36 Manufacturing Technicians jobs in Elizabethport

**Job Title: Quality Control Technician**
**Job Description**
We are seeking a dedicated Quality Control Technician for the 3rd shift to join our growing team. This role is integral in ensuring the production of high-quality food products in a safe and clean environment.
**Responsibilities**
+ Ensure new workers are trained accordingly.
+ Maintain housekeeping standards to ensure a clean and safe workplace.
+ Work closely with other Production Supervisors to ensure effective production handovers.
**Essential Skills**
+ Bi-lingual Spanish required for effective communication with production staff.
+ Positive attitude and pleasant personality for efficient communication with diverse populations.
+ Self-motivation and a results-oriented approach.
+ Understanding of principles, practices, and procedures of the food manufacturing environment.
+ Ability to lead and motivate others to achieve productivity goals.
**Additional Skills & Qualifications**
+ Experience in quality control, GMP, food manufacturing/packaging quality, inspection, packaging, and production.
**Why Work Here?**
Join a dynamic and growing company that has doubled in size over the last five years, offering a stable work environment with a structured and predictable workflow.
**Work Environment**
This position is located in the Cookies Production - Mixing/Mini Pan department, within a standard food production warehouse environment. You will work near moving equipment such as forklifts and machinery like conveyor belts and production machinery, with exposure to moderate to loud noise and fluorescent lighting. Cleanliness and sanitation are required. Shifts typically last 8-12 hours, and you may work during the day or night, surrounded by the smells of cookies and other food products. The facility manufactures products that may contain peanuts and tree nuts.
**Job Type & Location**
This is a Contract to Hire position based out of East Brunswick, New Jersey.
**Pay and Benefits**
The pay range for this position is $20.25 - $20.25/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave)
**Workplace Type**
This is a fully onsite position in East Brunswick,NJ.
**Application Deadline**
This position is anticipated to close on Oct 10, 2025.
**About Aerotek:**
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Job Title: Quality Control Specialist
Job Description
We are seeking a dedicated Quality Control Specialist to join our dynamic team in the cell and gene therapy sector. This role offers the opportunity to work at a brand new site, supporting our cutting-edge CDMO operations. The successful candidate will be trained in a variety of analytical methods and will be responsible for maintaining high-quality standards in a fast-paced environment.
Responsibilities
+ Perform and be trained in ELISA-based assays, Endotoxin testing, Flow Cytometry, and PCR analytical methods.
+ Support operations at both the Newark and Princeton locations.
+ Conduct quality inspections and manage materials, reagents, and live cells.
+ Interact effectively with clients and health authorities, ensuring clear communication and maintaining professional relationships.
Essential Skills
+ Master's Degree with 1+ years of experience in the pharmaceutical industry or GMP environment, focusing on analytical methods or Quality Control, OR a Bachelor's Degree with 2+ years of relevant experience.
+ In-depth knowledge and hands-on experience with analytical assays, including Flow Cytometry, PCR, and ELISAs.
+ Extensive Quality Control experience with a comprehensive understanding of compendial methods and regulatory guidance.
+ Ability and willingness to learn and perform microbiological assays as part of the evolving needs of the team.
+ Capability to thrive in a dynamic environment, manage multiple priorities, and adapt to evolving demands.
+ Willingness to travel between facilities and work flexible hours, including evenings, weekends, and shift-based schedules as operational needs dictate.
Additional Skills & Qualifications
+ Experience with LIMS, Endotoxin, Sterility, mycoplasma, and method qualification/validation, including supporting method transfer activities.
+ Familiarity with FDA, EMEA, ICH, USP, GMP guidelines, and cGMP regulations related to QC labs and cell-based product manufacturing.
+ Proven ability to support lab investigations, deviations, CAPAs, and change controls.
+ Knowledge of Gene/Cell therapy products, particularly in clinical production.
Work Environment
This role is based in a growing CDMO specializing in Cell/Gene Therapy at a brand new site. The work environment is dynamic, offering opportunities to work with the latest technologies in a supportive team-oriented setting. Flexible hours, including evenings and weekends, may be required to meet operational demands.
Job Type & Location
This is a Contract to Hire position based out of Princeton, NJ
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Newark,NJ.
Application Deadline
This position is anticipated to close on Oct 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

