24 Manufacturing jobs in Santa Clarita

**Job Title: Process Technician**
**Job Description**
We are seeking a dedicated Injection Molding Technician to join our team. In this role, you will be responsible for setting up, starting, and maintaining injection molding machines to ensure the delivery of high-quality products on time. Additionally, you will troubleshoot issues, perform mold and color changes, and collaborate with other departments to maintain efficient operations. While this position does not involve supervisory duties, you will be a crucial member of the production team.
**Responsibilities**
+ Set up and start injection molding machines.
+ Perform basic maintenance and troubleshoot issues.
+ Change molds and colors as needed.
+ Ensure materials are stocked and machines meet safety, quality, and efficiency standards.
+ Collaborate with other teams to solve problems and improve processes.
+ Maintain a clean and organized work area.
+ Document machine settings and repairs.
**Essential Skills**
+ Mechanical skills and problem-solving ability.
+ Basic knowledge of injection molding.
+ Willingness to train others and act as a backup Mold Setter.
+ Completion of molding and safety training (Paulson, Forklift, LOTO).
+ Comfortable using computers and reading instructions.
+ Ability to work overtime and pass pre-employment screenings.
**Additional Skills & Qualifications**
+ High school diploma or GED preferred.
+ 1-2 years of injection molding experience.
+ Capability to stand for long periods and lift up to 50 pounds.
+ Experience in assembly, production, and use of hand and power tools in a manufacturing setting.
+ Familiarity with work orders.
**Work Environment**
The role is set in a production environment around machines. Employees are expected to maintain a professional demeanor and adhere to safety protocols at all times.
**Job Type & Location**
This is a Contract position based out of Santa Maria, California.
**Pay and Benefits**
The pay range for this position is $21.00 - $26.00/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 Santa Maria,CA.
**Application Deadline**
This position is anticipated to close on Oct 22, 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.

HELP US BRING THE GIFT OF HEALTH TO LIFE.

Working at Pharmavite is an experience like no other. With a focus on complete nutrition for all, each endeavor is urgent and every day counts. You'll have the opportunity to work on the #1 selling national vitamin and supplement brand, Nature Made, as well as an exciting portfolio of other products that are shaping the future of the healthy living industry. Consumer-driven innovation, high quality products and a promising portfolio, all driven by a team with a shared sense of purpose -- that's Pharmavite. Join us to bring the gift of health to life.

T his role is not available for sponsorship, including I-983 participation.

Position Summary:

The Manufacturing Data Manager is responsible for the development of the broader manufacturing data strategy, supporting and continuous improvement of the Manufacturing Execution System (MES) platform and other key data systems across manufacturing operations.

The focus of the role will ensure key manufacturing data is visible to stakeholders at all levels within manufacturing. This role works closely with the Pharmavite IT, manufacturing, quality, and external vendors to maintain and expand MES capabilities in alignment with business objectives.

In addition, this role is a key contributor in defining the MES strategic direction to allow visibility and integration of manufacturing data across the Pharmavite manufacturing network. This individual is passionate about creating information to produce data-driven results and the positive impact it can have within the Manufacturing organization. The individual needs to be entrepreneurial in spirit as well as be capable of translating data technologies into opportunities, providing a competitive advantage to Pharmavite. The role includes leading the definition of our manufacturing data technology strategy as well as the development of data collection and governance strategy, oversight of the configuration and customization of MES and other key data applications, ensuring solutions align with manufacturing requirements, seeding the future investment plans, and developing process information projects.

Critical Success Factors:

• Being passionate about production data collection and where it can provide business value through collection and visibility
• Has demonstrated subject matter expertise in 'process data collection and configuration' in a like/similar industry and has experience developing and delivering these projects with success.
• The individual keeps abreast of current data systems and automation, Internet of Things (IOT), Artificial/Augmented Intelligence (AI), Industry / Pharma 4.0 and other system driving value through data.
• Has demonstrated the ability to translate aspects of production processes into practical data collection solutions as well as the business value into investment planning and approval process.
• Ability to collaborate cross-functionally to define robust user requirements and functional specifications, providing fit-for-purpose information and/or automation solutions while maintaining the right balance between user requirements, solution platforms, and the capability of end users.
• Has an entrepreneurial mindset to investigate, influence, and proliferate the use of data systems within manufacturing to enable and drive continuous improvement.

Responsibilities:

The role of a Manufacturing Data Manager involves overseeing the implementation and management of MES platforms within a manufacturing environment. Key responsibilities include:

