25 Manufacturing Technicians jobs in Oceanside

Quality Control Manager- Camp Pendleton

Competitive Salary and EMPLOYER PAID INSURANCE!

EMI Services is hiring a Quality Control Manager (QCM) to work directly with the project manager, the operations manager, the safety supervisor, as well as the United States Government. This position assures quality services to customers: reports performance levels and degrees of compliance with an established QC program. The QCM is required to test and inspect services and work performed for compliance with contract requirements and performance standards. Evaluate data and write reports to validate or indicate deviations. Recommend modifications or necessary actions to achieve optimum quality. Monitor building conditions for possible QC issues or violations, in conjunction with the Safety Supervisor. Also, monitor work assignments and projects for safety or health issues. In addition, the QCM produces and analyzes reports and makes recommendations for quality improvements, as well as, investigates complaints and report's findings to the project manager. The ideal EMI Quality Control Manager promotes quality and customer services excellence.

Salary

Starting at $100,000 (DOE) plus employer paid insurance!

Key Responsibilities

* Work closely with Project Manager, FSM, SSHO, subcontractors and QCI Staff
* ALL aspects Quality Control Inspection and documentation of Service and Maintenance work
* Develop and maintain quality surveillance and tracking system for maintenance shops and subcontractors
* Develop and implement QC plan, ensuring environmental plan compliance, performance monitoring, analysis and reporting
* Advise the Project Manager on quality control and environmental program status, strategies, issues and potential problem areas
* Monitor and track specialized qualifications or credentials such as licenses, certificates, degrees or training needed by personnel
* Enforce all regulatory, base and company specific safety rules
* Manage Quality Control Inspectors
* Lead monthly QCM with Government
* Execute additional duties and responsibilities as assigned and/or required to complete the project

Essential Skills

* Effective oral and written communication skills
* Strong organizational, interpersonal skills
* Type; operate a personal computer, with emphasis on accuracy, mental alertness, and neatness
* Demonstrated ability to work accurately, follow procedures and schedules, and prioritize multiple tasks
* Ability to read and understand blueprints, specifications, and contract requirements
* Proficiency with all MS Office products (Word, Excel, Access, PowerPoint)
* Ability to work successfully in a team environment, aligning with company culture and processes
* Must possess a strong work ethic and values that are above-reproach
* Understand and adhere to policies and procedures as set by EMI Services
* Promote and maintain a positive image of EMI Services
* Maintain confidentiality of information related to EMI Services, our customers, vendors and employees
* Be adaptable and flexible in work situations. Establish priorities to ensure completion of tasks in a timely manner
* Inform the Project Manager of all pertinent problems, irregularities, and other important information within area of responsibility
* Adhere to safety policies and procedures to include proper use of personal protective equipment

About Us

When you work at Chugach Government Solutions (CGS), you join a proud legacy of supporting missions while sustaining culture.

The federal division of Chugach Alaska Corporation, CGS has been supporting critical missions as a government contractor for over 25 years. Our focus is to support facility maintenance, IT/technical services, construction and education. We are proud to have built, and continue to foster, an incredibly talented team spanning across the globe in hundreds of different fields - each team member proud to serve our country with first-class business services, while also making a difference for our Chugach shareholders.

At CGS, empowering employees is a part of our core, and that focus is one of the ways we build and foster high-performing teams. We empower our employees through competitive compensation and benefits package, professional growth opportunities, truthful communication, and more!

If you are looking for an opportunity to serve something bigger than yourself; if you want your day job to be one that creates meaningful value; if you are looking for an environment that highly values employees and respects individual differences - then Chugach Government Solutions may be the right fit for you!

Job Overview

Responsible for the overall management of the task order's Quality Control program. Conduct inspections of the entire Task Order functions to ensure compliance with the Statement of Work (SOW), QC, published schedules, and task order requirements, including work in progress, finished work and complete inspection reports/documentation to support findings. Will perform routine and ongoing safety training to staff. Evaluates staff and ensures that all CCS personnel are trained in maintenance activities and are following standard operating procedures. Interacts professionally with contractors, vendors and corporate staff members, maintains effective working relationships in cooperation with the CCS management team to meet the mission objectives. Keeps Project Manager appraised of unique situations and problems encountered. Responsible for compliance issues as they apply to the functional operation of the task order. Implement and maintain the Quality Control (QC) Plan tailored to the specifics of the task order encompassing all facets of the operation.