First for a reason:
**At First Student, we are a family of 60,000+ employees who take pride in safely transporting more than 5 million students and passengers to and from their destinations each day! Our family of brands include Transco, Total Transportation, Maggies Paratransit, and GVC II. Our employees are at the forefront of safety and innovation; they create and implement the most advanced training and technology the transportation industry has to offer.**
Maintains and fuels all para-transit vehicles in conjunction with para-transit operations center. Performs light maintenance as necessary to buildings and grounds.
+ Job Description **Major Responsibilities**
+ Opens the gates to the lot and checks para-transit parking areas to ensure all can be dispatched in a timely manner. Re-positions any vehicles that may impede the traffic in the yard.
+ Opens the fuel island, takes accurate stick and meter readings, and turns in inventory sheets at the end of the day.
+ Maintains accurate records and completes Bulk Fuel Receiving Report, Fuel Variance Report, Closing Month-end Report and Meter Calibration Report.
+ Notifies the Manager or designee when a fuel delivery is required and ensures that accurate stick readings are taken before and after delivery. In addition, ensures that proper procedure is followed during delivery.
+ Checks and fills the oil, antifreeze, power steering, transmission fluid, brake fluid, windshield washer fluid and belts on vehicles being fueled. Ensures that adequate supplies to perform checks are maintained at the fuel island. Communicates with the shop foreman regarding supplies and oil inventory dispensed into equipment.
+ Twice a week, checks tires for damage and proper air pressure. Tire damage must be reported to the shop immediately.
+ Inspects all vehicles during fueling or on a regularly scheduled basis for physical damage. Any damage will be reported immediately to the Manager or designee.
+ Maintains the required inventory in the spill barrel and notifies the Manager any time supplies are used or replaced.
+ In the event of a fuel spill, takes all necessary steps to contain the spill. The Manager or designee must be notified immediately.
+ Maintains adequate inventories and supplies to make minor repairs and facilitate the washing of vehicles.
+ Cleans interiors and exteriors of vehicles as required to maintain cleanliness of the fleet.
+ Performs maintenance of buildings and grounds to include yard cleanliness, grass and weeds or any other yard projects that are assigned as necessary.
+ Performs any other management requests or directives as requested. **Minimum Education or Certifications Required**
+ High school diploma or equivalent **Minimum Experience or Skills Required**
+ Ability to effectively prioritize tasks and manage time effectively.
+ Ability to appropriately interact with employees of all levels including drivers, customers, senior management, client representatives, union officials, and public.
+ Work extended hours regularly, including weekends and holidays to meet the business needs.
+ Demonstrate regular and consistent attendance and punctuality. **Physical Requirements and Working Conditions**
+ The position requires the employee to work outdoors in varying, seasonal weather conditions.
+ Must be able to drive company or personal vehicle to review driver performance, meet clients, and for other company related purposes
+ Use full range of hearing, speech, and vision
+ Use fingers (manual dexterity) handling paperwork
+ Stoop, crouch, squat, or kneel when performing inspections of any type
+ Bend at knee, hip, waist when performing duties
+ Stand while performing inspections
+ Be subject to wet, cold, or hot environmental conditions
+ Write reports in a coherent, legible way **Disclaimer** Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. This job description reflects management's assignment of essential functions, it does not prescribe or restrict the tasks that may be assigned.
_In the state of Washington, all technician and driving positions, including but not limited to van drivers and any other position requiring employees to drive a company-owned vehicle, are considered safety-sensitive and are therefore subject to drug and alcohol testing, including cannabis._
_All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. First is also committed to providing a drug-free workplace. First will consider for employment qualified applicants with criminal histories consistent with the requirements of the San Francisco Fair Chance Ordinance, Los Angeles Fair Chance Ordinance, and any other fair chance law. Philadelphia's Fair Criminal Record Screening Standards Ordinance Poster is at this link or upon request_ _ _._

