BAG Production Tech
Manufacturing Technician Job 35 miles from Novato
Linde is seeking qualified applicants for our BAG Production Technician position. The primary function of the BAG Production Technician is to ensure safe and reliable production at the Wilmington, CA Air Separation Plant. The BAG Production Technician works in a team environment where individuals are empowered to set priorities and complete different activities with minimal supervision.
Primary Responsibilities:
Successful candidates must be able to understand principles of all Government and Linde Environmental Permits, Regulations and Policies.
This is a full-time position in Southern California, supporting the Air Separation Plant in Wilmington. This is a 12-hour rotating Shift position.
Follow safe work permit processes, policies and procedures.
Ensure safety and hazard recognition through the use of HWP is implemented and effective for all personnel involved in your actions.
Take leadership of LOTO for the facility.
Understand and ensure compliance with all Praxair and Governmental Environmental Permits, Regulations, and Policies.
Understand Production KPIs and work towards achieving these goals - included in individual performance rating.
Understand and Conduct water test on cooling tower and boilers: make necessary adjustment needed to keep in control.
Understand the theoretical aspects of the process and adjust controls towards achieving desired flows, pressures, and purities.
Utilize the EAM Maintenance program to maintain compliance in areas covered by CMMS.
Understand P&ID and control loop input-output logic.
Understand Process Loop interaction and impact on the process (i.e. basic air separation principles).
Knowledge of Switchgear relay flags and functionally rack in-out breakers.
Safely move Tractor-Trailers within the plant property.
Assist in the training and development of new employees.
Ensure customer quality requirements are met for ALL products: maintain Quality Program.
Understand and follow all SMP, SOP, COP, OSS, OPS alerts and Technical Bulletins.
Where required: understand and resolve fill zone and back-up system issues.
Understand what parameters the analyzer must function under (i.e. Reference gas flows, product gas flows).
Review QA logs and COC's for errors.
Perform QA testing and unload Argon Railcars into Storage Tanks
Complete Railcar inspections.
Complete all LMS training modules and OJT for assigned job per assigned timeline.
Qualifications:
High School Diploma or equivalent is required.
Associates in Applied Sciences Degree or equivalent apprenticeship preferred.
Motivated, self-starter capable of effectively managing multiple tasks and priorities.
Relevant computer and technical skills.
Must be able to work overtime and weekends as required.
Must have strong, written, verbal and interpersonal communication skills.
Must have a current and valid driver's license.
Must be able to meet the physical demands of the job.
Lift 50 pounds.
Climb stairs and ladders.
Work in tight and closed spaces.
Be able to wear all required personal protective equipment.
About Linde:
Linde is a leading global industrial gases and engineering company with 2023 sales of $33 billion. We live our mission of making our world more productive every day by providing high-quality solutions, technologies and services which are making our customers more successful and helping to sustain and protect our planet.
The company serves a variety of end markets including aerospace, chemicals, food and beverage, electronics, energy, healthcare, manufacturing, and primary metals. Linde's industrial gases are used in countless applications, from life-saving oxygen for hospitals to high-purity & specialty gases for electronics manufacturing, hydrogen for clean fuels and much more. Linde also delivers state-of-the-art gas processing solutions to support customer expansion, efficiency improvements and emissions reductions.
For more information about the company and its products and services, please visit ************* .
We offer a comprehensive competitive benefits package including paid holidays and vacation, health, dental, disability, life insurance, 401(k) (with matching), and pension benefits.
At Linde, we strive to create a work environment that treats all employees with respect, supports new thoughts and ideas, encourages growth and development, celebrates our differences, and embraces inclusion. Linde is committed to remaining an employer of choice for the diverse, ever-increasing pool of global talent.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, protected veteran status, pregnancy, sexual orientation, gender identity or expression, or any other reason prohibited by applicable law.
Linde thanks all applicants in advance for their interest; however, only those applicants who are being considered for an interview will be contacted.
Pay commensurate with experience. Pay range: $53,301 - $78,175.
Nondestructive Examination (NDE) Engineering Technician II (ESC)
Manufacturing Technician Job 39 miles from Novato
Requisition ID # 162560
Job Category: Maintenance / Construction / Operations
Job Level: Individual Contributor
Business Unit: Electric Engineering
Work Type: Onsite
Applied Technology Services (ATS) is an internal service provider performing technical services for PG&E. The Nondestructive Examination (NDE) unit provides technical NDE expertise, consultation, special project inspections and examinations in both the laboratory and in the field. The methods and tools used to support various projects include Gamma and X-Ray conventional and computed radiography, conventional and automated ultrasonic testing using straight beam, shear wave, phased array and TOFD, magnetic particle testing, liquid penetrant testing, remote video inspection using push cameras and crawlers, CWI visual inspections, surface laser scanning, infrared thermography, field chemistry analysis, acid etching, and in-situ tensile/yield strength testing.
Projects are performed in support of Gas Operations, Hydro Generation, Nuclear Power Generation and Electric Operations. Specific Gas Operation projects include gas pipeline inspections in support of internal/external corrosion direct assessment and in-line (ILI) inspection programs. Hydro Generation projects include pressure boundary, penstock, and rotor inspections. PG&E's Diablo Canyon nuclear power plant requires ATS support for the main turbine, feed-water piping, and conduit inspections on an annual basis.
Position Summary
This position is represented by the Engineers & Scientists of California (ESC) subject to collective bargaining.
The NDE Engineering Technician II shall have the skills and knowledge to set up and calibrate equipment to conduct inspections and to interpret, evaluate, and document results in accordance with company procedures written with respect to applicable codes, specifications, and standards. The individual shall be thoroughly familiar with the scope and limitations of the test method and shall exercise assigned responsibility to effectively communicate inspection results to project engineering and/or management. This position is responsible for the safe and efficient execution of nondestructive inspections within the PG&E service territory.
This position will require 50% of the NDE Engineering Technician's time to be spent at work sites throughout the Northern California service territory. Technicians are dispatched from the San Ramon office location daily with overnight stays near the work site being required on a limited basis.
This position is the mid-level, fully experienced, and skilled level of Engineering Technician for hands-on work.
