Quality assurance specialist jobs in Elkhart, IN - 73 jobs
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Quality Assurance & Compliance Manager
Voyant Beauty 4.2
Quality assurance specialist job in Elkhart, IN
Voyant Beauty believes our people are more than just employees; they're the driving force behind everything we achieve. Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual's contribution is valued and celebrated. We invest in their growth, providing opportunities for development and advancement within our dynamic team.
Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products. We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs. This can include skincare, haircare, bath and body products, fragrances, and more. Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life.
Safety is a core value at Voyant Beauty. We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel.
If you're seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you. Come join us and be a part of our journey.
A Brief OverviewThe Quality Assurance & Compliance Manager will oversee all aspects of quality operations at a high-volume manufacturing facility. This role ensures compliance with regulatory standards, internal specifications, and customer expectations by managing quality systems, compliance programs, and continuous improvement initiatives. The position requires leadership, strategic alignment with business objectives, and the ability to foster a high-performance culture within a regulated manufacturing environment.What you will do
Lead, mentor, and develop the QA team; align quality objectives with business goals and regulatory requirements; serve as a key member of site leadership influencing cross-functional decision-making.
Manage investigations (NCPs, deviations, CAPA), change control, plant procedures (Level I-III), and annual product reviews. Ensure effective governance of quality systems.
Lead internal audit program, act as site contact for external audits (customer/regulatory), ensure audits (Internal & external)/regulatory inspection readiness, prepare responses, and drive sustainable CAPA implementation.
Maintain compliance with FDA, GMP, ISO, and other standards; monitor/report KPIs (CAPA effectiveness, audit scores, complaints, training); present updates to leadership and stakeholders.
Oversee calibration, quality training (onboarding, cGMP, role-specific modules), and complaint handling investigations with trend analysis.
Champion Lean, Six Sigma, and other quality methodologies; identify systemic issues and implement preventive/corrective actions to enhance efficiency.
Support corporate initiatives related to quality and compliance.
Collaborate with cross-functional teams to resolve product integrity issues.
Participate in strategic projects, including systems upgrades and policy harmonization.
Represent the facility in corporate, customer facing or external quality forums.
Travel (up to 10-15%) for audits, training, and corporate meetings.
Some duties may vary slightly by location.
Education Qualifications
Bachelor's degree in chemistry, Engineering, Life Sciences, or related field; Master's (Preferred)
Experience Qualifications
7-9 years of progressive QA experience in regulated manufacturing (OTC, pharma, cosmetics, personal care) with 3+ years in leadership. (Preferred)
7-9 years FDA regulations, GMP, ISO standards, electronic QMS platforms. (Preferred)
7-9 years proven success leading audits, managing CAPA, and driving compliance initiatives. (Preferred)
7-9 years communication, analytical, leadership, and problem-solving abilities. (Preferred)
Skills and Abilities
Deep understanding of FDA, GMP, ISO, and related compliance frameworks. (High proficiency)
Ability to oversee CAPA, deviations, audits, training, calibration, and complaint handling. (High proficiency)
Ability to mentor, coach, and foster high-performance culture. (High proficiency)
Skilled in preparing for, leading, and responding to external/internal audits. (High proficiency)
Apply CI methodologies to reduce risk and enhance efficiency. (High proficiency)
Root cause analysis, trend analysis, and data-driven decision-making. (High proficiency)
Clear, persuasive communication across functions and with stakeholders. (High proficiency)
Ability to prioritize, manage timelines, and deliver cross-functional quality initiatives. (High proficiency)
Licenses and Certifications
Auditor certification (ASQ CQA, ISO Lead Auditor) (Preferred)
To Staffing and Recruiting Agencies: Our company does not accept unsolicited curriculum vitae's or applications from agencies. We are not responsible for any fees related to unsolicited curriculum vitae's or applications and explicitly reserve its right to contact candidates presented in such unsolicited curriculum vitae's or application.
Our company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, color, national origin, sexual orientation, age, disability or veteran status. Voyant Beauty will consider requests for accommodations due to a disability impacting a qualified employee's ability to perform the essential functions of their position consistent with applicable laws. In addition to federal law requirements, Voyant Beauty complies with applicable provincial and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
$70k-100k yearly est. 53d ago
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QA/QC Construction Manager - South Bend, IN
Explore DLB Associates
Quality assurance specialist job in South Bend, IN
QA/QC Construction Manager
Salary
We recognize job-board ranges may not reflect our pay bands; we often out-compete those ranges for well-qualified candidates.
Job Summary
The QAQC Construction Manager (QCM) serves as the contractor/owner's on‑site advocate throughout the project to ensure all work is performed in conformance to the standards required of quality, schedule, and scope. This role combines classic construction manager and owner's representative duties (owner advocacy, contract oversight, risk management, stakeholder communication) with deep QAQC field leadership across electrical, mechanical, and controls systems in mission‑critical environments.
The QCM is vital during the L1-L3 phases-design validation, procurement, and construction-ensuring installations meet project requirements and are fully documented for a seamless handoff to the commissioning team. This role does not execute commissioning tests (L4-L5) but ensures the site is commissioning‑ready by enforcing quality standards and resolving issues early.
Essential Functions
Construction Management, Owner Advocacy & Project Oversight
Act as the contractor and/or owner's “eyes and ears” on site, ensuring all decisions and field activities align with the client's Quality Control Specifications (CSPEC) and programmatic expectations.
Lead proactive risk identification and escalation pathways, emphasizing early detection and resolution of quality issues to maintain project momentum and commissioning readiness.
Facilitate cross-functional communication among the owner, designers, contractors, equipment manufacturers and vendors, and trade partners to ensure consistent interpretation and execution of the project quality standards.
Support contract administration and regulatory compliance, coordinating with legal and project management teams to resolve disputes or clarify scope where quality deviations are involved.
QAQC Field Leadership (L1-L3 Focus)
Monitor field execution to ensure installations meet project requirements, drawings, specifications, and applicable codes, with strict adherence to the client's QAQC framework.
Ensure field-level activities-including inspections, documentation, and issue tracking-are conducted in accordance with the client's commissioning plan of record and QAQC program.
Enforce HSE/LOTO requirements and site safety policies in coordination with contractor and client teams.
Readiness for Commissioning
Ensure all pre-functional checklists, QAQC documentation, and punch lists are complete and accurate before turnover to the commissioning team.
Validate that equipment start-up prerequisites and vendor documentation are in place to support Cx activities.
Drive early issue resolution to prevent delays in L4-L5 commissioning.
Document Control & Technical Reviews
Review shop drawings, submittals, RFIs; verify contractor quality requirements are flowed down to vendors; assist in maintaining the field document control system (drawings, tests, inspections, vendor data, as‑builts).
Use common tools (Procore, BIM 360/ACC, Bluebeam, MS Project/P6, Excel/PowerPoint/Teams) for traceability and dashboarding.
Reporting & Metrics
Maintain accurate inspection/test records; monitor and report status to stakeholders; facilitate root‑cause analysis for non‑conformance and track dispositions to closure; generate metrics to communicate site quality compliance.
Requirements
Position Requirements
Strong working knowledge of electrical, mechanical, and controls system principles in mission‑critical environments.
Proficiency with MS Office (Excel, Word, Outlook, PowerPoint, Teams); exceptional organization and file management.
Ability to leverage AI and emerging technologies to streamline workflows and drive innovation.
Clear, concise communication (technical and non‑technical) with the ability to represent the owner directly with contractors and clients.
Demonstrated ability to manage schedule inputs and enforce quality standards across multiple stakeholders.
Education & Experience
Bachelor's degree in engineering, construction or related discipline
OR
Two years hands‑on install/testing/validation/troubleshooting of mechanical, controls, and/or electrical infrastructure plus a minimum of 5 additional years of related experience.
Certifications & Safety
Ability to achieve NFPA 70E and/or OSHA training as required; strict adherence to HSE/LOTO policies.
