank * Maintains a culture of risk management and control, supported by effective processes in alignment with risk appetite Employee/Team Accountabilities: * Participates fully as a member of the team, supports a positive work environment that promotes service to the business, quality, innovation and teamwork and promotes timely communication of issues/points of interest * Provides thought leadership and/or industry knowledge for own area of expertise in own area and participates in knowledge transfer within the team and business unit * Keeps current on emerging trends/developments and grows knowledge of the business, related tools and techniques * Participates in personal performance management and development activities, including cross training within own team * Keeps others informed and up-to-date about the status/progress of projects and/or all relevant or useful information related to day-to-day activities * Contributes to team development of skills and capabilities through mentorship of others, by sharing knowledge and experiences and leveraging best practices * Leads, motivates and develops relationships with internal and external business partners/stakeholders to develop productive working relationships * Contributes to a fair, positive and equitable environment that supports a diverse workforce * Acts as a brand ambassador for your business area/function and the bank, both internally and/or externally Physical Requirements: Never: 0%; Occasional: 1-33%; Frequent: 34-66%; Continuous: 67-100% * Domestic Travel - Occasional * International Travel - Never * Performing sedentary work - Continuous * Performing multiple tasks - Continuous * Operating standard office equipment - Continuous * Responding quickly to sounds - Occasional * Sitting - Continuous * Standing - Occasional * Walking - Occasional * Moving safely in confined spaces - Occasional * Lifting/Carrying (under 25 lbs.) - Occasional * Lifting/Carrying (over 25 lbs.) - Never * Squatting - Occasional * Bending - Occasional * Kneeling - Never * Crawling - Never * Climbing - Never * Reaching overhead - Never * Reaching forward - Occasional * Pushing - Never * Pulling - Never * Twisting - Never * Concentrating for long periods of time - Continuous * Applying common sense to deal with problems involving standardized situations - Continuous * Reading, writing and comprehending instructions - Continuous * Adding, subtracting, multiplying and dividing - Continuous The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties and skills required. The listed or specified responsibilities & duties are considered essential functions for ADA purposes. #LI-AMCBCorporate Who We Are: TD is one of the world's leading global financial institutions and is the fifth largest bank in North America by branches/stores. Every day, we deliver legendary customer experiences to over 27 million households and businesses in Canada, the United States and around the world. More than 95,000 TD colleagues bring their skills, talent, and creativity to the Bank, those we serve, and the economies we support. We are guided by our vision to Be the Better Bank and our purpose to enrich the lives of our customers, communities and colleagues. TD is deeply committed to being a leader in customer experience, that is why we believe that all colleagues, no matter where they work, are customer facing. As we build our business and deliver on our strategy, we are innovating to enhance the customer experience and build capabilities to shape the future of banking. Whether you've got years of banking experience or are just starting your career in financial services, we can help you realize your potential. Through regular leadership and development conversations to mentorship and training programs, we're here to support you towards your goals. As an organization, we keep growing - and so will you. Our Total Rewards Package Our Total Rewards package reflects the investments we make in our colleagues to help them and their families achieve their financial, physical and mental well-being goals. Total Rewards at TD includes base salary and variable compensation/incentive awards (e.g., eligibility for cash and/or equity incentive awards, generally through participation in an incentive plan) and several other key plans such as health and well-being benefits, savings and retirement programs, paid time off (including Vacation PTO, Flex PTO, and Holiday PTO), banking benefits and discounts, career development, and reward and recognition. Learn more Additional Information: We're delighted that you're considering building a career with TD. Through regular development conversations, training programs, and a competitive benefits plan, we're committed to providing the support our colleagues need to thrive both at work and at home. Colleague Development If you're interested in a specific career path or are looking to build certain skills, we want to help you succeed. You'll have regular career, development, and performance conversations with your manager, as well as access to an online learning platform and a variety of mentoring programs to help you unlock future opportunities. Whether you have a passion for helping customers and want to expand your experience, or you want to coach and inspire your colleagues, there are many different career paths within our organization at TD - and we're committed to helping you identify opportunities that support your goals. Training & Onboarding We will provide training and onboarding sessions to ensure that you've got everything you need to succeed in your new role. Interview Process We'll reach out to candidates of interest to schedule an interview. We do our best to communicate outcomes to all applicants by email or phone call. Accommodation TD Bank is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, status as a protected veteran or any other characteristic protected under applicable federal, state, or local law. If you are an applicant with a disability and need accommodations to complete the application process, please email TD Bank US Workplace Accommodations Program at ***************. Include your full name, best way to reach you and the accommodation needed to assist you with the applicant process.

