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Kratos Unmanned Aerial Systems (KUAS), a division of Kratos Defense, is renowned for its expertise in developing, delivering, integrating, and supporting high-performance, cost-effective, jet-powered Unmanned Aerial Systems (Targets and Tactical). Keyword: Develops/improves manufacturing processes, coordinates engineering changes, manages product introductions, CAD tools, Dfx, engineering BOMs.

YEAR

Kratos Defense & Security Solutions, Inc., is a leading defense technology company focused on unmanned systems, satellite communications, cyber security/warfare, microwave electronics, missile defense, training, and combat systems. Our customers include the U.S. federal government, foreign governments, commercial enterprises, and state and local government agencies. At Kratos, we prioritize affordability as a cornerstone of our technology. We leverage proven, cutting-edge methodologies and technology to minimize costs, streamline schedules, and mitigate risks, ensuring timely delivery of cost-effective solutions to market.Kratos Unmanned Aerial Systems (KUAS), a division of Kratos Defense, is renowned for its expertise in developing, delivering, integrating, and supporting high-performance, cost-effective, jet-powered Unmanned Aerial Systems (Targets and Tactical). As a mid-tier defense contractor, we've demonstrated agility and innovation in providing aircraft to the US military and global allies and partners. Our track record of delivering top-notch jet-powered subscale targets has established us as a go-to defense contractor capable of delivering capabilities at an affordable price.At KUAS, we prioritize innovation, collaboration, and growth. Our team collaborates to cultivate a supportive and dynamic workplace, fostering creativity and promoting professional development while honoring personal and family lives. Join our team and help shape the future of unmanned technology within the defense industry today!GENERAL JOB SUMMARY:Develops, implements, and improves manufacturing and industrial processes to effect maximum product throughput and optimum resource efficiency. Coordinates engineering changes to existing product lines and manages new product introductions. Sets work standards, work-flows, and defines resource requirements for assigned programs. Is expected to apply and champion Lean Manufacturing methodologies in all areas of the manufacturing cycle. Works closely with other engineers and other functional departments to ensure schedule, systems, and part/process data integrity.ESSENTIAL JOB FUNCTIONS:Manufacturing Engineer ALLThe duties and responsibilities listed below apply to all levels of Manufacturing Engineers. Each level of Manufacturing Engineer has additional duties and responsibilities listed.<ul><li>Works with customer released or KUAS released drawings and/or CAD models, engineering BOMs, and other engineering specifications to develop, implement and improve manufacturing processes.</li><li>Creates or participates in engineering and manufacturing reviews and communicates effectively as a technical contributor.</li><li>Implements and executes producibility concepts and understands DfX of products and processes.</li><li>Collaborates well with internal and external resources to resolve technical issues.</li><li>Develops and documents the manufacturing process in detail with an emphasis on visual media, ease of training, and standardized format.</li><li>Responsible for disposition of discrepant or non-conforming product.</li><li>Has familiarity with CAD tools, manufacturing execution systems, ERP, and other commonly used software.</li><li>Designs, coordinates and validates workstation layouts with an emphasis on ergonomics, single piece or small batch flow, visual aids, Poke Yoke (mistake proofing), 5S, and zero-defect policies.</li><li>Calculates and communicates shop floor staffing based on production requirements. Provides OTJ training or mentoring and may provide certification for processes to production associates.</li><li>Works with materials management to develop and implement effective inventory methodologies.</li><li>Reviews and designs in-process handling equipment for the safe and expeditious transportation of parts, inventory, and/or tooling.</li><li>Identifies tooling requirements and coordinates the manufacturing of tools/fixture.</li><li>May identify issues with production personnel and recommend mitigation actions.</li><li>Responsible to generate, review, and maintain cost, schedule, and technical performance operational targets and standards.</li><li>Other duties may be assigned.</li></ul>Manufacturing Engineer I<ul><li>Works on projects of basic complexity that effect program outcomes.