25 Manufacturing jobs in Manteca

**Immediate hiring need for a Manufacturing Engineer**
For immediate consideration, please apply directly to this job posting AND email me at habels @actalentservices.com with the following:
1) Word copy of resume
2) 2-3 professional references
3) 4-5 brief bullet points highlighting technical qualifications
Job Description
We are seeking a skilled Manufacturing Engineer to join our innovative and dynamic team. The role involves conducting time studies, analyzing production data, and leading efficiency improvement projects. You will work closely with cross-functional teams to ensure project alignment and monitor key performance indicators to drive continuous improvement.
Responsibilities
+ Develop and implement robust manufacturing processes for existing products.
+ Ensure a seamless transition from product development to full-rate production, ensuring process stabilization.
+ Develop and qualify new tooling and equipment to enhance production capabilities.
+ Design and draft workspace layouts, including materials and equipment, using computer-aided design (CAD) software.
+ Update risk documents (FMEA's) and Quality Control Plans for New Product Introduction.
+ Conduct verification and validation (IQ/OQ/PQ) of processes, machines, and equipment to meet company procedures and regulatory requirements.
+ Create and maintain routers and standards for manufacturing processes.
+ Troubleshoot product and process-related issues, performing root cause analysis and implementing corrective and preventative action plans.
+ Collaborate with vendors to identify and implement operational equipment and automation solutions.
+ Develop and manage project plans for major operational improvement activities.
Essential Skills
+ Minimum of 2 years of experience working as a Manufacturing Engineer in the medical device industry.
+ Experience in process development and process improvement.
+ Supporting Design Transfer and process improvement for class III medical devices, including catheters.
Additional Skills & Qualifications
+ Bachelor's Degree in Engineering or a related field.
+ Proven experience in manufacturing process validation.
+ Excellent communication and technical writing skills for preparing reports and collaborating with cross-functional teams.
Work Environment
This role operates within a global leader in medical device manufacturing, focusing on cardiovascular and endovascular solutions. Join a team of 8 on the 2nd Shift, working Monday to Friday from 2:00pm to 11:00pm, with limited overtime expected. The environment is collaborative and fast-paced, offering flexible work hours and a career path due to the company's accelerated growth.
Job Type & Location
This is a Contract to Hire position based out of Irvine, California.
Pay and Benefits
The pay range for this position is $45.00 - $55.00/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 Irvine,CA.
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.

**Immediate hiring need for a Manufacturing Engineer**
For immediate consideration, please apply directly to this job posting AND email me at ayami @actalentservices.com with the following:
1) Word copy of resume
2) 2-3 professional references
3) 4-5 brief bullet points highlighting technical qualifications
Job Description
We are seeking a skilled Manufacturing Engineer to join our innovative and dynamic team. The role involves conducting time studies, analyzing production data, and leading efficiency improvement projects. You will work closely with cross-functional teams to ensure project alignment and monitor key performance indicators to drive continuous improvement.
Responsibilities
+ Develop and implement robust manufacturing processes for existing products.
+ Ensure a seamless transition from product development to full-rate production, ensuring process stabilization.
+ Develop and qualify new tooling and equipment to enhance production capabilities.
+ Design and draft workspace layouts, including materials and equipment, using computer-aided design (CAD) software.
+ Update risk documents (FMEA's) and Quality Control Plans for New Product Introduction.
+ Conduct verification and validation (IQ/OQ/PQ) of processes, machines, and equipment to meet company procedures and regulatory requirements.
+ Create and maintain routers and standards for manufacturing processes.
+ Troubleshoot product and process-related issues, performing root cause analysis and implementing corrective and preventative action plans.
+ Collaborate with vendors to identify and implement operational equipment and automation solutions.
+ Develop and manage project plans for major operational improvement activities.
Essential Skills
+ Minimum of 2 years of experience working as a Manufacturing Engineer in the medical device industry.
+ Experience in process development and process improvement.
+ Supporting Design Transfer and process improvement for class III medical devices, including catheters.
Additional Skills & Qualifications
+ Bachelor's Degree in Engineering or a related field.
+ Proven experience in manufacturing process validation.
+ Excellent communication and technical writing skills for preparing reports and collaborating with cross-functional teams.
Work Environment
This role operates within a global leader in medical device manufacturing, focusing on cardiovascular and endovascular solutions. Join a team of 8 on the 2nd Shift, working Monday to Friday from 2:00pm to 11:00pm, with limited overtime expected. The environment is collaborative and fast-paced, offering flexible work hours and a career path due to the company's accelerated growth.
Job Type & Location
This is a Contract to Hire position based out of Irvine, California.
Pay and Benefits
The pay range for this position is $45.00 - $55.00/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 Irvine,CA.
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.