• Leads the development of the MES strategy & data roadmap.
• MES platform support & troubleshooting, software capability & configuration SME, testing, change management, collaboration on customization, upgrades & integration.
• Acting as the primary subject matter expert on the MES platform, offering insights and guidance to optimize its utilization.
• Guides the manufacturing community on how key manufacturing data can be developed into usable reports.
• Leads the 'MES and Manufacturing Data Center of Excellence' and leads the development of data governance processes to set standards across the manufacturing network.
• Engaging with plant personnel to gather requirements, identify challenges, and explore opportunities for system optimization, enhancement, and training.
• Creates comprehensive training materials and conducts training sessions to ensure effective use of the MES and other data systems.
• Managing the rollout of new features, coordinating efforts with corporate and plant teams to ensure seamless integration.
• Aligning user requests with organizational goals, prioritizing improvements, and feature enhancements accordingly.
• Monitoring system updates, promptly communicating changes and improvements to relevant stakeholders.
• Collaborating with technical teams to integrate and test new functionalities, ensuring a unified user experience across the system.
• Providing guidance and expert advice to corporate and plant management on leveraging system capabilities to drive process and productivity enhancements.
• Mentoring manufacturing managers and leaders in the adoption of new technologies to foster continuous development
• Works with production work centers to identify opportunities and develop rationales for business cases/investments
• Collaborates closely with Pharmavite IT, procurement, and operations to determine strategic partners in data automation and production equipment integration execution and support.
• Drive skills and capability in being able to support, configure data systems as required across the manufacturing network.
• Work with 3rd parties and Pharmavite IT, for systems customization and drive configuration capabilities internal to Manufacturing Operations
• Contributes to investment planning and master planning, ensuring system development investments are clearly represented in Pharmavite's short- and long-range investment plans.
• Working closely with Pharmavite IT, leads the development of standards within Pharmavite, including data governance and integrity along with system and hardware architecture. Influences equipment controls standards and data system asset deployment standards.
• Leads, advises, and trains others in the configuration, implementation, and analysis of information at multiple levels.

Education:

• Requires a Bachelor's degree, ideally in a chemical or process engineering or computer science-related major with a minimum of 5 years' experience or 10 years of equivalent experience in a manufacturing environment.

Certification:

• Lean certification is a plus.

Experience:

• Automation of both packaging and batch manufacturing equipment experience is desired in a similar industry.
• Programming experience with various control systems is a plus.
• Understanding the importance of critical process parameters and their value in controlling a robust manufacturing process is advantageous
• Has a working knowledge of Process Control systems (PCS), Building Management Systems (BMS), and Environmental Management Systems (EMS).
• Experience with TrakSYS from Parsec Automation is highly desirable.
• Experience in Kepware-based OPC server integration and programming is desired.
• Experience improving processes through integrated information systems and providing actionable data for decision making (OEE, SPC, etc.)
• Knowledge of SQL, HTML, JAVA, C#, CSS, and other programming languages is helpful.
• Understanding of Microsoft Power BI reporting and integration with shopfloor data collection systems required.
• Experience in integrating discrete controls system.
• Some understanding of Microsoft Fabric would be advantageous
• A basic understanding of AI systems and how they may provide benefits in a production environment is beneficial.

Knowledge/Skills/Abilities:

• Has the ability to lead the collaboration of peers spanning multiple sites, ensuring common ways of working and standards are maintained.
• Proven success in recognizing business needs and creating and implementing solutions.
• Has the capability to discern where the business value is in driving data collection & data visibility.
• Good financial acumen, understands and can articulate concepts like IRR, ROI, COGS, etc.
• Has an entrepreneurial mindset to be able to navigate obstacles required to drive change and level up the use of data technology within Pharmavite manufacturing.
• Ability to collect and assess data and translate data into robust business cases and form actionable solutions through to reporting utilized by the end user.
• Ability to apply technologies while maintaining the right balance of flexibility for end users.
• Ability to be able to coach on the successful delivery of data system projects
• Able to influence others without positional authority
• Ability to lead project teams as well as be a good team member on large projects
• Good project management skills
• Good communication/interpersonal skills.

Physical Requirements:

• General office environment, ability to sit for long periods of time. Ability to move about an office.

Environment:

• Exposure to disagreeable elements is moderate.

Safety:

• The incumbent must be able to perform this job safely in accordance with standard operating procedures and good manufacturing practices without endangering the health or safety of themselves or others.

Supervisory Responsibilities:

• The position currently has one direct report, but will need to be able to work and influence in a matrixed environment

Travel:

• Occasional travel to company facilities is required, estimated at approximately 15-20% of the time

OUR OFFER

Here, career paths aren't predefined, and bureaucratic limitations don't exist -- you have the opportunity to grow, learn from industry pioneers, and develop the way you want to. Pharmavite is investing more in the development of our team -- to help us deliver on our purpose and help you achieve your career aspirations. Our environment is geared to fuel curiosity, encourage experimentation, and generate learning as this is the way we develop ourselves and our organization.

Pharmavite is committed to meeting the needs of our employees and their families with a Total Rewards package that's as comprehensive as the vitamins and supplements we deliver to consumers. With competitive compensation programs and standout benefits, we provide employees with optimal health and well-being -- as well as peace of mind. These rewards -- plus our new recognition program -- ensure employees feel supported both at work and home.

National Target Base Pay Range: $112,000.00 - $90,000.00

The salary range for this position is based on national standards. For candidates in California and the New York metro, the Target Base Pay Range is 124,000.00 - 212,000.00, to reflect the cost of living and market conditions in those areas.

Actual compensation will take into account a wide range of factors that are unique to each candidate, including but not limited to geographic location, education, experience, qualifications and job-related skills. It is not typical for an individual to be hired above the midpoint of the range for their role, and compensation decisions depend on the facts and circumstances of each case. This information is provided to applicants in accordance with state and local laws.