</li><li>Implements Manufacturing and/or Engineering Change Orders.</li><li>Reviews and updates manufacturing work instructions.</li><li>Collaborates with Quality Engineering to determine inspection criteria and methods.</li></ul>Manufacturing Engineer II<ul><li>Works on projects of medium complexity which impact aspects of programs.</li><li>Works with IPT and Program managers to ensure schedule and contractual integrity.</li><li>May coordinate the work of other engineers and production specialists.</li><li>Reviews and approves Engineering Design changes.</li><li>Coordinates tool maintenance, repair, and inspection.</li><li>Implements new product design into the manufacturing system.</li><li>Constantly reviews equipment, technology, processes, and manufacturing methods to identify opportunities for improvements.</li></ul>Manufacturing Engineer III<ul><li>Works on projects of advanced complexity that have significant program impact.</li><li>Works with IPT and Program managers to ensure schedule and contractual integrity.</li><li>Establish & maintain material, process, and workmanship specifications.</li><li>Develop and implement tooling for all phases of production.</li><li>A subject matter expert for manufacturability of product, process, and tooling.</li><li>May mentor junior level manufacturing engineers.</li></ul>Manufacturing Engineer IV<ul><li>Independently works on projects of advanced complexity that have major organizational impact.</li><li>Maintain reliable and safe manufacturing systems while improving production rates, efficiencies, yields, costs, and changeovers.</li><li>Responsible for material evaluation, testing, and implementation for production operations. Includes assisting Engineering and Supply Chain with material obsolescence and or selection.</li><li>Evaluate and improve on processes in manufacturing systems.</li><li>Research and purchase new manufacturing technology.</li><li>Advise on corrective actions.</li><li>Responsible to establish & maintain material, process, and workmanship specifications.</li><li>Will mentor lower-level manufacturing engineers and act as a liaison to other functional organizations.</li></ul>SUPERVISORY RESPONSIBILITY:NoneCOMPENSATION:$80,000 - $140,000 Keyword: Develops/improves manufacturing processes, coordinates engineering changes, manages product introductions, CAD tools, Dfx, engineering BOMs Required Experience: KNOWLEDGE, SKILLS & ABILITIES:EDUCATION AND EXPERIENCE:Required:Each successive level of Manufacturing Engineer builds on the identified typical qualifications listed for the previous level(s) Manufacturing Engineer.Manufacturing Engineer I<ul><li>Requires BS degree in a technical field, (Manufacturing Engineer preferred).</li><li>A minimum of 1-2 years of progressive/technical experience.</li><li>May be required to obtain and maintain a U.S. security clearance at the appropriate level (requires U.S. Citizenship).</li></ul>Manufacturing Engineer II<ul><li>Requires BS degree in a technical field (Manufacturing Engineering preferred).</li><li>A minimum of 2-5 years of progressive/technical experience.</li><li>May be required to obtain and maintain a U.S. security clearance at the appropriate level (requires U.S. Citizenship).</li></ul>Manufacturing Engineer III<ul><li>Requires BS degree in a technical field (Manufacturing Engineering preferred).</li><li>A minimum of 5-7 years progressive/technical experience.</li><li>May be required to obtain and maintain a U.S. security clearance at the appropriate level (requires U.S. Citizenship).</li></ul>Manufacturing Engineer IV<ul><li>Requires BS degree in a technical field (Manufacturing Engineering preferred).</li><li>A minimum of 7-10 years progressive/technical experience.</li><li>Material and/or Process Engineering experience.</li><li>May be required to obtain and maintain a U.S. security clearance at the appropriate level (requires U.S. Citizenship).</li></ul>Preferred:<ul><li>Experience with composite manufacturing, i.e. lamination, machining, and bonding.</li><li>Experience in lean manufacturing methods.</li><li>CATIA v5.</li></ul>WORK ENVIRONMENT/PHYSICAL REQUIREMENTS:<ul><li>Standing on a hard surface, walking. Some lifting (not over 50 lbs.).</li><li>Office and manufacturing environment.</li><li>May work extended hours or weekends.</li><li>Employee may generate, handle, manage, or work around hazardous materials and hazardous wastes.</li><li>May be required to lift up to 50 pounds in accordance with KUAS General Safety Training guidelines.</li></ul>TRAVEL REQUIREMENTS:<ul><li>0-25% May be required between other KUAS locations.</li></ul>#LI-Onsite From: Kratos Defense