**Overview**
Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.
**Responsibilities**
The Manager of Manufacturing Engineering will plan, direct, and coordinate activities for the sustainment of commercial manufacturing to ensure that goals or objectives are accomplished within the prescribed time frame and funding parameters of the manufacturing engineering group by performing the following duties personally or through subordinate supervisors.
**Responsibilities**
+ Manage technical activities of engineers and technicians to sustain commercial manufacturing; assign duties/projects to staff by reviewing/aligning with company goals and objectives.
+ Hiring, training, and performance management of sustaining Manufacturing Engineering.
+ Overall management, direction, coordination, and evaluation of Manufacturing Engineering.
+ Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws.
+ Resolve technical issues in manufacturing using a hands-on approach.
+ Lead continuous improvement projects by creating project plans, establishing objectives and priorities, determining timelines and milestones, and assessing resource requirement
+ Manage engineering resources to resolve Non-Conformances (NC) and/or Corrective Actions/Preventative Action (CAPA) activities. This may include investigation, root cause analysis and/or propose solutions/disposition of materials
+ Assist in complaint investigations (as needed). Perform other duties as assigned.
+ Interface with Operations Management to review project goals and priorities
+ Formulate the sustaining activities for the Manufacturing Engineering department and organize staff according to business needs.
+ Support company goals and objectives, policies and procedures, and FDA regulations.
**Qualifications**
**Qualifications**
+ Bachelor's degree in engineering (Mechanical, Biomedical, Chemical, or related field)
+ 8+ years related work experience, including 2+ years of previous supervisory experience, or equivalent work experience
+ 5+ years' experience in the medical device/pharmaceutical field or in a related area.
+ Excellent written and verbal communications skills; ability to interact with all levels of management.
+ Ability to review and write/edit technical documents.
+ Strong Root Cause Analysis and analytical skills.
+ Strong interpersonal skills, effective interaction with Ops and other cross‐functional management to drive projects forward.
+ Proficiency in MS Word, MS Project and Excel required.
+ High attention to detail and accuracy is required.
+ Ability to perform multiple tasks concurrently with accuracy.
+ Work includes potential exposure to chemicals.
**Pay / Compensation**
The expected pre-tax pay rate for this position is $111,650 - $159.500. Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge and location.
**Preferred Qualifications**
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one-s identity. All our teammate-s points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming.
**JOIN OUR TALENT COMMUNITY**
Joining our Talent Community is a great way to receive company news and updates, as well notifications on career opportunities and events that interest you! Please tell us more about yourself so we can align you with future opportunities that match your background, skills and interests.
**Job Locations** _US-CA-Irvine_
**ID** _ _
**Category** _Manufacturing_
**Position Type** _Regular Full-Time_
CORDIS is proud to be an equal opportunity employer, values diversity in all its forms is and committed to fostering an inclusive work environment. We are committed to advancing our culture of belonging, where all teammates feel seen, heard, and appreciated and encouraged to be their authentic selves. Our team is invested in attracting, retaining and growing top talent. Our Teammates are the core of our innovation and success. Cordis is an inclusive, engaging place to work and grow a career. CORDIS is committed to offering reasonable accommodations, upon request, to job applicants with disabilities. If you need assistance or an accommodation due to a disability, please contact

**Manufacturing Engineer II**
Engineering
Irvine, CA, US
Pay Rate Low: 47.00 | Pay Rate High: 50.72
+ Added - 10/09/2025
Apply for Job
Exciting development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest Medical device company in the world - with complementary businesses in Surgical and Vision Care.
Proactive 18 month Contract **Manufacturing Engineer** II to drive process improvements and boost efficiency across our production lines. You'll work hands-on with product design, tooling, and equipment, using data-driven insights to enhance quality and streamline operations.
**_Location:_** Irvine, CA (Onsite)
**_Duration_** _:_ 18 months
**Pay:** $47.00 to $50.72 DOE
**Benefits** : Medical, Dental, Holiday, PTO 401K matching
**Key Responsibilities:**
+ Develop and optimize manufacturing processes based on product requirements.
+ Improve workflow, space utilization, and equipment layouts.
+ Design and execute tests to ensure product and process quality.
+ Analyze costs, production schedules, and future capacity needs.
+ Support engineering documentation, reports, and data analysis.
+ Ensure compliance with safety and regulatory standards.
+ Collaborate with vendors and operators to troubleshoot and enhance systems.
+ Guide and mentor technicians during development and implementation phases.
**Qualifications:**
+ Degree in Engineering or a related field (Advanced degree preferred).
+ Strong ability to read mechanical, electrical, and PCB drawings.
+ Experience with Life Cycle Management, Engineering Changes, V&V, and technical documentation.
+ Self-starter with strong decision-making and risk-assessment skills.This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH#LI-DNP:
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