Base pay is only one component of our total rewards offerings, and we will take the full offering into consideration when presenting an offer of employment. Our total rewards package for this position may also include an annual performance bonus, Medical, dental, and vision benefits, 401K match, and other wellness benefits.

Visit Pharmavite.com/careers to learn more about our mission and discover an opportunity that's right for you. Health and wellness begins with us.

Pharmavite is an equal opportunity employer. We prohibit employment discrimination and harassment based on race, color, religion, age, sex, sexual orientation, gender, national origin, and any other basis protected by state and federal law. Pharmavite recruits, hires, employs, trains, promotes, and compensates individuals solely based on job-related qualifications and abilities.

Pharmavite also provides reasonable accommodation to qualified individuals with disabilities or based on a sincerely held religious belief, in accordance with applicable laws. If you need to inquire about an accommodation to complete the application process, please email

Disclaimer

The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications of employees assigned to this job.

CALIFORNIA FAIR CHANCE ACT:

Qualified Applicants with arrest or conviction records will be considered for Employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

JOB ALERT FRAUD:

We have become aware of scams from individuals, organizations, and internet sites claiming to represent Pharmavite in recruitment activities in return for disclosing financial information.

Our hiring process does not include text-based conversations or interviews and never requires payment or fees from job applicants. All of our career opportunities are regularly published and updated on Pharmavite.com's Careers section.

If you have already provided your personal information, please report it to your local authorities. Any fraudulent activity should be reported to:

#WIM

Job Description: Manufacturing Engineering Technician

The Senior Manufacturing Engineering Technician provides manufacturing expertise while setting up and conducting complex product evaluation, creating process documentation, operations support, and small scale process development. Ensures high quality process development of Meggitt products/components.

Job Core Responsibilities

• Interpret drawings, procedures and process documents to support Operations with their procedures
• Support Manufacturing Engineering department in execution of development and product evaluation activities
• Provides significant expertise in the creation of product test plans, procedures and reports
• Designs and develops special test rigs and advises on methods of testing
• Performs process validation test programs to ensure products/systems meet design specs
• Acts as a resource for operations to explain drawing and process requirements
• Support equipment maintenance team with
• advanced diagnostics of our equipment
• Performs analysis and troubleshooting to determine root causes of failures of product and equipment
• Select and procure tooling and equipment using purchase requisitions and approval for expenditure process
• Consistent exercise of independent judgment and discretion in matters of significance
• Knowledge of welding and brazing development and qualification
• Regular, consistent and punctual attendance is required. May need to work nights and weekends, variable schedule(s) and additional hours as necessary

Job Specifications

Education : Combination of relevant education and work experience or degree in Engineering or equivalent that will allow successful performance of job expectations

Years Experience: 7+ years of relevant experience

Skills:

• Excellent test engineering knowledge to improve products by applying best practices and experience
• Ability to provide significant expertise on complex product/process issues and to act as a resource for colleagues
• Experience in a manufacturing environment with raw material processing, and assembly
• Effective interpersonal skills to drive tasks to completion
• Email, ERP, Word, Excel, PowerPoint experience
• Excellent communication skills, both written and verbal and ability to communicate difficult concepts and negotiate well with others

Plusses:

• AutoCad and Solidworks

#LI-BP1
#LI-Onsite
Seniority Level: Mid level
Salary: $80,000-$90,000
Job Function: Technician
Industry: Manufacturing
Employment Type: Contract
Location: Simi Valley, CA