PG&E is providing the hourly rate range that the company in good faith believes it might pay for this position at the time of the job posting. This compensation range is specific to the locality of the job. The actual hourly rate paid to an individual will be based on multiple factors, including, but not limited to, specific skills, education, licenses certifications, experience, market value, geographic location, collective bargaining agreement, and internal equity.
Under the terms of the collective bargaining agreement, the hourly rate range for this position is $56.94 to $63.03, subject to collectively bargained wage increases.
Responsibilities
Technicians travel to PG&E facilities in locations throughout the service territory and perform field testing &measurements such as:
Perform all laboratory and field assignments, maintenance and repairs, calibrations, and investigations of a difficult nature on a wide variety of materials and equipment; perform other investigative work as directed.
Prepare reports on results of inspections
Perform inspection in the lab or field with minimal to no supervision
May direct the work of other employees
Qualifications
Minimum:
Associate in Science degree or equivalent education and experience in NDE
2 years of experience performing nondestructive testing on structures, systems or components
Desired:
Documented training and on-the-job hours for the direct certification to Ultrasonic, Radiographic, Liquid Penetrant, and/or Magnetic Particle Level II examiner in accordance with ASNT CP-189
3 years of experience working as a certified Level II examiner with a focus in Ultrasonic Thickness Testing (UT(T), AUT, PAUT)
Current ANST NDE Level III certification(s)
Directly related experience with gas pipeline integrity management programs
Current IRRSP or Radiographers State Card
Previous nuclear power generation inspection experience to include unescorted access
Current AWS CWI and API 510, 570, 653 certifications
ASNT ACCP certifications, CSWIP, PCN certifications
Working knowledge of various PAUT instruments (Olympus or Zetec)
Inspection experience utilizing automated UT systems and interpreting collected data
Inspection experience performing Advanced Ultrasonics including TOFD
Knowledge and familiarity with the use of codes and standards to include ASME Section III, V, VIII, XI, 31.1, 31.3,31.8, API 1104, API 5L, AWS D1.1
Acid etching and hardness testing data collection experience
Ability to interpret and evaluate results with respect to applicable codes, specifications, standards, and company procedures
Knowledgeable with Microsoft Office and Adobe software applications to compile final inspection reports
Bed Technician, FT Days
Manufacturing Technician Job 49 miles from Novato
Under direct supervision of the POM Manager, the Bed Technician performs general inspection, testing, corrective and preventative maintenance of patient beds and gurneys.
PIH Health is a nonprofit, regional healthcare network that serves approximately 3 million residents in the Los Angeles County, Orange County and San Gabriel Valley region. The fully integrated network is comprised of PIH Health Downey Hospital, PIH Health Good Samaritan Hospital, PIH Health Whittier Hospital, 37 outpatient medical office buildings, a multispecialty medical (physician) group, home healthcare services and hospice care, as well as heart, cancer, digestive health, orthopedics, women's health, urgent care and emergency services. The organization is nationally recognized for excellence in patient care and patient experience, and the College of Healthcare Information Management Executives (CHIME) has identified PIH Health as one of the nation's top hospital systems for best practices, cutting-edge advancements, quality of care and healthcare technology. For more information, visit PIHHealth.org or follow us on Facebook, Twitter, or Instagram.
Required Skills
Knowledge and experience in maintaining and repairing a variety of beds and gurneys.
Strong communication skills; excellent telephone manner; strong English and grammar skills.
Strong organizational skills; detail oriented; accurate.
Strong analytical and problem solving skills.
Ability to work with minimal supervision, and under the pressure of deadlines.
Strong knowledge and experience with testing bed systems- mechanical, electrical, and hydraulic.
Required Experience
Required:
High School, GED or trade school graduate preferred with courses in arithmetic, mathematics, and electricity.
Minimum (3) years of experience in hospital bed maintenance and repairs.
Demonstrate competence in complex bed systems.
Requires a valid California Driver's License.
LA City Fire Card within six (6) months of employment
Preferred:
Hospital experience
Intermediate level computer skills; specifically in Microsoft Word, Excel and Outlook.
Ability to read maintenance manuals and schematics
Strong knowledge in Hill-Rom and Stryker equipment.
Address
1225 Wilshire Boulevard
Salary
27.44-45.27
Shift
Days
FLSA Status
Non-Exempt
Zip Code
90017
Production Technician - Robotics
Manufacturing Technician Job 24 miles from Novato
Sentien Robotics is a cutting-edge technology company, redefining what's possible with unmanned aerial systems (UAS) and robotics. Our mission is to deliver innovative solutions for critical industries like surveillance, environmental monitoring, infrastructure inspection, and national security through persistent aerial flight, multi-UAS coordination, and full lifecycle automation.
Role Description
As a Production Technician, you'll assemble, troubleshoot, and maintain robotic systems, ensuring they meet our high standards of quality and safety. You'll work closely with engineers and follow detailed assembly instructions, contributing directly to the success of our groundbreaking technology.
Responsibilities
• Assemble mechanical, electrical, and robotic components.
• Manage inventory and prepare components for assembly.
• Conduct quality checks throughout the production process.
• Diagnose and resolve assembly issues and perform preventive maintenance.
• Interpret technical drawings and maintain accurate records.
• Support critical hardware demonstrations with customers as needed
Qualifications
• Experience with hand and power tools in a production setting.
• Ability to read mechanical drawings and schematics.
• Strong attention to detail and organization skills.
• Prior experience in robotics or automation is a plus.
• Technical degree or certification preferred.
Why Sentien Robotics?
Join us in shaping the future of robotics. You'll be part of a fast-paced, innovative team working on impactful real-world projects with opportunities for growth and professional development.
US Hourly Range
$32-$40 USD
Manufacturing Technician
Manufacturing Technician Job 23 miles from Novato
Title: Manufacturing Tech
Duration: 1 year contract
Responsible for clinical manufacturing of monoclonal antibodies (mAB) Drug substance within the Cell Culture Technology Center (CCTC). Collaborates closely with biological development (BD) and Manufacturing Science and Technology (MSAT) for new product introductions and ensure platform alignment.