**Be visionary**
Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins.
**Job Description**
Teledyne Energetics is comprised of Teledyne Electronic Safety Products (TESP) and Teledyne RISI Inc. (RISI). TESP specializes in developing solid state Electronic Safe & Arms for Military, Space, and Commercial (Oil Exploration/Production). RISI specializes in developing EBW and EFI detonators that integrate into Electronic Safe & Arms.
Well established supplier of interconnect systems and High Voltage components for the aerospace industry in the Tracy, CA is seeking a **Manufacturing (Mechanical) Technician.**
**Responsibilities:**
+ Demonstrated ability to read and follow engineering notes, sketches, and drawings.
+ Experience with mechanical diagnostic equipment, maintaining area controls, assisting with mechanical diagnostic calibration and alignment, testing prior to experiment execution, and performing data recovery after experiment execution
+ Provide operations, maintenance, design, fabrication, assembly support, and maintain systems documentation and experimental records.
+ Manage the tool identification, configuration control, storage and scheduled maintenance
+ Experience in general machining processes with the ability to operate hand/power tools.
+ Fabricate, assemble, and disassemble moderately complex mechanical components and systems, using work control process and procedure requirements while working under general supervision.
**Requirements:**
+ Associate degree in Mechanical or Manufacturing Engineering or equivalent from community college or trade-technical school
+ 1-4 years related experience working with machines, presses, and power tools.
+ Excellent analytical and reasoning skills
+ Excellent communication skills both written and oral
+ Ability to lift 50 lbs in a safe and controlled manner.
+ MS Word, Excel, and Powerpoint
+ AutoCAD, Inventor, and/or SolidWorks preferred
In our efforts to maintain a safe and drug-free workplace, Teledyne RISI requires that candidates complete a satisfactory background check and pass a drug screen prior to employment.
Due to the type of work at the facility and certain access restrictions, successful applicants must be a "US Person" (US Citizens, US Nationals, lawful permanent residents, asylees or refugees).
Please note the salary range posted is a general guideline for this job level and location. When extending an offer, a variety of factors are considered such as responsibilities of the position, relevant education and experience, certifications, knowledge and skills.
**Salary Range:**
$37,200.00-$49,600.000
**Pay Transparency**
The anticipated salary range listed for this role is only an estimate. Actual compensation for successful candidates is carefully determined based on several factors including, but not limited to, location, education/training, work experience, key skills, and type of position.
Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions.
Teledyne is an Equal Opportunity/Affirmative Action Employer. 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, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws.
You may not realize it, but Teledyne enables many of the products and services you use every day **.**
Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.

**What you will do-**
+ ⁠Lead complex manufacturing process design and improvement activities to ensure the safety and efficacy of components and finished medical devices
+ Independently lead qualification, verification, and validation (QVV) of manufacturing processes, equipment, and product lines for medical device production
+ Troubleshoot and resolve issues related to product safety, quality, cost, delivery, and process performance
+ Drive engineering initiatives and new product development, including technology development, process studies, Six Sigma projects, materials testing, and intellectual property generation
+ Design and develop manufacturing equipment in compliance with safety regulations such as OSHA and EPA standards
+ Participate in design control efforts, including risk analysis (FMEA), design reviews, and validation protocols
+ Lead supplier sourcing and evaluation efforts to assess capability, quality, and effectiveness of external partners and service providers
+ Direct controlled environment operations, including cleanroom design, equipment maintenance, and troubleshooting
+ Mentor and train cross-functional teams, including engineers, technicians, and operators, while also supporting post-market surveillance and product performance reviews
+ Lead and coordinate cross-functional project teams, manage timelines, define goals, evaluate engineering tests and experiments, and identify opportunities for process optimization and cost savings
**What you need-**
+ Bachelor's degree in engineering or related - required
+ 4+ years of experience - required
+ Ability to work well with others in a team setting
+ Ability to conduct complex statistical, geometric, and mathematical calculations
+ Ability to read, understand, create engineering drawings on common engineering software
+ Ability to mentor Engineers and other technical staff
+ Proficient in Microsoft Office applications
+ Proficient in use of Minitab, or similar, statistical software - preferred
$87,600.00 - $186,700.00 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

Crystal Creamery is currently looking for Lab Technician for our Dairy Manufacturing Plant in Modesto.