Kratos Defense

Manufacturing Engineer I - IV

Aerospace and Defense

Bill of Materials (BOM)

CAD/CAM (Computer-Aided Design/Computer-Aided Manufacturing)

CATIA CAD

Communication Skills

Computer Workstations

Corrective Action

Cyber Warfare

Data Processing

Data Quality

Documentation

ERP (Enterprise Resource Planning)

Electronic Warfare

Energy Efficiency

Engineering

Engineering Change Management

Engineering Change Order

Ergonomics

Establish Priorities

Federal Government

Hazardous Materials/Substances

Identify Issues

Internet Security

Internet/IP Telephony

Lean Manufacturing

Local Government

Machine Tool

Machining

Maintenance Services

Manufacturing

Manufacturing Engineering

Manufacturing Execution Systems (MES)

Manufacturing Methods

Manufacturing Process Engineering

Manufacturing Systems

Manufacturing Technology

Manufacturing/Industrial Processes

Materials Analysis

Materials Engineering

Materials Management

Materials Testing

Mentoring

Microwaves

Problem Solving Skills

Process Engineering

Process Improvement

Process Manufacturing

Product Design

Product Management

Product/Service Launch

Proofreading

Quality Engineering

Requirements Management

Risk Management

Satellite Communications

Security Clearance

State Government

Supply Chain

Technical/Engineering Design

Time Management

Tool and Die Manufacturing

Training/Teaching

United States Citizen

United States Military

Willing to Travel

Pereless

FEED

Experienced RequiredBachelor's degree in a relevant scientific discipline (biology, biochemistry, immunology, etc.) with 3+ years of experience in quality control testing, analytical development, or GMP; OR a Master's degree in relevant scientific disciplines with 1+ years of experience . Work ConditionsMany roles must be able to work at either Orca Bio Sacramento location (3400 Business Dr. or 7910 Metro Air Pkwy) based on operational needs, as well as regularly participate in video-based meetings.