Key Responsibilities:
Facility Maintenance & Compliance:
Maintain the manufacturing floor to GMP standards, ensuring it remains audit-ready.
Organize and manage disposables, including the disposal of expired items and restocking of everyday materials and equipment.
Conduct routine facility checks and upkeep using the Encompass system.
Environmental Monitoring:
Support environmental monitoring activities during processing, including the handling and testing of environmental monitoring plates.
Ensure adherence to aseptic techniques and processes for maintaining Class B, C, and D cleanroom standards.
Equipment Maintenance:
Perform regular cleaning and maintenance of manufacturing equipment, such as biosafety cabinets, microscopes, incubators, pH conductometers, and flex cell counters.
Monitor and maintain equipment logs to ensure consistent performance.
Documentation & Compliance:
Review and update DSD shift books and ensure accurate documentation entries on a monthly basis.
Support process documentation in compliance with GDP standards.
Operational Support:
Spend approximately 50% of time on the manufacturing floor and 50% on administrative tasks.
Assist with training team members in GMP compliance, environmental monitoring, and operational protocols.
Qualifications:
Education: Bachelor's degree in a relevant scientific discipline required.
Experience:
Hands-on experience in manufacturing or as a manufacturing technician.
Strong understanding of GMP, GDP, and pharmaceutical/biotechnology operations.
Familiarity with environmental monitoring and aseptic techniques.
Experience with SAP and cell culture or cell therapy processes is a significant advantage.
Technical Skills:
Proficiency with analytical equipment, including microscopes, biosafety cabinets, flex cell counters, and incubators.
Knowledge of Class B, C, and D cleanroom standards is highly preferred.
Exact compensation may vary based on several factors, including skills, experience, and education.
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.
Manufacturing Associate I
Manufacturing Technician Job 37 miles from Novato
Role Title: Manufacturing Associate I
Department: Manufacturing
Supervisor: MFG Manager
FLSA: Exempt
CORE VALUES
Respect ● Passion ● Teamwork ● Integrity ● Honesty ● Commitment ● Collaboration
ROLE SUMMARY
The MFG Associate I is responsible for the manufacturing of Polaris' drug substance and/or drug product portfolio. This includes support and collaboration with manufacturing customers and partners, including Quality, MSAT, Facilities, and management, that results in safe, high quality, and continuously improving production, while maintaining full compliance with current Good Manufacturing Practices, and Polaris' corporate principles, quality policies, and standards. This position supports fermentation, purification (CLF), and aseptic fill suite (AFS) areas of manufacturing.
ROLE RESPONSIBILITIES
Daily GMP Manufacturing operation activities in the cleanroom and AFS
Daily Manufacturing support, cleaning, autoclave and parts wash
Work closely with Manufacturing leadership team, MSAT, Quality, and Scheduling to meet short and medium term objectives
Responsible for escalations as needed
Drive a culture of continuous improvement
Develop area technicians in both expertise and production knowledge
Comply with cGMP and GDP regulations
Order and dispense raw materials
Perform inventory cycle counts and site fit-for-use inspections
Perform revision and creation of SOP's, batch records, or associated protocols under a change control program
Perform deviation initiation, investigation, resolution, and CAPA
Maintain Polaris' right-to-operate: Ensure cGMP production of products in compliance with all applicable Health Authority requirements and Polaris' Quality Management System Maintain inspection readiness, and serve as an area SME during inspection tours
Ensure systems and processes are properly maintained to ensure staff's safety, product quality, and continuity of supply
Ensure that staff are appropriately trained and qualified for the activities they perform prior to execution
Ensure on-site presence for their staff and themselves
Work overtime (including outside of normal business hours) as needed per business requirements
JOB REQUIREMENTS
Bachelor's degree, preferably in Life Sciences or engineering with 2-3 years of relevant work experience, or associates degree and 4+ years of relevant work experience, or high school diploma and 5+ years of relevant work experience
Knowledge of large molecule biopharmaceutical manufacturing processes and equipment
Ability to work on-site full-time as required
Ability to lift and carry up to 40 pounds
Work overtime as required, including outside of normal business hours
Ability to stand for a prolonged period operating manufacturing equipment, including in an ISO5 cleanroom
5*Manufacturing Associates
Manufacturing Technician Job 34 miles from Novato
Hi Network,
Our client, based in South San Francisco, is currently looking for 5 Manufacturing Associates for a short-term contract to start End of February for 6 - 8 weeks.
The successful candidates must have the following skills:
Experience using standard laboratory equipment such as balances and mixers,
Manual operations,
Documentation of work,
Proficient in using MS Word and Excel,
Operation of process equipment,
Compliance with GMPs.
Please send me your updated resume if you are interested in applying for the role.
Thanks!
Quality Assurance Technician
Manufacturing Technician Job 41 miles from Novato
$31 - $35 per hr
Shift: M-F 8:30-5
4-5 month contract - this role will NOT extend as the site is closing
REQUIRED:
Min of 2+ years of manufacturing QA experience
Experience with finished product testing, inspection, batch record review/product release - must have all
biotech, pharma, medical device industry experience highly preferred
SCOPE:
The Quality Assurance Technician is located at and supports the Hayward, CA manufacturing site.
PRIMARY RESPONSIBILITIES:
• Support manufacturing by performing duties such as incoming, in-process and final inspections, DHR review and completion, product release, etc.
• Authorize release of material, subassembly and product.
• Prevent release of suspect or known nonconforming products and materials.
• Ensure all activities are performed in accordance with Quality System requirements, work instructions and regulatory requirements.
• Follow detailed process steps without deviation.
• Initiate deviations (NCR) as needed upon occurrence and collect information for investigation.
• Collaborate with other functional teams to identify, investigate and resolve product quality issues.
• Conduct training to Quality Systems processes as defined within the learning management system.
Rad Tech
Manufacturing Technician Job 32 miles from Novato
Bass Surgery Center is offering a $5,000.00 Sign On Bonus
Bass Surgery Center in Walnut Creek is searching for a Rad Tech to join our family.
Perform the described duties in the primary work area and demonstrate competency in the following:
IV and contrast administration, orthopedic radiology, pediatric radiology, operating room Radiology, GI Radiology.