Physical Demands
The following physical demands must be met by the employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is:
Frequent manipulation of small parts/tools
Periods of stationary work
Movement through data center and outdoor environments (heat/cold/precipitation), including tight spaces
Stair/ladder access
Occasional overhead/under‑equipment positioning
Occasional lifting up to 50 lbs
Reasonable accommodation available
Travel / Relocation Requirements
Must have a valid driver's license and the ability to rent vehicles.
Travel between 75-100% in various support roles until extended project assignment is received, this may include travel to any of the 50 US states.
Extended project assignment is defined as a project location where a continuous onsite presence is required in excess of 6 months. Project assignments are typically between 9 months and 4 years; however, shorter temporary relocation assignments may be required depending on location and client agreement.
If candidate is not local to a project site - the ability to relocate to the project location within 1 - 3 months of extended project assignment unless the project location supports 100% travel.
Project locations are within the 50 US States.
Benefits
DLB Associates offers a very competitive benefits package; highlights include
Choice of comprehensive medical plans (including two PPO-style plans and a HDHP w/ HSA option)
Flex spending accounts (FSA)
Dental and vision plans
Comprehensive medical, dental and vision benefits extended to spouse / domestic partner and dependent children up to age 26
401k with company match and self-directed brokerage account option
PTO including additional paid time off during the last week of the year
Company paid life insurance coverage for employees and their eligible dependents
Short and long-term disability, AD&D coverage
Professional development opportunities, tuition reimbursement and professional licensing assistance
Paid parental leave after one year of employment
DLB Associates is an EEO/Affirmative Action Employer and participates in the E-Verify program with the Department of Homeland Security. We encourage diversity in our workforce.
Are you ready to challenge yourself and redefine standards in the AEC industry? Apply now and join our award-winning team!
NOTICE TO THIRD PARTY AGENCIES:
DLB does not accept unsolicited resumes from recruiters, employment agencies, or other staffing services. Unsolicited resumes include any resume or hiring document sent to DLB in the absence of a signed Service Agreement where DLB has expressly requested recruitment/staffing services specific to the position at hand. Any unsolicited resumes, including those submitted to hiring managers or other business leaders, will become the property of DLB and DLB will have the right to hire that candidate without reservation - no fee or other compensation will be owed or paid to the recruiter, employment agency, or other staffing service.
$73k-110k yearly est. 60d+ ago
Senior Manager, Quality Assurance
Alpha Baking Company 4.2
Quality assurance specialist job in La Porte, IN
Key Responsibilities
Lead, coach, and develop the QA team to ensure strong execution of quality and food safety responsibilities across all shifts.
Ensure compliance with applicable FDA, USDA, and state food safety regulations and customer requirements.
Oversee facility audits including third-party certifications (e.g., BRC, SQF, AIB), customer inspections, and internal GMP reviews.
Manage and continuously improve programs related to HACCP, HARPC, allergen control, sanitation, pest control, traceability, and product hold/release.
Collaborate with Operations, R&D, Maintenance, and Sanitation to proactively resolve quality issues and drive root cause corrective actions.
Lead or support investigations related to product complaints, deviations, and non-conformances.
Ensure documentation and data integrity across all QA systems, including product testing, calibration records, and process control charts.
Develop and monitor quality KPIs and present metrics to plant and corporate leadership.
Partner with HR to ensure QA training programs are maintained and effectively implemented.
Support implementation of corporate and customer-driven quality initiatives at the site level.
Qualifications
Bachelor's degree in Food Science or related field.
Minimum 5-7 years of progressive QA/Food Safety experience in a food manufacturing environment, with at least 2 years in a leadership role.
Strong knowledge of FSMA, HACCP, GMPs, and food safety regulatory compliance.
Experience with bakery or high-volume food manufacturing environments strongly preferred.
Demonstrated success leading teams and managing third-party audits.
Strong analytical and problem-solving skills; data-driven decision-making required.
Excellent communication and cross-functional leadership skills.
Proficiency with QA software systems, Microsoft Office Suite, and ERP platforms (e.g., SAP, Plex, etc.).
Working Conditions
Based full-time on-site at the LaPorte Bakery.
Must be available to support QA coverage across all shifts as needed.
Exposure to a manufacturing environment with variable temperatures and allergens.
$100k-129k yearly est. 10d ago
QA Compliance Specialist
Lebermuth Co 3.7
Quality assurance specialist job in South Bend, IN
Full-time Description
Lebermuth Company is currently looking for a Quality Assurance Compliance Specialist to join our team. Lebermuth Company, a family-owned leader in the fragrance and flavor industry, has been blending tradition with innovation for over a century. Specializing in essential oils, fragrances, and flavors, Lebermuth is dedicated to quality and integrity. Our commitment to excellence is evident in our personal touch, sustainable practices, and customer-centric approach.
Summary:
The QA Compliance Specialist is responsible for administering and coordinating quality programs to ensure compliance with FDA, FSMA, SQF, HACCP, and other applicable state and federal regulations. This role partners with procurement and cross-functional teams to maintain a robust supplier quality program and supports continuous improvement initiatives across the organization.
Essential Duties & Responsibilities:
Serves as the primary SQF Practitioner and PCQI; oversees Verification & Validation, Document Control, Foreign Material Management, and Environmental Monitoring programs.
Manages Pest Control Programs and 3rd party contractors supporting Quality and Food Safety initiatives.
Facilitates 3rd-party laboratory testing for raw materials and finished products to meet EPA/FDA and certification requirements (e.g., Organic).
Responsible for managing the Supplier Approval Program by overseeing supplier level approvals, partnering with regulatory team to maintain accurate and current supplier data, and administering the Supplier Approval Database to ensure compliance and program integrity
Administers the Alchemy training program; collaborates with QEHS and other departments on annual training needs.
Leads internal auditing program; communicates schedules and results to leadership.
Facilitates corrective and preventive action (CAPA) processes to drive continuous improvement.
Supports Regulatory department during governmental, third-party, and customer audits.
Promote food safety culture by maintaining a clean and organized workspace and adhering to all quality and safety standards within the department to ensure the safe production and shipment of quality food products
Performs other duties as assigned to support compliance and quality objectives.
Requirements
Qualifications:
Education: Bachelor's degree in food science, Quality Assurance, Business, or related fields of study, or an equivalent combination of education and experience.
Experience: 2+ years of related experience and/or training; Knowledge base representative of the position includes experience with SQF, cGMP and HACCP programs.
Certifications: SQF Practitioner, PCQI, and HACCP.
Functional Skills: Strong planning, organizational, and executing skills are required; technical aptitude, with lean thinking/process improvement skillsets, are needed to problem-solve and enhance the operations; excellent forward-thinking, prioritization, analytical, and detail-oriented skills are required to manage multiple data points. Analytical problem solving, effective communication and partnership development
Technology Aptitude/Skills: Basic knowledge of computer and keyboard functions. Strong working knowledge and experience with MRP/ERP systems and familiarity with regulatory-related programs. Proficiency with Microsoft Office products, particularly Excel.
Language Skills: Strong verbal and written communication skills. Demonstrates advanced group presentation skills, presents information effectively and responds to questions from owners and management teams Ability to read, analyze and interpret professional journals, technical procedures, governmental regulations, and chemical hazard information and safety procedures. Ability to write correspondence that is professional in both content and tone. Ability to effectively present information and respond to questions.
Leadership/Behavior Skills: Self-motivated to stay focused on quality and output goals; strong work ethic and values, sound judgement, dependable, focused on the customer and processes; high level of accuracy and attention to detail with the flexibility to move to priorities throughout the operation areas, following all Safety requirements
Culture Match Behaviors: Enjoys and thrives in a fast-paced, high-growth environment, with a huge drive to create an impact while also being an effective listener, respectful problem-solver and a collaborative continuous learning team member.
Physical and Sensory Demands / Environmental Conditions / Equipment Used
This role routinely uses standard office equipment such as computers, phones, electronic devices, photocopiers, filing systems/cabinets and fax machines.