First for a reason:
**At First Student, we are a family of 60,000+ employees who take pride in safely transporting more than 5 million students and passengers to and from their destinations each day! Our family of brands include Transco, Total Transportation, Maggies Paratransit, and GVC II. Our employees are at the forefront of safety and innovation; they create and implement the most advanced training and technology the transportation industry has to offer.**
**Job Summary:**
Responsible for maintaining and fueling all paratransit vehicles in support of the operations center. Also performs light maintenance on buildings and grounds as needed.
$17.00/hr
**Major Responsibilities:**
+ Open facility gates and inspect paratransit parking areas to ensure all vehicles are ready for timely dispatch. Reposition any vehicles obstructing yard traffic.
+ Open the fuel island, take accurate stick and meter readings, and submit inventory sheets at the end of the shift.
+ Maintain accurate fuel-related records, including:
+ Bulk Fuel Receiving Report
+ Fuel Variance Report
+ Closing Month-End Report
+ Meter Calibration Report
+ Notify Manager or designee when a fuel delivery is needed. Take accurate stick readings before and after delivery and ensure proper fuel delivery procedures are followed.
+ Check and top off fluids during fueling, including:
+ Oil
+ Antifreeze
+ Power Steering Fluid
+ Transmission Fluid
+ Brake Fluid
+ Windshield Washer Fluid
+ BeltsMaintain adequate supplies at the fuel island and communicate inventory needs to the shop foreman.
+ Inspect tires twice a week for damage and proper inflation; report any damage to the shop immediately.
+ Inspect all vehicles during fueling or as scheduled for physical damage; report findings to the Manager or designee.
+ Maintain spill kit inventory; notify the Manager when supplies are used or need replacement.
+ In the event of a fuel spill, follow proper containment procedures and notify the Manager or designee immediately.
+ Maintain inventory and supplies to perform minor repairs and vehicle washing.
+ Clean vehicle interiors and exteriors as required to maintain fleet cleanliness.
+ Perform light maintenance on buildings and grounds, including yard cleanup, grass/weed control, and other assigned projects.
+ Carry out additional duties as assigned by management.
**Minimum Education/Certifications:**
+ High school diploma or equivalent required.
**Minimum Experience/Skills Required:**
+ Strong time management and task prioritization skills.
+ Ability to interact professionally with all levels of employees, including drivers, customers, senior management, union officials, and the public.
+ Must be able to work extended hours, including weekends and holidays, as needed.
+ Regular and reliable attendance and punctuality are essential.
**Physical Requirements and Working Conditions:**
+ Must be able to work outdoors in varying weather conditions throughout the year.
+ May be required to drive company or personal vehicle for operational duties.
+ Must be able to:
+ Hear, speak, and see clearly.
+ Use manual dexterity for paperwork and inspections.
+ Stoop, crouch, squat, or kneel to perform vehicle inspections.
+ Bend at the knees, hips, and waist.
+ Stand for extended periods during inspections.
+ Work in wet, cold, or hot conditions.
+ Write clear and legible reports.
**Disclaimer:**
This job description is not intended to be all-inclusive. Management reserves the right to assign or reassign duties and responsibilities at any time. It outlines essential functions but does not limit the tasks that may be assigned.
_In the state of Washington, all technician and driving positions, including but not limited to van drivers and any other position requiring employees to drive a company-owned vehicle, are considered safety-sensitive and are therefore subject to drug and alcohol testing, including cannabis._
_All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. First is also committed to providing a drug-free workplace. First will consider for employment qualified applicants with criminal histories consistent with the requirements of the San Francisco Fair Chance Ordinance, Los Angeles Fair Chance Ordinance, and any other fair chance law. Philadelphia's Fair Criminal Record Screening Standards Ordinance Poster is at this link or upon request_ _ _._

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:

People Leader

All Job Posting Locations:

Raritan, New Jersey, United States of America

Job Description:

Janssen Pharmaceutical, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Supervisor, QC Release (S-W Day Shift) in Raritan, NJ!

At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at and follow us @JanssenGlobal. Janssen Biotech, Inc. is part of the Janssen Pharmaceutical Companies.

Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy. This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR-T platform and investigational treatment.

Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our cell therapy products? Apply today for this exciting opportunity to be part of the #CAR-T team!

The QC Supervisor is responsible for overseeing day-to-day Quality Control activities for a designated functional laboratory, ensuring GMP compliance, accuracy, and timeliness of specified testing processes. They carry out duties in compliance with all local, state, and federal regulations and guidelines (including FDA, EPA, and OSHA) as well as all company and site policies and procedures. They will also support internal and external audits. They will typically guide daily work activities of 10-12 direct staff within a functional laboratory of the Quality Control department. They are responsible for interviewing, hiring, performance review, rewarding and disciplining employees, addressing complaints, and resolving conflict.