Perform Pain Blocks and Cholangiograms,
File and log in OR x-ray, keep Mini C-Arm logs up to date.
Report system of radiology findings to physician.
Strong teamwork skills, utilizing "down time" to perform other assigned tasks, including room turnovers, restocking warmer, specialty carts, etc.
Pay Range: $50.00 - $58.00 / hour
Wages are determined based upon a number of factors including, but not limited to, an individual's qualifications and experience.
Required Skills:
EDUCATION, TRAINING AND EXPERIENCE REQUIREMENTS:
- Graduate of an accredited program in Radiological Technology.
- Minimum 2 years of previous experience preferred.
- AART Registered, State of California MRT and CPR Current and Fluoroscopy permit required.
- Knowledgeable of local, state, federal and Joint Commission Regulations.
- Must possess independent decision making skills.
- Ability to prioritize and handle multiple projects.
- Excellent communication skills with the staff, physicians, patients and families.
- Must be able to communicate verbally and non-verbally in a professional way.
Familiarity with medical terminology and departmental supply items is required.
Licensure/Certification/Registration:
American Registry of Radiologic Technologists
CA Department of Health - Certified Medical Radiologic Technologist
Education and Experience:
1-2 years experience in C-Arm and Portable x-rays in operating room setting.
Employment practices will not be influenced or affected by an applicant's or employee's race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.
Quality Inspection Technician III
Manufacturing Technician Job 31 miles from Novato
We are looking for a meticulous and detail-oriented Incoming Quality Inspection Technician III ensure the quality levels of incoming materials and components. The ideal candidate will perform inspections based on blueprints, ECOs, and established operating procedures, ensuring that all materials meet required standards for acceptance. This role involves working closely with various departments to support quality assurance processes, maintain proper documentation, and ensure consistent product quality.
Key Responsibilities:
Perform inspection procedures to ensure the quality of incoming materials, working from blueprints, ECOs, or established procedures.
Use measuring instruments effectively to assess material quality and compliance.
Support and adhere to Calex Quality Assurance policies as required by ISO9001 standards.
Maintain daily monitoring and reporting of rejected or discrepant materials, hazardous materials, chemical compounds, shortages, and problem POs.
Conduct dimensional inspections of parts for Concord and other MPS warehouses that drop ship parts.
Complete first article inspections and standard dimensional inspections for fabricated parts (e.g., PC boards, baseplates, housings, connectors) for Concord and other warehouses.
Complete and document First Article Inspection (FAI) findings, filling out appropriate forms.
Issue Non-Conformance Reports (NCR) for discrepant parts and route them to relevant personnel.
Create MPS labels for each part and reel, ensuring that the correct manufacturer's lot codes and date codes are reflected.
Coordinate with planners, buyers, QAs, engineers, sales teams, and receivers from other MPS locations regarding POs, rejections, inquiries, and other issues.
Maintain solderability test and cross-section samples from PCB vendors for the current year and route them for maintenance after year-end.
Train backup personnel for incoming inspections.
Qualifications:
Experience performing inspections on incoming materials and components.
Proficiency in using measuring instruments and interpreting blueprints or specifications.
Familiarity with ISO9001 quality assurance standards.
Strong attention to detail and ability to maintain accurate documentation.
Excellent communication and collaboration skills to work effectively with internal teams.
Ability to train others and ensure consistent inspection practices.
Why Join Us:
Competitive pay range of $25.70/hr. - $27.16/hr.
Opportunity to work in a dynamic and collaborative environment.
Contribute to maintaining high-quality standards and ensuring smooth production operations.
Opportunity to be part of a dynamic team that values continuous improvement and world-class customer satisfaction.
Contribute to a high-performance culture focused on quality and excellence.
Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria.
If you are passionate about quality control and are looking to make an impact in a fast-paced manufacturing environment, we encourage you to apply!
Please submit your resume and cover letter detailing your relevant experience and qualifications to Alissa at ...@adeccona.com. Only shortlisted candidates will be contacted for further steps in the selection process.
Pay Details: $25.70 to $27.16 per hour
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
The California Fair Chance Act
Los Angeles City Fair Chance Ordinance
Los Angeles County Fair Chance Ordinance for Employers
San Francisco Fair Chance Ordinance
Manufacturing Technician, Fab (Night Shift)
Manufacturing Technician Job 24 miles from Novato
Overview Keysight is on the forefront of technology innovation, delivering breakthroughs and trusted insights in electronic design, simulation, prototyping, test, manufacturing, and optimization. Our ~15,000 employees create world-class solutions in communications, 5G, automotive, energy, quantum, aerospace, defense, and semiconductor markets for customers in over 100 countries.
Learn more about what we do.
Our powerful, award-winning culture embraces a bold vision of where technology can take us and a passion for tackling challenging problems with industry-first solutions.
Diversity, equity & inclusion are integral parts of our culture and drivers of innovation at Keysight.
We believe that when people feel a sense of belonging, they can be more creative, innovative, and thrive at all points in their careers.
Responsibilities Responsibilities Able to work 12 hour shifts on this schedule.
Able to stand and walk the entire shift.
Ability to handle chemicals Operate equipment dedicated to semiconductor manufacturing processes.
Be comfortable using computers and learning new computer programs.
Be comfortable using a computer and data system for data entry while following written instructions Implementation of continuous improvement and lean principles to optimize workflow.
Follow standard manufacturing and cleanroom protocol, including gowning and following good operating discipline.
Ability to sustain a high quality of work in a fast-paced cleanroom environment.
Excellent work ethics in terms of attendance, organization, and team skills.
Once proven efficient, ability to train others based on business needs.
This is a variable work schedule (VWS) where the employee works 3 days on, 4 days off, 4 days on, and 3 days off.
The hours are 9pm-9am.
