Automation Engineer Salary at Turbocam Inc BETA

Job Purpose To perform day to day duties of Quality Engineering. Job Responsibilities In performing their respective tasks and duties, all employees are expected to adhere to Albany's current values: Albany Wins Together, Count on Each Other, Own Your Actions, Care About Each Other, and Share Your Enthusiasm. Safety must always come first; we never compromise on safety for the sake of achieving another objective. Employees are also responsible for the health and safety of themselves and each other. Develop, implement, and maintain quality standards for manufacturing processes. Devise and implement methods and procedures for inspecting, testing, and evaluating production components and assemblies. Design and/or specify inspection and test methods and equipment. Develop and implement quality assurance test and perform statistical analysis for development & production programs. Lead Failure Mode Effect Analysis (FMEA) activities enabling improvements in process control and capability. Ini

Job Title: Quality Engineer Job Description We are seeking a dedicated and detail-oriented Quality Engineer to join our team. The successful candidate will help lead CAPA investigations, conduct root cause analysis, and manage audit programs compliant with ISO standards. This role involves developing documentation for new product launches, tracking quality metrics, and maintaining test equipment through calibration and standardization procedures. Responsibilities + Help lead CAPA investigations. + Conduct root cause analysis. + Manage audit program compliant to ISO standards. + Develop documentation compliant to ISO standards. + Track quality metrics. + Develop processes and documentation for new product launches. + Maintain test equipment through calibration and standardization procedures. Essential Skills + Quality engineering + CAPA + Root cause analysis + Minitab + Excel + Nonconformance Reviews + Corrective action + Preventative action + QMS + AS9100 + ISO 9001 + Audit Additional

Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life changing products to life. We are searching for a Quality Engineer to support manufacturing quality operations in a dynamic, fast-paced, medical device manufacturing environment. This environment includes the manufacture, inspection, and test of devices for design verification, design validation, and commercial production. How you will make an impact: Work cooperatively with other team members and in compliance with applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 to transition products from development to manufacturing. Use experience within medical devices, to provide guidance and assistance in the development of new production processes Drive the development, implementation, and approval of PFMEAs and control plans. Develop inspection processes and sampling plans acc

Join our client, a forward-thinking manufacturing facility specializing in cutting-edge devices, as a Document Control Specialist the 1st shift. You will work as part of a dynamic team that manufactures exciting products that help people. You will ma Control Specialist, Control, Specialist, Staffing

Alexander Technology Group is looking for a Quality Engineer for a client based in the Portsmouth, NH area. This is full-time (perm) On-site in Portsmouth, NH Key Responsibilities: Develop and maintain quality systems for combination products. Ensure compliance with FDA, ISO 13485, cGMP, and other standards. Lead risk assessments, root cause analyses, and corrective actions. Oversee testing, validation, and documentation processes. Collaborate with R&D, manufacturing, and regulatory teams. Conduct training on QA practices and support continuous improvement. Perform inspections and product testing to ensure quality standards. Qualifications: Bachelor’s in Engineering, Life Sciences, or related field. Strong knowledge of regulatory requirements and quality tools (e.g., Six Sigma, CAPA, FMEA). Excellent problem-solving and communication skills. Able to work independently in a small team environment. Preferred: Experience with design control, eQMS, and statistical tools. ASQ CQE certificat

At E Tech Group, joining our team means joining a group of passionate and forward-thinking experts. We're one of the largest engineering and system integration firms in the United States providing value for our clients through IT automation and control solutions for more than 25 years to the Life Sciences, Mission Critical, Metals, Material Handling, Consumer Products and Food & Beverage industries. Our national scale allows us to help our clients develop and implement standardized solutions at any of their facilities regardless of physical location or the local resources available at that site. The Senior Controls / Automation Engineer role requires an individual have a diverse engineering skill set with the ability to work independently to perform all aspects of process automation engineering and system integration, including initial concepts, specifications, design engineering, documentation, project implementation, testing, startup, and training of operating and maintenance personn

CSV/DeltaV Engineer Location: Portsmouth, NH Please note: We are only considering W2 candidates at this time. Applications from third-party vendors or C2C arrangements will not be considered. ADVENT Engineering is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Head-quartered near San Francisco, California, and with operations in the Eastern and Western US, Canada and Singapore, our company is involved in almost every facet of global pharmaceutical and biotechnology facility design and process engineering and quality system projects. ADVENT's services include process engineering, automation engineering, project engineering, facility/system design, start up and commissioning, validation and compliance consulting for distinguished and successful biotechnology and pharmaceutical manufacturing companies. The successful candidate will work with a group of engineers involved in the design, automation, commissioning and start-up of va

Job Description Job Description Document Control Specialist | Bedford, NH Responsibilities: Support change control administration, part number management, BOMs and BOM structure, and applying revision control within the Product Lifecycle Management (PLM) and Enterprise Resource Planning (ERP) systems Review all changes and in a timely manner with high level of detail Contribute to cross-functional improvement initiatives Provide input during weekly change board meetings to facilitate change review and closure Support the proper organization, filing, archiving, and secure destruction of all controlled documents whether electronic or paper Ensure all change requests and documents within the Quality Management System are reviewed by the appropriate department Review change orders for accuracy, completeness, and impact to other documents, products, processes, and the PLM or ERP systems Review documents for the proper formatting and editing prior to submitting for approval Provide Good Docu