Key Responsibilities:

• Manage analyst schedule to support Drug Product testing
• Review/approve QC laboratory data for validity and accuracy according to cGMP/cGLP standards
• Review/approve documents as a QC department subject matter expert (SME)
• Oversee timely completion of laboratory investigation of OOS/ invalid assays, CAPAs and change controls
• Ensure accuracy and completeness of executed analytical method transfer activities
• Set testing priorities and manage work assignments
• Mentor, train, and supervise quality control staff, as well as evaluate performance and provide opportunities for growth
• Communicate department objectives and metrics
• Support internal and Health Authority audits, as well as audit related investigations

Qualifications: Education:

• Minimum of a Bachelor’s or equivalent University degree required; advanced degree (MSc., Ph.D.) or focused degree in Biology, Biochemistry, or related scientific field is preferred

Experience and Skills:

Required:

• Minimum 6 years of relevant work experience
• Experience performing one or more of the following cellular and/or molecular based techniques: qPCR, Flow Cytometry, ELISA, Cell Culture, and/or Potency assays
• Knowledge of cGMP regulations and Good Documentation Practices (GDP)
• Detailed knowledge of Compendial (e.g., USP, EP, JP, etc.) requirements and standards for QC testing

Preferred:

• Proficient knowledge of analytical technologies used in a Quality Control laboratory and method transfer
• Experience leading, coaching, or supervising direct or indirect personnel or teams
• Work experience in Cell and/or Gene Therapy or Biologics
• Experience with LIMs and SAP or equivalent systems

Other:

• Requires ability and flexibility to work 10-hour shifts between the operational hours of 7AM-5PM (Sunday - Wednesday), and provide occasional support on the weekends or other shifts
• Requires the ability to meet the physical demands (lift up to 20 lbs, stand or sit for extended periods of time in a laboratory setting)
• Requires up to 5% domestic travel to other sites/locations

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit & 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 & 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, external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource.

The anticipated base pay range for this position is :

$91,000-$147,200

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation –120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year Holiday pay, including Floating Holidays –13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave – 10 days Volunteer Leave – 4 days Military Spouse Time-Off – 80 hours Additional information can be found through the link below.

QC Manager – Fairfield, NJ

Summary :

The QC Manager is primarily responsible for the daily operation of pharmaceutical Quality Control Laboratory. This position will manage the staff to schedule and perform all necessary testing to support manufacturing and release requirements. Responsible for training and personnel development. This is a hands- on position. In addition to managerial responsibilities, this position will be performing analytical testing including wet chemistry, GC, HPLC, etc. as needed

Responsibilities :

• Lead, coach and manage a team of analysts to ensure data integrity and performance to meet business objectives
• Train and develop analysts
• Formulate, document, and maintain quality control standards and on-going quality control objectives
• Schedule workload to meet release objectives and deadlines
• Review, interpret, analyze and report HPLC/GC/UV/FTIR data according to USP/NF/BP/EP/IP/JP/CEP/cGMP, and internal guidelines
• Author analytical methods and SOPs
• Clean, maintain, and troubleshoot HPLC/GC/UV/FTIR instruments
• Develop specifications and analytical methods as required
• Develop analytical methods to support product development projects
• Prepare analytical method validation protocols and reports
• Perform Laboratory Investigations, root cause analysis, CAPA, Change Controls, Validations, Stability Programs, APRs, statistical analysis, environmental monitoring of air, water, and surfaces, as needed.
• Manage the outsourcing process of testing to contract laboratories
• Ensure lab safety and manage chemical inventory
• Improve the compliance of the laboratory operations as well improve the efficiency and reduce the cost of the operations
• Perform duties of QC Analyst as needed including HPLC sample preparation and testing and any other testing requirements
• Audit the work of QC Analysts
• Other duties assigned by Management

Education :

• Bachelor’s degree in a scientific discipline (Chemistry preferred) with a minimum of 5 years’ experience in laboratory management OR Master’s degree in a scientific discipline (Chemistry preferred) with a minimum of 3 years’ experience in laboratory management

Experience Requirements:

• Experience with Empower 3
• Experience working in an FDA regulated environment
• Experience with GC sample preparation and testing
• Knowledge of USP Monograph testing, analytical method development & validation
• Knowledge of CFR & ICH Regulatory Guidelines
• Knowledge of cGMP processes, lab safety and GDP.

