3 Manufacturing jobs in Orange

**About us**
At ExxonMobil, our vision is to lead in energy innovations that advance modern living and a net-zero future. As one of the world's largest publicly traded energy and chemical companies, we are powered by a unique and diverse workforce fueled by the pride in what we do and what we stand for.
The success of our Upstream, Product Solutions and Low Carbon Solutions businesses is the result of the talent, curiosity and drive of our people. They bring solutions every day to optimize our strategy in energy, chemicals, lubricants and lower-emissions technologies.
We invite you to bring your ideas to ExxonMobil to help create sustainable solutions that improve quality of life and meet society's evolving needs. Learn more about our What and our Why ( and how we can work **together** .
**About Beaumont**
With a population of more than 118,000, Beaumont ,Texas, is located in the Gulf Coast region of the United States, on the Neches River, about 85 miles east of Houston, the nation's fourth largest city. Beaumont has been a home to the oil industry from the days of the Spindletop oil boom until today, and along with nearby Port Arthur and Orange, is part of the Golden Triangle industrial area on the Texas Gulf Coast. Those who live and work in Beaumont will find a close-knit community with friendly people and opportunities to explore the area at its many restaurants and businesses, as well as numerous museums and nature parks.
Built along the banks of the Neches River in 1903, the original ExxonMobil Beaumont refining facilities have grown into an integrated petrochemical complex on 2,700 acres and have contributed to the economic and social landscape of southeast Texas. In fact, 1 in 7 jobs in Jefferson County are linked to ExxonMobil, making it an integral part of the community. With a workforce of more than 5,500, the Beaumont complex includes a refinery, chemical plant, polyethylene plant and lubricant blending and packaging plant. The complex is part of ExxonMobil's current building and expansion plans for the U.S. Gulf Coast.
Not only does Beaumont produce Mobil 1, the world's leading synthetic motor oil, it is the only manufacturer of Mobil Aviation Greases. Other products include fuels and chemical compounds used in a diverse range of products, including plastics, Nylon, shrink wrap and more.
**Learn more about what we do in Beaumont** **here** **.**
**What role you will play in our team**
Our Chemical Process Engineers play a pivotal role in the successful operation of our plants and are responsible for initiating and leading improvements to unit performance in safety, production, and reliability in a dynamic team environment. You will think strategically, execute thoughtfully, and collaborate across many teams, levels, and situations. In this role, you will serve as a process technical resource, providing technical and operational expertise to address complex processes across business teams.
Process Engineers serve primarily to set longer term visons for unit performance and troubleshooting in addition to supporting day-to-day activities.
**What you will do**
Serve as a technical leader by:
+ Mentor less experienced engineers on design practices, unit health monitoring, and troubleshooting
+ Provide support of abnormal and non-routine operations, including unit Turnarounds
+ Aid in the development of long term vision and strategy for product line improvements
+ Organize and design plant testing and product trials
+ Influence others and drive toward solutions without direct authority
+ Work in a team environment with other engineering disciplines, operations, and mechanical personnel and interface with corporate technology support
+ Ability to interface with 3rd party vendors (cost optimizations as well as developing/driving solutions)
+ Lead/support incident investigations as technical lead
+ Provide support for developing and implementing various capital projects to drive margin or mitigate SHE risk
+ Provide assistance in the field during plant startups, shutdowns or upsets
+ Demonstrate courage of conviction to drive healthy tension for both business team and corporate technology support to promote fit for purpose outcome
**About you**
**Skills and Qualifications**
+ B.S. Chemical Engineering
+ 3-10 years of experience in refining and/or chemicals manufacturing roles
**Preferred Qualifications/ Experience**
+ Process design exposure
+ Familiarity with advanced control strategies/optimization software
+ Risk assessment and HAZOP experience
+ Understanding of safety relief limits (modelling and evaluations)
+ Understanding of modelling software (PROII, ASPEN, etc)
**Your benefits**
**An ExxonMobil career is one designed to last. Our commitment to you runs deep: our employees grow personally and professionally, with benefits built on our core categories of health, security, finance, and life.**
**We offer you:**
+ Pension Plan: Enrollment is automatic and at no cost to you. The basic benefit is a monthly annuity to be paid to you in retirement for the rest of your life
+ Savings Plan: You can contribute between 6% and 20% of your pay and are encouraged to enroll right away. If you contribute at least 6% to your savings plan, the Company will contribute a 7% match
+ Workplace Flexibility: We have several programs such as "Flex your Day", providing ad-hoc flexibility around when and where you work, as well as longer-term programs such as leaves of absence and part-time work
+ Comprehensive medical, dental, and vision plans
+ Culture of Health: Programs and resources to support your wellbeing
+ Employee Health Advisory Program: Provides confidential professional counseling for you and your family, including tools and resources promoting mental health and resiliency at no additional cost to you
+ Disability Plan: Income replacement for when you cannot work due to illness or injury occurring on or off the job. Enrollment is automatic and at no cost to you
More information on our Company's benefits can be found at .
Please note benefits may be changed from time to time without notice, subject to applicable law.
**Stay connected with us**
Learn more at our website ( us on LinkedIN ( and Instagram ( us on Facebook ( our channel at YouTube ( Opportunity Employer**
**ExxonMobil is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, citizenship status, protected veteran status, genetic information, or physical or mental disability.**
Nothing herein is intended to override the corporate separateness of local entities. Working relationships discussed herein do not necessarily represent a reporting connection, but may reflect a functional guidance, stewardship, or service relationship.
Exxon Mobil Corporation has numerous affiliates, many with names that include ExxonMobil, Exxon, Esso and Mobil. For convenience and simplicity, those terms and terms like corporation, company, our, we and its are sometimes used as abbreviated references to specific affiliates or affiliate groups. Abbreviated references describing global or regional operational organizations and global or regional business lines are also sometimes used for convenience and simplicity. Similarly, ExxonMobil has business relationships with thousands of customers, suppliers, governments, and others. For convenience and simplicity, words like venture, joint venture, partnership, co-venturer, and partner are used to indicate business relationships involving common activities and interests, and those words may not indicate precise legal relationships.
**Job ID :-81231**