Ability to operate keyboard and view computer screen occasionally.
Ability to write ideas/information in a logical flow occasionally.
Cognitive and reasoning ability to read, review and interpret work orders or processes on a frequent basis.
Ability to read and respond due to nature of the work on a frequent basis.
Ability to talk and communicate with others via phone, in-person, and/or computer frequently.
Ability to listen to others, solve problems, and respond frequently.
Ability to stand, sit, walk, climb, bend, stoop, kneel, crouch, reach, squat, twist, push, pull, and carry items frequently.
Ability to lift/move up to 15lbs sporadically.
Ability to work in a manufacturing environment with fluctuating temperatures and noise levels.
The employee is required to wear suitable Personal Protective Equipment such as safety glasses, hair/beard nets and steel toed shoes, as required.
Work schedule is generally 1st shift, generally Monday through Friday, but at times requires on-call and non-traditional work hours, to meet business needs
Salary Description Hourly Non Exempt
$59k-85k yearly est. 54d ago
Specialist, Quality Assurance
Apidel Technologies 4.1
Quality assurance specialist job in Portage, MI
Job Description
In support of the Product Field Action team, implement quality standards, ensure and execute compliance on every stage of the process. Assess potential risks, ensure compliance and give recommendations. Take responsibility for all quality control aspects of the process (intake, record documentation, destruction, internal and external customer communications).
Facilitates audits and regulatory inspections.
Coordinates quality trainings.
This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision.
Roles typically require a university degree or an extensive amount of practical knowledge gained through experience.
Job requires an understanding and application of procedures and concepts of own discipline.
The job requires the ability to make judgements based on practice and previous experience.
This job typically requires a degree or equivalent and no experience.
Hours:8:00am to 5:00pm
$33k-52k yearly est. 3d ago
Quality Assurance Coordinator
CDI Corporation 4.7
Quality assurance specialist job in Portage, MI
"Together We Make Life Better". Our quality engineering, sustainable solutions and safety record inspire everything we do. Our diverse and inclusive workforce allows all employees to feel valued and safe to give their opinions and improve our company.
Tata Consulting Engineers USA, LLC, (TCE), is a multi-disciplinary engineering organization offering a full range of integrated engineering design, project support, procurement and construction management services to the energy and chemicals industries.
Position Summary
Quality Assurance Construction Coordinator to implement quality assurance procedures for capital and expense projects managed by the customer's Project/Construction Focal point, and will lead the overall Quality Assurance program for the Construction Management team.
Responsibilities
* Assess current quality management systems and practices, identify gaps, and recommend closure action plans. Work with stakeholders to effectively implement quality management system elements.
* Development and maintenance of local and regional documents that support and compliment global quality specifications and guidelines.
* Train and coach Construction Management personnel on quality best practices and requirements.
* Network with global colleagues to stay current on incidents, improvements and best practices.
* Implementation standardization and measurement of the effectiveness of quality systems and work processes to ensure that the Global Construction Quality strategies are successfully maintained.
* Leads or participates in Quality related unplanned event investigations and ensures that actions effectively address root causes.
* Perform internal audits to assure conformance to work processes.
* Ensure that the required contractor Quality Control procedures are properly implemented and that the constructed facilities comply with the related requirements, codes, and specifications.
* Significant Safety visibility and activity, providing support to the Construction Manager.
* Verify the contractors' implementation of their Project QC plan, identify deficiencies.
* Work with construction team to initiate any required 'Request For Variance' and/or MOC.
* Ensure that installation is according to customer specifications and contract drawings.
* Complete Non-Conformance Reports and monitor all NCR's for status and to closure.
* Communicate nonconforming issues of customer procured equipment, tanks, vessels, etc. to the Regional Quality Manager.
* Lead process to obtain, review, and approve contractor provided quality plans, inspection and latest plans.
* Participate in lesson learned analysis.
* Work with Discipline Focal Points and implement improvement actions.
* Request metrics to the Discipline Focal Points.
Qualifications
* Familiar with or previous experience with construction documents such as isometrics, P&ID's, Owner piping codes, civil- underground, and structural steel drawings, rotating equipment and vessel drawings, electrical single line diagrams and architectural drawings, quality best practices, safety standards, ASME, API, AWS, and similar codes of construction.
* Multi discipline experience preferred including civil concrete and structural steel, mechanical/ piping, vessels, reactors, rotating equipment, electrical equipment such as transformers, motor control centers, termination of motors, power distribution
* Applicant must be willing at times to cover off hour work (night, weekend, or overtime) as applicable.
EEO Statement
Tata Consulting Engineers USA, LLC ("TCE") is an equal opportunity and affirmative action employer committed to promoting diversity, equity, and inclusion in our workplace. We do not discriminate on the basis of race/ethnicity, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, veteran's status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.
In compliance with federal law, all candidates hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form after acceptance of a formal TCE offer letter through our onboarding system.
Fraud Alert
Please be aware that there have been instances of fraudulent job offers being made in the name of TCE by unauthorized individuals or organizations. We want to make it clear that TCE will never ask for any type of payment information during our interview process. Please be advised during our company transition, all email communications from TCE will come from our business email addresses, which end in '@tatconsultingengineers.com'. If you receive any suspicious job-related emails from any other domain, please do not respond to them and disregard any requests for personal or financial information. If you have any concerns about the legitimacy of a job offer or communication, please contact us through our website at tataconsultingengineers.com
$63k-82k yearly est. Auto-Apply 60d+ ago
Quality Assurance - Clinical II
Lancesoft 4.5
Quality assurance specialist job in Kalamazoo, MI
Provides project support with current Good Manufacturing Practices to clinical supply packaging operations. Provides guidance on procedures and training necessary to be in complete compliance with current GMPs.
Additional Information
All your information will be kept confidential according to EEO guidelines.
$75k-97k yearly est. 1d ago
** Quality Control Lead I
Dwyer Instruments 4.3
Quality assurance specialist job in Kingsbury, IN
QC Lead I - Kingsbury Full-time/Part-time EMC-R54/64-6 Responsible for quality of all incoming products and material. Make sure all parts meet Dwyer specifications.
Essential Duties and Responsibilities:
Update all QC files as required.
Inspect Incoming material by following the QC procedures.
Strong understanding of AS400, can look up PO's, DMR's, IP's, and scrap.
Maintain an effective dialogue with all employees to foster good employee morale.
Organize work areas before, during and after assignments. Is responsible for general housekeeping and organization of workstations.
Parts must be inspected in a timely fashion to prevent down time on the lines. Limit withdrawals from the QC area.
Review Engineering Change Request (ECR's) to ensure files are updated accordingly.
Issue DMR's and advisories for defective products.
File claims with UPS/FedEx for damaged and missing products.
Verify ROHS certificates are included with shipments, contacts purchasing when missing.
Perform first article evaluations and works with line leads to get parts tested.
Key Performance Indicators (KPI's):
Limit mistakes by reviewing quality of own work and following instructions
Limit scrap by inspecting all incoming material and ensuring it meets the quality standards. Prevent bad parts from being taken to the lines.
Have strong organization skills.
Achieve Safety objective for the plant
Requirements
Required Skills / Experience / Equipment Operation:
Must be 18 years of age.
Must be a US citizen or have authorization to work in the US issued by the Department of Homeland Security.
Minimum of 2 years of service.
Physical/Mental Essential Functions:
Able to stand or sit for prolonged periods of time
Able to read/speak in English and follow verbal/written instructions
Able to count and sort
Able to interact/communicate with respect of fellow co-workers and management
Able to push/pull and reach above shoulders
Able to control operation of hand and/or foot
Able to turn wrist frequently in a repetitive motion
Able to lift/carry up to 50 pounds
Salary Description 20.69-
$60k-80k yearly est. 27d ago
Assurance Intern - Summer 2027
Rsm 4.4
Quality assurance specialist job in Mishawaka, IN
We are the leading provider of professional services to the middle market globally, our purpose is to instill confidence in a world of change, empowering our clients and people to realize their full potential. Our exceptional people are the key to our unrivaled, culture and talent experience and our ability to be compelling to our clients. You'll find an environment that inspires and empowers you to thrive both personally and professionally. There's no one like you and that's why there's nowhere like RSM.
