Product Management Consultant
Research And Development Technician Job 219 miles from Nipomo
Amplytics is seeking an experienced Product Management Consultant to join our team. In this role, you will partner with clients to drive product strategy, lead requirements gathering, and oversee the implementation of data-driven solutions. You will serve as the bridge between business stakeholders, technical teams, and executive leadership.
Key Responsibilities:
Product Strategy & Definition
Lead stakeholder engagement sessions to identify business problems, define product goals, and translate them into actionable requirements and features
Develop and maintain comprehensive product roadmaps based on business priorities and technical constraints
Drive feature prioritization through collaboration with Business and IT stakeholders and executive leadership
Data Management & Quality
Oversee data discovery initiatives, including documentation of data sources, systems of record, and potential collection issues
Establish data quality frameworks and validation processes
Lead the development of data flow documentation and process improvements
Implement quality assurance protocols for both data integrity and business logic validation
Process & Change Management
Create and maintain detailed process documentation
Identify and address potential roadblocks while leveraging existing enablers
Develop change management strategies to ensure successful product adoption
Continuously evolve roles and responsibilities in partnership with Business and IT leadership
Stakeholder Management
Foster strong relationships with cross-functional teams including business units, IT, and executive stakeholders
Facilitate working sessions and follow-up meetings to drive decision-making and resolve open issues
Support development and IT teams to ensure timely product delivery
Present recommendations and status updates to executive leadership
Required Qualifications
5+ years of product management experience, with at least 3 years in consulting or client-facing roles
Proven track record of delivering data-driven products and solutions
Strong understanding of data management principles and quality assurance methodologies
Excellent facilitation and stakeholder management skills
Bachelor's degree in Business, Computer Science, or related field; MBA preferred
Skills & Competencies
Outstanding analytical and problem-solving abilities
Exceptional communication and presentation skills
Strong project management and organizational capabilities
Experience with agile methodologies and product development frameworks
Ability to navigate complex organizational structures and drive consensus
Proven ability to manage multiple workstreams and priorities effectively
Amplytics is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
Energetic Material Chemist
Research And Development Technician Job 137 miles from Nipomo
Country:
United States of America Onsite
At Raytheon, the foundation of everything we do is rooted in our values and a higher calling - to help our nation and allies defend freedoms and deter aggression. We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today's mission and stay ahead of tomorrow's threat. Our team solves tough, meaningful problems that create a safer, more secure world.
Opportunity to work in Materials & Process Engineering in Tucson AZ. This position will offer a qualified candidate the opportunity to engage our energetic suppliers to review energetic materials and ingredients data and solve engineering problems for single use energetic devices (one-shots) used to enable the function and deployment of our deliverable products. While energetics will be the prime focus, a candidate will also be working to solve day to day chemistry problems in our laboratory. One needs to have hands on experience with all classes of energetic material used in one-shots including formulation and manufacture while also having excellent wet chemistry skills to support routine day to day analysis of materials used in the manufacture of our products. Chemistry problems in our laboratory involve performing chemical analysis on various materials (adhesives, polymers, tapes, composites, metals, and various other production materials).
What You Will Do:
Assess materials based on conformance to specifications or conducting root cause failure analysis, leveraging knowledge of instrumental analysis, including spectroscopy, chromatography and thermal analysis
Tasks will require quick turn of analysis working with a multi-discipline team, requiring careful attention to detail and can be repetitive at times
Review energetic material data, testing, processes, and obsolescence at our energetic suppliers' part of the time while also supporting our programs with analytical analysis of common materials problems onsite.
Candidate must be able to manage and coordinate a wide variety of simultaneous tasks within set schedule requirements, while spending much of their time in the laboratory.
Knowledge and understanding of energetic safety requirements will be required for this position
Due to the physical nature of the work, qualified candidates must also be able to lift 22 lbs.
Travel, potentially including international, to supplier locations may be required.
The Energetic Material Chemist job is in Tucson, AZ and the position is onsite.
Qualifications You Must Have:
Typically requires a Bachelor of Science degree in Chemistry and a minimum of 5 years of prior relevant experience. In absence of a degree, 9+ years of experience. An advanced degree in a related field may be substituted for additional years of experience
Experience with energetic materials specific analysis and testing, including safety evaluations.
Experience in Analytical Chemistry and Instrumental Analysis, including Infrared Spectroscopy, Chromatography and Thermal Analysis (ie: FTIR, DSC, DMA, TGA, GCMS, HPLC, GPC, etc..)
The ability to obtain and maintain a U.S. government issued security clearance is required. U.S. citizenship is required, as only U.S. citizens are eligible for a security clearance.
Qualifications We Prefer:
Able to troubleshoot analytical instrument problems, perform analysis and interpret data.
Good communication, interpersonal, planning, teaming and time management skills
Proficient in MS Office (Excel, Word, PowerPoint)
Demonstrated ability to work effectively independently and with individuals from diverse communities and cultures
Demonstrated ability to work with colleagues who represent a diversity of work and conflict resolution styles
Demonstrated ability to lead and complete large scale multi-disciplined scientific based projects including failure analysis investigations
Ability to write concise technical reports summarizing analyses
What We Offer:
Our values drive our actions, behaviors, and performance with a vision for a safer, more connected world. At RTX we value: Trust, Respect, Accountability, Collaboration, and Innovation.
Learn More & Apply Now!
RTX solves some of the toughest challenges in aerospace and defense. That requires expansive thinking and bold innovation - and that, in turn, requires a culture that is diverse, equitable and inclusive.
We embrace individuality and diversity of thought to fuel opportunity for our employees, our customers, and our communities. We work toward progress, knowing that a more inclusive world is critical to our mission. Not just in this moment, but always.
Please consider the following role type definition as you apply for this role. Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products.
#LI-SM4
The salary range for this role is 82,000 USD - 164,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills.Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window.
RTX is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class.
Privacy Policy and Terms:
Click on this link to read the Policy and Terms
Operations Product Development - Design Intelligence Analyst
Research And Development Technician Job 180 miles from Nipomo
Job Title: Operations Product Development - Design Intelligence Analyst
Duration: 12 months
Pay Rate Range: $70/Hour
Intelliswift Software Inc. conceptualizes, builds, and supports the world's most amazing technology products and solutions. Our team of rich experts from diverse backgrounds contributes to making Intelliswift one of the most reliable partners in IT and Talent solutions. We specialize in delivering world-class Digital Product Engineering, Data Management and Analytics, and Staffing Solutions services to Fortune companies, SMBs, ISVs, and fast-growing startups.
Skills:
As an Operations Product Development (OPD) Design Intelligence Analyst you will engage with the Client Engineering, Operations, Procurement, Marketing, and OPD Product Manager teams to help shape product design & sourcing strategies that enable best-in-class hardware products.