Salary Range: 90K - 110K

Work Model: Onsite/In-Office

Responsibilities

Essential Duties & Job Functions:

* Develop plans and procedures for QC programs.
* Review all site work to verify compliance in accordance with applicable plans and procedures.
* Responsible for the performance of subcontractors with respect to QC.
* Ensure records are maintained of all Permits/Licenses/Certifications and ensure operator certifications are current to operate respective equipment/machinery.
* Serve as a technical advisor for the Task Order Manager.
* As directed, performs a variety of procurement duties requiring an understanding of the government supply system, programs, policies, work methods, or other established guidelines.
* Assists in developing cost estimates, budgets, correspondence and status reports.
* Review all site work to verify compliance in accordance with applicable safety plans and procedures.
* Plan and organize work to meet schedules and timelines in an environment with constantly changing priorities.
* Performs other duties as assigned by the Project Manager or Safety Manager.
* Formulate and announce QC operating policies.
* Represent the Task Order Manager when authorized.
* Adherence to contract requirements and CCS policies.

Accountable For:

* Using progressive work and educational experience to increase knowledge and improve expertise.
* Completing all mandated training requirements per government and management directives.
* Adherence to established company safety policies and good industrial and office safety practices.
* Timely and cost-effective performance of duties.
* Harmoniously working with other employees and customers.
* Working with the Project Principals to fully coordinate all activities.
* Knowledge of Chugach policies and procedures as set out in Chugach Alaska Corporation Employee Handbook.
* Must have experience and working knowledge of ISO 9001:2015.
* Diversified knowledge of quality assurance principles and practices predominantly, but not exclusively, to the Marine Industry.
* Working knowledge of welding, corrosion control, engine repair, carpentry, painting, hydraulics, and general marine repair activities.
* Ability to perform well in high pressure situations.
* Solid problem solving, decision making and judgement.
* Exceptional written and oral communication skills.

Job Requirements

Mandatory:

* Must have completed at least three (3) years' Quality Management experience.
* Must have completed OSHA 30-Hour construction safety class or equivalent within the last three years
* Knowledge of OSHA and EM 385 standards for a variety of craft and labor activities.
* Understanding of Government contracts, correspondence, reports and records.
* Valid state driver's license with acceptable driving record (must provide current driving record).
* Mature judgment and ability to work with little or no supervision.
* Knowledge of equipment maintenance.
* Working knowledge in Microsoft programs, including but not limited to: Word, Power Point, Excel and Access or equivalent software program.
* Excellent communication skills, both oral and written.
* Excellent organizational skills.

Preferred:

* Professional CQM/OE certification in Quality Control.
* 5 years of Quality Management experience involving pool/training tanks, preparing and enforcing QMS programs on contracts of pools/training tanks scope and complexity.
* Maximo database experience.

Additional Eligibility Qualifications:

* Travel by plane, helicopter and/or boat to conduct work activities on an outer island as may be required.
* Ability to successfully pass any background checks, pre-employment physical requirements and drug testing required by the contract.
* This position is unaccompanied; and a Bachelor's Quarter (BQ) will be provided.
* Must be able to relocate to the United States Army Kwajalein Atoll, Marshall Islands.
* Must be able to obtain and maintain a U.S. passport.
* Must be able to obtain and maintain a DoD security clearance, which includes U.S. Citizenship or U.S. naturalization.
* Valid U.S. Driver's License required.

Working Conditions:

* Work includes both indoor and outside work. Outdoor work is subject to temperatures ranging between 80 - 95 degrees and inclement weather conditions.
* Employee use of personal protective equipment (PPE) is required for some situations. PPE includes, but is not limited to, head, foot, torso, respiratory, vision, and hearing protective devices.
* Subject to hazards that may cause personal bodily harm (diseases, cuts, bruises, dust odors and elevated noise levels).
* Work hours are subject to change, and the flexibility to work occasional non-duty hours or on weekends to support specific project or other requirements is essential.