The Lab Technician with general direction shall perform routine laboratory and administrative duties, assist other lab members professionally and respectfully, keep accurate and legible records, have the ability to prioritize work assignments effectively, in addition to reviewing work for quality and completeness.

The Lab Technician will also safely operate testing equipment involving potential chemical and temperature hazards, accurately identify and restock lab supplies to maintain a current lab supply and inventory rotation, prepare samples, media and solutions for testing, high acceptance of performing other related duties and projects as assigned.

Requirements

Job Duties:

• Operate, calibrate, and maintain laboratory equipment to include Foss FTIR, Brix, pH meter, EQA, CEM, scales, and pipettes.

• Perform organoleptic testing on required product samples including fresh and at code products

• Perform accurate physiochemical and microbiological preparation, testing, counting and examinations of raw materials, in process products, and finished goods.

• Approve release of in process and finished products including "first off" testing, while verifying adherence to stated specification.

• Record and enters data, creates COA's, and other reports, promptly and accurately.

• Maintain various production, raw material, testing, and quality control records in an organized manner.

• Report and take necessary action to prevent food safety and food quality issues from occurring.

• Perform pre-operational checks and sanitation inspections in adherence to filler release procedure.

• Perform environmental swabbing, line checks, allergen tests, special projects, and any other duties as assigned.

• Apply proper aseptic sample collection, transport, storage testing, and disposal.

• Follow all company Safety Policies, Good Lab Practices, Good Manufacturing Practices, and Standard Operating Procedures.

• Proficient in the use of standard computer software, i.e. Microsoft Outlook, Word, Excel, PowerPoint.

• Excellent written and verbal communication skills

• Knowledge of US customary units and metric system including weights and measures.

POSITION REQUIREMENTS:

• Bachelor's Degree in Food Science, Microbiology, Biology or related field or 2 years experience.

Crystal Creamery is an Equal Opportunity Employer and does not discriminate any employee or applicant because of race, color, religion, national origin, ancestry, marital or veteran status, disability, medical condition, sex, or age (as defined by applicable law).

Any offer of employment by Crystal Creamery may be contingent upon passing a background check, medical examination and or drug test.

To apply please visit click on careers and job openings.

Salary Description

23.00 to 27.60 DOE

**Overview**
Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.
**Responsibilities**
As a Senior Business Analyst, you will act as the bridge between our manufacturing/supply chain teams and our enterprise-application stack-chiefly JD Edwards EnterpriseOne (JDE) for ERP and Dassault Systèmes Enovia (3DEXPERIENCE) for product lifecycle management (PLM). You'll map business processes end-to-end, translate them into system requirements, and lead continuous improvement initiatives that boost productivity, quality, and margins across the shop floor and the full product lifecycle.
**Key Responsibilities**
+ Support On Site Subject Matter Expert (SME) for the R&D, Manufacturing and Supply Chain Applications.
+ Support On Site Subject Matter Expert (SME) with applications to ensure quality, compliance, and SLA/KPI adherence.
+ Work with other On Site Subject Matter Experts to interpret and gather requirements for IT Requests and Enhancements.
+ Work on projects where there is a need to bridge the gap between the site processes and needs to IT requirements and services to meet business requirements.
+ Investigate complex business problems in detail, to diagnose and provide effective and efficient alternatives.
+ Coordinate, Prototype, test, train, site personnel on applications and implement practical business solutions under multiple deadlines.
+ Participate and provide GxP validation support during FDA Computer Software Validation activities
**Qualifications**
+ 7+ years as a Business Analyst, Functional Consultant, or Systems Analyst in a manufacturing setting.
+ Bachelor's degree in industrial engineering, information systems, or similar discipline; or equivalent experience.
+ Hands-on expertise with JD Edwards EnterpriseOne Manufacturing & Supply Chain modules (E1 9.2 preferred).
+ Strong functional knowledge of Enovia/3DEXPERIENCE PLM, including BOM, change management (ECR/ECO), and CAD integrations.
+ Proven track record implementing or extending ERP-PLM integrations.
+ Deep understanding of discrete manufacturing workflows (MTS/MTO/ATO).
+ Ability to write functional specs, user stories, and test scripts; proficient with SQL for data validation.
+ Excellent facilitation, communication, and stakeholder-management skills.
+ Motivated to learn and ability to research and self-teach using online resources.
+ Experience in problem solving and process improvements.
**Preferred Qualifications 1**
Pay / Compensation
The expected pre-tax pay rate for this position is $94,600 - 127,600. Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge and location.
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.
Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one's identity. All our teammates' points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming.
**JOIN OUR TALENT COMMUNITY**
Joining our Talent Community is a great way to receive company news and updates, as well notifications on career opportunities and events that interest you! Please tell us more about yourself so we can align you with future opportunities that match your background, skills and interests.
**Job Locations** _US-CA-Irvine_
**ID** _ _
**Category** _Supply Chain_
**Position Type** _Regular Full-Time_
CORDIS is proud to be an equal opportunity employer, values diversity in all its forms is and committed to fostering an inclusive work environment. We are committed to advancing our culture of belonging, where all teammates feel seen, heard, and appreciated and encouraged to be their authentic selves. Our team is invested in attracting, retaining and growing top talent. Our Teammates are the core of our innovation and success. Cordis is an inclusive, engaging place to work and grow a career. CORDIS is committed to offering reasonable accommodations, upon request, to job applicants with disabilities. If you need assistance or an accommodation due to a disability, please contact

