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Qa automation engineer Jobs in Noblesville, IN

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Qa automation engineer • noblesville in

Last updated: 8 hours ago
QA Associate, 3rd Shift

QA Associate, 3rd Shift

INCOG BioPharma ServicesFishers, IN, US
Full-time
Working closely with the QA Operations Supervisor, the QA Associate will be instrumental in ensuring site compliance with Regulations, ISO Standards, organizations SOPs as well as support in champi...Show moreLast updated: 15 days ago
QA / Expeditor - Noblesville Chili's

QA / Expeditor - Noblesville Chili's

Chili's Grill & BarNoblesville, IN, US
Full-time +1
QA / Expeditor - Noblesville Chili's.Our Quality Assurance Specialists ensure each Guest receives perfectly prepared, high-quality food. They provide dependable, fast service that is absolutely Chili'...Show moreLast updated: 12 days ago
  • Promoted
QA Lead Engineer

QA Lead Engineer

Mesh SystemsCarmel, Indiana, United States
Full-time
Executive Summary : QA Lead Engineer.The Internet of Things (IoT) starts with.The transformational benefits promised by IoT and technologies like artificial intelligence, machine learning, and deep...Show moreLast updated: 4 days ago
  • Promoted
5703 - Controls Engineer (Vision) / Automation Engineer

5703 - Controls Engineer (Vision) / Automation Engineer

Verista, Inc.Fishers, IN, US
Full-time
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 heal...Show moreLast updated: 30+ days ago
Apptio Enterprise Field Sales Rep (Automation BSS)

Apptio Enterprise Field Sales Rep (Automation BSS)

IBMCarmel, IN, United States
Full-time
Introduction A Technology Sales Specialist role (what we internally call a, 'Brand Sales Specialist') within Automation means working for a leader in AI-Powered products. Envision helping clients cr...Show moreLast updated: 30+ days ago
Automation Engineer

Automation Engineer

Veracity SolutionsFishers, IN, US
Full-time
Java, Automation Scripting, REST / SOAP.Play a central role in enhancing our automation capabilities for testing our core platform. Collaborate with business analysts, developers and stakeholders to w...Show moreLast updated: 30+ days ago
  • Promoted
Sales Engineer / Automation Specialist

Sales Engineer / Automation Specialist

LINC SYSTEMS LLCWestfield, IN, US
Full-time
The Packaging Automation Specialist will drive and coordinate automation projects to support related field sales applications. This includes pre-sales work to recommend solutions uniquely suited to ...Show moreLast updated: 14 days ago
  • New!
API Automation Test Lead

API Automation Test Lead

Infosys Limited DigitalCarmel, IN, United States
Full-time
Job details Work Location Hartford, CT, Indianapolis, IN, Raleigh, NC, Richardson, TX, Tempe, AZState / Region / Province Arizona, Connecticut, Indiana, North Carolina, TexasCountry USASalary min 7...Show moreLast updated: 8 hours ago
Automation Engineer

Automation Engineer

Flexware InnovationFishers, IN, US
Full-time
Flexware Innovation is a leading technology integrator that helps forward thinkers in manufacturing and related industries build comprehensive and long-lasting solutions with ease.Founded in 1996 a...Show moreLast updated: 30+ days ago
  • Promoted
Factory Automation Application Engineer (Onsite)

Factory Automation Application Engineer (Onsite)

Evolution Motion SolutionsNoblesville, IN, US
Full-time
Factory Automation Application Engineer.Womack Machine Supply and Morrell Group have united to become Evolution Motion Solutions, an industry powerhouse in engineering and industrial solutions.With...Show moreLast updated: 30+ days ago
  • New!
Field Service Engineer - Automation

Field Service Engineer - Automation

Core ResourcesCarmel, IN, United States
Full-time
Field Service Engineer - Automation Job Summary.The Field Service Engineer - Automation will be responsible for the installation, commissioning, and servicing of industrial automation systems, incl...Show moreLast updated: 8 hours ago
Specialist QA

Specialist QA

Weil Group, IncCarmel, IN, United States
Full-time
SUMMARY Perform one or more of the following duties and responsibilities in support of Client's Quality Assurance program under minimal supervision. FUNCTIONS - Review and approve product MPs.Approv...Show moreLast updated: 30+ days ago
QA / Expeditor

QA / Expeditor

Chili'sNoblesville, IN
Full-time +1
Our Quality Assurance Specialists ensure each Guest receives perfectly prepared, high-quality food.They provide dependable, fast service that is absolutely Chili's! If you take pride in great team ...Show moreLast updated: 24 days ago
Automation (Controls) Engineer-Device Manufacturing

Automation (Controls) Engineer-Device Manufacturing

Eli LillyCarmel, IN, United States
Full-time
At Lilly, we unite caring with discovery to make life better for people around the world.We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work...Show moreLast updated: 30+ days ago
Controls Engineer – Industrial Automation OOJ - 32852