Are you interested in being part of an innovative team that supports Westinghouse's mission to provide clean energy solutions? At Westinghouse, we recognize that our employees are our most valuable asset and we seek to identify, attract and recruit the most qualified talent while recognizing and encouraging the value of diversity in the global workplace. About 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. We are committed to transparency and equity in all of our people practices. The base salary range for this position, which is dependent upon experience, qualifications and skills, is estimated to be $64,800 to $81,000 per year. #LI-Onsite Why Westinghouse? Our benefits package is tailored to meet the diverse needs of our employees, while also promoting wellness and career growth. The following are representative of what we offer: * Comprehensive Medical benefits which could include medical, dental, vision, prescription coverage and Health Savings Account (HSA) with employer contributions options * Wellness Programs designed to support employees in maintaining their health and well-being including Employee Assistance Program providing support for our employees and their household members * 401(k) with Company Match Contributions to support employees' retirement * Paid Vacations and Company Holidays * Opportunities for Flexible Work Arrangements to promote work-life balance * Educational Reimbursement and Comprehensive Career Programs to help employees grow in their careers * Global Recognition and Service Programs to celebrate employee accomplishments and service * Employee Referral Program Westinghouse Electric Company is the global nuclear energy industry's first choice for safe, clean, and efficient energy solutions. We enable our delivery of this vision by living our value system: * Safety and Quality * Integrity and Trust * Customer Focus and Innovation * Speed and Passion to Win * Teamwork and Accountability While our Global Headquarters are located in Cranberry Township, PA, we have over 11,000 employees working at locations in 19 different countries. You can learn more by visiting

JLL empowers you to shape a brighter way. Our people at JLL and JLL Technologies are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented people and empowering them to thrive, grow meaningful careers and to find a place where they belong. Whether you've got deep experience in commercial real estate, skilled trades or technology, or you're looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward. What this job involves This position provides comprehensive quality assurance support for pharmaceutical facility operations, ensuring all maintenance activities comply with company policies, client procedures, and FDA cGMP regulations. The Quality Specialist maintains the highest quality standards in regulated manufacturing environments while supporting continuous improvement initiatives and working closely with facility management teams and client quality control personnel. Your day-to-day tasks will include: * Executing Quality Compliance programs for cGMP manufacturing facilities and ensuring full regulatory adherence * Conducting facility self-assessments and vendor/supplier audits to maintain quality standards * Preparing and revising SOPs, change control documentation, investigations, and CAPAs * Developing training materials for facilities maintenance teams and maintaining personnel qualification files * Tracking and following up on quality events with department managers to ensure resolution * Supporting achievement of Key Performance Indicators outlined in Service Level Agreements * Interfacing with client quality control personnel to ensure proper documentation and SOP adherence Required Qualifications: * Bachelor's degree in Engineering or equivalent experience in related field * Minimum 5 years of experience in pharmaceutical, biotech, or life sciences sectors under GMP regulations * Minimum 4 years of regulatory quality and statutory compliance experience * Quality Assurance role experience in FDA-regulated manufacturing facilities * Strong knowledge of cGMP regulations as applied to maintenance and manufacturing equipment * Proficiency with Quality Engineering techniques, CMMS systems, and Quality Management Systems * Advanced computer skills including Microsoft Word, Excel, and PowerPoint Preferred Qualifications: * Auditing experience in pharmaceutical or regulated manufacturing environments * Experience with documentation control systems and change management processes * Background in facility maintenance operations within pharmaceutical settings * Knowledge of Quality Management Systems implementation and continuous improvement methodologies * Experience developing training programs for technical teams * Familiarity with client satisfaction survey processes and KPI management * Self-motivated and detail-oriented work style with ability to function independently in dynamic team environments This position does not provide visa sponsorship. Candidates must be authorized to work in the United States without employer sponsorship. Location: On-site -Portsmouth, NH If this job description resonates with you, we encourage you to apply, even if you don't meet all the requirements. We're interested in getting to know you and what you bring to the table! Personalized benefits that support personal well-being and growth: JLL recognizes the impact that the workplace can have on your wellness, so we offer a supportive culture and comprehensive benefits package that prioritizes mental, physical and emotional health. Some of these benefits may include: * 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 * Early access to earned wages through Daily Pay JLL Privacy Notice Jones Lang LaSalle (JLL), together with its subsidiaries and affiliates, is a leading global provider of real estate and investment management services. We take our responsibility to protect the personal information provided to us seriously. Generally the personal information we collect from you are for the purposes of processing in connection with JLL's recruitment process. We endeavour to keep your personal information secure with appropriate level of security and keep for as long as we need it for legitimate business or legal reasons. We will then delete it safely and securely. For more information about how JLL processes your personal data, please view our Candidate Privacy Statement. For additional details please see our career site pages for each country. For candidates in the United States, please see a full copy of our Equal Employment Opportunity policy here. Jones Lang LaSalle ("JLL") is an Equal Opportunity Employer and is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process - including the online application and/or overall selection process - you may email us at ******************. This email is only to request an accommodation. Please direct any other general recruiting inquiries to our Contact Us page > I want to work for JLL. Accepting applications on an ongoing basis until candidate identified.