At RSM, interns work with large and small companies in various industries. They develop strong working relationships with clients built on understanding their businesses and challenges. Interns work on multiple team engagements each year, including several pieces of any particular assignment - not just one part. Working in a mutually respectful team environment helps our associates perform at their best and integrate their career with their personal life.
Examples of the candidate's responsibilities include:
Understanding clients' needs and expectations, their business and industry, accounting and control systems, employees, company values and industry-related GAAP and GAAS issues
Developing an understanding of the RSM audit approach and tools
Assessing risks and evaluating the client's internal control structure
Performing substantive tests and tests of internal controls to identify and resolve accounting or reporting issues
Drafting financial statements under prescribed formats
Basic Qualifications:
90 credit hours completed
Working towards B.A. / B.S. degree or equivalent from accredited university
Accounting major
Travel to assigned client locations is required. Must have access to and ability to arrange for use of reliable modes of transportation to those locations
A minimum 3.0 GPA is preferred
At RSM, we offer a competitive benefits and compensation package for all our people. We offer flexibility in your schedule, empowering you to balance life's demands, while also maintaining your ability to serve clients. Learn more about our total rewards at **************************************************
All applicants will receive consideration for employment as RSM does not tolerate discrimination and/or harassment based on race; color; creed; sincerely held religious beliefs, practices or observances; sex (including pregnancy or disabilities related to nursing); gender; sexual orientation; HIV Status; national origin; ancestry; familial or marital status; age; physical or mental disability; citizenship; political affiliation; medical condition (including family and medical leave); domestic violence victim status; past, current or prospective service in the US uniformed service; US Military/Veteran status; pre-disposing genetic characteristics or any other characteristic protected under applicable federal, state or local law.
Accommodation for applicants with disabilities is available upon request in connection with the recruitment process and/or employment/partnership. RSM is committed to providing equal opportunity and reasonable accommodation for people with disabilities. If you require a reasonable accommodation to complete an application, interview, or otherwise participate in the recruiting process, please call us at ************ or send us an email at *****************.
RSM does not intend to hire entry-level candidates who require sponsorship now or in the future. This includes individuals who will one day request or require RSM to file or complete immigration-related forms or prepare letters on their behalf in order for them to obtain or continue their work authorization.
RSM will consider for employment qualified applicants with arrest or conviction records. For those living in California or applying to a position in California, please click here for additional information.
At RSM, an employee's pay at any point in their career is intended to reflect their experiences, performance, and skills for their current role. The salary range (or starting rate for interns and associates) for this role represents numerous factors considered in the hiring decisions including, but not limited to, education, skills, work experience, certifications, location, etc. As such, pay for the successful candidate(s) could fall anywhere within the stated range.
Compensation Range: $30 - $35 per hour
$30-35 hourly Auto-Apply 34d ago
Quality Assurance Engineering Intern
Land Vehicles Americas
Quality assurance specialist job in Elkhart, IN
Dometic is a global market leader in the mobile living industry. Millions of people around the world use Dometic products in outdoor, residential, and professional applications. Dometic Land Vehicles Americas is a trusted provider of high-end products for recreational vehicles, commercial passenger vehicles and overlanding vehicles in North America, Latin America, and the Caribbean. We are on a journey of continuous growth - now looking for our next star - a passionate Quality Assurance Engineering Intern within our Segment Product Quality capability. This position reports to Lead Segment Product Quality Manager and will work in Dometic location Elkhart.
At Dometic, we don't just offer internships, we provide opportunities to make a real impact, grow professionally, and discover your full potential. As a Segment Quality Engineer in the Segment Product Quality team, you will be involved in meaning work and hands on experiences such as...
Quality Data Analysis and Improvements
Sales RMA Data analysis to evaluate Good Will, Concealed Damage, Shipment Damage etc. filed returns to address, improve and take corrective actions as needed.
Amazon Returns Data Analysis to understand the reasons of escalating warranty cost and area of improvements.
Product Label Standardization for existing Products & Implementation
Per Dometic Product Label Standard and Retail Customer Specific requirements, all Dometic products must meet the requirements.
Project Measurable:
Report Top 3 Sales RMA drivers by cost and claim reasons identified during Sales RMA and Amazon Return analysis to Segment quality and PD engineering for resolution.
Complete the implementation of Product label Standardization- CWI Product List
Your main responsibilities
Investigate and evaluate all the existing products that are being sold to verify if they meet product label requirements.
Work with CWI Dometic Product list, Engage Engineering team, SQE team and the supplier to implement the new requirements of product labels.
Complete Vendor approval process (PPAP) for this change
Monitor Amazon Return Portal Daily ,Weekly and report to Segment Quality.
Evaluate and Analyze Sales RMA Returns and Amazon returns including final disposition of claim. Interact with quality group as required. Tests and inspects finished products returned. Compiles and documents data.
Assist Engineering Dept with special requests; testing and/or repairing items to regain functionality.
Perform other tasks as assigned by supervisor.
Provide input and assistance in warranty analysis activities performed by Segment Quality-Engineering team.
May enter data into computer systems for analysis and updating of database.
What do we offer?
The Dometic Internship Program is a professional learning experience that offers meaningful, practical work related to a student's field of study or career interest. Our program gives students the opportunity to collaborate with team members, have a meaningful project that allows you to have impact, career exploration and development, learn new skills, and get to know other interns.
$28k-44k yearly est. 46d ago
Quality Assurance Intern
Schafer Industries 3.3
Quality assurance specialist job in South Bend, IN
Schafer Industries is a premier supplier of off-highway axles and differentiated precision gearing solutions. Established in 1934, Schafer Industries has locations in South Bend, IN, Roscoe, IL, Fredericktown, OH and Blacklick, OH. Schafer Industries is one of the few manufacturers of integrated axle solutions in the off-highway electric vehicle market. Schafer serves customers in a variety of end markets including off-highway vehicles, recreational vehicles, aerospace, defense, oil & gas, material handling, powertrain, electric mobility, heavy duty trucking, agriculture, and construction. Our mission is to leverage world class capabilities to deliver superior products and services to maximize the value for our customers, employees, shareholders, and communities.
Why Work at Schafer Industries?
We are a growth-oriented company with a diversified customer base.
We are committed to a culture of safety and continuous improvement.
You will enjoy a collaborative work environment where your talents and opinions matter.
We provide training as well as opportunities to work on projects in support of your career development.
You will quickly see your impact when working with the team.
We live our values of Safety, Integrity, Responsibility to Others, Customer Focus, Continuous Improvement and Accountability in all that we do.
We have competitive pay and benefits to include 401(k) match and tuition reimbursement.
Job Summary
Perform activities related to the Quality Department including inspection, gauging, calibration, and document control. Opportunity to advance into the Engineering, CNC machinist, or Quality Technician positions.
Essential Functions:
Perform as an apprenticeship to advance into the technical position such as Engineering, CNC Machinist, or Quality Technician.
Support Quality Technicians with by collecting inspection samples, inspecting the features, and utilizing the measuring devices trained and approved by Quality leadership.
Support Gage/Calibration technician by collecting monthly due gages and help in calibration process as requested.
Support CMM technician by coordinating the movement of the material in and out of the CMM/GMM process.
Reading and interpreting the involute charts off of gear checking equipment.
Support document control process by monitoring and distributing the work instruction for the machine cells and update them per Quality leadership request.
Performing random floor audits for 6S, Gage usage, Document accuracy, and other Quality matters.
Collecting dimensional and visual data and recording to the appropriate documents.