Computer Skills:

• Proficiency in Microsoft Word
• Proficiency in Microsoft excel
• Proficiency in Empower 3

Other requirements:

• Has significant technical knowledge of scientific principles, theories, and practices of analytical chemistry in an FDA inspected pharmaceutical quality control laboratory.
• Able to perform complex mathematical problems
• In depth knowledge of all laboratory equipment, practices, and procedures
• Demonstrated managerial abilities
• Problem analysis, solving and resolution skills
• Has excellent oral and written skills
• Has excellent interpersonal skills
• Is self motivated
• Has a very high attention to detail
• Has a positive attitude
• Must speak, read, and write in English
• Able to lift 25 pounds
• Able to stand for extended periods

Hours :

• Standard: 8:30 AM to 5:00 PM, Monday through Friday
• Occasionally: Extended hours and/or Saturday and Sunday may be required as necessary to support manufacturing.

Job Type
Full-time

Description

About Us: Westrafo America is the first US based facility specializing in the design and manufacturing of high-quality transformers. We are committed to excellence and are looking to expand our team with dedicated professionals who share our passion for electrical engineering and manufacturing.

Position Overview: We are seeking a detail-oriented Quality Control Inspector to join our team. The ideal candidate will be responsible for ensuring that our transformers meet the highest quality standards and comply with industry regulations. This role is critical to maintaining our reputation for quality and reliability as we scale our operations.

Key Responsibilities:

• Conduct inspections of raw materials, in-process components, and finished products to ensure compliance with specifications and standards.
• Develop and implement quality control procedures and guidelines.
• Perform testing and analysis on transformers to identify defects or areas for improvement.
• Document inspection results and maintain accurate records of quality metrics.
• Collaborate with production teams to address quality issues and implement corrective actions.
• Conduct root cause analysis for quality defects and develop strategies for prevention.
• Ensure compliance with safety and regulatory standards in all quality control processes.
• Participate in continuous improvement initiatives to enhance product quality and operational efficiency.

Qualifications:

• High school diploma or equivalent; associate or bachelor's degree in engineering or a related field preferred.
• Previous experience in quality control or manufacturing, preferably in the electrical or transformer industry.
• Knowledge of quality control standards and methodologies (e.g., ISO 9001).
• Strong attention to detail and analytical skills.
• Proficient in using measurement tools and equipment (calipers, micrometers, etc.).
• Excellent communication and teamwork skills.
• Ability to work independently and manage multiple tasks effectively.

Benefits:

• Competitive salary and performance-based bonuses.
• Health, dental, and vision insurance.
• Retirement savings plan.
• Opportunities for professional development and career advancement.
• A dynamic and innovative work environment.

Job Type
Full-time

Description

About Us: Westrafo America is the first US based facility specializing in the design and manufacturing of high-quality transformers. We are committed to excellence and are looking to expand our team with dedicated professionals who share our passion for electrical engineering and manufacturing.

Position Overview: We are seeking a detail-oriented Quality Control Inspector to join our team. The ideal candidate will be responsible for ensuring that our transformers meet the highest quality standards and comply with industry regulations. This role is critical to maintaining our reputation for quality and reliability as we scale our operations.

Key Responsibilities:

• Conduct inspections of raw materials, in-process components, and finished products to ensure compliance with specifications and standards.
• Develop and implement quality control procedures and guidelines.
• Perform testing and analysis on transformers to identify defects or areas for improvement.
• Document inspection results and maintain accurate records of quality metrics.
• Collaborate with production teams to address quality issues and implement corrective actions.
• Conduct root cause analysis for quality defects and develop strategies for prevention.
• Ensure compliance with safety and regulatory standards in all quality control processes.
• Participate in continuous improvement initiatives to enhance product quality and operational efficiency.

Qualifications:

• High school diploma or equivalent; associate or bachelor's degree in engineering or a related field preferred.
• Previous experience in quality control or manufacturing, preferably in the electrical or transformer industry.
• Knowledge of quality control standards and methodologies (e.g., ISO 9001).
• Strong attention to detail and analytical skills.
• Proficient in using measurement tools and equipment (calipers, micrometers, etc.).
• Excellent communication and teamwork skills.
• Ability to work independently and manage multiple tasks effectively.