Physical Requirements:

* Work requires moving objects up to 50 pounds, standing, walking, bending, climbing stairs and ladders, and stretching with a good range of motion.
* Work may require heavy lifting, stooping, climbing, prolonged standing, prolonged sitting, and working with or in areas where a potential could exist for exposure to physical, chemical, or biological agents.

Proof of COVID-19 VACCINATION:

* In order to qualify for this position, you must be fully vaccinated prior to the start of your assignment and show proof of your vaccination status, unless you are legally entitled to an accommodation (religious or medical).
* The definition of fully vaccinated is that you have:



1.) Received a vaccine that is recognized by the governing entity and is either a.) Two doses of Pfizer BioNTech Vaccine b.) Two doses of AstraZeneca/Oxford Vaccine c.) Two doses of Moderna Vaccine (or) d. One dose of Johnson & Johnson Vaccine.

2.) Two weeks elapsed after the final dose was administered, which is either one or two doses depending on brand of the vaccination.

Reasonable Accommodation:

CGS will provide reasonable accommodations, according to applicable state and federal laws, to all qualified individuals with physical or mental disabilities. In compliance with the ADA Amendments Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a position with Chugach Government Solutions or any of its subsidiaries, please email

Equal Employment Opportunity:

Chugach is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, gender, sexual orientation, gender identity or expression, age, pregnancy, disability, genetic factors, protected veteran status or other characteristics protected by law.

Job Description

Job Description

SUMMARY Overview of the position

Responsible for reviewing digital files, proofs, and overlays to ensure content is built to required specifications and precise to established internal expectations, documented tolerances, print industry standards, procedures and/or published direction. Evaluate and review cards, provide direction for print accuracy or improvement. Quality Control is an extension of Prepress Production and works closely with a variety of internal departments to ensure quality and fiscal responsibility.

ESSENTIAL DUTIES AND RESPONSIBILITIES The following statements are intended to describe the general nature of the level of work being performed by an individual assigned to this job. Other duties may be assigned.

• Review print design engineering, product content, printability and make recommendations to ensure quality standards are attained.
• Assessed delivered information and implementation of direction received from designated Lead, Project Manager(s), Marketing, Legal, Design, Sports & Entertainment, Operations and written documentation from mechanicals, briefs, and costing documentation.
• Ensure the highest possible quality of files produced within lithographic pre-production environment. Quality Control Technician(s) will maintain a global view of these production procedures and make on-going recommendations to ensure tolerances are maintained and quality product files produced.
• Effective communication skills required demonstrate close mindfulness with organized practices. Responsible for interacting daily with Digital Operations Team Lead, Project Manager(s), Prepress Production personnel and Designers.’
• Support and adhere to internal Creative Departmental procedures and requirements to include but not limited to, assisting Prepress Production during production heavy cycles.
• Proficiency in the following software or systems: Adobe Creative Suite, MS Office, and Excel.
• Hands-on, energetic and motivated self-starter with the ability to work additional hours as required.

INTERACTION

This position will interact closely with the Director of Creative, Digital Operations Production Manager, Project Managers, Prepress Production, Designers, and other internal personnel.

EDUCATION/YEARS EXPERIENCE

• High School Diploma or equivalent. College Degree with an emphasis in Graphic Arts a plus.
• 1-2 years of experience in Prepress or related area, publishing, or relevant duties.
• Knowledge of Kodak Prinergy is a plus.