Knowledge, Skills, Abilities
High School Diploma or Enrollment in Engineering or Technical College preferred
Proficient in Microsoft Office programs
Problem solving/analysis
Detail Oriented
Initiative
Discretion
Motivated
Working Conditions:
Air conditioned/heated manufacturing facility with possible exposure to noise; dust; fumes; physical, chemical, and biohazards; solvents, oils, and detergents.
This job is to be performed at the designated facility 100% of the time unless directed otherwise by manager/supervisor.
$38k-58k yearly est. 2d ago
Quality Assurance Supervisor
Otter Base 4.1
Quality assurance specialist job in Goshen, IN
The Quality Assurance Supervisor is responsible for planning, coordinating, executing, and monitoring food safety and quality assurance programs within a manufacturing facility. This role supports the development, implementation, and maintenance of quality, sanitation, and food safety systems to ensure compliance with corporate standards, regulatory requirements, and industry best practices. The position partners closely with operations, maintenance, and leadership teams to promote a strong culture of food safety, quality, and continuous improvement.
Key Responsibilities
Plan, organize, and oversee quality assurance and sanitation activities to ensure compliance with food safety regulations and internal standards
Monitor compliance with quality, sanitation, GMP, and food safety policies on the production floor
Ensure completion and documentation of physical, chemical, and microbiological testing
Support facility readiness for internal audits, third-party audits, and regulatory inspections
Promote a strong food safety and quality culture across all departments
Champion workplace safety accountability for self and others
Core Duties
Oversee product sampling results, sanitation documentation, label compliance, and quality performance metrics
Coordinate and maintain HACCP plans, reviewing annually and updating as needed
Administer and document the facility environmental monitoring and sampling program
Lead SQF (Safe Quality Food) compliance, recordkeeping, and audit preparedness; serve as site SQF Practitioner
Manage procurement and inventory of laboratory and sanitation supplies within budget guidelines
Maintain quality and sanitation manuals to ensure policies and procedures remain current and compliant
Conduct and coordinate food safety, quality, and sanitation training for plant personnel
Support third-party audits and regulatory inspections through documentation, corrective actions, and system improvements
Lead internal quality assurance and sanitation self-assessments to maintain audit readiness
Investigate consumer complaints and oversee corrective and preventive actions
Coordinate quality hold product storage, disposition, and rework activities
Manage supplier quality documentation and review processes
Participate in cross-functional quality initiatives and training at multiple facilities
Communicate quality and sanitation risks, trends, and status updates to leadership
Provide leadership, coaching, and guidance to quality team members
Collaborate with operations and maintenance teams to ensure compliance with regulatory and corporate quality standards
Serve as backup support for Quality Manager responsibilities as assigned
Specialized ResponsibilitiesDairy Manufacturing Facilities
Provide technical support for production trials, sanitation programs, cGMPs, ingredient management, PMO compliance, and product wholesomeness
Oversee raw milk receiving programs, including testing, training, documentation, and regulatory compliance
Direct and schedule Quality Assurance laboratory staff to ensure compliance with regulatory, SQF, cGMP, and sanitation standards
Prepared Foods Manufacturing Facilities
Provide technical support for operations and corporate teams related to product trials, GMPs, sanitation, ingredients, and product performance
Direct and schedule quality assurance laboratory team members to ensure compliance with corporate standards, regulatory requirements, SQF, GMP, and sanitation programs
Qualifications
Bachelor's degree preferred; Food Science, Chemistry, Biology, Microbiology, or related field strongly preferred
Minimum of 3 years of supervisory experience in Quality Assurance within a food manufacturing environment
Strong knowledge of food safety systems including HACCP, SQF, GMP, sanitation, and regulatory compliance
Experience with sanitation programs and continuous improvement methodologies preferred
Proficiency in Microsoft Word, Excel, and PowerPoint
Strong data analysis, decision-making, and problem-solving skills
Ability to manage multiple priorities in a fast-paced manufacturing environment
Demonstrated sense of urgency and ability to work under pressure
Excellent written and verbal communication skills across all organizational levels
Strong organizational, project management, and attention-to-detail skills
Ability to work independently and collaboratively within cross-functional teams
$57k-78k yearly est. 11d ago
Quality Assurance Support
Refresco Careers
Quality assurance specialist job in Paw Paw, MI
Make a Difference in YOUR Career!
Our vision is both simple and ambitious: to put our drinks on every table.
We are the world's largest bottler for retailers and A-brands. Our products are distributed worldwide from our production sites in Europe and North America. Although our own branding may not appear on the labels of the beverages we produce, there is a good chance you are reading this while sipping one of our drinks.
Our ambition is to continually improve and it's what keeps us at the top of our game. We are solutions-based. We are innovative. We seek out new challenges and conquer them. This is our company ethos, but it's our people's too: Refresco is at the cutting edge of a fast-moving industry because we have passionate people pushing the boundaries of what's best.
Stop and think: how would YOU put our drinks on every table?
Essential Job Functions of QA Support Tech:
Adhere to all health and safety policies/procedures, Good Manufacturing Practices (GMPs) and wear the required personal protective equipment (PPE) while in the warehouse or production areas (including but not limited to hairnets/beard nets, safety glasses, hearing protection, hard toe and slip/oil resistant shoes, appropriate safety gloves, and seatbelts while operating forklifts).
Responsible to adhere to food quality and food safety as per the standard(s) provided by corporate, customer, and/or governing bodies (ex. SQF).
Ensure all products being run conform to the customer product specifications as outlined in SAP system, and conduct analysis on raw deliveries, finished batches and treated water.
Conduct chemical and physical analysis on raw and intermediate processing materials including packaging materials and determine status of materials as acceptable or unacceptable.
Evaluate finished products against current standards by performing audits to monitor all aspects of finished product and packaging integrity.
Investigate all out of specification conditions and make recommendations for corrective action and document.
Enter data into and confirm batches in SAP.
Check process control parameters to assure proper equipment application and operation is being maintained by performing secure seal, closure torque and seaming checks.
Effectively perform BBSO audits and provides feedback to the employee observed.
Can send professional emails as required to provide effective communication to all levels of the organization.
Understands how to generate a Process Order (COR1) and print batch sheet in emergency situations with Manager approval.
Able to train coworkers up to the Tier II skill level and actively participates in the training of new techs and uses SOPs and training matrix to track progress.
Knowledgeable of department KPIs and can clearly communicate continuous improvement opportunities in all QA processes.
Performs Root Cause Analysis and Reporting.
Stop any production which may be questionable in terms of Food Safety and immediately alert a member of the management team.
Maintain accurate, legible records of all tests and retests performed. Complete all other required reports (work orders, action reports, etc.) in a timely manner.
Perform analytical tests required to qualify ingredient batches for production.
Perform production line checks at specified intervals.
Ensure accurate test results by maintaining proper operation and calibration of laboratory equipment.
Maintain laboratory cleanliness at all times.
Report all out of specification results to designated leadership.
Complete special projects and other reasonable duties as assigned by leadership.
Has demonstrated Tier II skills have been sustained at an acceptable level with limited supervision.
Required Skills:
Working knowledge of Excel, Word, and SAP.
Exposure to using measurement tools and equipment (e.g., calipers, micrometers, CMM machines) preferred.
Organized and detail oriented, adaptable to change.
Ability to apply statistical methods to analyze data and identify trends.
High level of precision and accuracy in inspection and testing processes.
Familiarity with ISO, Six Sigma, GMP, and other relevant standards and regulations
Understanding of Food Safety Requirements.
Able to read and understand metric system.
Prior inspection experience in a laboratory setting.
Competencies:
Technical: Skilled in maintaining accurate and detailed records of inspections and tests
Integrity: Commitment to maintaining high ethical standards in all quality assurance activities.
Adaptability: Flexibility to adapt to changing production environments and requirements.
Communication: Clear and concise communication with production staff and management
Education and Experience:
Highschool diploma or equivalent.