Benefits:

• Competitive salary and performance-based bonuses.
• Health, dental, and vision insurance.
• Retirement savings plan.
• Opportunities for professional development and career advancement.
• A dynamic and innovative work environment.

**Job Description**
The QC/WIMS Clerk is responsible for processing accurate and timely transactions and conducting Quality Assurance of inbound/outbound product orders, including Train Provisioning Solution (TPS) services where applicable, while delivering excellent customer service to internal and external Amtrak customers and client partners.
COMPENSATION: The hourly rate for this position ranges from $22.00 to $22.00, that is the amount that Aramark expects to offer. This is Aramark?s good faith and reasonable estimate of the compensation for this position as of the time of posting.
BENEFITS: Aramark offers comprehensive benefit programs and services for eligible employees including medical, dental, vision, and work/life resources. Additional benefits may include retirement savings plans like 401(k) and paid days off such as parental leave and disability coverage. Benefits vary by location and are subject to any legal requirements or limitations, employee eligibility status, and where the employee lives and/or works. For more information about Aramark benefits, click here AramarkCareers - Benefits & Compensation ( is no predetermined application window for this position, the position will close once a qualified candidate is selected. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law, including, but not limited to, the Los Angeles County Fair Chance Ordinance for Employers, the California Fair Chance Act, and the San Francisco Fair Chance Ordinance to the extent that those laws apply to the opportunity.
**Job Responsibilities**
+ Enter data and process transactions in Warehouse Inventory Management System (WIMS) database.
+ Conduct Quality Assurance (QA) verification audits for both inbound and outbound orders, in the commissary (including cooler/freezer), at the Amtrak railyard/train platform, and on board Amtrak trains, effectively communicate and help resolve all discrepancies identified.
+ Ensure that the QA Process VPS Tools and Business Process SOPs are in compliance; communicate any deviations immediately to management.
+ Assist with problem solving, determining root causes to transactional issues and developing appropriate sustainable solutions.
+ May be asked to assist with Centralized Purchasing process as well as executing Warehouse to Warehouse Transfers.
+ Maintain files at the location, answer internal and external calls, use electronic equipment such as scanners, tablets, computers, printers, copiers, etc.
+ Participate in End of Month (EOM) inventory process and periodic cycle counts as required.
+ Utilize various reports (such as Negative Usage) to identify trends and areas for transactional process improvement.
+ Prepare communication materials for management and for the hourly staff including, but not limited to: bulletin boards, schedules, memos, etc.
**Qualifications**
+ Possess excellent verbal and written communication skills, including the ability to communicate professionally in person, by phone and through email.
+ Must be able to work in a fast-paced environment while interacting with staff at all levels, and remaining positive, proactive and resourceful.
+ Demonstrates initiative and the ability to work efficiently and independently.
+ Basic computer skills required, including use of technology (scanners, tablets, printers, copiers, etc.) and Microsoft Office programs, as well as cloud based systems.
+ Able to read and understand various reports and take appropriate action.
+ Must possess a high level of accuracy, attention to detail and is well organized.
+ An understanding of inventory flow and accountability.
+ Work well and collaboratively as part of a team, with a high level of professionalism and confidentiality
**Education**
**About Aramark**
**Our Mission**
Rooted in service and united by our purpose, we strive to do great things for each other, our partners, our communities, and our planet.
At Aramark, we believe that every employee should enjoy equal employment opportunity and be free to participate in all aspects of the company. We do not discriminate on the basis of race, color, religion, national origin, age, sex, gender, pregnancy, disability, sexual orientation, gender identity, genetic information, military status, protected veteran status or other characteristics protected by applicable law.
**About Aramark**
The people of Aramark proudly serve millions of guests every day through food and facilities in 15 countries around the world. Rooted in service and united by our purpose, we strive to do great things for each other, our partners, our communities, and our planet. We believe a career should develop your talents, fuel your passions, and empower your professional growth. So, no matter what you're pursuing - a new challenge, a sense of belonging, or just a great place to work - our focus is helping you reach your full potential. Learn more about working here at or connect with us on Facebook , Instagram and Twitter .