Depending on the shift, the VWS follows the schedule of: "Front Half Schedule" Sunday 9pm - Monday 9am, Monday 9pm-Tuesday 9am, Tuesday 9pm-Wednesday 9am And "Monday" à Sunday 9pm - Monday 9am "Tuesday" à Monday 9pm - Tuesday 9am "Wednesday" à Tuesday 9pm - Wednesday 9am "Thursday" à Wednesday 9pm - Thursday 9am Or "Back Half Schedule" Wednesday 9pm - Thursday 9am, Thursday 9pm - Friday 9am, Friday 9pm - Saturday 9am, Saturday 9pm - Sunday 9am And "Friday" à Thursday 9pm - Friday 9am "Saturday" à Friday 9pm - Saturday 9am "Sunday" à Saturday 9pm - Sunday 9am Qualifications Must have the ability to work in a multi-disciplinary organization by communicating effectively with supervisors, engineers, and maintenance personnel to ensure that manufacturing needs are being met.
Careers Privacy Statement *Keysight is an Equal Opportunity Employer.
* Keysight Technologies Inc.
is an equal opportunity employer.
Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.
Santa Rosa, California pay range: MIN $54,520.
00- MAX $90,870.
00 Note: For other locations, pay ranges will vary by region This role is eligible for our Keysight Results Bonus Program US Employees may be eligible for the following benefits: Medical, dental and vision Health Savings Account Health Care and Dependent Care Flexible Spending Accounts Life, Accident, Disability insurance Business Travel Accident and Business Travel Health 401(k) Plan Flexible Time Off, Paid Holidays Paid Family Leave Discounts, Perks Tuition Reimbursement Adoption Assistance ESPP (Employee Stock Purchase Plan)
Bioprocess Specialist 2, Manufacturing
Manufacturing Technician Job In Novato, CA
BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. BioMarin will continue to focus on advancing therapies that are the first or best of their kind.
BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. Come join our team and make a meaningful impact on patients' lives.
As a member of a Process Team, the Manufacturing BioProcess Specialist (BPS) will work closely with representatives from Manufacturing, Manufacturing Science & Technology, Engineering, and Quality as well as Automation, Validation, and other supporting Organizations in support of day to day plant operations. With a focus on execution of operations, the Manufacturing BPS will investigate deviation incidents, identify and implement corrective or preventive actions, and execute continuous improvement projects. As a member of a Process Team, the Manufacturing BPS will influence technical strategy and project prioritization.
The Manufacturing BPS role is a front-line Subject Matter Expert (SME) for the operational execution of a defined manufacturing process. As a SME, the Manufacturing BPS is expected to know how manufacturing systems (procedures, batch records, automation, equipment, biological processes) work in conjunction with operations floor staff to deliver quality product supply while using creativity and technical acumen to troubleshoot and develop plans to transform and mature those systems.
RESPONSIBILITIES
As a member of a Process Team, the Manufacturing BPS is responsible for the operations execution of a defined manufacturing process; Upstream or Downstream operations of one of BioMarin's products. This includes the following activities:
Respond to, and/or troubleshoot, operational issues and drive robust and compliant processes
In accordance with BioMarin policies and procedures, regulatory requirements, guidelines, and recommendations:
Investigate, manage, and own deviations in the Quality Management System as necessary to support the Process Teams
Use root cause analysis techniques to identify true root cause of incidents and determine appropriate Corrective and/or Preventive Actions
Manage and own related Change Records
Collaborate in a matrixed organization to contribute to comprehensive implementation plans for investigations and changes
Use defined metric processes to recognize potential deviations and escalate to MFG Management and QA
Drive continuous improvement initiatives
Develop and deploy GMP and/or Manufacturing-related training to Manufacturing floor staff
Write, modify, and implement GMP Procedures and Batch Records
EDUCATION AND EXPERIENCE
Required: Relevant experience in pharmaceutical or biopharmaceutical manufacturing
6+ years' experience in pharmaceutical or biopharmaceutical manufacturing with a BA or BS Degree in biological science or engineering
OR
4+ years' experience in pharmaceutical or biopharmaceutical manufacturing with a MS degree in biological science or engineering
REQUIRED QUALIFICATIONS
Operational knowledge of process automation and associated equipment
Familiarity with the underlying scientific principles that drive biologic protein manufacturing
Understanding of cGMP guidelines pertaining to biopharmaceutical processing and GMP compliance
Ability and willingness to work well in a team environment and independently with minimal guidance
Demonstrated Ability to:
Solve complex technical problems
Handle multiple tasks concurrently and be flexible and adaptable as needed, to support operations in a dynamic environment and to support the Process Team goals
Meet deadlines and drive projects without direct authority as the primary change agent
Strong technical writing ability
PREFERRED QUALIFICATIONS
Demonstrated ability to coach others to drive for results; guide team members in a way which best suits their work style
Effective at exploring alternatives to reach outcomes which gain the support and acceptance of all parties
Skilled at asking penetrating questions to define the problem accurately
Project Management experience
Operational Excellence and/or Six Sigma experience
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.
GMP Manufacturing Technician I/II/III -KIT Lab- Day Shift
Manufacturing Technician Job In Novato, CA
LGC Biosearch Technologies locations Petaluma and Novato, CA, as well as our sister site in Denmark, represent a focused, collaborative culture of producing mission-critical genomics components, primarily oligonucleotides and supporting reagents, for our diverse customer base. We believe in Science for a Safer World and have embodied our mission by supporting first responders during the COVID-19 pandemic where our Biosearch Technologies portfolio has been and continues to be enabling millions of PCR tests worldwide. We are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organization.
Job Description
The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management.
This will be in our Kit Lab in Novato. Techs do final dry down (lyophilizatoin), column packing for purification, aliquoting and kitting of product. This is an entry level role.
Shift: Monday-Friday, 5 x 8 hours, 0600-1430.
Perform manufacturing activities according to written protocols, as directed by the departmental supervisor, manager or director.
Maintain batch records, equipment logs and other production records as directed per company procedures.
Follow current Good Manufacturing Practices (cGMP) and close adherence to internal SOPs utilizing GDP practices.
Perform routine operation, maintenance, inspection and cleaning of equipment in accordance with operational instructions
Quick and effective diagnosis of routine problems in manufacturing steps
Initiate attention to operators and tag-outs per documented processes
Execute Deviation and Nonconformance action plans
Reporting of safety incidents or safety hazards to senior colleagues, supervisors or managers
Maintain a clean an orderly laboratory environment.