For over 40 years, Charles River Cell Solutions has worked to making a positive impact on the world by providing the highest quality cellular material and services to biotech and pharmaceutical companies and research organizations that are performing innovative research and developing novel cell-based therapies.
We recognize that our success depends on the vision and passion of our employees; that is why we are devoted to making Cell Solutions a rewarding and valuable place to work. We believe in making a difference, and at Cell Solutions, you will make a difference every day.
**Job Summary**
The Manufacturing Associate I will be responsible for assisting in the manufacturing of GMP products, Research Use Only products, and products for further manufacturing in controlled and un-controlled environments, utilizing guidance documents and batch records for process documentation. This individual shall assist in supporting core manufacturing requirements of the facility, including readying consumables, supporting and maintaining the in/outflow of critical manufacturing components, and contributing to document authorship.
Essential Responsibilities
+ Participate in aseptic production of human primary cells within the cleanroom suite using accompanying documentation according to GMP guidelines. Verifies entered data by reviewing and sending for correction/reentry of data. Assist with preparing products for dispensing into bags and unit dose packaging.
+ Performs tasks to prepare documentation for sampling site, incubator ID, batch number, and microbiological identification outside of clean room. Performs per-batch personnel monitoring on each sterile staff member. Performs weekly and per-batch environmental monitoring in sterile area(s). Reads and records the results.
+ Labels blood products, including assigning labels and recording information
+ Prepares equipment by performing sterile cleaning-in-place (CIP), servicing-in-place (SIP), and cleaning out-of-place (COP). Performs daily cleanings, monthly cleanings, and checks off on weekly cleanings, as well as ensuring removal of expired APIs.
+ Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks. Maintain proper control of operations by following SOP's, Manufacturing Procedures, GMP's, ISO requirements, OSHA guidelines, and other pertinent regulatory requirements.
+ Complies with all state and federal laws, rules, and regulations governing the practice of manufacturing and blood banking, including HIPAA. Stops at-risk behavior of others and self.
+ Demonstrates thorough knowledge of the job, completing all annual competencies and skill validations, all initial and on-going validations, and advanced media-fill verifications, and continuously attains new knowledge. Prepare, perform, and report proficiency testing. Maintain the ability to a pass cleanroom gowning qualification and work within manufacturing cleanrooms as necessary.
+ Use of the cell counter to generate QC data for in-process cleanroom operations. Record, interpret, review and report test results. Ability to use and analyze data from the flow cytometer for in-process cleanroom operations. Ability to recognize and investigate unacceptable test results.
+ Ability to identify and aid in the investigation of deviations.
+ Generate reports, store completed work in designated locations, and perform backup operations. Resolves discrepancies by using standard procedures or returning incomplete documents for resolution. Ability to review and complete all the documents/results needed for all the GMP product batch records.
+ Tracks and maintains raw materials, gowning supplies, and other inventory for the maintenance of the cleanroom and other supportive areas. Responsible for inventory and ancillary supply restocking, expiration date checking, monitoring controlled environments, physical inventory, loading and unloading of various stock items.
+ Performs maintenance and cleaning of cGMP/clean room areas. Assist all contractors to assure that work is done properly, and safety guidelines are observed. Supervise cleanroom maintenance work in or outside the cleanroom.
+ In addition to the aforementioned tasks, perform/execute other duties as assigned
**Job Qualifications**
To perform this job successfully, an individual must be able to perform each essential responsibility satisfactorily using the skills and abilities outlined in this job description. The requirements listed below are representative of the knowledge, skills, and abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
+ Meets department quality standards.
+ Good time management skills: ability to complete assignments within established timelines.
Education, Experience, and Licensure
+ High school diploma or equivalent required. College credits or college degree preferred.
+ 1+ years of experience of clinical and/or pharmaceutical lab experience.
+ Experience working within a GMP environment preferred.
+ Proficient use of Microsoft Office products including Word, Excel, Outlook, and PowerPoint.
+ Ability to quickly learn new software programs as needed.
Compensation Data
The pay rate for this role is $22.84 - $25.53 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
**About Charles River Cell Solutions**
Charles River Cell Solutions is a global leader and trusted brand in the customization of human-derived biological products and services for biomedical research, drug discovery, and cell and gene therapy development. Cell Solution's vertically integrated solutions support preclinical research, clinical studies from phases 1 to 3, and commercialization with high-quality RUO and GMP-compliant starting material and apheresis collections.
In January 2020, HemaCare was acquired by Charles River Laboratories, an early-stage contract research organization (CRO). Combined with Charles River's integrated, early-stage portfolio of discovery, safety assessment, and manufacturing support services, the acquisition creates a unique, comprehensive solution for researchers and cell therapy developers and manufacturers worldwide to help accelerate their critical programs from basic research and proof-of-concept to regulatory approval and commercialization. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs and enhances their productivity and effectiveness to increase speed to market. We work closely with our clients throughout the clinical process to maximize success and drive positive clinical outcomes.
Together, with over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical and biotechnology companies, government agencies, and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
At Cell Solutions, we are passionate about our role in improving the quality of people's lives. We have proudly supported the development of 100% of the current commercially available FDA-approved immunocellular therapies. Our mission is to provide a best-in-class portfolio of high quality, customizable human cellular material and services to support drug discovery, scientific research, and cell therapy. This resonates from our employees and impacts our customers because we know that every day is an opportunity to advance discoveries and make a difference in someone's life.
We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
**Equal Employment Opportunity**
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit

**Manufacturing Associate - Biotech**
Science & Research
Simi Valley, CA, US
Pay Rate Low: 25 | Pay Rate High: 30
+ Added - 18/08/2025
Apply for Job
Our client is a global, research-driven biotechnology company focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for additional Manufacturing Associates to join their different departmental teams. This is an amazing opportunity to work on cutting edge treatments and make a difference!
Located in Simi Valley, CA
**Type:** Contract
**Pay:** $25-30/hr
**All shifts available**
**Responsibilities include:**
+ Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment
+ Preparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)
+ Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance
+ Performing and monitoring critical processes with the ability to perform basic troubleshooting
+ Performing in-process sampling of equipment and operating analytical equipment
+ Performing washroom activities: clean small and large scale equipment used in production activities
+ Maintaining an organized and clean workspace
+ Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work
+ Initiating quality reports- Drafting and revising documents (SOPs, MPs)
**Requirements:**
+ BS degree from an accredited institution in a relevant scientific discipline
+ Laboratory experience from previous employment/academic programs
"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
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.