Understand evolving consumer electronic technologies and be able to identify features, manufacturing processes, and materials in collaboration with cross functional supply chain and engineering partners
Utilize engineering expertise to model component cost estimates
Identify and develop opportunities to optimize architecture, materials, processes, and supply chain for cost.
Support product feature/implementation scenarios, supply chain investigations, environmental assessments, etc.
Provide and maintain aggregate data on industry trends
Hold regular executive forums to review architecture analysis and drive opportunities for cost, process & design optimization
Education:
BS/BEng (Mechanical or Electrical Engineering degree preferred)
5-7 years in product Engineering, Operations, or other relevant experience.
Equal Employment Opportunity Statement
Intelliswift celebrates a diverse and inclusive workforce. We offer equal employment opportunities to all applicants and employees. All qualified applicants will be considered regardless of race, color, sex, gender identity, gender expressions, religion, age, national origin or ancestry, citizenship, physical or mental disability, medical condition, family care status, marital status, domestic partner status, sexual orientation, genetic information, military or veteran status, or any other protected basis under the law.
Americans with Disabilities Act (ADA)
If you require a reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please contact Intelliswift Human Resources Department
Other Employment Statements
Intelliswift participates in the E-Verify program.
Learn More
For information on Intelliswift Software, Inc., visit our website at *********************
R&D Engineering Manager
Research And Development Technician Job 255 miles from Nipomo
A leader in the Defense industry is looking for an expert in R&D, to develop new products. and lead a team of engineers, quality and test people.
Experience in Defense related products
Experience in Actuation systems will be given preference. Experience in developing electro-mechanical products a plus.
Ability to live or relocate to the Folsom area,
must be a US citizen,**
email resumes to ****************************
Medical Affairs Research Associate
Research And Development Technician Job 181 miles from Nipomo
Job Title: Medical Affairs Research Associate
Onsite Requirements:
Top Skill #1 - Someone with proven track record of working within Cardiology and working in the cardiac space.
Top Skill #2 - Experience in working with soft tissue (handling, histology and fixation, including staining and dissection).
Top Skill #3 - Previous experience with Bioinstrumentation laboratory equipment and experience in working with large animal (porcine/ovine, etc) and bench top models.
Job Description:
Summary:
Essential Duties and Responsibilities include the following. Other duties may
be assigned.
Independently works on in-vivo and bench models for the investigation of cardiac
products and how they perform in a simulated clinical use setting.
Independently identifies data outliers, prepares data for statistical analysis for in-vivo
study data
Assists in in-vivo protocol execution, may develop or be a part of developing new
processes/test fixtures or methods for medical device testing
Interfaces with internal customers within R&D, Medical Safety, and Quality
May be asked to assist in model development for proper statistical analysis of in-vivo,
clinical, and other parametric datasets
May be asked to assist in the production of mathematical and/or computational
modeling of cardiac systems using electromechanical design and controls
Responsible for ensuring personal and company compliance with all Federal, State, local
and company regulations, policies and procedures for Health, Safety and Environmental
compliance as well as develop a strong working knowledge of design controls and
quality assurance standards of procedure.
Has a working knowledge of good laboratory practices and operating room procedures
Willingness to develop an understanding of cardiac electrophysiology procedures and
the products used
Excellent oral and written communication skills are required.
Qualification Requirements:
To perform this job successfully, an individual
must be able to perform each essential duty well.
The requirements listed below are representative of the knowledge, skill, and/or ability required: Experience in working with soft tissue (handling, histology and fixation, including staining and dissection).
Previous experience with Bioinstrumentation laboratory equipment.
Experience in working with large animal (porcine/ovine, etc) and bench top
Strong working knowledge with all of the programs listed: MicroSoft office
(specifically Excel and Powerpoint), statistical analysis tools (such as SAS or
Minitab, R, SPSS), and working knowledge of Mathematical modeling MatLab
software or Prism.
Education and/or Experience:
A minimum BS in the Sciences or Engineering or
equivalent from an accredited Laboratory Science program, College or University.
At least 5-8 years of Laboratory experience (Industry and/or Hospital); and/or related
medical device development experience and/or training is required.
Experience in cardiology, cardiac biophysics and anatomy are preferred.
Other Skills and Abilities:
Computer skills is strongly required.
Good written and oral English communication skills essential.
Weekends, Domestic travel will be required at least 40%.
** 3rd party and subcontract staffing agencies are not eligible for partnership on this position. 3rd party subcontractors need not apply. **
Clinical Research Data Developer/Manager
Research And Development Technician Job 246 miles from Nipomo
Daily Responsibilities:
Manages all aspects of clinical database design and reporting.
Establishes and maintains policies and procedures for gathering, analyzing, and reporting clinical data.
Standardizes data management procedures and documents departmental operating procedures.
Prepare data analysis listings and activity, performance, or progress reports.
Process clinical data including receipt, entry, verification, or filing of information.
Prepare appropriate formatting for datasets as requested.
Design, manage, and validate clinical databases and large data repositories including designing or testing logic checks.
Design forms for receiving, processing, and tracking data.
Develop or select specific software programs for various research scenarios.
Write work instruction manuals, data capture guidelines, or standard operating procedures.
Train staff on technical procedures or software program usage.
Read technical literature and participate in continuing education or professional associations to maintain awareness of current database technology and best practices.
Provide support and information to functional areas as related to research.
Evaluate processes and technologies and suggest revisions to increase productivity and efficiency.
Develop technical specifications for data management programming and communicate needs to information technology staff.
Contribute to the compilation, organization, and production of protocols, clinical study reports, regulatory submissions, or other documentation.
Monitor work productivity or quality to ensure compliance with standard operating procedures.
Generate data queries based on validation checks or errors and omissions identified during data entry to resolve identified problems.
Confer with end users to define or implement clinical system requirements such as data release formats, delivery schedules, and testing protocols.
Develop project-specific data management plans that address areas such as data coding, reporting, or transfer, database locks, and workflow processes.
Compile NMCSD clinical data from a variety of sources.
Required Education & Experience:
Education:
A four-year baccalaureate degree is required in health informatics, computer science, computer engineering, statistics, business administration, or equivalent field.
Experience:
2+ years of data development/managing experience.
Preferred and Critical: Extensive experience in the NDR (National Data Repository) - requires specialized knowledge and how to pull the data.
Methodical and strategic thinking.
Project management skills.
Strong writing skills.
Computer literacy.
Excellent communication skills, both verbal and written.