REQUIREMENTS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

KNOWLEDGE, SKILLS AND ABILITIES

• Present understanding of Prepress and Print Industries’ standards, competent knowledge of established production tolerances. Familiarity with the 4/c process, to include, but not limited to: spot colors, varnish, foil, die cuts, deboss and/or embossing. Imposition software skills with a basic understanding of file standards for print production (bleed, trapping, color separation, resolution, etc.).
• Minimally an intermediate knowledge of Mac and applied software with verified results, fundamental knowledge of ripping and trapping of digital files through a Prinergy Workflow. The qualified applicant must possess acceptable computer skills; a working knowledge of Adobe Creative Suite is a plus. Additionally, basic to intermediate proficiency in the following software: Microsoft Word, Excel, and Outlook.
• Strong oral and written communication skills demonstrate close mindfulness with organized practices. Ability to articulate clearly with internal partners and not be afraid to ask questions.
• Effective organizational skills with the ability to manage multiple, high priority projects with dedicated attention to detail.
• Demonstrated ability to read, comprehend written instructions and follow pre-established guidelines.
• Utilize technology and maximize efficiency: Maintain education and ability of innovative techniques, technologies, and software capabilities. On an on-going basis, ensure we are maximizing our technology resources and making recommendations for improvements.
• Excellent interpersonal, problem solving and troubleshooting skills.
• Professional demeanor; collaborator orientation.
• Ability to perform duties under minimal supervision while exercising reasonable discretion and independent judgment.
• Manage time effectively, prioritizing duties and meeting deadlines. Ability to maintain flexible work hours. Work hours are mostly consistent, but production requirements require flexibility.
• Knowledge of the following areas would be desirable: NHL, Football and Basketball, and/or historical knowledge of pop culture, including comics and films spanning a multitude of trends.
• Hands-on, energetic and motivated self-starter

Job Description

Job Description

Since 1996, RQC, LLC. has been a leading player in Southern California's robust commercial and governmental Design-Build economy. Headquartered in beautiful Carlsbad, CA, we are a full-service Design-Build company. We offer management of projects throughout the United States, with our field operations' team members who work on location for each of our projects. We specialize in fast-track projects in new commercial construction for both public and private clients, with a primary focus in the Department of Defense market.

We are looking for Construction Quality Control Manager candidates to join our West Coast Field Operations team for military/federal projects located in San Diego County. Headquarter/Office assignment will be in Carlsbad, but specific construction project could be anywhere in San Diego County.

QC Manager's are responsible for planning, coordinating, and implementing a project-specific quality control program, executing its performance according to contract requirements, completing administrative documentation on time, and cultivating customer satisfaction with the client, all in alignment with RQ's Mission, Vision, and Values. Local candidates will be given preference depending on location of project, though relocation or travel to on-site management will be required for the QC Manager position. The QC Manager position must work on-site.

Pay: $100,000-$145,000 annually (depends on experience)

Fringe Benefits: Vehicle Allowance, Medical/Dental/Vision Benefits (UnitedHealthcare), Vacation/Sick/Holiday Pay, Bonus eligibility

Ideal Candidates will have the following experience:

• A graduate of a four year accredited college or university program within the discipline of Engineering, Architecture, Construction Management, Building Construction, or Building Science. A combination of equivalent work experience and training in the field may be qualifying.
• A minimum 5 to 10 years' experience as a Project Manager, Superintendent, QC Manager, Project Engineer, or Construction Manager with at least two years of continuous experience as a QC Manager required.
• A current USACE CQM for Contractors Certificate (or equivalent) is required.
• Specialty inspection training and licenses/certs highly desired.
• LEED AP, AP+ or Green Associate (GA) Certificate preferred.
• Level 1 EM 385-1-1, CRP, First Aid, OSHA 30-hour certifications required. Training can be provided.
• Computer literacy (Microsoft Office, Outlook, Internet, etc.) required.
• Specific software literacy (Viewpoint/Vista) preferred.

COMPANY PROFILE: RQC, LLC is a full service contracting and design firm that specializes in Design/Build projects for both public and private clients, with a primary focus on the Department of Defense. Our mission is "to provide our customers the best built environment while being the first choice of all stakeholders."

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, creed, gender (including gender identity and gender expression), religion (all aspects of religious beliefs, observance or practice, including religious dress or grooming practices) marital status, registered domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition (including cancer or a record or history of cancer, and genetic characteristics), sex (including pregnancy, childbirth, breastfeeding or related medical condition), genetic information, sexual orientation, veteran status, or any other basis or status protected by federal, state, or local law or ordinance or regulation.

