Quality Engineer Salary at Secant Group Llc BETA

Job Description Job Description ROLE: Quality Engineer ATTRACTIVE SKILLS/EXPERIENCES: Bachelor’s Degree in Engineering (Mechanical; Industrial) or related field (required) Experience (5+ years) of relevant quality engineering in a regulated setting Experience related to validation activities Proficiency with SAP and MS Office Proven knowledge of cGMP and ISO Standards (9001; 13485; 15378) Experience in pharmaceutical or glass forming industry (preferred) Demonstrated communication skills (written / oral) including the ability to read/speak English Ability and willingness to work in fast-paced, matrix structured organization SUMMARY / RESPONSIBILITIES: This Quality Engineer will plan, coordinate and implement quality projects related to continuous improvement, measurement system capability, pharmaceutical packaging initiatives and product introduction, to ensure satisfaction of total project objectives. Projects include process analysis, data analysis, process improvement, product intro

We Are: Accentures SAP practice, and we bring the New to life using design thinking, agile development methodologies, and the latest smart tech like IoT, automation, and AI. We even built myConcerto, a mix of SAP and Accenture that helps lead our clients to big wins. Ready to learn as much as you can? We train our people on "new" SAP like S/4HANA and Cloud, and we offer classes and support through our 50,000+ member community. Its also nice to know our hard work doesnt go unrecognized. Weve got over 70 SAP awardsmore than any other partnerand were the leading business partner for SAP SuccessFactors, SAP Ariba, SAP Hybris, SAP FieldGlass, SAP Concur, and more. Visit us here to find out more about Accenture's SAP practice. (https://www.accenture.com/us-en/services/sap-index) You Are: A transformation ace with the skills to help clients meet the challenges of digitization. Your superpower? Using your know-how, creativity and analytical powers to solve clients most complex business problem

Job Description We're looking for an Automation Engineer for our client, ZETA! ZETA is a privately owned global supplier of turnkey projects and is specialized in designing, engineering, development, manufacture, automation and maintenance of customized process solutions for liquid aseptic applications in the biopharma and biotechnology industry. ZETA is perceived in the marketplace as a solution and process systems provider. ZETA aspires to be considered for all major capital projects globally. ZETA is a single-source expert for engineering, automation, plant design and construction and is a best-in-class partner for customized system solutions. Continuous innovation and a right-first-time approach ensure the highest quality products and services for our customers. This is how we secure sustainable corporate development and maintain our competitiveness and profitability. Responsible for allocated work packages. Software development SPS, SCADA and PLS and database applications. Softwar

Avo Photonics (www.avophotonics.com) is a dynamic contract engineering services company that designs, develops, and manufactures custom opto-electronic products for a large customer base. Members of our staff have the opportunity to produce next generation products for a diverse range of markets including aerospace, military, medical, industrial, and communications. We seek a diligent, dedicated, and meticulous person who will help to further our success by supporting our aerospace quality system. An ideal candidate must take ownership over and strive for continuous improvement in the procedures and documentation that encompass our aerospace products. The candidate is expected to advise program managers and engineers on best-practice quality procedures, and should feel comfortable leading large-scale change within the programs they operate in. Proactivity, high attention to detail, and the ability to cooperate professionally within different levels of the organization are essential tra

The Opportunity: Avantor is looking for a Quality Engineer II to support our chemical manufacturing facility in Phillipsburg, NJ! The Quality Engineer II leads efforts in site quality assurance programs and improvement activities. He/she is responsible for identifying and implementing programs to ensure regulatory compliance with cGMPs, ICHQ7, IPEC guidelines, ISO regulations as well as FDA requirements. The Quality Engineer II is accountable for direct support of several systems, including CAPA, cGMP, Complaint Investigation and Response, ISO System, Stability, SPC (supporting the microelectronic, pharmaceutical and reagent product lines as necessary) and Validation. This is a full-time, onsite position in Phillipsburg, NJ (1st Shift, Monday – Friday). What we’re looking for  Education: Bachelor’s Degree in chemistry or a related field required Experience: Minimum of five (5) years of experience in quality engineering or a related role required Experience working within pharmaceutical

Description Home Search Jobs Job Description Automation Engineer Contract: West Point, Pennsylvania, US Salary: $50.00 Per Hour Job Code: 356362 End Date: 2024-12-26 Days Left: 12 days, 2 hours left Apply About the Role: The Workflow and Data Capture (WDC) team of Pharmacokinetics, Drug Metabolism and Bioanalysis (PDMB) in MRL is seeking a Lab Automation Specialist to support ongoing and new efforts to optimize data collection and use in inventing new medicines at a cutting-edge automated incubation lab at the client's site. The candidate will play a key role in developing and delivering connectivity solutions for data streams, laboratory instrumentation, robots, and data storage solutions. Responsibilities: Collaborate with laboratory scientists and automation lab specialists to connect instruments and systems, develop scripts, applications, and data infrastructure. Manage small projects from conception through completion with various stakeholders. Prioritize high-reward projects and

Quality Engineering Manager Our team is working with one of the fastest growing pharmaceutical companies in the industry on a dynamic Manager of Quality Engineering to lead their quality engineering buildout in New Jersey. This permanent role focuses on establishing robust engineering functions and developing systems to ensure product safety and efficacy. Your expertise will drive us to exceed industry standards through innovative practices. As the Quality Engineering Manager, you will ensure compliance with regulatory standards, manage quality processes, validation protocols, and investigations, and implement effective Corrective and Preventive Actions (CAPAs). You will collaborate across departments, provide training on Good Manufacturing Practices (cGMP) and data integrity, enhance team skills, manage risks, and maintain audit readiness, all while supporting our mission to deliver cutting-edge healthcare solutions. Key Responsibilities Ensure compliance with USP, FDA, and cGMP stand

"Develop and establish processes for analyzing supplier performance.” United Safety and Survivability Corporation is committed to delivering the most innovative and reliable safety and survivability solutions our customers can trust to protect life and property. As the global leader in our industry, we push boundaries by utilizing innovation to highly engineer and produce the next generation of safety and survivability technologies. At United Safety we’re solving our industry's most important problems with talented individuals who share our passion to change the world. Our culture is fast-paced, energetic and innovative. We work to build an inclusive environment in which everyone, regardless of gender, race, religion, age, or background, can do their best work. We are fully committed to continuous growth and advancement; we will reinvest profits and resources into our employees, our processes and product innovation. Job Title: Sr. Supplier Quality Engineer Department: Global Procuremen