Ability to meet deadlines
Clearance:
Candidates must be able to secure and maintain Tier 3 Non-Critical Sensitive security clearance
Principal R&D Engineer : Bioresorbable Scaffold For Peripheral Arterial Disease : Hybrid Bay Area
Research And Development Technician Job 173 miles from Nipomo
Principal R&D Engineer
Class III Bioresorbable Scaffold : PAD Intervention
Product Design / Development : V&V / Design Transfer
Hybrid Bay Area : Full Time Direct Hire
Our client is a rapidly growing Bay Area leader in the vascular intervention arena developing a novel 1st of its kind class III sirolimus coating bioresorbable scaffold aimed to improve the standard of treatment for below-the-knee (BTK) peripheral arterial disease (PAD).
This new stent platform is uniquely designed with an ultra-high molecular weight polylactic acid polymer to balance strength and flexibility as a well-needed advancement over traditional metal drug-eluting stents.
This new PAD stent innovation will be a much-welcomed alternative to below-the-knee amputation and could be a highly disruptive concept in a $2.5B+ US PAD market.
Current critical need is toward a new Principal R&D Engineer position responsible for developing and supporting new and existing technologies, products, equipment, and processes. The position plays a critical role in technical leadership and directly contributes to development and manufacturing of innovative vascular solutions through the product lifecycle.
Our client has just recently raised a substantial tranche of new financing to fund company-wide organizational expansion ensuring this new Principal R&D Engineer is well-resourced to complete their mission.
Responsibilities:
Product & Process Development
Develop concepts and prototypes for new and existing products and manufacturing processes.
Actively participate or lead user needs assessment process through interacting with KOLs, clinicians, and Clinical Affairs and Operations staff.
Create product, assembly, and parts specification, CAD models, and drawings.
Manage parts suppliers or contract manufacturers to create parts that meet specification.
Leadership and Management
Provide technical leadership to company teams. Provide training and mentorship to engineers and technicians. Educate Operations and Clinical Affairs teams on technical details and proper function/use of tools and devices.
Organize and execute development and improvement projects.
Develop and maintain comprehensive clinical and technical product knowledge. Recognize and understand competitive products including industry trends.
Product & Process Validation and Verification
Validate and verify device and parts designs and manufacturing processes through methodical scientific tests.
Write test protocols, conduct tests, and write test reports to document validation and verification activities.
Actively participate or lead risk assessment reviews and phase reviews for new and existing devices and processes.
Assist in resolving complaints in a prompt and effective manner to include proper device or process complaint investigations.
Participate in device performance evaluation through pre-clinical & clinical tests.
Manufacturing Knowledge Transfer and Training
Document manufacturing and testing processes for Operations to ensure consistent process output.
Assist in managing and training Operation staff on executing manufacturing and testing instructions.
Monitor manufacturing process output, root cause issues, and create solutions to increase process success.
Administrative Responsibilities
Support clinical by providing technical details for devices and procedures and participating in planning and monitoring clinical cases.
Participate in managing device production and inventory including device shipments, usage and return of product.
Communication
Maintains a high level of communication with cross functional team members and leadership.
Qualifications:
Educational Requirements
Bachelor's degree in engineering
Excellent interpersonal and written communication skills.
Experience
Minimum of 5 years of medical device development and manufacturing.
Experience in medical device development. Knowledge of regulated medical device industry and clinical environment.
Demonstrated understanding of anatomy, physiology, and pathway to care.
Stent/ Catheter/ Peripheral Vascular intervention experience is preferred.
IDE/PMA/regulatory experience with catheter, stent, drug delivery device.
Firm grasp of scientific and engineering concepts associated with materials, mechanics, heat transfer, flow dynamics, mechatronics, software UI either through undergraduate/graduate program or on-the-job training.
Hands on concept-to-prototype and tech transfer to manufacturing experience.
Hands on packaging/sterilization, V&V protocol/testing/reporting experience.
Hands on CAD/CAM/FEA, traditional machining, and rapid prototyping experience.
High degree of familiarity with preclinical and clinical operations.
Experience in managing prototyping/manufacturing schedule and staff.
Research Scientist- Process Development (Cell and Gene Therapy)
Research And Development Technician Job 246 miles from Nipomo
Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease. A Japan-based company, our goal is to make people smile by delivering breakthroughs where no adequate treatments currently exist, working from drug discovery to product development and commercialization. In North America, we are headquartered in Princeton, NJ, with offices in California, Massachusetts, and Ontario.
Summary:
The Research Scientist I/II, Process Development will support Kyowa Kirin's cell therapy pipeline programs in a highly collaborative environment. This position will play a key role in developing next-generation cell therapy programs from drug discovery to IND.
Essential Functions:
* Design, optimize and scale processes for pipeline projects
* Conduct experiments and analyze data to support process improvements
* Collaborate with R& D, quality assurance and manufacturing teams to ensure seamless process integration
* Maintain compliance with regulatory guidelines and internal standards
* Identify opportunities for automation and process enhancement
* Troubleshoot and resolve process-related issues in a timely manner
* Provide support for technology transfer to CMC/CRO/CDMO.
* Prepare necessary documentation for project reviews (proposals, monthly, quarterly, annual, or study reports), patent applications, publications, and/or animal, biosafety, or human subject protocols.
* Present individual research at group and project meetings and efficiently records experiments and data in laboratory notebooks, databases and monthly reports.
Requirements:
Education
Ph.D. in Biological Sciences, Immunology, Molecular Biology, Biochemistry, or closely related discipline
Experience
* Minimum five (5) years' biotech/pharma industry or academia experience in cell therapy process development.
* Extensive knowledge of cell therapy concepts and exploration, including in vitro and in vivo study experience
* Hands-on experience in developing and characterizing cell therapy products including HSC, iPSC and/or CAR-T.
* Familiarity with synthetic biology concepts and approaches including gene and/or base editing.
* Understanding of relevant Regulatory guidelines (GMP, ISO, ICH) is preferred.
* Familiarity with FDA regulatory requirements for Cell Therapy is desired.
* Experience with handling, culturing and differentiation of human stem cells to various types of immune cells is highly preferred.
* Experience with development of potency assays and other related QC release assays is highly desired.
Technical Skills
* Strong knowledge of Immunology, Hematology and/or Cancer Biology.
* Comfortable in a fast-paced environment and able to adjust workload based upon changing priorities.
* Excellent written, verbal, and listening communication skills: articulate and effective communicator and presenter.
* Self-motivating and creative, able to work within a team and collaborate proficiently with colleagues to achieve program goals.
* Demonstrated familiarity with flow cytometry and other immunostaining assays.
* Experience with gene modification and genome editing technologies.
* Experience in handling viral vectors.
* Stem cell culturing and differentiation into immune cells.
* Ability to manage a high-volume workload and adapt to workload based upon changing priorities.
* Solid proficiency in Microsoft Office Suite (Excel, Word, Outlook, etc.).
