Quality Assurance Analyst Jobs in Norwood, MA

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New Point of Care Testing Specialist (Lab) opening at a beautiful facility in the state of MA! Shift: Many different shift options available. Inquire for specifics. REQUIREMENTS: ASCP (or equivalent) required Background in laboratory work/leadership Strong work ethic and desire to succeed This is a permanent, full-time position with great pay and benefits. Click APPLY today. If you are interested in learning more, or if you are a laboratory professional looking for a new position, contact Marina - call/text or email your resume to Or book a 5 minute phone call here:

Profile Schneider Electric is a global leader in enterprise energy management systems. We are looking for a new team member who can help us advance our cloud-based energy management and information systems. As a member of this team you will work on strategic projects delivering world class enterprise software systems to a wide variety of customers. We are looking for a passionate and creative senior software tester with extensive Web software quality assurance experience to join our agile team of Business Analysts, Developers, Quality Assurance, Operations and Support. This role will play a crucial role in high quality and frequent deliveries of our cloud-based energy management system. The Sr. Software Tester will be primarily responsible for reviewing and analyzing requirements and system specifications, creating and executing (manual/automated) test cases, reviewing results, reporting and documenting technical issues to ensure client requirements are met. The successful candidate must strive to deliver high-quality software that is highly scalable, performant, interoperable and secure while aligned with client needs and business goals at the same time. Responsibilities & Key Tasks Analyze user stories/use cases/requirements for validity and feasibility Develop effective test strategies and plans. Design, create and manage test cases Design and develop automation scripts when needed Execute test cases for all levels of testing (system, integration and regression) Detect and track software defects and inconsistencies Reproduce, trouble shoot, verify fixes for customer reported issues (technical support tickets) Apply quality assurance principles throughout the Agile product lifecycle Other duties as assigned Skills and Qualifications Essential 5+ years of post-secondary work experience as a Software Tester or similar role Broad and extensive knowledge of software testing process and technologies Experience with testing Web applications hosted on the cloud Experience with system, integration, and regression testing Experience with user acceptance testing Experience with test management software Strong knowledge of software development cycle, software testing life cycle and bug life cycle Commitment to customer satisfaction and quality Analytical and skeptical mind and problem-solving aptitude Attention to detail Strong organizational skills Positive attitude, enthusiasm, and self-motivation Excellent written and verbal communication skills. Proven ability to learn quickly, multi-task and handle pressure to meet tight deadlines Desirable A strong understanding of software Agile methodologies, particularly Scrum Experience with automated testing Experience in Atlassian tools (Jira Software, Jira Service Desk, Confluence, etc) Experience with automation tools like Selenium, Test Complete and SoapUI Experience with working in distributed teams and with remote stakeholders Experience with SQL Server and Cosmos DB Experience with Cyber security principles Experience with BI tools such as Qlik or Tableau Looking to make an IMPACT with your career? When you are thinking about joining a new team, culture matters. At Schneider Electric, our values and behaviors are the foundation for creating a great culture to support business success. We believe that our IMPACT values - Inclusion, Mastery, Purpose, Action, Curiosity, Teamwork - starts with us. IMPACT is also your invitation to join Schneider Electric where you can contribute to turning sustainability ambition into actions, no matter what role you play. It is a call to connect your career with the ambition of achieving a more resilient, efficient, and sustainable world. We are looking for IMPACT Makers; exceptional people who turn sustainability ambitions into actions at the intersection of automation, electrification, and digitization. We celebrate IMPACT Makers and believe everyone has the potential to be one. Become an IMPACT Maker with Schneider Electric - apply today! €36 billion global revenue +13% organic growth 150 000+ employees in 100+ countries #1 on the Global 100 World's most sustainable corporations You must submit an online application to be considered for any position with us. This position will be posted until filled. Schneider Electric aspires to be the most inclusive and caring company in the world, by providing equitable opportunities to everyone, everywhere, and ensuring all employees feel uniquely valued and safe to contribute their best. We mirror the diversity of the communities in which we operate, and ‘inclusion' is one of our core values. We believe our differences make us stronger as a company and as individuals and we are committed to championing inclusivity in everything we do. This extends to our Candidates and is embedded in our Hiring Practices. You can find out more about our commitment to Diversity, Equity and Inclusion here and our DEI Policy here At Schneider Electric, we uphold the highest standards of ethics and compliance, and we believe that trust is a foundational value. Our Trust Charter is our Code of Conduct and demonstrates our commitment to ethics, safety, sustainability, quality and cybersecurity, underpinning every aspect of our business and our willingness to behave and respond respectfully and in good faith to all our stakeholders. You can find out more about our Trust Charter here Schneider Electric is an Equal Opportunity Employer. It is our policy to provide equal employment and advancement opportunities in the areas of recruiting, hiring, training, transferring, and promoting all qualified individuals regardless of race, religion, color, gender, disability, national origin, ancestry, age, military status, sexual orientation, marital status, or any other legally protected characteristic or conduct.

