Jobs in Orange, CA

Senior Attorney - Wage & Hour Class Action
Wilshire Law Firm is a distinguished, award-winning legal practice with over 18 years of experience, specializing in Personal Injury, Employee Rights, and Consumer Class Action lawsuits. We are dedicated to upholding the highest standards of Excellence and Justice and are united in our commitment to achieve the best outcome for our clients.
You will work side by side on a team of dynamic, collaborative, and client-focused professionals who are committed to delivering on our founding core values: Excellence, Teamwork, and Integrity.
The Opportunity
As our Senior Attorney in our Employment Class Action department, you will have the opportunity to fight for our clients and win the largest settlements and verdicts achievable in employee misclassification, overtime wage violations, time-shaving, failure to provide rest and meal breaks, and other worker rights violation cases.
Accountable for
Draft and prepare pleadings, motions, and other legal documents.
Develop Strategies to resolve cases favorably and cost-effectively for clients.
Take and defend depositions.
Develop and form arguments and represent clients in wage and hour matters.
Qualifications
Licensed and in good standing with the California State Bar.
At least 5 years of experience in Employment Class Action.
Superior analytical and legal research skills.
Excel in a fast-paced environment.
Ability to negotiate, research, and communicate both verbally and in writing.
Ability to exercise common sense in complex situations.
Adaptable and meticulous attention to detail.
Compensation
$180,000 - $280,000 based on experience, plus performance-based incentives
Benefits
Paid time off and paid holidays.
Opportunities for growth and advancement.
Team outings and sponsored events.
Referral bonus program.
Firm-paid Medical, Dental & Vision HMO with low-cost upgrades.
Paid Life and AD&D insurance.
401k.
FSA (Flexible Spending Account).
EAP (Employee Assistance Program).
Pet Insurance.
Strive for Excellence. Fight for Justice. Foster Unity.
Wilshire Law Firm celebrates being an equal employment opportunity provider to all people in accordance with all applicable laws. We are committed to providing reasonable accommodations to assist individuals with disabilities during the application process and to facilitate their performance of essential job functions throughout their employment.
Join Wilshire Law Firm
Los Angeles, Irvine, San Diego, Oakland, Sacramento, Riverside, Torrance

by Jobble

• Develop, implement, and maintain the Quality Management System (QMS).
• Plan, conduct, and coordinate internal and supplier audits to ensure compliance with regulatory and accreditation standards (e.g., CLIA, CAP).
• Manage document control, change control, CAPA, nonconformance management, complaint handling, and MDR/Vigilance activities.
• Coordinate proficiency testing programs and analyze results to identify trends and improvement opportunities.
• Ensure all required regulatory licenses and accreditations remain current.
• Maintain quality documentation, SOPs, and laboratory testing procedures.
• Prepare, analyze, and present quality metrics and reports for management review.
• Train and onboard new personnel; review training documentation and monitor ongoing competency of testing staff.
• Maintain working knowledge of laboratory protocols, specimen processing, equipment operation and maintenance, and data analysis.
• Review and approve product labeling, packaging, promotional materials, and technical documentation for regulatory compliance.
• Monitor changes in global regulations, standards, and guidance; assess impact and recommend updates to internal processes.
• Partner with cross-functional teams (R&D, manufacturing, engineering, clinical, marketing) to embed quality and regulatory requirements early in product development.
• Lead or support management reviews, regulatory and quality training programs, and continuous improvement initiatives.
• Prepare, submit, and maintain regulatory filings, documentation, and reports.
• Coordinate with regulatory and accreditation bodies to support product approvals, certifications, and inspections.
• Ensure compliance with internal health and safety policies; report and address violations as required.
• Participate as an external auditor on College of American Pathologists (CAP) inspection teams, as required by the CAP accreditation program.
  
  

• Bachelor's degree (required) in life sciences, biology, chemistry, engineering, pharmacy, or related field; Master's a plus
• 3+ years of laboratory experience, including experience with audits, compliance systems, and regulatory submissions.
• Strong knowledge of key regulations and standards: FDA QSR (21 CFR Part 820/211), ISO 13485/9001, EU MDR/IVDR, GMP, ICH guidelines, etc.
• Working knowledge of relevant regulatory frameworks
• Professional certification is a plus (i.e, Regulatory Affairs Certification – RAC, ASQ Certified Quality Auditor – CQA).
• CLS Generalist or CGMBS license preferred
• Proven knowledge of quality assurance terminology, software, methods, and tools.
• Previous experience with Laboratory Information Management Systems is preferred.
• Proficient in QMS software (i.e. MediaLab, TrackWise, MasterControl or similar)
• Strong analytical, problem-solving, and decision-making skills.
• Experience in compliance and/or regulatory and knowledge of laboratory standards and regulations
• Experience with Microsoft Office Suite; Word, Outlook, Excel
• Excellent written and verbal communication skills for agency interactions, technical writing, and cross-functional collaboration.
• Able to effectively present information and respond to questions from various stakeholders
  
  

Blue Chip Talent, in partnership with an automotive technology organization, is seeking a skilled Verification & Validation Engineer – Vehicle Electronics. This role is responsible for developing and executing validation test plans for electronic control units (ECUs) and ensuring module-level reliability under environmental and electrical stress conditions. The engineer will support design verification activities and lead cross-functional validation efforts through production readiness.