Annualized base salary ranges from $105,000 - $135,000 plus short term incentive bonus; actual salaries will vary and may be above or below this range commensurate with various factors including but not limited to experience, education, training, and merit.
KKNA and all of its employees have an obligation to act in accordance with the law and with integrity in all our operations and interactions
It is the policy of Kyowa Kirin North America, Inc. to provide equal employment opportunity to all qualified persons without regard to race, religion, creed, color, pregnancy, sex, age, national origin, disability, genetic trait or predisposition, veteran status, marital status, sexual orientation or affection preference or citizenship status or any other category protected by law.
When you apply to a job on this site, the personal data contained in your application will be collected and stored by Kyowa Kirin, Inc. ("Controller"), which is located at 510 Carnegie Center Dr. Princeton, NJ 08540 USA and can be contacted by emailing ****************************************. Controller's data protection officer can be contacted at usprivacyoffice@kyowakirin.com. Your personal data will be processed for the purposes of managing Controller's recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes. Such processing is legally permissible under Art. 6(1)(f) of General Data Protection Regulation (EU) 2016/679 ("GDPR") as necessary for the purposes of the legitimate interests pursued by the Controller, which are the solicitation, evaluation, and selection of applicants for employment.
Your personal data will be shared with Greenhouse Software, Inc., a cloud services provider located in the United States of America and engaged by Controller to help manage its recruitment and hiring process on Controller's behalf. Accordingly, if you are located outside of the United States, your personal data will be transferred to the United States once you submit it through this site. The transfer will be made using appropriate additional safeguards under the standard contractual clauses approved by regulators for transfers of personal data outside the European Union.
Your personal data will be retained by Controller as long as Controller determines it is necessary to evaluate your application for employment. Under the GDPR, if you are located in the European Union, you have the right to request access to your personal data, to request that your personal data be rectified or erased, and to request that processing of your personal data be restricted. You also have the right to data portability, and to lodge a complaint with an EU supervisory authority. If you have any questions about our use of your data, you may contact us by email at usprivacyoffice@kyowakirin.com.
Recruitment & Staffing Agencies
Kyowa Kirin does not accept agency resumes unless contacted directly by internal Kyowa Kirin Talent Acquisition. Please do not forward resumes to Kyowa Kirin employees or any other company location; Kyowa Kirin is not responsible for any fees related to unsolicited resumes.
#LI-TT1 #La Jolla
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R&D Engineer- SiPho
Research And Development Technician Job 178 miles from Nipomo
Client: Tower Semiconductor
R&D Engineer - SiPho
Duration: Permanent
Openings: 1
Salary: Flexible, $75,000-$170,000 depending on years of experience
Interview Process:
1st round: Microsoft Teams Interview
2nd round: Microsoft Teams Panel Interview
Role Overview:
Insight Global is hiring a R&D Engineer focused on Silicon Photonics for a leading Semiconductor company in Newport Beach, California. The R&D Engineer will be responsible for research, development, and improvement of existing and newly developed devices and process technologies for manufacture of Silicon Photonics-related devices in a Semiconductor wafer foundry. This individual will exercise independent judgement in developing methods, techniques, and evaluation criteria.
Day-To-Day:
Process technology development and implementation in a VLSI manufacturing, foundry environment.
Silicon photonic device design, characterization, and optimization.
Participate and coordinate experiments toward technology development and yield enhancement.
Work closely with process engineering team, test team, and customers to define goals and manufacturing solutions.
Design test structures in CAD and define tests for device characterization in ICCAP, Labview.
Provide support to resolve customer issues, problems, and questions.
Support transfer from development to production for processes variants.
Support process transfer to worldwide fabrication facilities when needed.
Basic Qualifications:
Bachelor's, Master's, or PhD degree in Electrical Engineering, Physics, Mat Sci, Chemical Engineering or related fields.
5+ years of experience in Silicon Photonics-related process and device development.
MUST BE AN EXPERT in Silicon Photonic and Optoelectronic devices.
Strong verbal and written communication skills. Strong problem solving and data analysis skills.
Technology requirements:
Optical simulation software (Lumerical)
Ability to read and edit mask layout data (Cadence Virtuoso)
Statistical data processing (R or JMP)
Device and process TCAD simulation tools (Medici, Sentaurus)
Semiconductor FAB lot management (PROMIS, Workstream)
Research And Development Engineer
Research And Development Technician Job 246 miles from Nipomo
VIE Technologies is revolutionizing industrial and utility operations with a fully autonomous and non-invasive predictive solution that minimizes maintenance losses, saves energy, reduces downtime, enhances product quality, and improves plant safety. Headquartered in San Diego, CA, our virtual expert combines cloud artificial intelligence with proprietary sensors to preemptively find hidden failure modes in electrical transformers and industrial machinery. VIE Technologies was founded in 2017 by technology veterans.
Role Description
This is a full-time hybrid role as a Research And Development Engineer at VIE Technologies. The role involves conducting research, testing, product development, and utilizing analytical skills to support the innovation and enhancement of our predictive solution. Essentially you are solving problems that are at intersection of Physics, signal processing, electrical/mechanical engineering and data science. Our strength is to adapt quickly to changing requirements and address varied variety of problems by bringing learning from different fields together. In addition to exploratory work, you will be hands on writing code, testing it with real world data and integrating your solution both on device and the cloud, while collaborating with SW engineers for efficient and scalable implementations.
This is a hybrid job. While we value flexibility, we would prefer a candidate who is able to frequently meet the other team members onsite in San Diego office for brainstorming, white board discussions as and when needed.
Qualifications
Master's or PhD in Electrical Engineering or any other related discipline. Background in electro-magnetic modeling with machine learning applied to scientific and engineering problems is highly desired.
Skilled in Python for developing advanced algorithms, including machine learning and signal processing. Familiarity with tools like TensorFlow or PyTorch is a plus.
Knowledge of power grid systems with transformers and switchgears, including operational metrics and fault diagnosis, is highly valued.
Experience with predictive maintenance, IoT-based sensor systems, condition monitoring systems for mechanical or electrical equipment, or handling large-scale data is a plus.
Familiarity with applying vibration analysis for fault detection and signal processing is a plus.
Proven experience working in multidisciplinary teams, collaborating with engineers and experts from various fields to create innovative solutions.
Comfortable working in a fast-paced, startup-like environment, adapting quickly to new challenges and shifting priorities while staying productive and creative.
Strong problem-solving skills with the ability to simplify complex technical ideas into clear and practical solutions.
Excellent communication skills, including presenting research insights and writing technical reports.
Self-starter and able to drive oneself in fast pace startup environment.
R&D Engineer II
Research And Development Technician Job 221 miles from Nipomo
DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES.
RECRUITERS: DO NOT CONTACT.