**Dreaming big is in our DNA. It's who we are as a company. It's our culture. It's our heritage. And more than ever, it's our future. A future where we're always looking forward. Always serving up new ways to meet life's moments. A future where we keep dreaming bigger. We look for people with passion, talent, and curiosity, and provide them with the teammates, resources and opportunities to unleash their full potential. The power we create together - when we combine your strengths with ours - is unstoppable. Are you ready to join a team that dreams as big as you do?**
**SALARY:** $25 per hour + housing & travel stipends based on eligibility
**SHIFT:** Rotating shifts, including nights & weekends
**COMPANY:**
Michelob ULTRA. Cutwater Spirits. Budweiser. Kona Brewing Co. Stella Artois. Bud Light. That's right, over 100 of America's most loved brands, to be exact. But there's so much more to us than our top-notch portfolio of beers, seltzers, and more. We are powered by a 19,000-strong team that shares our passion to create a future with more cheers. We look for people with talent, curiosity, and commitment and provide the teammates, resources and opportunities to unleash their full potential. The power we create together - when we combine your strengths with ours - is unstoppable. Are you ready to join a team that dreams as big as you do?
**ROLE SUMMARY:**
Our University Programs are crafted to fast-track the careers of future leaders, allowing current students to gain exposure to a variety of roles and challenges in our Brewery and Manufacturing Operations. We believe in learning by doing. We value curious and ambitious people who are open and willing to embrace opportunities in different locations across our company.
If this sounds like you, then we encourage you to apply to our Supply (Brewery & Manufacturing Operations) Internship. In your internship, you will have the opportunity to have an in-depth exposure to our Brewery and/or Manufacturing Operations and obtain relevant experiences right from the start. The internship takes place over the course of 10-weeks; however, we are flexible to adjust as necessary based on the external environment and business need. Throughout the program, Supply Interns will gain an in-depth view of the manufacturing side of the business while experiencing either the corporate headquarters, the Supply (Brewery) or Can Plant Operations (MCC) organizations, as well as flexing creative and analytical muscles through project work.
Interns can be placed in various different areas of the Supply business; from working in our Brewing Department where they will have close ties to the process in which BEER is made, our Packaging Department to work with how the BEER is packaged in cans bottles or kegs, our Technical Operations group to work with teams on how the cans are made, or you may have the opportunity to work on our Corporate Team and help implement an initiative for process improvements across our Supply locations.
**JOB RESPONSIBILITIES:**
+ Bring your authentic self to work every day, lead with humility and drive top performance in a fast-paced industrial manufacturing environment.
+ As an intern you will be assigned project(s) that will result in process improvement and be responsible for reporting on deliverables to senior leaders of the company.
+ Use Lean Manufacturing techniques to accomplish tasks within project scope
+ Shift work may be required to understand the full scope of the project.
+ Train and gain a full understanding of the process your project focus will be on
+ Build relationships with operators and technicians in respective areas for aid in projects
+ Development opportunities to help boost skillset and build long-term leadership potential.
+ Upon successful completion of the intern, you will be given the opportunity to present your final project(s) and results to our members of the Supply leadership team.
**JOB QUALIFICATIONS:**
+ Current university student with a GPA of 3.0 or greater.
+ A background in Engineering or Science is preferred, but all majors are accepted.
+ Geographical & Functional mobility - open to experiencing different functions and locations across the U.S. for this internship.
+ Our breweries are 24/7 - 365 day a year facilities which requires alternating shift work. **Must have flexibility to work varying shifts including weekends, holidays, & overtime based on business need.**
+ Must have the ability to walk up and down elevated catwalks and stairs, stand for long periods of time, and work in all environmental conditions including extreme temperatures.
+ Ability to leverage data and insights to provide effective solutions to complex problems.
+ Can demonstrate leadership capabilities in previous work experience and/or extracurricular activities.
+ Self-motivated to drive results and deliver above and beyond expectations.
+ Ability to collaborate, be an active listener, seek diverse opinions and input from others, and foster an inclusive environment.
+ Embraces ambiguity and thrives in a fast-paced environment. Able to effectively manage several projects and teams at once, while being agile in the face of setbacks and change.
+ Questions the status quo, seeks opportunities to improve processes, not afraid of change and willing to take calculated risks.
+ As a general rule, the Company does not offer practical training positions for F-1 visa holders nor sponsor individuals for purposes of obtaining temporary work visas (e.g., H-1B) or permanent residency ("Green Cards"). Individuals who require sponsorship will be removed from the selection process.
**WHY ANHEUSER-BUSCH:**
At Anheuser-Busch, our purpose is to create a future with more cheers. For more than 165 years, we have delivered a legacy of brewing great-tasting, high-quality beers that have satisfied beer drinkers for generations. 99 percent of the products we sell in the U.S are made in the U.S. with more than $00 million in high-quality ingredients sourced from American farmers and more than 7 billion in goods and services purchased from U.S. suppliers, and we have invested nearly 2 billion in our 100 facilities across the country over the past five years. Through these investments, and as a leading American manufacturer and the nation's top brewer, we drive economic prosperity nationwide through investments in our people, facilities, and communities. We are the only brewer that invests in the U.S. at this scale.
**WHY ANHEUSER-BUSCH:**
Anheuser-Busch is here for the times that matter. The moments where we celebrate, defy challenges, dream of the brighter future we are building today- and all the moments in between. We are a company that brings people together for richer conversations, sweeter celebrations and stronger communities.
As the leading global brewer, Anheuser-Busch InBev is committed to finding innovative ways to continually improve. It's this kind of thinking that creates a unique work environment by rewarding talent and encouraging forward thinking. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status or any other characteristic protected by applicable law.
**REQUIRE ADDITIONAL ASSISTANCE?**
Anheuser-Busch is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you are a qualified individual with a disability, or a disabled veteran, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access the Anheuser-Busch Careers website as a result of your disability. We will make a determination on your request for reasonable accommodation on a case-by-case basis.
If you need an accommodation or assistance in using the Anheuser-Busch Careers website, please email .
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Job DescriptionJob Description

JSG is hiring a Calibration Technician - Aerospace for 1st shift in Simi Valley, CA.