2 - 4 years of experience in Quality within a manufacturing environment.
Laboratory experience required.
In plants co-packaging alcoholic beverages, sensory tasting must be at least 21 years old.
Working Conditions:
Work Schedule: Weekdays, weekends, afternoon, evening, and overnight may be required. Overtime scheduled as needed.
Work Environment: Operating in a fast-paced production plant with numerous moving parts. Noise levels require hearing protection and temperatures can get very hot and/or relatively cold (laboratory is temperature controlled). The environment is structured and supervised.
Travel Requirements:
0% travel anticipated.
Physical Requirements:
R = Rarely (0-15%) O = Occasionally (16-45%) F = Frequently (46-100%)
Physical Demand
R
O
F
Stand or Sit
X
Stoop, kneel, crouch, or crawl
X
Lifting up to 50 lbs. (minimum 5 lbs)
X
Carry weight, lift
X
Walking
X
Driving
X
Climb (stairs/ladders) or balance
X
Visual/Sensory: This position requires attention to detail, requiring attention with one or two senses at a time.
Mental Stress: There is pronounced pressure from deadlines, production quotas, accuracy, or similar demands.
Other Duties:
This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.
A Career with Refresco
Refresco offers a competitive salary and comprehensive benefits, which include:
Medical/dental/vision insurance
Life insurance
401(k) savings plan with company match
Paid holidays and vacation
Well-being benefits
Discount programs
Join Refresco TODAY and enjoy a rewarding CAREER!
Equal Opportunity Employer
Refresco is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to
race, color, ancestry, religion, sex, national orientation, sexual orientation, age, marital status, disability, gender identity, gender
expression, Veteran status, or any other classification protected by federal, state, or local law.
$39k-79k yearly est. 60d+ ago
Quality Coordinator
Champagne Metals
Quality assurance specialist job in Middlebury, IN
Job Description
Join Our Team as a Quality Coordinator - Where Precision Meets Passion
Are you an organized, detail-oriented professional looking for a role where your skills can truly shine? If you have quality coordinator experience and a keen eye for detail apply now!
Pay: $18-$21 per hour (or more with experience - let's talk!)
Shifts: 1st
What You'll Do:
-Take initiative
- Inspect materials during production to ensure top-notch quality.
- Review and complete claim forms for rejected materials.
- Use tools such as tape measures, micrometers, and calipers to inspect and measure materials.
- Confidently inspect questionable materials and make sound decisions.
- Leverage basic Microsoft Office skills to keep everything on track.
- Outlook for emails.
What You Bring:
- Quality control experience.
- Ability to work independently with minimal supervision.
- Strong attention to detail and a passion for precision.
Why Champagne Metals?
At Champagne Metals, we're more than just a company - we're a family. We value our employees and demonstrate this with amazing benefits:
- Paid Time Off: 15 days of PTO in your first year.
- 401(K) Matching: We match 5% to help you secure your future.
- Health Coverage: Premiums paid by us, including Blue Cross Blue Shield health insurance.
- Supportive Team: A quality-driven culture where your work truly matters.
If you're ready to make an impact and grow with a company that values you, apply today! Your next career adventure awaits.
$18-21 hourly 13d ago
QA Technician III
8427-Janssen Cilag Manufacturing Legal Entity
Quality assurance specialist job in Warsaw, IN
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at *******************
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Business Enablement/Support
All Job Posting Locations:
Warsaw, Indiana, United States of America
Job Description:
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.
Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.
About MedTech
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at *******************/medtech
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at *******************/.
We are searching for the best talent for QA Technician III
JOB SUMMARY
QA Technician III performs inspections on incoming products and materials.
DUTIES & RESPONSIBILITIES
In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
Perform all job duties in full accordance with the Worldwide Policies on Information Asset Protection, maintain password(s) as Confidential, and protect Critical Business Information.
Incumbent knows, understands, incorporates and complies with all applicable laws and regulations relating to DePuy's business activities and Policies and Procedures of the Health Care Compliance Program and Code of Conduct.
Works independently to complete routine and complex inspections using applicable sampling plans, control plans to verify product and services conform to quality and other engineering and Quality Assurance requirements.
Troubleshoot and problem solve quality issues utilizing basic research and analysis techniques.
Functions as technical resource and “go-to” person regarding quality issues with their specific area.
Recommends new sampling procedures and inspection methods
Conducts training for lower level inspectors
Maintains accurate inspection records, filing systems and appropriate documentation to conform to all quality and GMP regulations.
Performs sterile release activities including review of documentation and products (as assigned).
Initiates nonconforming records for products not meeting specifications.
Responsible for communicating business related issues or opportunities to next management level
Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable
Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
Performs other duties assigned as needed
EXPERIENCE AND EDUCATION
A minimum of High School Diploma or equivalent is required
4 years of related experience is required
REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS
Experience working in inspection/manufacturing/operations is preferred.
The ability to perform "hands on" troubleshooting and problem solving is required.
Knowledge of standard inspection techniques (i.e. calipers, micrometers, etc.) is required.
Strong analytical, communication, negotiation, skills.
Ability to interact with, influence, and lead cross-functional, cross-business unit teams is required.
Strong tactical planning and execution abilities, including strong organization skills is required.
Experience taking initiative with innovative ways to problem solve in a fast-paced, changing business environment is required.
Results driven, decisive, proactive, and responsive
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (********************************) or contact AskGS to be directed to your accommodation resource
Required Skills:
QA Documentation, QA Inspection, Technical Maintenance, Technical Quality Assurance
Preferred Skills:
Accountability, Administrative Support, Compliance Management, Controls Compliance, Execution Focus, ISO 9001, Persistence and Tenacity, Process Oriented, Quality Control (QC), Quality Standards, Quality Systems Documentation, Quality Validation, Report Writing, Teamwork, Technologically Savvy
$28k-43k yearly est. Auto-Apply 5d ago
Product Development Quality Leader
Zoetis 4.9
Quality assurance specialist job in Kalamazoo, MI
Zoetis's Veterinary Medicine Research and Development (VMRD) Product Quality group is seeking highly skilled, detail-oriented, and forward-thinking Quality Leaders who will be active members of vaccine, biopharma and pharma co-development teams providing input on co-development strategy (clinical/PK supplies, design of experiments, analytical method development and transfer, registration batch manufacture, submission planning, etc.) throughout the lifecycle of a project including transfer to Zoetis Global Manufacturing & Supply (GMS).
Their goal will be to assure that long-term product sustainability is a process design deliverable by guiding co-development teams with a quality mindset. Knowledge from product and process development is the basis for establishing an approach to control of the manufacturing process that results in products with the desired quality attributes. The Quality Leaders will help to ensure that during process/product development, variation, impact of variation and control of variation is understood and well documented. The successful candidate will make sure that the appropriate level of quality and compliance is applied across all aspects of the process design stage of process validation, collaborating with both VMRD and GMS. Quality Leaders will be involved in key decision making and supportive processes of the co-development team such as risk assessments, determination of Critical Process Parameters, Critical Quality Attributes (specifications) and control strategies. The close partnership with GMS will continue across the qualification and verification phases of validation to ensure seamless transition of product quality to commercial manufacturing.
The Quality Leaders will foster a culture of excellence and harmonize practices across diverse projects. They will be responsible for the review and approval of GMP documentation (batch records, protocols, reports, stability, etc.) for each project and for the maintenance and continuous improvement of the VMRD Quality Management System policies in accordance with regulatory requirements, Zoetis standards and industry best practices.
Each Quality Leader will be responsible for supporting multiple projects and interfacing with partner groups in the co-development teams across the organization in both VMRD and GMS. These include global development teams, regulatory, GMS quality, formulation, chemistry, analytical, bioprocess development, PK/PD, clinical, CROs, etc.