Responsibilities:
The R&D Engineer will use engineering knowledge to design, develop, verify and validate product designs in support of company's strategic plan. Contribute as part of a cross‐functional team in product design and development, process development and optimization, and verification & validation testing to support product transfer to manufacturing.
Responsibilities:
Prepare documentation to support quality system for design functions (project plans, concept document, FMEA, design input, test results, drawings, etc.)
Prepare technical documentation, including manufacturing instructions, test methods, drawings, BOMs, protocols, and reports to support design control activities.
Perform Verification and Validation (V&V) and may draft protocols/reports for approval.
Work with engineers & QA to create new components, assemblies, or tools.
Conducts testing to verify that the design meets the engineering specifications.
Document engineering work in compliance with the company's quality system.
Identifies hazards and mitigates risk associated with identified hazards in Design and Process FMEA. Assess failure modes and conduct technical risk analysis.
Compiles and analyzes data, identifies causes, draws conclusions, generates reports.
Provide hands‐on, technical execution in the prototyping and development of devices.
Manages processes and ensures that activity goals are achieved.
Training and/or providing work direction to technicians and less experienced engineers.
Support the development of specifications for tooling and fixturing according to company quality standards.
Qualifications:
Education & Experience:
Engineering degree desired or equivalent experience in related job field.
2+ yrs Biomedical product or medical device development experience (catheter experience desirable).
Working knowledge of mechanical design principles and FDA regulated medical device design controls a plus.
Proficient in CAD software, preferably SolidWorks.
Familiarity with statistical analysis of raw data is required, proficiency in Minitab is preferred.
Understanding of IEC60601 requirements/constraints for mechanical system design is preferred.
Experience managing suppliers and/or contract manufacturers a plus.
Hands-on mechanical prototyping, verification, and failure analysis skills.
Familiarity with design control according to 21 CFR 820 or ISO 13485, engineering change orders (ECO), Corrective Actions and Preventive Actions (CAPA) preferred.
Skills & Abilities:
Proficient in Risk Management according to ISO 14971.
Knowledge of ASME Y14.5 GD&T.
Excellent interpersonal, communication, and documentation skills are required.
Proven self-starter who runs towards critical issues, ambiguous requirements, or loosely defined challenges with a demonstrated ability to rally teams to achieve business results.
Takes initiative and acts quickly to drive solutions.
Strong interpersonal, organizational and communication skills.
A flexible team player, focusing on shared goals with a positive results‐oriented attitude.
QC Scientist II
Research And Development Technician Job 181 miles from Nipomo
The Quality Control Analyst is responsible for conducting the cell-based potency assays(CBPA) of biologics for release and stability of both commercial and late-stage biologics under current good manufacture practice(cGMP).
He/She will prepare all documentation associated with the cGMP testing and independently or in a team setting execute protocols in support of manufacture of biologics product.
The position is responsible for cGMP compliance of the quality control CBPA laboratory, ensuring that all cell Based Potency Assays testing is performed according to the FDA, foreign MOH and requirements.
Major Responsibilities:
· Perform cGMP testing in support of the manufacture of biologics products.
· Generate, compile, and evaluate data for technical reports to support commercial and clinical supplies.
· Review and approve raw data and laboratory logbooks/worksheets.
· Perform cell culture and cell banking.
· Manage critical reagents and supplies.
· Write quality systems records including laboratory investigations, change controls, non-conformances.
· Support regulatory inspections where needed. ·
Perform and execute activities supporting CBPA lab such as equipment validation, equipment preventive maintenance. ·
Generate and update SOPs.
Regulated Responsibilities (including cGMP and EHS):
Client is regulated company and the incumbent is expected to be fully compliant with all criteria established by governmental agencies, Ministry of Health, and legislative requirements including, but not limited to: the FDA, European Community (EC), ISO 13485 - Medical Devices, European Economic Community Medical Device Directive (MDD), Canadian Medical Device Regulations (CMDR), OSHA, Sarbanes-Oxley, EPA, DOT, EEOC, and ADA. Incumbent will work to ensure that the company is in compliance with all environmental, health and safety requirements and assure our business practices enhance the welfare of our customers, employees and the community in which we operate.
Qualifications:
· Proficiency in TrackWise, Microsoft Project, and Excel.
· Experience in a GMP regulated environment.
· Experience in bioassays, Chemi-ELISA preferred.
· Experience with aseptic cell culture and cell banking preferred.
Top 3-5 skills, experience or education required
1. MS in Chemistry/Biochemistry/Cell Biology or a related Biological Science field with 3+ years of relevant industrial experience or BS in Chemistry/Biochemistry/Cell Biology or a related Biological Science field with 5+ years of relevant industrial experience.
2. Experience in a cGMP regulated environment required.
3. Experience with the application of aseptic cell culture and 96-Well format bioassay techniques for potency determination of proteins and their degradation and modification products
About US Tech Solutions:
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 ************************
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Recruiter Details:
Name: Shivangi
Email: *********************************
Internal Id: 25-29766
Manufacturing Scientist II
Research And Development Technician Job 252 miles from Nipomo
Wondering what's within Beckman Coulter Diagnostics? Take a closer look.
At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.
Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges.
The Manufacturing Scientist II for Beckman Coulter Diagnostics is responsible is responsible creating batch records and specifications to support product batches, manufacturing those according to the specifications, and coordinating delivery to the end customer. Additional responsibilities include being a Core Team member on R&D product development teams. Supports manufacturing operations with scientific expertise to ensure successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization; failure investigation of commercialized products; support processes to ensure performance within expected parameters. Includes laboratory roles.
This position is part of the Microbiology Operating Company located in West Sacramento and will be a fully on-site position. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.
You will be a part of Microbiology Operations and report to the Director of Technical Operations responsible for Manufacturing and Technical Operations. If you thrive in a multifunctional, leadership, fast paced, supporting role and want to work to build a world-class Microbiology supply chain organization-read on.
In this role, you will have the opportunity to:
Create batch records and specifications according to the requirements provided by internal customers
Create part numbers and complete change orders for Piloting document control
Write Supply Chain plans and reports
Execution of product transfers to production
Complete product cost estimates and develop bill of materials for new products
The essential requirements of the job include:
Bachelor's degree in Life Science or Engineering with 2+ years of experience
Experience with Design Transfer of new products into Manufacturing
Excellent interpersonal, oral, and written communication and problem-solving skills
Experience with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP)
Experience in a manufacturing environment is preferred
It would be a plus if you also possess previous experience in:
Computer proficiency, including Word and Excel
Supporting continuous improvement initiatives
The salary range OR the hourly range for this role is $74,000-$90,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit ****************
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
The EEO posters are available here.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.