This role will be based in our Cambridge, MA location until our new state of the art facility located in Burlington, MA is ready Vericel Corporation, a leader in advanced therapies for the sports medicine and severe burn care markets, has an exciting opportunity for a top performing QA professional looking to join and contribute to a commercial stage company with an established portfolio of unique advanced cell therapies and specialty biologics. Reporting directly to Quality Management at Vericel, this is a great opportunity to join a high growth company with a strong balance sheet supported by a talented team of professionals who are committed to improving the lives of the patients we serve. POSITION SUMMARY Responsible for the oversight of QA activities which include but are not limited to batch record review, media disposition, label issuance, archiving and final product packaging and release activities. The individual must be able to gown into classified manufacturing ISO 7 clean room areas, to conduct inspection of final product. DUTIES AND RESPONSIBILITIES Perform, as well as ensure that the review of batch records and release of intermediates is performed within required timeframes outlined in SOPs. Responsible for the packaging and final batch disposition. Responsible for inspection of final product within an ISO 7 cleanroom Support day to day operations, including batch record review, label issuance, archiving and verification with supervision oversight and in a timely manner. Follow oral and written procedures for review and release of intermediate and final product. Support projects as a QA resource. Identifies deficiencies and works with cross functional departments to remedy them. Communicate issues that have occurred, resolutions, or discussions with QA team and Management. Identify, address, and/or escalate compliance problems and issues and provides recommendations for process improvements within the department. Become a Qualified Trainer for QA Operations Review of Validation requalification of equipment and reviewing validation discrepancy forms. Write, conduct periodic review and revise Standard Operating Procedures. Provide oversight to QA Specialist I and II and ensuring compliance. Participate in audits and represent QA as an SME for specified areas. Accountable for timely project completions to meet business needs. Independently make decisions on minor issues on behalf of junior staff. Act as QA Reviewer which entails managing deviations/events, CAPAs and tasks within TrackWise. This includes participating in root cause analysis or hosting a root cause analysis meeting. Participate in Change Controls as SMEs and action item owners for QA. Generate, evaluate, and report quarterly event trending metrics. Generate and present metrics for QMR, PPR and Dashboard Reporting. Manage and investigate product complaints. Participate in risk assessments, root cause analysis, and data interpretation. QUALIFICATIONS, EDUCATION AND EXPERIENCE Bachelor's degree plus a minimum of 4-6 years of industry relevant experience or Master's Degree plus a minimum of 2-4 years of industry relevant experience. Strong interpersonal skills and ability to work in a team environment. Strong written and verbal communication. Strong organization and time management skills. Proficient in MS Office. Working knowledge of cGMP regulations. Preferred Qualifications: Experience in overseeing a team and projects. Knowledge of electronic batch records, ERP systems, and Quality Management Systems (TrackWise and Veeva). Ability to interpret Quality standards for implementation and review. WORKING CONDITIONS AND PHYSICAL DEMANDS Ability to lift and transport up to 30 lbs. Must be able to work one weekend day. Must be able to support rotating holiday coverage. Must be able to gown into classified manufacturing ISO 7 clean room areas, to conduct inspection of final product. Must be able to gown into CNC areas EEO Statement All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. Vericel Corporation is an Equal Opportunity/Affirmative Action Employer. Vericel Corporation is VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state.