Controls Engineer – Industrial Automation OOJ - 32852

Hatch Global SearchNoblesville, Indiana, US
Full-time
Quick Apply
An essential responsibility of a controls engineer involves designing and implementing control systems.These systems help in the automation of industrial processes, enhancing their efficiency and r...Show moreLast updated: 30+ days ago
Building Automation Engineering Manager - Hybrid Remote

Building Automation Engineering Manager - Hybrid Remote

CBRE Group, IncCarmel, IN, United States
Remote
Full-time
About the Role : As a CBRE Automation Engineering Manager, you will lead all aspects of operation and maintenance of all building automation systems. This job is part of the Engineering and Technical ...Show moreLast updated: 30+ days ago
Engineer - Automation

Engineer - Automation

BioSpaceCarmel, IN, United States
Full-time
Job DetailsAt Lilly, we unite caring with discovery to make life better for people around the world.We are a global healthcare leader headquartered in Indianapolis, Indiana.Our employees around the...Show moreLast updated: 30+ days ago
Lead Quality Engineer (Test Automation)

Lead Quality Engineer (Test Automation)

DeloitteCarmel, IN, United States
Full-time
Lead Quality Engineer (Test Automation)Role Overview : As a Quality Engineer specializing in test automation, you will actively engage in your quality engineering craft, taking a hands-on approach t...Show moreLast updated: 30+ days ago
Building Automation Systems Project Manager

Building Automation Systems Project Manager

SiemensCarmel, IN, United States
Permanent
Here at Siemens, we take pride in enabling sustainable progress through technology.We do this through empowering customers by combining the real and digital worlds. Improving how we live, work, and ...Show moreLast updated: 30+ days ago
QA Associate, 3rd Shift

QA Associate, 3rd Shift

INCOG BioPharma ServicesFishers, IN, US
15 days ago
Job type
  • Full-time
Job description

Description

Working closely with the QA Operations Supervisor, the QA Associate will be instrumental in ensuring site compliance with Regulations, ISO Standards, organizations SOPs as well as support in championing and developing organization's Quality Mindset, as well as a culture of efficiency, attention to detail, and on time delivery. The QA Associate will need to provide support with identifying operational and quality gaps.

The Quality Assurance Associate will exemplify excellent interpersonal skills and be capable of developing productive, customer-centric working relationships with colleagues, internal customers, and partners. The QA Associate will demonstrate excellent written and oral communication skills with the ability to clearly and concisely articulate complex issues to a range of target audiences. The QA Associate will thrive in a team environment but will also work autonomously utilizing strong self-management and organizational skills. The QA Associate will value process owners and subject matter experts and will possess a demonstrated ability in influencing positive outcomes without direct reporting authority.

Essential Job Functions :

  • Maintain a Quality Assurance presence and provide process confirmation on the manufacturing floor.
  • Review and approve documentation for Quality approval, including but not limited to on-floor batch record review, logbooks, work orders, procedures, etc.
  • Collaborate with Manufacturing / Operations team and lead or provide support with investigations to resolve equipment and process related deviations.
  • Support other QA personnel with batch record reviews, material release, etc.
  • Prioritize and coordinate his / her time in balancing production timelines with product quality assurances.
  • Exercise rapid decision-making in the preliminary evaluation of the scope and impact of deviating events, requirements for product segregation, and the implementation of initial corrective actions or escalate the issue to Manager for resolution.
  • Provide support as needed in a cross-functional capacity on deviation investigative processes using root cause analysis tools, report writing, and mitigation development using risk analysis tools.
  • Exemplify and take proactive approaches in terms of safety expectations, practice positive intervention, and enforce best practices that align to SOPs, compliance requirements, quality guidelines, and site goals.
  • Utilize various paper and automated systems (Veeva, SCADA, BMS, CMMS, LIMS, lab instrument software, etc.) to ensure data integrity for site policies, procedures, and batch records.
  • Use technical skills and applied statistics to analyze and track deviations and to identify sources of variability and error site processes.
  • Ability to manage multiple projects in a fast-paced environment.

Special Job Requirements :

  • This position will support primarily third shift (11 : 00pm-7 : 30am) with occasional weekend support, dependent on operations' needs.
  • Bachelor's Degree required or equivalent; degree preferred to be in Science (Chemistry, Biology, Biochemistry, Microbiology etc.)
  • Minimum of 2 years with experience working as Quality in a GMP Manufacturing environment, and / or as an Operator within a Pharmaceutical Manufacturing environment.
  • Moderate knowledge of regulations and quality systems such as deviations, Non-Conformance, CAPA, etc..
  • Understanding of Good Documentation Practices (GDPs) and its criticality.
  • Excellent written and verbal communication skills.
  • General computer skills evidenced by hands-on work with computerized Operations equipment (SCADA); and reporting and data analysis software (Word, Excel, Visio, JMP, Minitab, etc.).
  • Additional Preferences :

  • Hands-on experience with aseptic manufacturing.
  • Experience with Continuous improvement, Six Sigma, and / or Lean principles.
  • Additional info about INCOG BioPharma Services :

    At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design : focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.

    If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.

    INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.

    By submitting your resume and details, you are declaring that the information is correct and accurate.