Research And Development Engineer
Research And Development Technician Job 246 miles from Nipomo
The Design Engineer for the Research and Development Department must have the ability to research, design and detail mechanical and electromechanical products and systems, as well as direct and coordinate activities involved in fabrication, operation, application, installation, and repair of mechanical or electromechanical products and systems.
Type: 6 month Contract to Hire
Contract Pay Rate: 32/hrly - 35/hrly
Permanent Pay Rate: Same pay rate not to exceed 36/hrly + Benefits
Schedule: Hybrid - 2 Days onsite
Location: Chula Vista, CA
*Qualified candidates must have a Bachelor of Science degree, preferably in Mechanical Engineering.
Responsibilities for the R&D Design Engineer
Design and detail recycling machinery from concept to series production under consideration of manufacturability, serviceability, and costs.
Modification of machines to fit individual applications.
Generate accurate, detailed manufacturing drawings in SolidWorks software, and complete in a manner consistent with company design guidelines and industry GD&T standards.
Close interaction with production, vendors, and other related departments to deliver a high-quality product on time and on budget.
Consult with engineers and managers regarding materials, specifications, and design criteria to ensure models and drawings are developed per customer and system requirements.
Communicate with vendors to gather necessary information about parts and applications and provide detailed information to the purchasing department.
Define and coordinate fabrication and installation activities to ensure products and systems conform to engineering, design, and customer specifications.
Synthesize complex or diverse information; collect, research, and interpret data; define production procedures and design required fixtures / devices; generate creative solutions; apply design principles; utilize engineering tools like FEA simulation, engineering formulas; demonstrate attention to detail.
Minimum requirements for the R&D Design Engineer:
Bachelor of Science degree in Mechanical Engineering.
2-3 years of professional experience in 3D modeling and drafting in SolidWorks.
Knowledge of mechanical parts, hydraulics, and pneumatics.
Understanding of manufacturing processes such as sheet metal forming, welding, machining, assembly.
Proactive, solution and detail oriented, good communication skills.
Fluent in English.
For other opportunities available at Akkodis go to **************** If you have questions about the position, please contact ********************************
Equal Opportunity Employer/Veterans/Disabled
Benefit offerings include medical, dental, vision, term life insurance, short-term disability insurance, additional voluntary benefits, 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. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs which are direct hire to a client
To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit **********************************************
The Company will consider qualified applicants with arrest and conviction records.
R&D Engineer II
Research And Development Technician Job 176 miles from Nipomo
This is a hands-on individual contributor position with responsibility for the following areas: support concept/design development, component/material sourcing, design verification and validation, project engineering, and early manufacturing engineering, in accordance with the company's Quality System and customer requirements. Salary range: $99,000 - $148,000
Job Details/Responsibilities
1. Concept Development: Able to provide input to the development of unique solutions to complex problems that solve clinical challenges, as well as engineering challenges as they relate to product and manufacturing.
2. Design Development: Able to provide to take a concept to reality, converting prototype materials into manufacturable components and assemblies. This includes decisions on whether to insource or outsource certain assembly processes, based on capability, and cost. This includes the ability to determine best options for manufacturing, whether injection molded, machined, or otherwise, knowing what will help to make a component or material that meets the functional needs at a reasonable price.
3. Component and Materials Sourcing: Able to identify suppliers for individual components and materials, and support specification development, procurement, component inspection, and resolution of non-conformances related to receipt of first lots.
4. Verification and Validation Efforts: Able to drive efforts that test the frozen design against the market and technical requirements of the finished good,
a. Can establish, and release protocols to test the design against the customer requires specification or the product specification
b. Drive the build(s) of traceable lots of finished goods that can be tested under the released protocols.
c. Coordinate and/or lead testing the finished goods per the released test methods, as defined in the released protocols. Tests to include simple visual inspections and dimensional measurements using equipment such as Instrons, leak testers, and other complex pieces of equipment.
d. Ensures effective data collection, data analysis, document drafting, and report releasing based on the requirements established in the protocol.
Job Responsibilities (continued)
5. Project Engineering: As part of a project team, or on an individual basis contribute to the development of detailed specification, construction of prototypes for new products or current product enhancements. Design product testing protocols. Set up and run product testing and protocols in accordance with project plans. Research and recommend vendor and material choices for product. Required to prepare and deliver status reports.
6. Manufacturing Engineering: Support Manufacturing Engineering group in process validation activities. Design and qualify tooling and equipment for the timely and cost-effective manufacture of products. Work directly with Production and Quality Assurance Personnel to ensure that manufacturing documentation is in accordance with the Quality Systems.
7. Supervision: May be required to train Assemblers and Technicians in the project group.
8. Regulatory Compliance: Provide support in engineering testing and documentation that is in accordance with regulatory requirements for approvals of products by the U.S. and foreign regulatory agencies.
9. Responsibilities to the Quality System: Support the Quality System and Quality Policy. Be aware of Quality System procedures and requirements including regulatory requirements and training requirements for position activities. Inform responsible personnel of concerns involving product quality.
10. Intellectual Property: Ensures technical activities are properly documented in lab notebook. Participates in and contributes to technical discussion sessions to generate new intellectual property.
11. Safety: Perform all activities and documentation related to employee health and safety and ensure compliance with all legal and regulatory requirements. Performs job functions in a safe and effective manner.
12. Other Duties: As assigned.
Working Conditions/Physical Requirements
This position is located in Campbell, California and requires 10-20% travel to Terumo facilities and other destinations such as hospitals or suppliers.
Knowledge, Skills and Abilities (KSA)
1. Demonstrated skill in analytical problem solving; ability to systematically investigate issues and implement fixes under general supervision.
2. Demonstrated skill in technical writing; ability to write low level documents such as Manufacturing Process Instructions and Component Specifications under general supervision. Ability to generate higher level documents such as Protocols and Reports under regular supervision.
3. Basic understanding of key regulations/standards for medical product manufacturing and development: 21 CFR 820 (Quality System Regulation), 21 CFR 803 and 804 (MDR regulations), ISO 13485, ISO 14971, and MDD 93/42/EE.
4. Ability to execute established procedures and protocols under general supervision.
5. Ability to train Assemblers and Technicians to applicable standards.
6. Ability to manage small projects under regular supervision.
7. Proficiency using general business software like Microsoft Office and Windows applications; Word, Excel, PowerPoint, Project.
8. Skilled in the use of CAD software such as AutoCAD, SolidWorks, Pro Engineer (preferred).
9. Skilled in the use of statistical analysis software such as Excel or Minitab.
10. Knowledge of data collection, analysis, and documentation techniques.
11. Knowledge of Design Control procedures and requirements, including risk management.
Qualifications/ Background Experiences
Bachelors degree in sciences, Engineering or related discipline required, Masters degree preferred, or equivalent combination of education, training and experience.
Minimum of 2 years previous experience in design, manufacturing or quality engineering required.