Pay rate: $30+ DOE 

Job Duties:

• Coordinate and oversee onsite vendor calibration activities, ensuring all calibrations are completed to schedule.
• Identify and manage equipment requiring off-site evaluation, ensuring timely shipment, follow-up and return.
• Review and approve calibration certificates for accuracy, compliance, and traceability to NIST, NADCAP standards.
• Ensure calibration compliance with relevant quality standards, including AS9100, ISO 9001, and customer-specific requirements.
• Participate in internal and external audits, providing documentation for traceability.
• Complete Defective Gage Reports and coordinate repair/replacement of defective gages
• Review calibration recertification for release
• Managing and scheduling onsite calibration services
• Create and manage purchase orders for calibration services and equipment through internal procurement systems
• Assist in sourcing and evaluating suppliers for metrology and calibration equipment based on quality, delivery times, costs, and reliability.
• Maintain a current inventory and calibration schedule using a calibration tracking systems. Indysoft background is a plus
• “Restrictions imposed by federal export control laws may limit this job opportunity to candidates who are a 
• A high school diploma, or equivalent, is required; Associate’s degree in Metrology, Engineering Technology, or related field .
• 5+ years of Quality Experience in the Aerospace or Automotive industry with a focus on conventional machining and assembly operations.
• CMM Proficiency: Operate and program Coordinate Measuring Machines (CMMs) to inspect, validate, and measure master gages. experience with software like Zeiss Calypso or equivalent tools.
• Background in gauge classification for procurement

Company DescriptionOur people and culture make JSG a great place to work. JSG’s mission is to empower people, help our clients reach their goals, and hire motivated individuals.

Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with 40 years of experience investing in people and companies. We are always looking for great people to join our team—we want to see your success here at JSG! We can be found locally in more than 30 offices throughout the United States and Canada. JSG continues to work diligently to offer our clients and candidates world-class service and diversified offerings to fit their evolving needs.

We offer medical, dental, vision, life insurance options, 401(k), weekly pay, and more.

Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to , , , sex, , , , , , marital status, protected veteran status, or any other characteristic protected by law.Company DescriptionOur people and culture make JSG a great place to work. JSG’s mission is to empower people, help our clients reach their goals, and hire motivated individuals.

Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with 40 years of experience investing in people and companies. We are always looking for great people to join our team—we want to see your success here at JSG! We can be found locally in more than 30 offices throughout the United States and Canada. JSG continues to work diligently to offer our clients and candidates world-class service and diversified offerings to fit their evolving needs.

We offer medical, dental, vision, life insurance options, 401(k), weekly pay, and more.

Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to , , , sex, , , , , , marital status, protected veteran status, or any other characteristic protected by law.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

The Opportunity

This position works out of our Sylmar, CA or Waukegan, IL locations within the Business Solutions & Service IT Organization.

As the Application Technol

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:

• Career development with an international company where you can grow the career you dream of.

• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

• An excellent retirement savings plan with a high employer contribution

• Tuition reimbursement, the Freedom 2 Save ( student debt program, and FreeU ( education benefit - an affordable and convenient path to getting a bachelor's degree.

• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

The Opportunity

This position works out of our Sylmar, CA or Waukegan, IL locations within the Business Solutions & Service IT Organization.

As the Application Technology Lead (Manufacturing) you'll have the chance to implement and build a technology focused team within our TS3 Manufacturing IT Organization. The role will focus on Manufacturing Execution System BASIS and Platform technologies delivery and support. You will work with our business customers to ensure key technologies are delivering required value to the organization.

What You'll Work On

• Build and maintain multiple DEV, QA and prod environments for a J2EE application (FTPC -MES by Rockwell Automation) running on JBOSS and tomcat. Maintain the same code base across all environments with documented or automated deployment processes.

• Deploy and maintain various application components on JBOSS, IIS and tomcat technologies. Monitor and maintain these technologies at optimal performance levels and manages SLAs for the functionality.

• Maintain and manage various application related services like data transfer and data purge at optimal levels.

• Collaborate and partner with infrastructure teams (network, Oracle, Windows /Linux) to deliver and deploy MES and other manufacturing systems.

• Responsible for creating and maintaining a DR (Disaster Recovery) plan for MES and related systems. Lead yearly testing plans for DR set-up by collaborating with infra and business teams.

• Partner with the functional groups within the IT organization to communicate and clarify business needs, contribute to development of long-range system /platform plans, and ensure products and services are aligned with business needs.

• Maintain server infrastructure compliant to Cyber security standards. Manage folder and user permission standards for access to various file types. Define plans and paths to remediate if not compliant.

• Manage semi-annual code pushes for enhancements to all QA and prod environments and manage related documentation in a validated environment

• Create and maintain robust and validated processes for making changes / incidents to core MES components (Linux /Windows/JBOSS) and application related changes. Create and manage proper documentation for DWI (departmental work instructions) and SOPs and processes should be followed by him and the team.