Quality Analyst Micro 3-6 Months Billerica, MA Max PR: $30.00 Perform testing on incoming materials, finished products and stability studies in QC Laboratory. Job Responsibilities Perform routine QC testing in accordance with SOPs and cGMP guidelines. Some supervision required. Perform verification of data to ensure accuracy. Perform approval upon discretion of supervisor. Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment. Utilize a range of electronic systems such as LIMS and document/equipment management software. Author SOP changes; participate in change controls, CAPAs, other quality systems. Resolve routine problems by utilizing appropriate resources. Assist in investigations. May assist on special projects as needed. Help with continuous improvement. Train on and maintain knowledge of current regulatory requirements and relevant internal procedures. Team player who can work independently with quality and attention to detail. Good communication skills both oral and written, professional conduct. Effectively and efficiently participate in assigned tasks in a quality manner. Actively promote safety rules and awareness. Reports and takes initiative to correct safety & environmental hazards. Work with potentially hazardous chemical, radiological and/or biological materials on a daily basis. Demonstrate good safety practices at all times including the appropriate use of protective equipment. *In case of absence the “Reports to” Manager above or a peer incumbent will function as a backup for this position. Education & Qualifications Typically requires 1-3 years of previous experience in the pharmaceutical industry, related GMP environment, or equivalent. Previous experience preferred. Requires a BA/BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and experience. Familiar with aseptic technique Perform routine Environmental Monitoring and utilities testing Perform sterility, microbial limits and Endotoxin testing, identify and trend microorganisms Some non-routine travel may be required. Flexibility with scheduling requirements-may include shifts, overtime, weekends and holiday coverage, including during adverse weather conditions. Must be able to lift 50 lbs.

Veeva QMS QA Lead Duration: Long Term Contract Required qualifications to be successful in this role • Bachelor's degree in Life Sciences, Computer Science, Engineering, or related field. • Minimum of 8 years of experience in quality assurance and validation within the pharmaceutical industry. • Extensive experience working with Quality Management Systems (QMS) and tools such as Veeva or Trackwise. • Strong experience with validation processes and documentation, including IQ, OQ, PQ, and use of HP ALM for test management and traceability. • In-depth knowledge of GxP, 21 CFR Part 11, and other relevant pharmaceutical regulations. • Proven ability to lead and manage both offshore and onshore validation and QA teams. • Excellent project management skills with the ability to manage multiple projects simultaneously. • Strong problem-solving skills and the ability to mitigate risks effectively. • Excellent written and verbal communication skills, with the ability to collaborate across different functions and regions. • Experience managing external audits and ensuring regulatory compliance readiness Manish Prabhakar Email: ****************************** Phone: ************ |VLink Inc.

Akkodis is seeking a Scientific Business Analyst for a contract position with a client located in Boston, MA. The successful candidate will collaborate with several analytical teams to implement a new scientific data capture and processing tool. You will also work within the operations, interfacing also with IT developers. Our client has an electronic laboratory notebook under development based on Agile approach, requiring flexible thinking to integrate new ways of working in the context of digitalization (data analytics). Pay/Salary Range: $55.00/hr - $70.00/hr Business Analyst job responsibilities include: • Support digital template generation considering platforms technology specificities, to reach adequate data structuration • Capture new features to be developed in the tool to meet business needs (Agile mode). Communication/interaction between users and developers • Ensure the tool roll-out according to project milestones through regular & formalized interactions with key users in the platforms, and appropriate monitoring indicators • Maintain continuous scientific awareness to get deep understanding of software functioning QUALIFICATIONS: • You have a scientific and/or IT background, including scientific data structuration and processing • Three to five years of relevant experience • Knowledge in the use of Azure, AHA!, and SAP tools • Knowledge in reporting/data management tools (as Power Bi, and Spotfire, etc.) If you are interested in this Scientific Business Analyst job in Boston, MA, then please click APPLY NOW. For other opportunities available at Akkodis go to **************** If you have questions about the position, please contact Roderick Grays at ************ or ************************** Equal Opportunity Employer/Veterans/Disabled Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit ********************************************** The Company will consider qualified applicants with arrest and conviction records

Job Title: Embedded Software Functional Tester with Medical Domain experience We are seeking a highly skilled Embedded Software Functional Tester to join our dynamic team. Key Responsibilities: 7 to 9 years of experience in software verification and testing activities. Design, develop, and execute comprehensive test plans, test protocols, and test cases for verification and validation of embedded software. Collaborate with cross-functional teams to understand project requirements and define test cases. Identify or develop software test tools to verify system software and validate software tools used for verification. Formulate test methods for verification and validation purposes and develop/maintain test automation frameworks (e.g., Python Scripts). Conduct design verification/tests on new or existing products in the development cycle to verify software. Knowledge and experience in validation and verification protocols for medical devices (e.g., ISO's IEC 62366:2007) is desired. Suggest improvements in testing methods and tools for enhanced efficiency and accuracy. Provide technical guidance to a team of test engineers. Skills Required: Strong experience in software testing, verification, and validation. Hands-on experience with test automation frameworks and tools. Familiarity with medical device standards and validation protocols. Proficiency in Python scripting for automation. Excellent problem-solving and communication skills. -- Shailendra Rajak Raas infotek corporation 262 Chapman road, Suite 105A, Newark, DE-19702 Phone no. ************, Ext. 145 Email id: ******************************** LinkedIn:linkedin.com/in/shailendra-r-9904ba27b