Experience working under quality systems designed to meet governmental regulations such as FDA QSR, ISO 13485, and the MDD required.
Experience in a start-up environment preferred.
Experience with catheter-based medical devices preferred.
We provide competitive and comprehensive benefit options that allow you to design your own plan based on your individual needs which include: paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program. Salary range: $99,000 - $148,000
Chemist I (Industrial)
Research And Development Technician Job 121 miles from Nipomo
Chemist I (Industrial) - Valencia & Burbank, CA
Company Benefits
100% employer paid medical and dental
401(k) matching contribution
Generous PTO and paid holidays
Long-term disability
Life and AD&D
Health Care and Dependent Care Flex Spending
Tuition reimbursement
Profit-sharing program
Pay: $26.89 - $28.39 hourly
Position is Onsite
Company Overview
Contributing to Saving Lives
The Eckert & Ziegler Group is one of the world's largest providers of isotope technology for medical, scientific, and industrial use. The core businesses of the Group are Diagnostic Nuclear Medicine Imaging, Cancer Therapy, and Industrial Radiometry.
Business Segment Overview
Eckert & Ziegler Isotope Products provides sealed and unsealed radiation sources and materials for Medical Imaging sources; Industrial sources for measurement and analysis; Oil Well Logging sources and related products; Reference, Calibration and Environmental Monitoring sources and solutions; Bulk radioisotopes for pharmaceutical, therapeutic and industrial product manufacturing; Services for collection, recycling and disposal of sources and low-activity waste; Sources for industrial Non-Destructive Testing; High-Activity radiation sources for radiation processing and sterilization; Medical and Industrial irradiators for blood irradiation, sterilization or calibration.
The Job
Eckert & Ziegler Isotope Products seeks a Chemist I (Industrial) to join our team. Each Chemist is assigned production work orders to complete. The chemist is responsible for all work orders assigned to him/her by the group lead. While the director and lead provide oversight, the work is scheduled and processed by the chemist so that production deadlines are met, and quality is instilled in the product.
Duties:
Transfer, pipetting, and weighing
Epoxy mixing and pouring
Logging radionuclide and activities used in Microsoft D365
Daily cleaning and maintenance of production labs and facilities
Gamma camera scanning
Communication with other groups within the company to ensure timely product manufacture
Requirements:
Minimum education (or substitute experience) required: Bachelors or AA degree in related field + 6 months related experience (college coursework or internal experience is accepted).
Minimum experience required: 6 months related experience (college coursework or internal experience is accepted).
Abilities and skills required:
Experience in handling standard laboratory equipment such as pipettors, balances, mixers, and ovens are a plus.
Experience working with containment apparatus such as hoods and gloveboxes is also a plus.
Excellent manual dexterity and a steady hand are essential.
Knowledge of Microsoft Excel, Word, Outlook, and Access
Must be safety-oriented, neat, and clean.
Possess sound judgment and decision-making ability.
Ability to lift 30 pounds.
Capable of completing daily duties and orders unsupervised.
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
To apply please click on the link below or copy and paste into your browser.
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(To view, please copy and paste into your browser)
Compensation details: 26.89-28.39 Hourly Wage
PI8cf1e438c687-26***********4
Research And Development Engineer
Research And Development Technician Job 166 miles from Nipomo
Research and Development Engineering is responsible for the development and lifecycle management of products through medical device design control processes and good engineering and documentation practices. The Infusion Preparation and Delivery (IPD) platform seeks a hardworking and passionate leader to develop and drive technical strategies. Demonstrates working knowledge of Engineering principles and their application in solving standard technical problems. Demonstrates working knowledge of product design, development, and design control processes. Demonstrates knowledge to provide design documentation to support global Regulatory filing strategies. Applies basic statistical techniques and utilizes design of experiments with moderate guidance. Works with moderate guidance to achieve project objectives. Flexible work arrangements allow our team members to collaborate remotely and onsite to experiment, discover, create, and simply connect with others toward a common purpose.
Job Responsibilities:
• Lead R&D deliverables throughout the medical device design control process for intravenous infusion sets and connection devices
• Collaborate within a cross-functional team to plan, develop, modify, implement, and support IPD products through the application of rigorous engineering practices
• Engineer robust products through strong understanding and application of engineering fundamentals and DFSS principles.
• Develop technical plans and guide the team to develop design inputs, conduct analytical and empirical feasibility studies, refine product configurations and designs, verify and validate subsystems and systems, concurrently transfer designs alongside Manufacturing and Operations, and provide design documentation to support global Regulatory filing strategies
• Execute design verification testing to confirm design outputs meet design input requirements.
Required Qualifications:
• BS - Mechanical Engineering, Materials Engineering or Biomedical Engineering
• Work experience of 5 years or 3 years plus an advanced degree
• Critical thinking - able to work with moderate guidance in own area of knowledge.
• SolidWorks or equivalent CAD tool
• Experience with medical device design control processes and creating and maintaining design control documentation.
Chemical and Biological Technicians
Research And Development Technician Job 24 miles from Nipomo
Work in the cutting edge of the STEM field. Hone your chemistry and biology skills as you work with cutting edge equipment to prevent contamination or injury from hazardous materials.
Similar Jobs: Occupational Safety, Chemical and Biological Technicians
Engineering Technician II
Research And Development Technician Job 20 miles from Nipomo
Job Category: Service Contract Act Time Type: Full time Minimum Clearance Required to Start: Secret Employee Type: Regular Percentage of Travel Required: Up to 10% Type of Travel: Continental US * * * CACI has a great opportunity for a Vandenberg Space Force Base (VSFB) SATCOM Engineering Technician to provide Mission Essential support to the Satellite Control Network Tracking Station Operations Remote Site and Mission Partners (STORMS) contract which operates and maintains the SATCOM terminal at VSFB.
What You'll Get To Do:
* Performs operations and corrective/preventive maintenance on telecommunications equipment and circuits, RF equipment, secure communications equipment and computerized systems.
* Documents operations, performance testing, troubleshooting and maintenance activities in job registers and databases.
* Completes paperwork for equipment and spares inventories, and reports.
* Occasionally ascends/descends a ladder on antenna towers, at heights of 40 feet or more, and constantly positions self to work on equipment mounted lower in racks.
You'll Bring These Qualifications
* Education: AA/Vocational/Tech plus 3 years of experience (7 years of experience in lieu of degree) with managing/overseeing geographically separated Air Force/DoD contract operations, maintenance, and base operations functions
* Satellite Control Network (SCN) knowledge
* Interfacing with active-duty military and civil service personnel
* Must be a US Citizen
* Active Secret Security Clearance
Required Skills:
* Technically competent
* Self-motivated
* Attention to detail
* Ability to work independently
* Effective, professional interpersonal skills
* Strong team player
* Hardworking
Preferred Additional Skills:
* CompTIA Security+ certification
* Experience in troubleshooting at a system and circuit card / module level, coordinating and participating in RF and telecommunications troubleshooting efforts, and customer service for the Department of Defense.