I.T. Excel is a new breed of service firm - an industry-focused consulting and integration firm offering a broad range of solution offerings to clients from a broad range of Industries. ITE is an end-to-end global consulting & solutions company with over 250 employee .We help companies bring improved focus to IT and how it aligns with the business, executes on its priorities and balances between innovation and efficiency. We have successfully shared with many of our clients the strategies, approaches and techniques necessary to transform IT capability and enable the implementation of business strategy. We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Job Description RELOCATION IS A MUST AND 4 WEEKS MANDATORY IN-PERSON TRAINING IN RESTON, VA Title: Jr. Validation Engineer/QA Analyst/ Jr. QA Tester/Business Analyst/BA Description : WE ARE LOOKING FOR FRESH GRADUATES FOR QA and Validation POSITIONS. Qualifications : BS in Biomedical Engineering/ BS in Chemical Engineering/ Computer Science/ MS Computer Science/ BBA/ MBA/ Engineering degree required from an accredited university or college. Minimum Experience: Recent college graduates with no experience or graduates with few years of experience preferred. Computer literate and familiar with the use of word processing, spreadsheet, and basic database applications preferred. Employment Benefits: Competitive Base Salary: Base Pay of $55,000 - $58,000 / Yr with periodic reviews (usually every 6 months) and increments. I.T. EXCEL is an E-VERIFIED Company . Clients: We mostly work with Fortune 50 companies. We have existing contracts/partnership with Amgen, Aventis, Alfa Physician Resources, Baxter, Bank of America, Bank One, Biogen, Cisco Systems, Citi Bank, Citizens Bank, Cymbal, Deutsche Bank, Eli Lilly, Freddie Mac, Fannie Mae, GMAC Insurance, IBM, ING Direct Bank, Johnson & Johnson, JP Morgan & Chase, LL Bean, Liberty Mutual, Nasdaq, Navimedix, Nextel, Pfizer, State Farm Insurance, Schering Plough, Wells Fargo, Verizon, 3 COM and many more. Health Insurance: ITE provides all its full-time employees with medical insurance. Health Insurance coverage (PPO Plan) is offered by Anthem Blue Cross Blue Shield, one of the leading healthcare companies in the United States. This allows easy access to dependable healthcare, through a large network of physicians and hospitals, spread across the United States. We are also working on adding other benefits like Dental/Vision Workers Compensation: Workers' compensation insurance is provided to all employees, covering them against work related injuries and/or disabilities. Relocation Assistance: We offer our employees Relocation Assistance, to help them with the relocation costs while starting their project at client site Qualifications Qualifications : BS in Biomedical Engineering/ BS in Chemical Engineering/ Computer Science/ MS Computer Science/ BBA/ MBA/ Engineering degree required from an accredited university or college. Minimum Experience: Recent college graduates with no experience or graduates with few years of experience preferred. Computer literate and familiar with the use of word processing, spreadsheet, and basic database applications preferred. Additional Information Skills/Abilities/Competencies Required: Must be ambitious, have strong work ethic, and a willingness to learn Be a fast learner with strong problem solving skills Demonstrated strength in verbal and written communication Positive & winning attitude Excellent communication and interpersonal skills Ability to understand and effectively communicate at all management levels, technical dependencies, timeline impact and risks Employment Benefits: Competitive Base Salary.