Key Responsibilities: Develop and Execute Verification Protocols: Create and implement formal software verification and validation protocols based on product specifications, ensuring alignment with both user needs and regulatory requirements. Test Planning: Develop comprehensive test plans that define the scope and criteria for verification and validation, tailoring them to the specific requirements of each development cycle. Cross-Department Coordination: Collaborate with Software QA teams and other internal departments to guarantee that the product meets both functional and user expectations. This includes facilitating communication and feedback loops across teams. R&D Collaboration: Work closely with the R&D team to support activities such as data collection, issue reproduction, documentation, and the triage of problems. Provide technical expertise to ensure efficient resolution of identified issues. Functional Testing Development: Design and execute functional testing protocols, including unit tests, integration tests, white-box, and black-box testing approaches to ensure product robustness. Verification Compliance: Ensure the completeness of software verification efforts and adherence to applicable standards, including client's internal quality management system and industry regulations. Other Duties: Perform additional tasks as assigned to support the overall goals of the software development and validation process.

QA Engineer Remote 6-Month Contract to Hire $60-70/hr $120-130K with 10% bonus Are you well-versed in hands-on experience with testing in ETL and Data warehousing? And are you looking for your next opportunity? This opportunity will enhance your skills in ETL tools like DBT and Automation tools like Validator with a company closing the gap between healthcare and financial systems. This role will be heavy within a migration project so get ready for this awesome opportunity! THE COMPANY This world-class technology, information, and internet company is modernizing the business of healthcare through its platform. This company is committed to championing Data and AI through its platform. Does this excite you? THE ROLE Testing in ETL and Data warehouses such as Snowflake. Hands-on with ETL tools like DBT. Documenting QA efforts such as acceptance criteria, Source-target mapping, RTM, test plans, test cases, test results, bug reporting, etc. Testing SQL reports, paginated reports, etc. Working independently as a full QA resource and adaptability to work in multiple teams at the same time. YOUR SKILLS AND EXPERIENCE A successful Lead Data Engineer within this role will likely have the following skills and experience: Bachelor's degree in Business Administration, Computer Science, Data Systems or Data Analysis preferred Rich experience in functional, integration, end-to-end, regression, performance, and user acceptance testing (3+ Years). Hands-on experience with testing in ETL and Data warehouse (Snowflake is preferred) (2+ Years). Experience in automation tools like Validator. Experience documenting QA efforts such as acceptance criteria, Source-target mapping, RTM, test plans, test cases, test results, bug reporting, etc. Must have worked on migration projects.

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future ready. We offer accelerated, global growth opportunities for talent that's bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out ************************ What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth and variety in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We hire the best and trust them from day 1 to deliver global impact, handle teams, and be responsible for the outcomes while our leaders support and mentor you. We are a profitable, rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries; healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly different experience for you. If this excites you, then apply below Business Analyst You will be responsible for: Your impact: Experienced analytics consulting professional, who can handle a breadth of medical analytics projects and Document Business Requirements liasioning with stakeholders of the medical affairs function Maintain all the know how's including but not limited to - Data Mapping and business rules for KPIs arising from Medical Data sources, Veeva CRM & Master Data Management (MDM) along with few ad-hoc spreadsheet-based sources as defined by stakeholders Translate business requirements related to KOLs, MSLs, Scientific Share of Voice among others to technical specifications Provide technical and business leadership/ mentorship to junior team members; groom them for additional responsibilities Acquire, implement and provide knowledge transfer to Client's stakeholders or another external stakeholder as instructed by Client's NA on the business requirements with extensive documentation Collaborate with other members within the team to innovate through automation / new ideas / capabilities / tools Lead client communication, providing clients with periodic updates and insights / recommendations through appropriate channels (conference calls / emails) Meaningfully communicate insights and information to a broad group of stakeholders through excellent oral and written communication Assist in the creation of dashboards, reports, and visualizations that provide actionable insights to commercial teams Work with technical teams to support data integration efforts, ensuring accurate and consistent data flow across systems, including CRM, medical analytics and MDM Perform data validation and analysis to ensure the quality of data being used for analytics and reporting, identifying discrepancies and working to resolve them Support the mapping of source data to target systems, ensuring proper data lineage and governance practices are followed Act as a liaison between business stakeholders, data engineers, and technical teams, ensuring clear communication of business needs and technical solutions Participate in project meetings, providing updates on project progress, issues, and risks Help bridge the gap between business and technical teams by explaining complex technical concepts in simple terms to non-technical stakeholders Develop and maintain project documentation, including business requirement documents, functional specifications, and data flow diagrams Assist in creating detailed use cases and test scenarios for medical analytics solutions About you: 8+ years of experience with Graduate/Post-Graduate/ MBA Experience working with Tableau, SQL, knowledge of data sources like Veeva CRM, and medical data sources , MDM Experience in pharmaceutical analytics & medical affairs is a must have Experience in data visualization platforms like Tableau Experience of working in Agile environment a plus Ability to derive KPIs from data sets to create reports and dashboards Strong presentation and communication skills" EQUAL OPPORTUNITY Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate's merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