• Responsible for high system up-time of MES system and other related manufacturing system integrations with SAP, Windchill etc. Provide leadership on outage calls and work with infra team to restore application functionality quickly and seamlessly.

• Set-up monitoring for system uptime on application servers and web servers and application components like JBOSS, tomcat by using dashboards and scripting and reduce critical line down incidents.

• Ability to triage performance issues on JBOSS, Linux and other systems by partnering with infra groups like Linux, network, Citrix and windows teams.

• Collaborate with operations and technology leaders on system upgrades and enhancements.

• Create a compelling roadmap for system upgrades of the MES system and making sure it is well documented and complete within the guidelines of SLC and within timelines.

• Create and manage projects for system upgrades and system set-up by collaborating various stake holders.

• Support Design and Development of enhancements to Rockwell FTPC platform including reports

• Responsible for aligning technology solutions with business strategies, working principally with senior management.

• Acts as the principal designer for major systems and their subsystems utilizing a thorough understanding of available technology, tools and existing designs.

• Integrate manufacturing systems with other applications and shop floor equipment

• ITIL process understanding and deploy implement IT changes to manufacturing systems

• Work with pnuts and java code to program business rules and enhancements

• Level 3 support for Manufacturing Execution Systems

Required Qualifications

• B.S. in Computer Science or similar engineering discipline

• 8+ years' experience in developing (Java, Pnuts) and deploying solutions

• 8+ years' experience with developing manufacturing solutions in FTPC preferred

• 5+ years' experience with writing complex queries in SQL

• 3+ years' experience in managing production systems

• Bachelor's degree in engineering or computer science (preferred)

• Detailed understand of Cloud architecture, and infrastructure tools that support these technologies.

• 5+ years' experience deploying applications and code with various application technologies like JBOSS, WebLogic, WebSphere, tomcat and IIS.

• 3+ years creating shell scripts to automate deploying code and monitoring applications or using tools like Splunk for log management.

• Create, manage and monitor various environments like dev, QA and production from an application landscape and responsible for uptime SLAs.

• 9+ Years experience in IT application management or devops role and setting up related processes.

• Experience with IQ/OQ/PQ, authoring validation documents and execution mostly for code deployment.

• Manage a team of 3-5 direct/indirect reports.

• 15% Travel Required.

Preferred Qualifications

• Maintain and managing applications in Life Sciences industry with all related regulations and documentation

• Strong understanding of java and J2EE frameworks from an application standpoint

• Understanding and administration of middle-ware technologies like TIBCO, BIZTALK or JMS messaging services

• Developing reports/dashboards in PowerBI leveraging fabric.

• Understanding of MES and manufacturing preferably FTPC from Rockwell automation or Camstar.

• ITIL process in high regulated environments

• Familiarity with large scale ERP/MES Systems deployments

• Vendor management experience

• PMP certification will be nice to have

• Experience with global scale manufacturing systems (i.e. Rockwell) development, integration, and support.

• Excellent verbal and written communication skills

MISC:

• This is an onsite role; this is NOT a remote role/opportunity.

Apply Now (

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: (

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at , on Facebook at , and on Twitter @AbbottNews.

ogy Lead (Manufacturing) you'll have the chance to implement and build a technology focused team within our TS3 Manufacturing IT Organization . The role will focus on Manufacturing Execution System BASIS and Platform technologies delivery and support. You will work with our business customers to ensure key technologies are delivering required value to the organization.

What You'll Work On

• Build and maintain multiple DEV, QA and prod environments for a J2EE application (FTPC -MES by Rockwell Automation) running on JBOSS and tomcat. Maintain the same code base across all environments with documented or automated deployment processes.

• Deploy and maintain various application components on JBOSS, IIS and tomcat technologies. Monitor and maintain these technologies at optimal performance levels and manages SLAs for the functionality.

• Maintain and manage various application related services like data transfer and data purge at optimal levels.

• Collaborate and partner with infrastructure teams (network, Oracle, Windows /Linux) to deliver and deploy MES and other manufacturing systems.

• Responsible for creating and maintaining a DR (Disaster Recovery) plan for MES and related systems. Lead yearly testing plans for DR set-up by collaborating with infra and business teams.

• Partner with the functional groups within the IT organization to communicate and clarify business needs, contribute to development of long-range system /platform plans, and ensure products and services are aligned with business needs.

• Maintain server infrastructure compliant to Cyber security standards. Manage folder and user permission standards for access to various file types. Define plans and paths to remediate if not compliant.

• Manage semi-annual code pushes for enhancements to all QA and prod environments and manage related documentation in a validated environment

• Create and maintain robust and validated processes for making changes / incidents to core MES components (Linux /Windows/JBOSS) and application related changes. Create and manage proper documentation for DWI (departmental work instructions) and SOPs and processes should be followed by him and the team.

• Responsible for high system up-time of MES system and other related manufacturing system integrations with SAP, Windchill etc. Provide leadership on outage calls and work with infra team to restore application functionality quickly and seamlessly.

• Set-up monitoring for system uptime on application servers and web servers and application components like JBOSS , tomcat by using dashboards and scripting and reduce critical line down incidents.

• Ability to triage performance issues on JBOSS, Linux and other systems by partnering with infra groups like Linux, network, Citrix and windows teams.