Title: Quality Assurance Engineering Intern Internship Time Frame: Summer 2026 About Trimble's Internship Program As a Trimble intern, you will gain valuable hands-on experience, and be provided with challenging, meaningful tasks that will give you insight into what it's like working full-time as a valued member of a team. Our internships are designed to prepare you for your career journey, while growing as a professional through lunch and learns, professional development courses, team-building activities, and social networking events with other interns, whether you are in person or remote. Over the course of your internship, we want you to feel like you belong, innovate, and grow personally and professionally. Join Trimble's community to have a global impact where we value you, your experience, and your skills to propel your career forward. Do you have a passion for QA and want to contribute to delivering high-quality, scalable, and performant platforms and products within a collaborative environment at the B2W division? What You Will Do You will contribute to testing software platforms and products that serve the heavy civil construction domain. Clients who use our software are in the business of building roads, bridges, dams, stadiums, tunnels, etc. These products have desktop, web, and mobile aspects. All platforms/products are built on the Microsoft technology stack using .NET. You will test software platforms and products that are built on the Microsoft tech stack. Your goal is to deliver high quality solutions which perform and scale well. You will be part of a team which operates using SCRUM methodologies. Develop and execute comprehensive test plans and test cases for web, mobile, and related services. Perform various testing activities to identify and document defects, ensuring overall product quality. Collaborate with cross-functional teams including developers, product managers, and UX to understand requirements and ensure test coverage. Embrace a quality-first mindset in collaborating with the team to continuously improve processes and to raise the bar in regards to our quality standard. Conduct exploratory testing to uncover issues that may not be captured by existing test cases. Document and track defects through resolution, ensuring thorough communication and follow-up. Testing of REST APIs using tools such as Postman is a plus. What Skills & Experience You Should Bring Degree in Computer Science, Software Engineering, Information Systems, or Data Analytics Relevant coursework or project experience in testing web, desktop, or mobile applications Experience in Jira, SQL, Microsoft tech, and Playwright Automated testing and dev coding experience is a plus Eagerness to learn and enthusiastic attitude Learning and Mentorship: Mentorship from senior QA engineers. Exposure to different aspects of the software development lifecycle. Opportunities for growth and learning About Job Location This role requires onsite presence. There are no travel expectations. About B2W B2W Software is a vendor of software solutions to the heavy civil construction domain and has been in business for 35 years. It was acquired by Trimble during September 2022, and is now a division of Trimble. We are located in the town of Portsmouth in the state of New Hampshire. Visa sponsorship is not available for this position. Candidates must already possess authorization to work in the United States of America without the need for employer sponsorship. Compensation: Trimble provides the following compensation range and general description of other compensation and benefits that it in good faith believes it might pay and/or offer for this position. This compensation range is based on a full time schedule. Trimble reserves the right to ultimately pay more or less than the posted range and offer additional benefits and other compensation, depending on circumstances not related to an applicant's sex or other status protected by local, state, or federal law. Hiring Range $25.58-$32.67 Pay Rate Type Hourly Bonus Eligible? No Commission Eligible? No Benefits: Trimble offers comprehensive core benefits that include Medical, Dental, Vision, Life, Disability, Time off plans and retirement plans. Most of our businesses also offer tax savings plans for health, dependent care and commuter expenses as well as Paid Parental Leave and Employee Stock Purchase Plan. If this position is identified above as commission- or bonus-eligible, the terms of the commission plan or discretionary bonus plan for which you are eligible will be provided following the employee start date. How to Apply: Please submit an online application for this position by clicking on the ‘Apply Now' button located in this posting. Application Deadline: Applications could be accepted until at least 30 days from the posting date. At Trimble, we are committed to fostering a diverse, inclusive, and equitable workplace where everyone can thrive. Guided by our core values-Belong, Innovate, and Grow-we embrace and celebrate differences, knowing they make us stronger and more innovative. We are proud to be an equal opportunity employer, welcoming individuals of all backgrounds and advancing opportunities while embracing race, color, gender identity, sexual orientation, religion, disability, veteran status, or any other protected and diverse characteristic. We are committed to offering our candidates and employees with disabilities or sincerely held religious beliefs the ability to seek reasonable accommodations in accordance with applicable law and/or where it would not constitute undue hardship for Trimble. For more, please see Trimble's Code of Business Conduct and Ethics at ***************************** under “Corporate Governance.” Our mission to transform the way the world works starts with transforming how we work together. By actively listening, asking questions, and taking intentional actions, we cultivate a culture that provides equitable opportunities for everyone to contribute and grow. Trimble's Privacy Policy If you need assistance or would like to request an accommodation in connection with the application process, please contact ********************.