All candidates considered for hire must provide evidence of identity and U.S. work authorization at the time of hire. Additionally, all candidates must successfully pass a drug screening and commercial criminal background check, including a stricter Department of Defense background check, for access to job site at military base (if applicable for position being hired for).

Job Posted by ApplicantPro

About the Job

Background

McKenna Boiler Works, Inc. ( is a 5th generation family run rapidly growing ASME Section I, IV & VIII equipment manufacturer that engineers and builds pressure vessels for a variety of different industries. McKenna Boiler Works, Inc. provides engineering services to ASME standards for the highest quality fabrication or repair of pressure vessels and non-code tanks.

The Role

As a McKenna Boiler Works, Inc. Quality Control Manager, you evaluate product and workmanship requirements and review designs and blueprint specifications to assure on-time delivery of our first in class metal fabricated products. You are a quality expert with ASME welding experience and have a proven track record of being hands on and maintaining ASME quality management systems. You will spearhead the new implementation of a quality system from the ground up.

Each vessel that we build will have its own mechanical and quality requirements, and you will ensure that each particular set of requirements are adhered to during product fabrication, completion, and customer delivery.

With your engineering, manufacturing, welding, and/or metal fabrication background you are able to supervise staff to define, measure, analyze, improve and control the full manufacturing process through to customer delivery. For additional information on our product lines, please refer to our website.

Responsibilities

* Monitor weld procedures or ASME code requirements, to verify compliance with company, customer, and code specifications.
* Inspect welded sub-assemblies and assemblies at designated points of the manufacturing process for ASME hold points.
* Maintain compliance to ASME weld procedures and train shop foreman and your direct reports in QC measurements, weld procedures, materials traceability and all other ASME documentation requirements including shop traveler generation and various different data reports that our vessels require. POC for collaborating with AI inspectors for code jobs.
* Maintain all quality records for the Company.
* Perform visual and mechanical inspection of products in accordance with company drawings for the different ASME BPVC sections, code requirements and/or engineering blueprints.
* Conduct both onsite and offsite factory acceptance test (FAT) to customer specified QC documents.
* Participate in tri-annual review of ASME stamp certifications.
* Partner with the Engineering department to review (and correct) all shop fabrication drawings before they are released to the floor.
* Oversee and manage inventory, receiving, shipping, and packaging personnel to ensure compliance with Company PO and safe delivery of our customer's product as it leaves the factory.
* Prepare and maintain various ASME QC records both for fabricated equipment as well as ASME documentation for our welding staff (e.g. WPS, PQR, and weld qualification testing, and continuity records) including responding to supplier/customer corrective action, and respond to non-conformances, either internally generated or customer generated.
* Work closely with manufacturing, engineering, vendors and office staff to review quality problems and insure problem-free production.
* Support and manage the final assembly department to successfully perform its functions.

Minimum Qualifications

* Bachelor of Science degree in Manufacturing Engineering or technical degree from four-year college or university OR have significant work experience in manufacturing, welding, metal fabrication, and machining experience
* 3+ years of experience in working with Quality systems, programs, audits and procedures.
* 5+ years in the fabrication and / or manufacturing industries
* In depth knowledge of ASME and AWS codes
* Knowledgeable in ASME inspection process - incoming inspection, material certification and marking requirements and in-process inspection
* ASME Knowledge in code sections for hydrostatic testing, and be able to generate ASME records (required data reports, shop travelers, etc.)
* Ability to read and interpret engineering blueprints and verify or add weld symbols and finish callouts
* Ability to use measurement instruments, including pressure gauges, calipers, micrometers, and weld reinforcement gauges.
* Ability to verify completeness and accuracy of the information recorded.
* Ability to work, schedule and interact with Authorized ASME Inspections and present documents for their review, sign-off, etc.
* Familiar with continuous improvement initiatives such as Lean and Six Sigma and ISO 9001 a plus
* Possess a craftsman's eye for cosmetically pleasing equipment to meet our customers' high expectations.
* Ability to effectively present information and respond to questions from other managers and departments including customers regarding testing procedures and results to resolve problems.
* Must be a self-starter who has excellent written and verbal communication skills.
* Proficient in relevant software, working within ERP Systems, must be highly proficient in Excel, Word and Powerpoint.