**Overview**
MedAlliance, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs. MedAlliance is headquartered in Switzerland, with offices in Germany, Singapore, UK and the United States (Irvine, CA).
If you love a challenge and are ready to have a direct, positive impact on the lives of millions, then this is the place for you. Join us, and let's improve the wellbeing of millions, together.
We are the people behind the people who keep saving lives.
This position is responsible for the production of high-quality medical devices mostly in a clean room environment. This position includes formulation of polymers and spray coating formulations, production of a medical device using microscope and operation of various equipment and machinery.
**Responsibilities**
Ensure activities comply with GMPs, set up coating machines, coat, inspect and fold balloon catheters, prepare excipient formulations and spray coating formulations, test formulation, package sterile and non-sterile finished good or semi-finished good, identify supplies that need to be replenished, build components needed for top level Work Orders, other duties as assigned. Complete cleaning activities as required.
+ Operating machinery to produce medical device to meet the specifications.
+ Following manufacturing instructions and update the relevant job documentations accurately for traceability.
+ Product packing and sterilization preparation.
+ Product inspection using microscope.
**Qualifications**
+ High School or equivalent education.
+ Preferable 12 months experience in a medical device or other regulated manufacturing industry.
+ Ability to read, comprehend, and follow written procedures. Understand and follow verbal instructions.
+ Fluent in English.
+ Ability to utilize Microsoft Excel and other computer software packages.
+ Ability to be able to communicate ideas, problems and solutions to manufacturing supervisor and management.
+ Ability to work in a team environment.
+ Ability to work overtime and/or weekends, according business need.
+ Light work. Requires walking, lifting a maximum of 10 to 15lbs., lifting above head, bending, twisting, pushing, stretching, squatting, pulling, reaching, standing, climbing, and carrying.
+ Position requires standing for an extended period of time.
+ Dexterity and physical condition to perform some level of repetitive motion tasks and maintain pace of a continuous production process.
+ Adequate eyesight to ensure effective inspection of product, labeling and packaging. (Use of corrective lenses are acceptable).
+ Physical coordination/flexibility to allow gowning for clean room environments.
+ Ability to work with chemicals to mix products and clean manufacturing areas.
Pay / Compensation
The expected pre-tax pay rate for this position is $21.00 - $24.00 per hour
Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge and location.
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.
Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one's identity. All our teammate's points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming.
**JOIN OUR TALENT COMMUNITY**
Joining our Talent Community is a great way to receive company news and updates, as well notifications on career opportunities and events that interest you! Please tell us more about yourself so we can align you with future opportunities that match your background, skills and interests.
**Job Locations** _US-CA-Irvine_
**ID** _ _
**Category** _Manufacturing_
**Position Type** _Regular Full-Time_
CORDIS is proud to be an equal opportunity employer, values diversity in all its forms is and committed to fostering an inclusive work environment. We are committed to advancing our culture of belonging, where all teammates feel seen, heard, and appreciated and encouraged to be their authentic selves. Our team is invested in attracting, retaining and growing top talent. Our Teammates are the core of our innovation and success. Cordis is an inclusive, engaging place to work and grow a career. CORDIS is committed to offering reasonable accommodations, upon request, to job applicants with disabilities. If you need assistance or an accommodation due to a disability, please contact