Qualifications
Associate Degree is required.
1 year of equivalent industry lab experience and training and/or demonstration of ability to meet the requirements of a GMP Technician is preferred.
Knowledge of HPLC, MS, Purifiers, Spectramax, SpeedVacs, Liquid Handlers, TFF, Pipettes, experience or knowledge preferred.
Ability to add, subtract, multiply, and divide all units of measure, using whole numbers, common fractions, and decimals.
Microsoft Office, Outlook, Word, and Excel, use of a web browser - Unicorn and Empower a plus.
Self-motivated with the ability to work independently as well as on teams
Professional presence and strong attention to detail is required
Technical proficiency that enables effective execution of documented procedures
Able to multi-task work in a fast-paced environment.
Strong communication and problem solving abilities are necessary.
Additional Information
What we offer (US based-employees):
Competitive compensation with strong bonus program
Comprehensive medical, dental, and vision benefits for employees and dependents
FSA/HSA Pre-tax savings plans for health care, childcare, and elder care
Deductible Buffer Insurance and Critical Illness Insurance
401(k) retirement plan with matching employer contribution
Company-paid short- and long- term disability, life insurance, and employee assistance program
Flexible work options
Pet Insurance for our furry friends
Enhanced Parental leave of 8 additional weeks
PTO that begins immediately
Town Hall monthly meeting onsite/virtual, Cheer program where employees are recognized for outstanding work, Company wide social events, frequent catered lunches and much more!
The typical pay range for this role is:
Minimum: $ 20.91/ Hourly
Maximum: $ 34.855/ Hourly
This range represents the low and high end of the anticipated salary range for the California -based position. The actual base salary will depend on several factors such as: experience, skills, and location.
Manufacturing Associate
Manufacturing Technician Job In Novato, CA
Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity.
To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com
Job Description
One to the top pharmaceutical company is looking for 10 manufacturing professionals.
PROCESS KNOWLEDGE:
Understanding of process theory and equipment operation
Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, protein purification and formulation of bulk drug substance
Support initiatives for process optimization
Identify and elevate processing issues and support solutions
Demonstrated proficiency Gain experience with automation systems (LIMS, MES, PI, etc.)
TECHNICAL DOCUMENTATION:
Provide feedback and/or suggested changes to operational procedures
Assist in the incorporation of new technologies, practices and standards into procedures
Capable of writing and reviewing process documents
QUALITY AND COMPLIANCE:
Understanding of cGMPs as related to Commercial Operations
Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.)
BUSINESS:
Ability to participate on projects and contribute to outcomes
Capability to learn and support new business systems (Track wise, ERP, etc.)
Support trending of defined department metrics
Additional Information
All your information will be kept confidential according to EEO guidelines.
IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 619-727-5167 ASAP! I want to know more about your preferences.
If in case you know someone who might be interested for this, feel free to pass it along. I look forward to hearing from you!
manufacturing Technician
Manufacturing Technician Job 24 miles from Novato
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description:
Purifies proteins in a regulated FDA licensed and ISO certified facility and performs cross-functional activities associated with downstream production runs in collaboration with Bulk Fill and QC testing groups. The role may include special projects such as process development and validation activities where scientific research principles are applied.
Primary responsibilities:
Purify recombinant proteins to ensure commercial product demands are met:
1. Works as part of the purification team to perform purification, filtration, and centrifugation operations according to standard operating procedures.
2. Executes laboratory operations including dispensing of chemicals, volumetric and gravimetric measurements, making accurate dilutions, and preparing solutions.
3. Performs SAP duties that include cycle counting, reservations, issuing to process orders, and charging of expiring raw materials.
4. Performs equipment preventative maintenance tasks, column packing, and column testing procedures.
5. Ability to multi-task and become proficient at purifying 14 different proteins and make conjugates.
6. Responsible for ordering raw materials and components, as required.
7. Maintains a safe and well-organized work environment and complies with safety procedures.
Follow regulatory requirements:
1. Adheres to valid manufacturing procedures, manufacturing operations, and current good manufacturing practices (cGMP) and ISO requirements.
Documentation:
1. Responsible for the completion and review of batch records and logbooks, which requires legible, clear, and concise data entry.
2. Completes all training documentation within a pre-defined timeframe.
Analytical Testing:
1. Analyzes in-process samples generated from purification activities.
2. Operates lab equipment such as pH meters, balances, centrifuges, spectrophotometers, HPLC systems, and densitometers.
Skills:Must have an understanding of protein purification processes.
• Experience following and writing instructions.
• Very good verbal and written communication skills.
• Computer knowledge required with experience using MS Word and Excel.
• Able to document work accurately and has excellent organizational skills.
• Experience with preparation of reagents following instructions.
• Delivers quality products and services on time to all customers.
• Must be attentive to detail.
• Effectively manages time.
• Considers how all daily manufacturing activities impact product quality.
• Monitor processes and products to identify opportunities for continuous improvement.
• Able to lift and push up to 35 lbs.
1. Works well in a team environment to manufacture production lots.
2. Complies with cGMP and ISO requirements.
3. Maintains accurate documentation related to manufacturing processes.
Education:BA/BS in the sciences (Biology, Engineering, or related field) or 2 years of relevant experience
Languages:English Read Write Speak
Additional Information
Best Regards,
Anuj Mehta
************
GMP Manufacturing Technician I/II/III -KIT Lab- Day Shift
Manufacturing Technician Job In Novato, CA
LGC Biosearch Technologies locations Petaluma and Novato, CA, as well as our sister site in Denmark, represent a focused, collaborative culture of producing mission-critical genomics components, primarily oligonucleotides and supporting reagents, for our diverse customer base. We believe in Science for a Safer World and have embodied our mission by supporting first responders during the COVID-19 pandemic where our Biosearch Technologies portfolio has been and continues to be enabling millions of PCR tests worldwide. We are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organization.
Job Description
The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management.
This will be in our Kit Lab in Novato. Techs do final dry down (lyophilizatoin), column packing for purification, aliquoting and kitting of product. This is an entry level role.