Preferred Qualifications

* Knowledge of ASME Section I, IV or VIII Division 1 pressure vessel code.
* Experience with welding and joint design of carbon steel, process piping and/or other AWS, BPE code specifications.

Benefits

* Competitive Salary
* Vacation Pay
* Sick Pay (3 days)
* Holiday Pay
* Medical/Dental/Vision Benefits
* 401k Plan

Pay: $55,000 - $130,000 a year

EQUAL OPPORTUNITY EMPLOYER -- McKenna Boiler Works, Inc. does not discriminate on the basis of age, sex, sexual orientation, religion, national origin, marital status or disability status in its employment actions, decisions, policies and practices.

McKenna Boiler Works, Inc. is a 100 year old rapidly growing forward thinking turnkey solution provider for customers with steam or hot water needs. We have a great team of individuals that bring a variety of backgrounds to our manufacturing, service, mechanical and rental businesses. We are looking for top tier talent to help lead this company in achieving it's goals.

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Job Description

Job Description

Eastridge Workforce Solutions is a leading provider of workforce management solutions, committed to connecting skilled professionals with meaningful career opportunities.

Job Title: Quality Control Technician – Laboratory Testing

Location: Carlsbad, CA

Department: Quality Control / Chemistry

Reports To: QC Supervisor

Position Overview

Seeking a Quality Control Technician to perform laboratory-based testing and documentation for in-process and finished product evaluations. This role includes routine SOP-driven testing as well as participation in special assignments, method validations, and quality investigations. The technician will work cross-functionally to support core QC Chemistry functions such as raw material verification, stability testing, and product release activities.

Key Responsibilities

• Perform and document quality control testing on in-process and final product samples.
• Execute first article and final product testing in accordance with established procedures.
• Support raw material evaluations, stability programs, and special studies.
• Participate in method validation, process improvement, and product development efforts.
• Maintain accurate and complete testing records and data logs for internal audits and regulatory review.
• Uphold laboratory housekeeping standards and ensure consistent organization of workspaces.
• Follow internal procedures and regulatory guidelines related to quality systems, safety, and equipment use.
• Assist in onboarding and training of new QC personnel.
• Communicate test results and quality observations to cross-functional teams in a timely manner.

Cross-Functional Interactions

• Quality & Manufacturing: Coordinate results with production schedules and product release timelines.
• R&D and Engineering: Provide testing support for product development and process validation.
• Materials & Supply Chain: Collaborate on raw material tracking and availability.
• Regulatory and Quality Assurance: Support documentation and traceability requirements.

Work Environment

• Work is performed in laboratory, office, and manufacturing environments.
• Exposure to biological materials, chemicals, and standard laboratory hazards.
• Use of PPE required per internal safety policies.
• Flexibility in working hours may be needed to support production timelines.

Physical Requirements

• Regular lifting of up to 20 lbs.
• Prolonged periods of standing, walking, or sitting at a laboratory bench.
• Visual acuity required for sample evaluations and data entry.

Qualifications

Education:

• Bachelor's degree in Chemistry, Biology, or a related scientific field preferred.

Experience:

• 0–2 years in a laboratory or manufacturing quality control role.
• Background in medical device, diagnostics, or high-volume production environments strongly preferred.

Skills:

• Proficient in reading and interpreting SOPs, test methods, and technical drawings.
• Working knowledge of GMP/GLP, ISO, and QSR standards.
• Strong organizational skills with attention to detail.
• Capable of prioritizing tasks in a fast-paced setting.
• Comfortable working both independently and as part of a team.
• Effective written and verbal communication skills.
• Proficiency with MS Office (Excel, Word) or equivalent software for documentation and reporting.