More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks.With our purified, high-precision investigational cell therapies we hope to not only replace patients' bloodand immune systems with healthy ones, but also restore their lives. We have built a state-of-the-art, 100,000-square-foot manufacturing facility in Sacramento, CA (7910 Metro Air Pkwy) to ensure the consistent and reliable delivery of our high-precision cell therapy products. This site is essential to advancing our clinical pipeline and supporting future commercial availability of our life-saving therapies. The Specialist, Quality Assurance position is a key role in meeting the quality policy through their management of the different quality systems, including production records and deviation system management. The ideal candidate will be responsible for managing the quality systems, including deviations, change control, corrective and preventive actions (CAPA), and document management. Additionally, this role involves making timely batch disposition decisions to ensure quality standards are met before product release, supporting the rapid processing times required by our product. You will have the unique opportunity to make a difference in the lives of many patients as Orca Bio develops next-generation cell therapies. Physical Demands <ul><li>Production Associate Roles: Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment. </li><li>Most roles must be able to meet cleanroom gowning requirements, including wearing full gowning (face coverings, gloves, hoods, goggles) for extended periods, as needed. Use of cosmetics (makeup, painted nails), jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed. </li></ul>Work Conditions<ul><li>Many roles must be able to work at either Orca Bio Sacramento location (3400 Business Dr. or 7910 Metro Air Pkwy) based on operational needs, as well as regularly participate in video-based meetings. Also, may be required to work scheduled overtime, weekends, or holidays based on business needs. </li></ul>Responsibilities Quality System Management: <ul><li>Oversee the management of quality systems including deviations, change controls, CAPAs, and document control. </li><li>Ensure that all deviations are investigated thoroughly and timely, identifying root causes and implementing effective corrective actions. </li><li>Review and approve change controls to ensure compliance with regulatory requirements and internal procedures. </li><li>Maintain and improve CAPA processes to ensure effective resolution of quality issues. </li></ul>Batch Disposition: <ul><li>Evaluate batch records and associated documentation to make informed batch release decisions. </li><li>Collaborate with manufacturing and quality control teams to ensure all products meet regulatory and quality standards before release. </li><li>Monitor and document any quality issues related to batch production and implement corrective measures as necessary. </li></ul>Document Management: <ul><li>Maintain the document management system to ensure all quality-related documents are accurate, current, and compliant with regulatory standards. </li><li>Conduct regular reviews of quality documentation to ensure adherence to established protocols and procedures. </li></ul>Regulatory Compliance: <ul><li>Stay informed of current regulations, industry trends, and best practices in pharmaceutical quality assurance. </li><li>Assist in preparing for internal and external audits, ensuring that all quality systems and documentation are audit-ready. </li></ul>Training and Support: <ul><li>Provide training and guidance to staff on quality systems, processes, and compliance requirements. </li><li>Serve as a point of contact for quality-related inquiries and issues, fostering a culture of quality within the organization. </li></ul>Continuous Improvement: <ul><li>Participate in continuous improvement initiatives to enhance the effectiveness and efficiency of quality systems and processes. </li><li>Identify areas for improvement within quality operations and suggest appropriate solutions. </li><li>Track completion of quality records and maintain metrics. </li><li>Perform other duties as requested by supervisor/manager to support Quality </li><li>Work collaboratively with cross-functional teams, including manufacturing, research and development, and quality assurance, to support the overall quality of cell therapy products. </li></ul>General Requirements<ul><li>Communicate effectively with team members and contribute to a positive and collaborative work environment </li><li>Actively participate in group and project teamwork; project and process improvements </li><li>Strong organizational skills and the ability to manage multiple tasks concurrently </li><li>Willingness to learn and adapt in a fast-paced, dynamic environment </li><li>Adhere to cGMP policies and procedures, including documentation activities </li><li>Able to wear appropriate personal protective equipment </li><li>Willingness to work overtime as required </li></ul>Experienced Required<ul><li>Bachelor's degree in a relevant scientific discipline (biology, biochemistry, immunology, etc.) with 3+ years of experience in quality control testing, analytical development, or GMP; OR a Master's degree in relevant scientific disciplines with 1+ years of experience </li><li>Understanding of FDA regulations, GMP compliance, and quality system processes </li><li>Experience in quality control or GMP within a cell therapy or biopharmaceutical manufacturing environment is preferred </li><li>Able to meet project and testing timelines </li><li>Detail-oriented with a commitment to data integrity and accuracy, and an ability to identify problems with data management </li><li>Able to work collaboratively to respond to changing priorities and challenges </li><li>Ability to work both independently and collaboratively with a multi-disciplinary team in a fast-paced and regulated environment </li><li>Prior experience doing internal audits and document control management </li></ul> $75,000 - $90,000 a year The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. Full-time employment positions will also be eligible to receive pre-IPO equity and annual bonus, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include subsidized daily lunches and snacks at our on-site locations. Who we are We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them. We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility. We innovate on a path that hasn't been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren't afraid to ask "why not" and challenge the status quo. We maintain a start-up culture of camaraderie and leadership by example, regardless of title. We're proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers. Notice to staffing firms Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Weekend Manufacturing Jobs in West Sacramento, CA

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Weekend Manufacturing Jobs in West Sacramento, CA

Manufacturing Engineer I - IV Kratos Defense

Specialist, Quality Assurance - Weekend Shift (Friday-Monday) Orca Bio

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