Title: Quality Assurance Associate 2nd Shift Shift: 2nd Shift, 3 pm to 11pm Monday through Friday Status: 6-12 month contract Hourly rate: $55 an hour Please note, this is Quality Assurance role and not a QC role. Qualified candidates must have experience working in a QA role on the manufacturing floor. Additionally, this contract cannot be done on C2C or offer sponsorship of any kind. Quality Assurance Associate This individual in this office-based role will maintain on site quality presence at GMP facility in Lexington, MA by providing support for clinical phase manufacturing, batch record review and quality issue resolution. Will also support incoming raw material/excipient release, document management and training systems. Primary function is to assure the quality of manufactured products is in compliance with all applicable regulations, guidelines and internal procedures. Responsibilities: • Proactively promote GMP, GDP, and compliance concepts. • Support incoming raw material release. • Support Supply Chain and Manufacturing with dispensing of raw material for batch production. • Support QC, Analytical Research and Development (ARD) with CoA review, approval, and filing. • Perform quality oversight of clinical phase manufacturing executional compliance with GMP, including issuance of production batch records, line clearance, QA on the floor presence, raw material, component, and in-process material checks. • Support batch documentation review, deviations/investigations, change control and issue resolution for Intermediate and Drug Product (DP) Disposition. Qualifications: Minimum of BA/BS in a science related field • Minimum of 5 years of related work experience in pharmaceutical, biotech or medical industry • Knowledge of Good Manufacturing Practices (GMPs), Good Documentation Practices and application within pharmaceutical development.

Looking for a BA with required experience in data projects and pharmaceuticals. For the position, the immediate need is to support financial data warehouse and related reporting so financial understanding is preferred. PowerBI skills would also be preferred. Need someone who can attend meetings with our IT business partner, and frequently lead meetings, with our financial team, understand what they do with financial planning, actuals, reporting, be able to define as-is and to-be processes, define requirements, and work with the technical team to provide the solution, lead operations support/hypercare of it (with supporting tech team) after go-live. There will be opportunities to support the external marketing, HR, or commercial and marketing areas in the future, though initially the highest priority is financial reporting” Pharmaceutical experience is preferable

JOB REQUIREMENTS: Five or more years of operations support and process management experience within the asset management or financial services industry, specific experience with requirements gathering related to RPA processing preferred but not necessary. Experience with configuring Xceptor and Automation Anywhere Robotic Process Automation tool, other tools such as Blue Prism or UiPath) is plus. Excellent interpersonal, communication, and management skills. Experience designing and delivering presentations and training to diverse audiences, including senior management, technical and non-technical personnel. Extensive experience in Agile project lifecycle management. Strong technical, analytical, and business knowledge. Excellent technical understanding of underlying relevant technical architecture and business processes. Strong project management skills, proven analytical skills and demonstrated ability to make independent decisions. Ability to multi-task and shift priorities as circumstances warrant. Bachelor's degree in business or technology preferred.