Compensation

Base Hourly Rate: $20.00

Benefits : Use this link bit.ly/4cGUQSh to learn more about benefits available to Eastridge’s temporary employees.From time to time Eastridge’s clients may offer additional benefits to Eastridge employees while on assignment.Information about those benefits will be communicated when applicable.

Eastridge Workforce Solutions is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We celebrate diversity and are committed to creating an inclusive environment for all employees. Please note that Eastridge is unable to provide visa sponsorship to applicants.

Certain clients require Eastridge to perform background checks and Eastridge will consider qualified applicants with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.

#IPRO

Job Description

GLAUKOS - QUALITY CONTROL INSPECTOR I - 2ND SHIFT (SAN CLEMENTE, CA)

How will you make an impact?

The Quality Control Inspector I will be responsible for all aspects of inspection (receiving, in-process and final). In addition, this position will provide QSR support for other QA activities such as calibration, environmental monitoring, product testing, label control, etc.

What will you do?

Receiving Inspection

• Receiving inspection of components following procedures, specifications and drawings.
• Utilize a variety of standard metrology equipment, including: Optical comparator, height gauge, master height gauge, CMM, Vision Metrology System (VMS, e.g., Smartscope), calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, durometer, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc.
• Read engineering drawings and interpret geometric dimensioning and tolerancing.
• Review associated paperwork, complete inspection records using good documentation practices, and release components.
• Program the Smartscope to run automatic routines for multiple part inspections. (Level 2 and higher)
• Write clear and concise procedures for inspection of components, machined tubing, etc. (Level 2 and higher)
• Carefully handle and process extremely small components without damaging them.

In-Process Inspection

• Perform Line Clearance for Operations activities
• Inspect and release labeling
• Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures.
• Perform inspections on components and assemblies in manufacturing

Final Inspection

• Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures.
• Perform final inspection on finished goods
• Inspect finished goods for proper labels, packaging, tamper seals and product in accordance with procedures.
• Coordinate final inspection activities with outside vendors, i,e, LAL, peel testing
• Perform in-house peel testing on sealed packages
• Maintain sample retain area

Other Duties

• Work with engineering in the design of high quality inspection / metrology fixtures.
• Support equipment and process validation activities by inspecting process outputs
• Conduct periodic compliance audits of manufacturing operations and procedures for cGMP compliance.
• Ensures on a daily basis quality records and company practices are compliant with internal procedures and regulations.
• Coordinate the monthly environmental monitoring of the cleanrooms.
• Coordinate quarterly dose audits.

How will you get here?

• High School Diploma required.
• 0-2 years industry experience.
• Medical device experience and working knowledge of QSR a must
• Experience working in a clean room and/or performing in-process assembly and manufacturing verification inspections desirable
• Attention to detail and accuracy a must
• Must have excellent documentation skills
• Team player, good written/oral communicator
• Must be organized and able to coordinate activities with outside vendors

#GKOSUS

About Us

Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible.

Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.

Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases.

Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.

Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do.

Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol "GKOS". Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts.

Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer . All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Job Description

GLAUKOS - QUALITY CONTROL INSPECTOR I - 2ND SHIFT (SAN CLEMENTE, CA)

How will you make an impact?

The Quality Control Inspector I will be responsible for all aspects of inspection (receiving, in-process and final). In addition, this position will provide QSR support for other QA activities such as calibration, environmental monitoring, product testing, label control, etc.

What will you do?

Receiving Inspection

• Receiving inspection of components following procedures, specifications and drawings.
• Utilize a variety of standard metrology equipment, including: Optical comparator, height gauge, master height gauge, CMM, Vision Metrology System (VMS, e.g., Smartscope), calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, durometer, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc.
• Read engineering drawings and interpret geometric dimensioning and tolerancing.
• Review associated paperwork, complete inspection records using good documentation practices, and release components.
• Program the Smartscope to run automatic routines for multiple part inspections. (Level 2 and higher)
• Write clear and concise procedures for inspection of components, machined tubing, etc. (Level 2 and higher)
• Carefully handle and process extremely small components without damaging them.