Shift: Monday-Friday, 5 x 8 hours, 0600-1430.
Perform manufacturing activities according to written protocols, as directed by the departmental supervisor, manager or director.
Maintain batch records, equipment logs and other production records as directed per company procedures.
Follow current Good Manufacturing Practices (cGMP) and close adherence to internal SOPs utilizing GDP practices.
Perform routine operation, maintenance, inspection and cleaning of equipment in accordance with operational instructions
Quick and effective diagnosis of routine problems in manufacturing steps
Initiate attention to operators and tag-outs per documented processes
Execute Deviation and Nonconformance action plans
Reporting of safety incidents or safety hazards to senior colleagues, supervisors or managers
Maintain a clean an orderly laboratory environment.
Qualifications
Associate Degree is required.
1 year of equivalent industry lab experience and training and/or demonstration of ability to meet the requirements of a GMP Technician is preferred.
Knowledge of HPLC, MS, Purifiers, Spectramax, SpeedVacs, Liquid Handlers, TFF, Pipettes, experience or knowledge preferred.
Ability to add, subtract, multiply, and divide all units of measure, using whole numbers, common fractions, and decimals.
Microsoft Office, Outlook, Word, and Excel, use of a web browser - Unicorn and Empower a plus.
Self-motivated with the ability to work independently as well as on teams
Professional presence and strong attention to detail is required
Technical proficiency that enables effective execution of documented procedures
Able to multi-task work in a fast-paced environment.
Strong communication and problem solving abilities are necessary.
Additional Information
What we offer (US based-employees):
Competitive compensation with strong bonus program
Comprehensive medical, dental, and vision benefits for employees and dependents
FSA/HSA Pre-tax savings plans for health care, childcare, and elder care
Deductible Buffer Insurance and Critical Illness Insurance
401(k) retirement plan with matching employer contribution
Company-paid short- and long- term disability, life insurance, and employee assistance program
Flexible work options
Pet Insurance for our furry friends
Enhanced Parental leave of 8 additional weeks
PTO that begins immediately
Town Hall monthly meeting onsite/virtual, Cheer program where employees are recognized for outstanding work, Company wide social events, frequent catered lunches and much more!
The typical pay range for this role is:
Minimum: $ 20.91/ Hourly
Maximum: $ 34.855/ Hourly
This range represents the low and high end of the anticipated salary range for the California -based position. The actual base salary will depend on several factors such as: experience, skills, and location.
Manufacturing Bioprocess Technician
Manufacturing Technician Job 34 miles from Novato
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************
We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.
Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.
Job Description
Duties:
Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for Cell Culture Purification that may include process monitoring, sampling, harvesting, purification, formulation and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP).
Essential Technician:
Operate systems that clean and sterilize tanks and filtration systems.
Prepare solutions for the production process.
Review documentation and check all calculations (e.g. tickets, labels, equipment reading).
Trouble shoot equipment and process problems.
Comply with safety requirements, cGMP, SOP and manufacturing documentation.
Use of automation to perform production operations.
Provide support to Manufacturing to meet production demands.
Operate automated systems for equipment operation.
Assemble and prepare equipment for production.
Exhibit detail oriented documentation skills
Communicate effectively and ability to work in a team environment.
Exhibit professional interpersonal skills.
Work with coworkers and supervisor to effectively troubleshoot minor equipment and process issues.
Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters a positive safety culture in which no one gets hurt.
Job Matrix
A good working knowledge of biopharm technology and processes.
Trained and skilled in all operational procedures of at least one manufacturing department.
Demonstrated ability to independently document and record information related to the process.
Occasionally makes routine decisions based on experience. Identifies and suggests solutions to common basic problems.
Recognizes non-routine problems, investigates and suggests potential solutions.
Judgment is required in resolving problems and making routine recommendations.
Ability to recognize deviation from accepted practices is required.
Supplementary Responsibilities:
Operate bioreactors, centrifuges, other harvest systems and protein purifications units.
Operate and clean fixed tank and filtration systems
Operate large scale column chromatography systems.
Operate small-scale cell culture areas and systems by operating cleaning, set up, and maintaining 20L bioreactors; inoculating and maintaining spinner seed cultures using aseptic techniques, maintaining cell banks; and performing general seed lab operations.
Perform Solution Preparation activities (media and buffer make-up)
Clean, assemble, and sterilize equipment using glass washers and autoclaves.
Perform automated CIP and SIP of fixed equipment.
Qualifications
Degree in Life Sciences or engineering and 1 year related experience
Or Associate Degree and 3 year experience
Or High school and 5 years' experience
Biotech certificate from approved program
Additional Information
Sneha Shrivastava
Sr Technical Recruiter
862 - 579 - 4236
Manufacturing Technician - Bioprocess
Manufacturing Technician Job 37 miles from Novato
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.
Join Lonza in Vacaville, CA, as a Manufacturing Technician - Bioprocess and be part of a hard-working team dedicated to producing innovative bio-therapeutic medicines. This role offers an ambitious opportunity to collaborate with highly automated production systems and contribute to our world-class operations. At Lonza, we strictly follow cGMP and SOP standards, ensuring our processes meet the highest regulatory requirements.
Shift Model: 3-4-3
Shift Hours: 7:00a-7:00p or 7:00p-7:00a
Key responsibilities:
Operate and maintain production systems in a cGMP environment, ensuring inspection readiness and compliance with regulatory standards.
Manage inventory and process systems, maintaining accurate records and ensuring safety and environmental protocols are followed.
Participate in the production of mammalian cell culture products across various areas, including upstream (seed train, media preparation, fermentation, harvest) and/or downstream (buffer preparation, chromatography, filtration).
Perform dispensing of components, handle hazardous materials, and clean/sterilize equipment and fixed tank systems.
Support Right-First-Time operations with detailed documentation and timely issue resolution.
Use automation for production tasks, meet production demands, and collaborate effectively with the team.
Key requirements:
High School Diploma or GED Required
AS/BS/BA in Biological Sciences, Physical Sciences, or Engineering preferred.
Proven ability to work in a fast-paced, regulated environment.
Strong attention to detail and dedication to flawless documentation practices.