# 98123 - Sanford, Maine, United States TESTING Equal Opportunity Employer Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status (United States positions), or any other characteristic protected by law. Are you interested in working for Colgate-Palmolive? You can apply online and attach all relevant documents such as a cover letter and resume or CV. Applications received by e-mail are not considered in the selection process. Become part of our team. We look forward to your application. Colgate-Palmolive is a leading global consumer products company, tightly focused on Oral Care, Personal Care, Home Care and Pet Nutrition. Colgate sells its products in over 200 countries and territories around the world under such internationally recognized brand names as Colgate, Palmolive, elmex, Tom's of Maine, Sorriso, Speed Stick, Lady Speed Stick, Softsoap, Irish Spring, Protex, Sanex, Elta MD, PCA Skin, Ajax, Axion, Fabuloso, Soupline and Suavitel, as well as Hill's Science Diet and Hill's Prescription Diet. For more information about Colgate's global business, visit the Company's web site at ******************************** To learn more about Colgate Bright Smiles, Bright Futures oral health education program, please visit *************************** To learn more about Hill's and the Hill's Food, Shelter & Love program please visit ************************ To learn more about Tom's of Maine please visit *************************** Reasonable accommodation during the application process is available for persons with disabilities. Please contact Application_Accommodation@colpal.com with the subject "Accommodation Request" should you require accommodation.

As a Regulatory Operational Compliance Specialist, you will be part of a team that ensures operational compliance with our Regulatory and business partners to support a portfolio of veterinary and water diagnostics in the Animal Healthcare industry. This is an opportunity to build and improve existing processes to partner with global trade and regulatory partners worldwide. Your primary responsibilities will include submitting import permit applications, supplier outreach, product change management/risk assessments, and supporting global licensing/registration activities as well as Global Trade Import/Export through product analysis and documentation. This is a hybrid role requiring being onsite at our Westbrook facility 8 days a month. What you can expect in this role: * Coordinate regulatory documents, ensuring that submissions are timely and regulatory objectives are met. * Research scientific and regulatory information in order to write, edit, and review product documentation. * Compile materials required for support of submissions, license renewals, and annual registrations. * Keep informed of professional and global regulatory information. * Performs the coordination and preparation of document packages to support regulatory submissions for new and mature products to ensure alignment and compliance with local and regional registration requirements as well as with company policies from all areas of company as well as internal audits and inspections. * Monitors and improves tracking/control systems. Partner with other regulatory personnel to keep abreast of regulatory procedures and changes that can impact operations. May direct interaction with regulatory agencies on defined matters. * Recommends strategies for submissions of regulatory permits or approvals. What you need to succeed: * Bachelor's degree or equivalent combination of education and experience required, in life sciences is preferred with 3-5 years of experience in regulatory operational compliance. * Self-starter, with ability to work independently, initiates and coordinate projects and meet deadlines within a changing, fast-paced environment. * Strong collaboration and teamwork. * Excellent problem-solving skills, sound judgment and strong interpersonal, presentation and communication skills. * Pays close attention to detail, handles confidential information with discretion and possesses a "can do" attitude. * Goal and team-orientated, able to handle difficult issues in a professional, assertive and proactive manner and history of developing cross-functional relationships within an organization. * Practical, business-oriented approach to problem-solving, tempered by an appreciation of legal complexity and risk. * Occasionally participates in process improvements across teams and organizations. * In addition to your current areas of expertise, you will have the opportunity to learn and grow your skills within a wide variety of disciplines. What you can expect from us: * Salary range starting at $72,000 based on experience * Opportunity for annual cash bonus * Health / Dental / Vision Benefits Day-One * 5% matching 401k * Additional benefits including but not limited to financial support, pet insurance, mental health resources, volunteer paid days off, employee stock program, foundation donation matching, and much more If you're looking for a role that'll challenge you, offer a variety of work and learning, while helping an amazing industry, we'd love to hear from you! Why IDEXX? We're proud of the work we do, because our work matters. An innovation leader in every industry we serve, our team members help pet owners worldwide keep their companion animals healthy and happy, ensure safe drinking water for billions, and help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a collaborative global workforce. Our culture is one that embraces challenges and encourages learning and discovery. At IDEXX, you'll be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Knowing our work has a meaningful impact on the health and well-being of pets and people is what motivates us every day. If meaningful work and a sense of purpose are at the top of your list, you'll find it here. Let's pursue what matters together. About the job location: If you're thinking about relocating for this role, here are a few things to know about living in Maine (often called "Vacationland"). The Westbrook, ME area provides great access to active downtown areas and the outdoors, with the coast and numerous mountains and hiking trails nearby. You'll also find a number of large companies like ours in the area, creating a vibrant work culture. You can learn more on the Portland tourism website: ************************************************************** IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply. IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited by local, state, or federal laws. While we appreciate our staffing partners, we are unable to accept unsolicited agency resumes. #LI-CAG