In-Process Inspection

• Perform Line Clearance for Operations activities
• Inspect and release labeling
• Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures.
• Perform inspections on components and assemblies in manufacturing

Final Inspection

• Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures.
• Perform final inspection on finished goods
• Inspect finished goods for proper labels, packaging, tamper seals and product in accordance with procedures.
• Coordinate final inspection activities with outside vendors, i,e, LAL, peel testing
• Perform in-house peel testing on sealed packages
• Maintain sample retain area

Other Duties

• Work with engineering in the design of high quality inspection / metrology fixtures.
• Support equipment and process validation activities by inspecting process outputs
• Conduct periodic compliance audits of manufacturing operations and procedures for cGMP compliance.
• Ensures on a daily basis quality records and company practices are compliant with internal procedures and regulations.
• Coordinate the monthly environmental monitoring of the cleanrooms.
• Coordinate quarterly dose audits.

How will you get here?

• High School Diploma required.
• 0-2 years industry experience.
• Medical device experience and working knowledge of QSR a must
• Experience working in a clean room and/or performing in-process assembly and manufacturing verification inspections desirable
• Attention to detail and accuracy a must
• Must have excellent documentation skills
• Team player, good written/oral communicator
• Must be organized and able to coordinate activities with outside vendors

#GKOSUS

About Us

Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible.

Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.

Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases.

Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.

Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do.

Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol "GKOS". Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts.

Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer . All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Job Description Summary

At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy (RLT) to cancer patients. We are looking for dedicated and enthusiastic professionals to join our new manufacturing site in Carlsbad! Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner. Shift: Shift schedule will be phased in as the site approaches go-live. We are planning for 12-hour rotating shifts which will include at least one weekend day.

Job Description Key Responsibilities:

• Executes all activities related to the manufacturing of RLT products. Responsibilities include operating and maintaining grade A isolators, focusing on KPI goals as well as ensuring adherence to all state, federal and Novartis radiation safety guidelines.
• Responsible for successful on-time completion of required training curriculum comprising of the necessary Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications and other relevant training including Health, Safety & Environment (HSE) for the specific role.
• Supports all technical aspects related to production readiness including manually cleaning the cell and performing sterilization of the isolators.
• Conducts routine and dynamic environmental monitoring as required.
• Prepares all materials while maintaining material identity in accordance with the batch monitoring system as defined by procedure.
• Facilitates a culture of "speaking up" and ensuring all cGMP compliance activities are followed.
• Prepares applicable documents and records such as batch records, shipping documents, and training materials.
• Given the time sensitive nature of the product, this position will require unplanned overtime to ensure process continuity and completion.

Essential Requirements:

• Bachelor of Science strongly preferred. If the applicant does not have a degree, a minimum of 2 years of experience in a cGMP or aseptic environment is required.
• External candidates: 2+ years of experience in aseptic pharmaceutical manufacturing. Preferably in drug product filling operations.
• Current Novartis Associates: Must be a Production Technician for a minimum of 12 months including prior RLT experience and be qualified in at least two critical production isolator tasks.
• Knowledge of cGMP regulations and FDA guidance applicable to aseptic manufacturing.
• Proficient in MS Office applications.

• Flexibility to don clean room garments and personal protective equipment (PPE).
• Near vision performance should be the equivalent of 20/20 with no impairment of color vision. The use of corrective lenses to achieve the desired visual acuity is permitted.
• Makeup, jewelry, nail polish, perfume/cologne and other potential microbial sources are prohibited in restricted areas.
• Ability to lift or carry up to 35 pounds.

Benefits and rewards: Read our handbook to learn about all the ways we'll help you thrive personally and professionally:

The pay range for this position at commencement of employment is expected to be between $27.78 to $1.58 per hour; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

EEO Statement: The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

Accessibility and reasonable accommodations: The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@ or call +1 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Salary Range: 57,800.00 - 107,300.00

Skills Desired: Assembly Language, Cooperation, Efficiency, Electronic Components, Flexibility, General HSE Knowledge, Good Documentation Practice, Installations (Computer Programs), ISO (International Organization For Standardization), Job Description, Knowledge Of GMP, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Nuclear Medicine, Physics, Product Distribution, Production Line, Scheduler