Work effectively with the diverse community of researchers and management to capture business need, workflow, and value Participate in global outreach, collaboration initiatives, and projects supporting a diverse and dynamic research community at Company Participate in documenting business process workflow, create diagrams to support and communicate Support global stakeholder management processes including communication Engage with the business owners, users and service providers of existing solutions to aid in assessment and planning for lifecycle, improvement, expansion, or transition processes Provide input and data in support of planning, prioritization and budget process for IT projects Support communication of strategies, ideas, and goals to senior management Participate in the coordination and creation of product/service documentation and training Participation in the creation of foundational service design documentation Special projects as required Requirements 3-4 years of Business Analysis experience Bachelor's degree in computer science, engineering, a related field, or equivalent experience Experience working in the scientific environment, especially one that is related to drug development is preferred Practical experience understanding, collecting, and documenting requirements and use cases. Proven success enabling customer success through thoughtful analysis and communication Additional Requirements Strong organization and attention to detail Strong interpersonal skills and the ability to act as a trusted advisor and consultant Strong analytical thinking and problem solving Perform well in a fast-changing environment

Job Description This Software Test Engineer will test Windows based Medical Device software, ensuring regulatory compliance by developing and executing detailed test cases based on design requirements. Key Responsibilities: Develop and execute detailed test cases based on system requirements and designs. Create and maintain manual test scripts and tools. Manage test configurations and set up test environments. Perform functional, integration, system, and regression testing within Agile processes. Identify, track, and resolve defects. Assist in analyzing design issues and test failures for regression testing. Maintain test protocols and requirement traceability. Skills and Qualifications: Familiar with FDA-regulated software development processes. Skilled in test planning and manual test execution. Proficient in programming/scripting (e.g., C#, C++, Java, Python). Experienced in Agile, bug tracking, code repositories, and requirements tracing. Strong analytical, communication, and attention-to-detail skills. Team player with initiative and self-motivation. Education and Experience: BS in Engineering, Science, or related field. 5+ years in software testing on product teams. Experience in medical devices or regulated industries. Company DescriptionThe experts at Connected Systems Partners, Inc. have decades of successful experience providing technology recruiting and staffing services for Fortune 500 companies to new business start-ups. We specialize in Embedded Software, Firmware, Hardware/Electrical, QA/test Engineering, Mechanical and Engineering Technicians, in MA, NH, CT and RI. Since our founding in 2011, Connected Systems Partners has been providing a superior level of service to the technology workforce, looking to advance their careers and organizations looking to add contract, contract to hire, or permanent talent to their teams. Get Connected!Company DescriptionThe experts at Connected Systems Partners, Inc. have decades of successful experience providing technology recruiting and staffing services for Fortune 500 companies to new business start-ups. \r We specialize in Embedded Software, Firmware, Hardware/Electrical, QA/test Engineering, Mechanical and Engineering Technicians, in MA, NH, CT and RI.\r Since our founding in 2011, Connected Systems Partners has been providing a superior level of service to the technology workforce, looking to advance their careers and organizations looking to add contract, contract to hire, or permanent talent to their teams. \r Get Connected!

TRANSLATING IN THE AIR When we receive or intercept data in the air, it's critical for us to understand it in order to act accordingly. Responsible for translating intelligence communications, Airborne Cryptologic Language Analysts utilize fluent foreign language skills to analyze messages obtained during flight. Providing threat warnings and actionable intelligence that can assist in mission planning, these highly skilled specialists are critical to keeping our missions successful and our Airmen safe. REQUIREMENTS You must meet several requirements before joining the Air Force. These concern your background, overall health and other standards set by the Air Force, Department of Defense and federal law.Minimum Education You must be 17-42 years of age, a U.S. citizen and obtain a qualifying ASVAB score. High School Students may start their application as early as the end of their junior year. Applicants who are non-graduates or non-alternate credential holders must obtain an AFQT Test score of 65 or higher on the ASVAB. ASVAB SCORE REQUIREMENTS 72 General (G) Qualifications A minimum score of 62 on the Predictive Success Model. No record history of temporomandibular joint pain or disorder Height no less than 59 inches and no more than 80 inches Successful completion of a polygraph test Completion of a current Single Scope Background Investigation (SSBI) Demonstrated proficiency in a designated language, or successful graduation of the Defense Language Institute in a designated language Completion of Aircrew Fundamentals Course, Airborne Cryptologic Linguist Course, and designated Survival Schools Completion of Initial Qualification Training with a valid aviation qualification Completion of 7.5 weeks of Basic Military Training Must be at least 17, but has not reached age 42 on the date of enlistment