Expectation that colleague will adhere to being present on-site ≥50% of the time
Responsibilities:
As part of the core co-development team, represent VMRD Product Quality through product development. Provide strategic input and participate in highly matrixed cross-functional teams with operational leaders to prioritize processes and roadmaps and drive innovation. Collaborate to develop and implement innovative solutions to improve business processes, reduce compliance risk, while driving efficiency.
Interpret and stay updated on relevant regulation and guidelines from health authorities.
Ensure that all processes, documentation, facilities, and products comply with requirements. Assure adherence to appropriate GMP practices with a forward-looking perspective to anticipate and address emerging challenges across the business lines.
Ensure a proactive and adaptive approach to evolving project needs. Champion the implementation of efficient and compliant processes. Foster a culture of quality and continuous improvement.
Use a quality-embedded mindset and practical knowledge of industry, customer requirements, and general business environment to define appropriate actions.
Operate within quality management systems to lead, own, and drive investigations, corrective/preventive actions, and change control activities in the design phase
Partner with Quality Operations in GMS during the qualification and verification phases of product lifecycle to ensure a seamless approach to process transfer and to knowledge management.
Identify opportunities for automation and integrating technological solutions to simplify compliance tasks and improve quality.
Demonstrate resilience in the face of challenges, maintaining composure and guiding the team through periods of change.
Basic Qualifications:
Bachelor's degree
Experience across technical (chemistry, analytical, formulation, bioprocess development, etc) disciplines with a demonstrated track-record of constructive influence on product development teams.
10+ years pharmaceutical industry experience.
Preferred Qualifications:
Masters/Graduate Degree
Quality Operations experience Strong leadership skills.
Ability to work independently at a high level.
Strong interpersonal skills and accountability in day-to-day interactions.
Full time RegularColleague
Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.
Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.
$100k-128k yearly est. Auto-Apply 60d+ ago
QA/QC Technician, MI
Pero Family Farms Careers
Quality assurance specialist job in Benton Harbor, MI
Job DescriptionDescription:
Title: QA/QC Technician
Reports To: QA/QC Manager
Type: Full-Time | Onsite | Non-Exempt
Pero Family Farms is a market share leader with over a century of dedication, commitment and integrity. Operating since 1908, Pero is the farm trusted by retailers and consumers alike. We are a fully integrated farming operation, with departments that specialize in organic farming, logistics, global supply chain management, national sales operations, food processing operations, and strategic marketing functions. Our operation includes over 35,000 acres spanning across the East Coast of the United States from Florida to New York, with distribution and production facilities in several different states. We pride ourselves in maintaining a strong family heritage and tradition that has been dedicated to quality, innovation, and excellent customer service that has been feeding America's families for over a century. Our family's passion for farming remains unwavering, with a vision to continue the tradition for many generations to come, whilst maintaining the reverence and trust it has established with the American consumer. As we expand our offering to include an assortment of organic vegetable options; we have become one of the largest organic vegetable growers in the country and we are looking to grow our workforce family. Join us in continuing and strengthening our position as a market share leader dedicated and trusted by retailers and consumers alike.
JOB SUMMARY
It is the Quality Assurance/Quality Control Technician's responsibility to ensure compliance with all relevant regulatory requirements and guidelines, ensure compliance with all customer expectations, internal quality, and Food Safety Standards and Policies.
Requirements:
PRIMARY FUNCTIONS
Inspect inbound/outbound product
Take temperatures and cultures of product
Document all inspections and data as needed
Perform assigned tasks related to quality and food safety
The QA/QC Technician will be responsible for making sure company products are safe and meet or exceed company quality standards, and fully comply with food regulations.
Monitor and enforce organic handling practices.
Critical Control Point testing of HACCP program
To effectively operate PAA pumps, sanitizing outlets, and performs testing to assure Organic wash requirements are met
To effectively operate chlorine pumps, sanitizing outlets, and performance of testing to assure chlorination wash requirements are met
Sample pulling for shelf life, microbiological, and customer requirements
Pre-Operational testing of sanitation to include: ATP testing of surfaces, and evaluations of cleaning practices
To effectively monitor and test all metal detection units for assurance of metal free production
Packaging and seal testing, relative to container type - such as vacuum, pressure, or bubble testing
Calibrations on weight scaled, thermometers, and all applicable testing tools or detectors
GMP (Good Manufacturing Practices) monitoring of operation to ensure food-safe environment
Color code enforcement; sanitation, organics, allergens, others as required
Hold and release program
Rework program
Shelf-life evaluation and sensory testing as required
Paperwork filing
Work with soap's other cleaning chemicals
Other duties as required
PHYSICAL REQUIREMENTS
Required to stand, sit, walk for long periods of time
Frequent use of hands for simple firm, grasping and writing
Occasional bending, stopping, reaching, and climbing
Occasional Lifting, carrying 5 pounds to 50 pounds
Occasionally using cutting utensils (I.E Knives, peeler, etc.)
Exposure to product fumes such as onions, peppers etc.
Exposure to varying temperatures of 45 degrees or less
Exposure to chemicals such as chlorine, etc.
Works overtime as required
Other duties as required
SKILLS & REQUIREMENTS
Food Quality inspection experience, produce experience preferred
Good communication skills, including basic written and spoken English, to ensure understanding of safety procedures and documentation
Computer skills -
Basics: Microsoft Excel, Word, PowerPoint, Office
Industry Specific: Famous
HACCP certification or have participated in HACCP training
Must be able to follow complex verbal and written instructions and be able to work independently to evaluate and resolve Quality-related problems and identify and communicate short term remedial actions.
Must have a high level of problem-solving skills.
COMPANY BENEFITS/PERKS
401(k)
Health, Dental, Vision Insurance and more
Paid Time Off (PTO)
The company (Pero) reserves the right to alter, amend, expand or contract these duties and responsibilities as the companies needs evolve.
$30k-45k yearly est. 29d ago
QA Compliance Specialist
Lebermuth, Inc. 3.7
Quality assurance specialist job in South Bend, IN
Lebermuth Company is currently looking for a Quality Assurance Compliance Specialist to join our team. Lebermuth Company, a family-owned leader in the fragrance and flavor industry, has been blending tradition with innovation for over a century. Specializing in essential oils, fragrances, and flavors, Lebermuth is dedicated to quality and integrity. Our commitment to excellence is evident in our personal touch, sustainable practices, and customer-centric approach.
Summary:
The QA Compliance Specialist is responsible for administering and coordinating quality programs to ensure compliance with FDA, FSMA, SQF, HACCP, and other applicable state and federal regulations. This role partners with procurement and cross-functional teams to maintain a robust supplier quality program and supports continuous improvement initiatives across the organization.
Essential Duties & Responsibilities:
* Serves as the primary SQF Practitioner and PCQI; oversees Verification & Validation, Document Control, Foreign Material Management, and Environmental Monitoring programs.
* Manages Pest Control Programs and 3rd party contractors supporting Quality and Food Safety initiatives.
* Facilitates 3rd-party laboratory testing for raw materials and finished products to meet EPA/FDA and certification requirements (e.g., Organic).
* Responsible for managing the Supplier Approval Program by overseeing supplier level approvals, partnering with regulatory team to maintain accurate and current supplier data, and administering the Supplier Approval Database to ensure compliance and program integrity
* Administers the Alchemy training program; collaborates with QEHS and other departments on annual training needs.
* Leads internal auditing program; communicates schedules and results to leadership.
* Facilitates corrective and preventive action (CAPA) processes to drive continuous improvement.
* Supports Regulatory department during governmental, third-party, and customer audits.
* Promote food safety culture by maintaining a clean and organized workspace and adhering to all quality and safety standards within the department to ensure the safe production and shipment of quality food products
* Performs other duties as assigned to support compliance and quality objectives.
Requirements
Qualifications:
Education: Bachelor's degree in food science, Quality Assurance, Business, or related fields of study, or an equivalent combination of education and experience.
Experience: 2+ years of related experience and/or training; Knowledge base representative of the position includes experience with SQF, cGMP and HACCP programs.