About this role:

The Quality Control Lead will support the execution of critical quality activities including Device History Record (DHR) review, Receiving Inspection (RI), and calibration/preventive maintenance record audits. This role ensures compliance with quality system procedures and drives operational excellence by contributing to quality metrics, supporting audits, and performing hands-on inspections as needed.

Key Responsibilities:

Documentation Review & Records Management

• Review and approve Device History Records (DHRs) for sub-assemblies and Finished Goods (FG) to ensure compliance with GMP and procedural requirements.
• Review and approve RI documentation for completeness and traceability prior to material release.
• Audit calibration and PM records to ensure documentation accuracy and equipment qualification compliance.
• Maintain records in alignment with Good Documentation Practices (GDP) and submit them for document control archival.

Receiving Inspection & Inventory Support

• Assist RI team with incoming inspection of raw materials and components as needed to meet throughput targets.
• Perform physical inspection, labeling, and QAD transactions to release accepted lots.
• Perform and reconcile on-hold qualified material inventory.
• Participate in MRB inventory control; reconcile physical inventory vs. system (QAD).
• Initiate and assist in investigations of non-conforming material, support segregation, quarantine, and documentation of disposition.

Floor Audits & Compliance Monitoring

• Conduct routine Gemba walks in production, warehouse, receiving, and MRB to ensure labeling and identification compliance.
• Monitor cleanliness, organization, and status segregation of materials.
• Support monthly Laboratory Assessments and equipment inventory audits.

Quality Metrics and KPIs

• Support and contribute to the following departmental metrics and KPIs:
• RI Throughput – Number of lots/materials inspected and released per day/week/month.
• Right First Time (RFT) – Percentage of records or inspections completed without rework or error.
• Calibration Compliance Rate – Percentage of equipment calibrated on time.
• Preventive Maintenance (PM) Compliance – Timeliness of PM activities performed vs. scheduled.
• NC Trending Metrics – Number and type of non-conformances raised from DHR/RI/FA audits.
• Inspection Lead Time – Average time from material receipt to inspection completion.

Operational Support

• Perform RI and final acceptance inspections based on workload prioritization.
• Interface with manufacturing, materials, engineering, and quality teams to resolve issues and ensure continuous flow.
• Escalate quality risks or systemic issues to leadership in a timely manner.

Audit Readiness & Support

• Retrieve and prepare DHR, RI, calibration, and PM records for internal and external audits.
• Act as audit escort or subject matter resource for inspection-related questions.

Team & Continuous Improvement

• Participate in quality improvement initiatives, lean activities, and training programs.
• Cross-train on inspection procedures contribute to process standardization.
• Maintain a collaborative and supportive work environment.

About you:

• Minimum 5 years in Medical Device Quality Assurance or equivalent regulated industry.
• Proficient in 21 CFR Part 820, ISO 13485, and GDP/GMP.
• Experience in DHR review, receiving inspections, and use of basic measurement tools.
• Skilled in Microsoft Excel, QAD (or equivalent ERP), and electronic documentation systems.
• Strong attention to detail, time management, and problem-solving skills.

What’s in it for you:

This is a regular full-time position with competitive compensation package, excellent benefits including medical, dental, and vision insurances (all of which start on your first day), health savings account employer contributions (when enrolled in high deductible medical plan), cafeteria plan pre-taxed benefits (FSA, dependent care FSA, commute reimbursement accounts), travel reimbursement for medical care, noncontributory basic life insurance & short/ long term disability.

Additionally, we offer:

• emotional health support for you and your loved ones
• legal / financial / identity theft/ pet and child referral assistance
• paid parental leave, paid holidays, travel assistance for personal trips and PTO!

iRhythm also provides additional benefits including 401(k) (with company match), an Employee Stock Purchase Plan, pet insurance discount, unlimited amount of LinkedIn Learning classes and so much more!

FLSA Status: Nonexempt

As a part of our core values, we ensure a diverse and inclusive workforce. We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives. iRhythm Technologies, Inc. is an Equal Opportunity Employer. We will consider for employment all qualified applicants with arrest and conviction records in accordance with all applicable laws.

iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures, including those who may have any difficulty using our online system. If you need such an accommodation, you may contact us at

About iRhythm Technologies

iRhythm is a leading digital healthcare company that creates trusted solutions that detect, predict, and prevent disease. Combining wearable biosensors and cloud-based data analytics with powerful proprietary algorithms, iRhythm distills data from millions of heartbeats into clinically actionable information. Through a relentless focus on patient care, iRhythm’s vision is to deliver better data, better insights, and better health for all.

Make iRhythm your path forward. Zio, the heart monitor that changed the game.