* Background in operations and maintenance of DSCS/WGS satellite communications equipment.
* Background maintaining communications / electronics equipment.
* Previous experience supporting government and/or Department of Defense customers.
What We Can Offer You:
* We've been named a Best Place to Work by the Washington Post.
* Our employees value the flexibility at CACI that allows them to balance quality work and their personal lives.
* We offer competitive benefits and learning and development opportunities.
* We are mission-oriented and ever vigilant in aligning our solutions with the nation's highest priorities.
* For over 60 years, the principles of CACI's unique, character-based culture have been the driving force behind our success.
This position is contingent on funding and may not be filled immediately. However, this position is representative of positions within CACI that are consistently available. Individuals who apply may also be considered for other positions at CACI.
____________________________________________________________________________
What You Can Expect:
A culture of integrity.
At CACI, we place character and innovation at the center of everything we do. As a valued team member, you'll be part of a high-performing group dedicated to our customer's missions and driven by a higher purpose - to ensure the safety of our nation.
An environment of trust.
CACI takes pride in fostering a diverse and accessible culture where every individual feels supported to chart their own path. You'll have the autonomy to take the time you need through a unique flexible time off benefit and have access to robust learning resources to make your ambitions a reality.
A focus on continuous growth.
Together, we will advance our nation's most critical missions, build on our lengthy track record of business success, and find opportunities to break new ground - in your career and in our legacy.
Your potential is limitless. So is ours.
Learn more about CACI here.
____________________________________________________________________________
Pay Range:
This posting is for a position covered by the Service Contract Labor Standards (SCA). The pay and benefits provided for this position will meet or exceed the minimum required amounts detailed in the wage determination issued by the Department of Labor and made applicable to this position, as incorporated into CACI's government contract for the work location.
Minimum Required Hourly Wage:
$23.05
There are a host of other factors that can influence final salary including, but not limited to, geographical location, relevant prior work experience, specific skills and competencies, education, and certifications. Our employees value the flexibility at CACI that allows them to balance quality work and their personal lives. We offer competitive compensation, benefits and learning and development opportunities. Our broad and competitive mix of benefits options is designed to support and protect employees and their families. At CACI, you will receive comprehensive benefits such as; healthcare, wellness, financial, retirement, family support, continuing education, and time off benefits. Learn more here.
CACI is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, age, national origin, disability, status as a protected veteran, or any other protected characteristic.
Engineering Technician II
Research And Development Technician Job 20 miles from Nipomo
Engineering Technician IIJob Category: Service Contract ActTime Type: Full time Minimum Clearance Required to Start: SecretEmployee Type: RegularPercentage of Travel Required: Up to 10%Type of Travel: Continental US* * *
CACI has a great opportunity for a Vandenberg Space Force Base (VSFB) SATCOM Engineering Technician to provide Mission Essential support to the Satellite Control Network Tracking Station Operations Remote Site and Mission Partners (STORMS) contract which operates and maintains the SATCOM terminal at VSFB.
What You'll Get To Do:
Performs operations and corrective/preventive maintenance on telecommunications equipment and circuits, RF equipment, secure communications equipment and computerized systems.
Documents operations, performance testing, troubleshooting and maintenance activities in job registers and databases.
Completes paperwork for equipment and spares inventories, and reports.
Occasionally ascends/descends a ladder on antenna towers, at heights of 40 feet or more, and constantly positions self to work on equipment mounted lower in racks.
You'll Bring These Qualifications
Education: AA/Vocational/Tech plus 3 years of experience (7 years of experience in lieu of degree) with managing/overseeing geographically separated Air Force/DoD contract operations, maintenance, and base operations functions
Satellite Control Network (SCN) knowledge
Interfacing with active-duty military and civil service personnel
Must be a US Citizen
Active Secret Security Clearance
Required Skills:
Technically competent
Self-motivated
Attention to detail
Ability to work independently
Effective, professional interpersonal skills
Strong team player
Hardworking
Preferred Additional Skills:
CompTIA Security+ certification
Experience in troubleshooting at a system and circuit card / module level, coordinating and participating in RF and telecommunications troubleshooting efforts, and customer service for the Department of Defense.
Background in operations and maintenance of DSCS/WGS satellite communications equipment.
Background maintaining communications / electronics equipment.
Previous experience supporting government and/or Department of Defense customers.
What We Can Offer You:
We've been named a Best Place to Work by the Washington Post.
Our employees value the flexibility at CACI that allows them to balance quality work and their personal lives.
We offer competitive benefits and learning and development opportunities.
We are mission-oriented and ever vigilant in aligning our solutions with the nation's highest priorities.
For over 60 years, the principles of CACI's unique, character-based culture have been the driving force behind our success.
This position is contingent on funding and may not be filled immediately. However, this position is representative of positions within CACI that are consistently available. Individuals who apply may also be considered for other positions at CACI.
____________________________________________________________________________
What You Can Expect:
A culture of integrity.
At CACI, we place character and innovation at the center of everything we do. As a valued team member, you'll be part of a high-performing group dedicated to our customer's missions and driven by a higher purpose - to ensure the safety of our nation.
An environment of trust.
CACI takes pride in fostering a diverse and accessible culture where every individual feels supported to chart their own path. You'll have the autonomy to take the time you need through a unique flexible time off benefit and have access to robust learning resources to make your ambitions a reality.
A focus on continuous growth.
Together, we will advance our nation's most critical missions, build on our lengthy track record of business success, and find opportunities to break new ground - in your career and in our legacy.
Your potential is limitless. So is ours.
Learn more about CACI here.
____________________________________________________________________________
Pay Range:
This posting is for a position covered by the Service Contract Labor Standards (SCA). The pay and benefits provided for this position will meet or exceed the minimum required amounts detailed in the wage determination issued by the Department of Labor and made applicable to this position, as incorporated into CACI's government contract for the work location.
Minimum Required Hourly Wage:
$23.05
There are a host of other factors that can influence final salary including, but not limited to, geographical location, relevant prior work experience, specific skills and competencies, education, and certifications. Our employees value the flexibility at CACI that allows them to balance quality work and their personal lives. We offer competitive compensation, benefits and learning and development opportunities. Our broad and competitive mix of benefits options is designed to support and protect employees and their families. At CACI, you will receive comprehensive benefits such as; healthcare, wellness, financial, retirement, family support, continuing education, and time off benefits. Learn more here.
CACI is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, age, national origin, disability, status as a protected veteran, or any other protected characteristic.