• Collaborate with operations and technology leaders on system upgrades and enhancements.

• Create a compelling roadmap for system upgrades of the MES system and making sure it is well documented and complete within the guidelines of SLC and within timelines.

• Create and manage projects for system upgrades and system set-up by collaborating various stake holders.

• Support Design and Development of enhancements to Rockwell FTPC platform including reports

• Responsible for aligning technology solutions with business strategies, working principally with senior management.

• Acts as the principal designer for major systems and their subsystems utilizing a thorough understanding of available technology, tools and existing designs.

• Integrate manufacturing systems with other applications and shop floor equipment

• ITIL process understanding and deploy implement IT changes to manufacturing systems

• Work with pnuts and java code to program business rules and enhancements

• Level 3 support for Manufacturing Execution Systems

Required Qualifications

• B.S. in Computer Science or similar engineering discipline

• Understanding of java and J2EE frameworks from an application standpoint

• 8+ years experience in developing (Java , Pnuts) and deploying solutions

• 8+ years experience with developing manufacturing solutions in FTPC preferred or Camstar

• 5+ years experience with writing complex queries in SQL

• 3+ years experience in managing production systems

• Bachelor's degree in Engineering or Computer Science (preferred)

• Detailed understand of Cloud architecture, and infrastructure tools that support these technologies.

• 5+ years' experience deploying applications and code with various application technologies like JBOSS, WebLogic, WebSphere , tomcat and IIS.

• 3+ years creating shell scripts to automate deploying code and monitoring applications or using tools like Splunk for log management.

• Create, manage and monitor various environments like dev, QA and production from an application landscape and responsible for uptime SLAs.

• 9+ Years experience in IT application management or devops role and setting up related processes.

• Experience with IQ/OQ/PQ, authoring validation documents and execution mostly for code deployment.

• 15% Travel Required.

Preferred Qualifications

• Maintain and managing applications in Life Sciences industry with all related regulations and documentation

• Understanding and administration of middle-ware technologies like TIBCO, BIZTALK or JMS messaging services

• Understanding of MES and manufacturing preferably FTPC from Rockwell automation

• ITIL process in high regulated environments

• Familiarity with large scale ERP/MES Systems deployments

• Vendor management experience

• PMP certification will be nice to have

• Experience with global scale manufacturing systems (i.e. Rockwell) development, integration, and support.

• Excellent verbal and written communication skills

The base pay for this position is $128,000.00 - $256,000.00. In specific locations, the pay range may vary from the range posted.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call or email

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials
**Job Description**
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
**Discover Impactful Work:**
The Senior Manager Manufacturing Engineering will lead strategy and performance of off-the-shelf equipment and custom automation in diagnostic/medical device operations.
**A day in the Life:**
Automation Strategy & Leadership
+ Develop and implement a world-class automation roadmap for diagnostic product manufacturing.
+ Provide technical leadership for the selection and integration of physical automation platforms (e.g., robotic liquid handling systems, industrial filling and packaging, robotic packaging, SCADA).
+ Champion standardization, modularity, and scalability of automation solutions.
+ Lead, train, and mentor the team through Practical Process Improvement (PPI).
+ Identify areas for improvement and cost savings through equipment lifecycle management.
**Project Execution**
+ Coordinate end-to-end automation projects-from concept, justification, timelines, budgets, prioritisation, URS generation, vendor selection, design/build, FAT/SAT, installation, CQV (commissioning, qualification, and validation).
+ Drive improvements in efficiency, repeatability, and data integrity through automation upgrades or new installations.
**Team Management**
+ Lead, mentor, and develop a multidisciplinary team of automation and process engineers, technicians, and system integrators.
+ Define performance objectives, training needs, and career development plans for the team.
**Compliance & Risk Management**
+ Ensure the team, process, and systems align with applicable regulations (FDA, 21 CFR Part 820, Part 11, ISO 13485, IVDR, ISO 17025).
+ Own or support equipment/software validation protocols and risk assessments (e.g., FMEA).
+ Support internal and external audits (e.g., FDA, Notified Bodies).
**Multi-Functional Collaboration**
+ Partner with R&D and Manufacturing Sciences to enable design-for-automation in new product development.
+ Collaborate with QA, IT, and CSV teams to ensure systems are qualified, maintained, and detailed appropriately.
+ Support tech transfer and scale-up activities by integrating automation into new or existing production lines.
+ Manage cross-functional projects from initiation to completion.
**Keys to Success:**
**Education**
+ Bachelor's or master's in engineering (e.g., Electrical, Mechanical, Automation, or equivalent).
**Experience**
+ 8+ years of experience in automation engineering, with 5+ years in people management roles.
**Knowledge, Skills, Abilities**
+ Demonstrated experience with automation in diagnostics, medical devices, or life sciences manufacturing.
+ Project management experience a plus.
+ Process Engineering experience a plus.
+ Six Sigma experience a plus.
**Benefits**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
**Compensation and Benefits**
The salary range estimated for this position based in California is $143,000.00-$214,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
+ A choice of national medical and dental plans, and a national vision plan, including health incentive programs
+ Employee assistance and family support programs, including commuter benefits and tuition reimbursement
+ At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
+ Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
+ Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.