Certifications: SQF Practitioner, PCQI, and HACCP.
Functional Skills: Strong planning, organizational, and executing skills are required; technical aptitude, with lean thinking/process improvement skillsets, are needed to problem-solve and enhance the operations; excellent forward-thinking, prioritization, analytical, and detail-oriented skills are required to manage multiple data points. Analytical problem solving, effective communication and partnership development
Technology Aptitude/Skills: Basic knowledge of computer and keyboard functions. Strong working knowledge and experience with MRP/ERP systems and familiarity with regulatory-related programs. Proficiency with Microsoft Office products, particularly Excel.
Language Skills: Strong verbal and written communication skills. Demonstrates advanced group presentation skills, presents information effectively and responds to questions from owners and management teams Ability to read, analyze and interpret professional journals, technical procedures, governmental regulations, and chemical hazard information and safety procedures. Ability to write correspondence that is professional in both content and tone. Ability to effectively present information and respond to questions.
Leadership/Behavior Skills: Self-motivated to stay focused on quality and output goals; strong work ethic and values, sound judgement, dependable, focused on the customer and processes; high level of accuracy and attention to detail with the flexibility to move to priorities throughout the operation areas, following all Safety requirements
Culture Match Behaviors: Enjoys and thrives in a fast-paced, high-growth environment, with a huge drive to create an impact while also being an effective listener, respectful problem-solver and a collaborative continuous learning team member.
Physical and Sensory Demands / Environmental Conditions / Equipment Used
* This role routinely uses standard office equipment such as computers, phones, electronic devices, photocopiers, filing systems/cabinets and fax machines.
* Ability to operate keyboard and view computer screen occasionally.
* Ability to write ideas/information in a logical flow occasionally.
* Cognitive and reasoning ability to read, review and interpret work orders or processes on a frequent basis.
* Ability to read and respond due to nature of the work on a frequent basis.
* Ability to talk and communicate with others via phone, in-person, and/or computer frequently.
* Ability to listen to others, solve problems, and respond frequently.
* Ability to stand, sit, walk, climb, bend, stoop, kneel, crouch, reach, squat, twist, push, pull, and carry items frequently.
* Ability to lift/move up to 15lbs sporadically.
* Ability to work in a manufacturing environment with fluctuating temperatures and noise levels.
* The employee is required to wear suitable Personal Protective Equipment such as safety glasses, hair/beard nets and steel toed shoes, as required.
* Work schedule is generally 1st shift, generally Monday through Friday, but at times requires on-call and non-traditional work hours, to meet business needs
Salary Description
Hourly Non Exempt
$59k-85k yearly est. 55d ago
QA/QC Coordinator
CDI Corporation 4.7
Quality assurance specialist job in New Carlisle, IN
"Together We Make Life Better". Our quality engineering, sustainable solutions and safety record inspire everything we do. Our diverse and inclusive workforce allows all employees to feel valued and safe to give their opinions and improve our company.
Tata Consulting Engineers USA, LLC, (TCE), is a multi-disciplinary engineering organization offering a full range of integrated engineering design, project support, procurement and construction management services to the energy and chemicals industries.
Position Summary
Quality Assurance Construction Coordinator to implement quality assurance procedures for capital and expense projects managed by the customer's Project/Construction Focal point, and will lead the overall Quality Assurance program for the Construction Management team.
Responsibilities
Assess current quality management systems and practices, identify gaps, and recommend closure action plans. Work with stakeholders to effectively implement quality management system elements.
Development and maintenance of local and regional documents that support and compliment global quality specifications and guidelines.
Train and coach Construction Management personnel on quality best practices and requirements.
Network with global colleagues to stay current on incidents, improvements and best practices.
Implementation standardization and measurement of the effectiveness of quality systems and work processes to ensure that the Global Construction Quality strategies are successfully maintained.
Leads or participates in Quality related unplanned event investigations and ensures that actions effectively address root causes.
Perform internal audits to assure conformance to work processes.
Ensure that the required contractor Quality Control procedures are properly implemented and that the constructed facilities comply with the related requirements, codes, and specifications.
Significant Safety visibility and activity, providing support to the Construction Manager.
Verify the contractors' implementation of their Project QC plan, identify deficiencies.
Work with construction team to initiate any required 'Request For Variance' and/or MOC.
Ensure that installation is according to customer specifications and contract drawings.
Complete Non-Conformance Reports and monitor all NCR's for status and to closure.
Communicate nonconforming issues of customer procured equipment, tanks, vessels, etc. to the Regional Quality Manager.
Lead process to obtain, review, and approve contractor provided quality plans, inspection and latest plans.
Participate in lesson learned analysis.
Work with Discipline Focal Points and implement improvement actions.
Request metrics to the Discipline Focal Points.
Qualifications
Familiar with or previous experience with construction documents such as isometrics, P&ID's, Owner piping codes, civil- underground, and structural steel drawings, rotating equipment and vessel drawings, electrical single line diagrams and architectural drawings, quality best practices, safety standards, ASME, API, AWS, and similar codes of construction.
Multi discipline experience preferred including civil concrete and structural steel, mechanical/ piping, vessels, reactors, rotating equipment, electrical equipment such as transformers, motor control centers, termination of motors, power distribution
Applicant must be willing at times to cover off hour work (night, weekend, or overtime) as applicable.
EEO Statement
Tata Consulting Engineers USA, LLC ("TCE") is an equal opportunity and affirmative action employer committed to promoting diversity, equity, and inclusion in our workplace. We do not discriminate on the basis of race/ethnicity, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, veteran's status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.
In compliance with federal law, all candidates hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form after acceptance of a formal TCE offer letter through our onboarding system.
Fraud Alert
Please be aware that there have been instances of fraudulent job offers being made in the name of TCE by unauthorized individuals or organizations. We want to make it clear that TCE will never ask for any type of payment information during our interview process. Please be advised during our company transition, all email communications from TCE will come from our business email addresses, which end in '@tatconsultingengineers.com'. If you receive any suspicious job-related emails from any other domain, please do not respond to them and disregard any requests for personal or financial information. If you have any concerns about the legitimacy of a job offer or communication, please contact us through our website at tataconsultingengineers.com
$52k-67k yearly est. Auto-Apply 38d ago
Quality Coordinator
Champagne Metals
Quality assurance specialist job in Middlebury, IN
Join Our Team as a Quality Coordinator - Where Precision Meets Passion
Are you an organized, detail-oriented professional looking for a role where your skills can truly shine? If you have quality coordinator experience and a keen eye for detail apply now!
Pay: $18-$21 per hour (or more with experience - let's talk!)
Shifts: 1st
What You'll Do:
-Take initiative
- Inspect materials during production to ensure top-notch quality.
- Review and complete claim forms for rejected materials.
- Use tools such as tape measures, micrometers, and calipers to inspect and measure materials.
- Confidently inspect questionable materials and make sound decisions.
- Leverage basic Microsoft Office skills to keep everything on track.
- Outlook for emails.
What You Bring:
- Quality control experience.
- Ability to work independently with minimal supervision.
- Strong attention to detail and a passion for precision.
Why Champagne Metals?
At Champagne Metals, we're more than just a company - we're a family. We value our employees and demonstrate this with amazing benefits:
- Paid Time Off: 15 days of PTO in your first year.
- 401(K) Matching: We match 5% to help you secure your future.
- Health Coverage: Premiums paid by us, including Blue Cross Blue Shield health insurance.
- Supportive Team: A quality-driven culture where your work truly matters.
If you're ready to make an impact and grow with a company that values you, apply today! Your next career adventure awaits.
$18-21 hourly 12d ago
Learn more about quality assurance specialist jobs
How much does a quality assurance specialist earn in Elkhart, IN?
The average quality assurance specialist in Elkhart, IN earns between $31,000 and $80,000 annually. This compares to the national average quality assurance specialist range of $41,000 to $97,000.
Average quality assurance specialist salary in Elkhart, IN