Ability to determine and successfully implement solutions to process issues.
Excellent collaboration and communication skills.
The hourly rate for this position ranges between $25.10 --- 27.88. Shift differentials may apply. Compensation for the role will depend on a number of factors, including the successful candidate's qualifications, skills, competencies, experience, and job-related knowledge.
Full-time employees receive a comprehensive benefits package including performance-related bonus, medical and dental coverage, 401k plan, life insurance, short-term and long-term disability insurance, an employee assistance program, paid time off (PTO), and more.
Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
Manufacturing Technician II (1601)
Manufacturing Technician Job 31 miles from Novato
Calex Manufacturing Inc., which was acquired by Murata Power Solutions in 2018, has been in business for more than 50 years, designing and manufacturing DC-DC power converters for automotive, transportation and industrial applications. In recent years, Calex has been developing products for emerging markets such as drones, autonomous driving, hybrid and electric vehicles, in addition to the legacy products.
Calex is located in beautiful Northern California, approximately 50 miles north of San Jose and 30 miles east of San Francisco. Our corporate facility is in the city of Concord which is within easy commute distance of affordable housing, a rare trait for the Bay Area.
Position Summary
This position is expected to follow well-defined methods and procedures, using some degree of judgement and interpretation. Typical activities include set-up, loading, and operation of light manufacturing machinery and inspection of SMT assemblies.
Job Duties/Responsibilities
Prepare and pull parts for jobs.
Solder parts using soldering iron or wave solder machines.
Inspect for potential failures (solder bridges, incorrectly inserted parts, etc.).
Read and interpret drawings.
Complete manufacturing documentation correctly.
Set up and verify equipment performance, as assigned by team leader.
Receive units from burn-in, inspect and cup.
Attach ground wires.
Encapsulate units with potting compound.
Put headers on units.
Stamp job numbers on units.
Mechanical and cosmetic inspections.
Kit and enter jobs.
Process backorders in the computer.
Count inventory and enter control transactions into the Calex computer system.
Set up SMT equipment for previously programmed models.
Load and operate SMT equipment which includes the pick and place machine, the stencil machine, and the reflow oven.
Inspect and rework SMT assemblies for workmanship under microscope.
Program and set up light guided insertion machine.
Understand, support, and practice the Calex Quality Assurance policy as required by ISO 9001.
Other work related duties as assigned.
Experience Required
High school diploma or equivalent
At least 18 months of related experience preferred
Must be able to frequently lift up to 20 pounds, detect odors, crouch, crawl, climb, or balance
Physical Requirements
While performing the duties of this job the employee is regularly required to stand, sit, walk, talk, hear and use hands to operate equipment and handle materials and parts. Occasionally required to detect odors, stoop, kneel and reach with hands and arms and to crouch, crawl, climb or balance. Must be able to frequently lift up to 20 pounds. Specific vision abilities required by this job include close vision and color vision.
Work Environment
While performing essential responsibilities, the employee regularly works near moving parts, is exposed to fumes or airborne particles and to toxic or caustic chemicals. Occasionally exposed to vibration and extreme heat. The noise level is usually moderate.
Competencies Building and Supporting TeamsCommunicating EffectivelyDelivering High Quality WorkEvaluating and Implementing IdeasPrioritizing and Organizing WorkSupporting Organizational GoalsCompensation Data
Pay range for this role is $22.45/hour - $24.18/hour.
Compensation and Benefits:
Our benefit package is comprehensive and includes Medical Insurance; Dental Insurance; Vision Insurance; 401(K); Flexible Spending Accounts; Paid Vacation/Holidays; Short Term Disability; Long Term Disability; Tuition Reimbursement.
Quality Technician
Manufacturing Technician Job In Novato, CA
General Description
OMW is a highly respected contract manufacturing company specializing in precision machining of custom metal and plastic parts for some of the world's largest aerospace, electronics, and healthcare companies. We have recently been ranked one of the Top 100 Fastest Growing Private Companies in the Bay Area, by the San Francisco Business Times. The Fast 100 List will be featured in a special print edition of the San Francisco Business Times. To support our rapid growth, we are looking to fill new positions and are looking for team members who are challengers, teammates, strategic thinkers, customer-oriented achievers, and game changers with a desire to create a long term partnership with OMW.
Experience Required: Must have Excellent written English skills and ability to read and write reports and documentation. Direct machining or manufacturing experience in aerospace and avionics highly desirable. CMM programming experience is highly desirable. Experience and aptitude using windows PC software, including Excel and Word. Some background in Quality Management Systems such as ISO 9001 & AS9100 is a plus. Knowledge of Basic GD&T principals.
Skills required: The ability to use calipers, micrometers, pin and thread gages, height gages, microscopes, comparators, and other measurement equipment (training available). Must be able to operate automated CMM after training and prepare FAIR documentation. Ability to read engineering prints and interpret tolerancing and dimensions (including geometric tolerancing).
Specific Responsibilities:
Prepare FAIR and other QC documentation.
Operate and program CMMs for quality inspections (can train).
Prepare shop floor inspection reports and perform first article inspections on in-process parts.
Perform final QC signoffs and inspections on completed parts.
Keep parts from "escaping" with unacceptable defects. Work to continuously lower company's defect rate.
Handle customer and internal non-conformances. Interface with company's software systems.
Compensation based on experience. Benefits include 100% company paid healthcare for the employee (85% for family), generous paid time off accrual, retirement plan with company contribution, educational support, bonuses, and more. Please email your resume or job history to email provided in header. Suitable candidates will be contacted for interviews.
This position requires use of information or access to production processes subject to national security controls under the U.S. export control laws and regulations (including, but not limited to, the International Traffic in Arms Regulations (ITAR) and the Export Administration Regulations (EAR)). To be qualified to work for OMW Corporation, a successful applicant must be a U.S. Person, as defined in those regulations, and able to supply evidence of that qualification prior to starting work. The U.S. export control regulations define a U.S. Person as a U.S. Citizen, U.S. National, U.S. Permanent Resident (i.e., “Green Card Holder”), and certain categories of Political Asylees and Refugees.
OMW Corporation is an equal opportunity employer and drug-free workplace.