Job Description Our clean energy client is looking for an experienced, start-up-mindedsoftware automation test engineer. You will build an automation framework for their software to enable hardware-in-the-loop (HIL) testing. You will work with development to identify weak points and design creative ways to break software and uncover potential problems. You will also present test suites and results to customers to communicate the status and coverage of their testing. You should see yourself as a generalist software engineer. While your primary responsibility will be software testing, you should be comfortable learning and contributing quickly to DevOps and UI/UX. Responsibilities: Build automation frameworks and test cases for hardware-in-the-loop testing Link test cases to requirements to provide traceability Prepare test results and identify and document issues Use creative testing to uncover problems that would otherwise make it to deployment Work as part of Agile teams to deliver testing that is in line with software development Helping develop systematic software engineering practices such as code reviews, design reviews, unit tests, module tests etc. Requirements: Bachelor's degree in Engineering or higher Commercial experience developing and deploying test cases and test automation frameworks in a corporate setting Experience working on Python, C# or equivalent testing languages Experience working on NI Labs or other HIL testing equipment A couple of years working with software tools like Jira, BitBucket/Git, Confluence, etc. Experience working with AWS IoT tools and cloud products (Greengrass, Kinesis/Firehose, S3) a plus Experience working in automotive industry is preferred

Job Description Verista’s 600 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities. Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day. Company Culture Guidelines & Values: We empower and support our colleagues We commit to client success at every turn We have the courage to do the right thing We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged. We constantly acquire new skills and learn from our experiences to enhance our collective expertise Senior Automation Engineer Responsibilities: Support staff - on site resources Setup and troubleshooting activities MES Responsibilities - Set up master data (BOMs, BOPs, etc.) Syncade administrative settings Testing MES integrations - simulating commands, etc. Set up printers - configuration and testing Set up scales - configuration and testing Set up barcode scanners - configuration and testing PCS Responsibilities - Support troubleshooting Additional Potential Responsibilities: Support the scope, deliverables, schedule, and project team for BoMs, BoPs of automation projects. Participate in the development and evaluation of RFP and bidder/vendor analysis for General contracting and engineering services when design build method used. Works directly with project controls to prepare and update project status, schedule, resource, and cost reports within Oracle based tools (OPPM & P6) for the use of numerous BMRN departments. Identify and oversee system integrations. Coordinate/support engineering and automation design, commissioning, qualification, and the QA Validation groups as appropriate. Proactively look for and recommend improvements in site processes and procedures. Represent the Capital Project Automation group with good communication and presentation skills Provide status reports on Projects to Automation Management as required Requirements Demonstrated experience with Syncade Experience with MES -Master Data setup and administration, and with integrations Ability to work with minimal direct supervision: meet deadlines, prioritize assignments, provide recommendations and effectively communicate updates. Experienced with communicating with in supporting Executive Management as well as providing direction support for multiple projects simultaneously. Must be very organized and possess strong verbal and written communications skills. Must be proficient with Internet navigation, Microsoft Office (Outlook, Word, PowerPoint, Excel, Project, Teams, Sharepoint), Adobe Acrobat Should be flexible to working outside the core business hours (occasionally on short notice, and a limited basis) as needed. Proven ability to manage multiple and fast-moving priorities. Ability to work well in a fast-paced collaborative team environment within a rapidly evolving business environment. Skilled at solving multi-dimensional problems with both quantitative and qualitative variables. Ability to lead and influence others in support of company objectives. Excellent decision making and cross functional team building skills. Solid understanding of GMP, GLP, and non-GMP project requirements Able to read and understand engineering plans and specifications. Benefits Why Choose Verista? High growth potential and fast-paced organization with a people-focused culture Competitive pay plus performance-based incentive programs Company-paid Life, Short-Term, and Long-Term Disability Insurance. Medical, Dental & Vision insurances FSA, DCARE, Commuter Benefits Supplemental Life, Hospital, Critical Illness and Legal Insurance Health Savings Account 401(k) Retirement Plan (Employer Matching benefit) Paid Time Off (Rollover Option) and Holidays As Needed Sick Time Tuition Reimbursement Team Social Activities (We have fun!) Employee Recognition Employee Referral Program Paid Parental Leave and Bereavement For more information about our company, please visit us at Verista.com For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future. $80,465 - $121,170 *Verista is an equal opportunity employer.