Job Duties

• Develop detailed design verification and validation (DV&PV) test plans across all program phases
• Execute validation activities aligned to program milestones to ensure production readiness
• Generate and maintain test coverage reports and validation documentation
• Provide early design feedback focused on testability and validation strategy
• Create Design for Testability (DFT) reports for ECU hardware
• Lead technicians during durability, environmental, electrical, and functional testing
• Coordinate lab resources and manage validation schedules across cross-functional teams
• Drive root cause investigations for non-compliant test results using data-driven analysis

Skills & Experience

Required:

• BS or MS in Electrical Engineering or related technical field
• 5+ years of experience in electronics characterization and validation testing
• Hands-on experience with design verification and validation methodologies (DVP&R, PVP&R)
• Proficiency with lab instrumentation including oscilloscopes, power supplies, electronic loads, and digital multimeters
• Experience operating thermal chambers and vibration tables for environmental testing
• Experience performing data analysis and generating technical reports using Python

Desired:

• Experience querying and analyzing data using SQL
• Experience working in Databricks or similar data platforms
• Experience with automated test equipment (ATE) systems

Blue Chip Talent is an award-winning and woman-owned talent solutions provider based out of Bloomfield Hills, Michigan. For over 30 years, we’ve specialized in IT, Engineering, and Professional Services staffing—now serving clients in 37 states and counting. We connect the market's elite talent with top employers, pairing exceptional white-glove service with proven hiring results to drive innovation and fuel growth.

We offer industry-leading benefits options and are proud to be an Equal Opportunity Employer (EOE) that values merit-based recruitment centered around technical ability, skillset, and alignment with our employing partners.

At CGH we are seeking motivated professionals to join our growing sales team. Whether you’re looking for a full-time career path or part-time flexibility, this role offers comprehensive training from top-performing sales leaders and a steady stream of qualified leads (no cold calling).

You will have the opportunity to build strong client relationships, provide personalized life insurance solutions, and grow your income potential in a supportive, tech-enabled environment.

Licensing support is provided for candidates not yet licensed.

Ideal Candidates:

• Previous experience in sales (insurance, finance, real estate, or related fields)
• Strong communication and relationship-building skills
• Self-driven and goal-oriented, with a desire to grow professionally
• Comfortable using digital tools to manage prospects and sales activity
• Willing to obtain a life insurance license (licensing assistance provided)
• Flexible availability and ability to work independently

Learn how we started!

If you’re ready to advance your career in a dynamic, high-growth industry, we encourage you to apply today.

This opportunity is only for citizens or permanent residents with independent work authorization (no work visas).

Quality Inspector CMM Programmer Anaheim, CA $30-$38/hr

Summary

The Quality Inspector will evaluate product conformity by measuring or otherwise comparing product to customer requirements, primarily using a Romer Arm, and/or CMM. Will also have programming responsibilities.

Responsibilities

• Perform visual and precision mechanical inspection of raw materials and finished products.
• Able to use standard mechanical measuring tools (Calipers, Micrometers, Plug & Ring Gages, Gage blocks, Height gage, etc.)
• Program and inspect part dimensions using Romer Arm and/or CMM.
• Ability to read and interpret engineering drawings, standards and specifications.
• Familiar with ANSI/ASME Y14.5.
• Proficient shop math skills, including some trigonometry.
• Ability to prepare and complete documentation such as inspection reports using Microsoft Excel.
• Ability to prepare and complete FAIs per AS9102 requirements
• Good communication skills and ability to coordinate interdepartmental tasks.
• Identify quality issues and recommend corrective actions
• Ability to prioritize multiple assignments and exercise independent judgment.
• All other dues and responsibilities as assigned by Supervisor.

Requirements

• High school diploma or (GED)
• Bachelor’s degree preferred
• Some aerospace QA experience required
• 2+ years mechanical inspection or quality assurance experience
• 1+ year experience using CMM or Romer Arm for part dimension inspection.
• 1+ year experience programming CMM or Romer Arm preferred.
• Knowledge of AS9100, ISO 9001:2015, Lean Manufacturing, Quality Management Systems, Root Cause Analysis is a plus
• Proficiency in English and basic computer skills, including the use of the internet and Microsoft Office
• Strong understanding of quality control standards and procedures
• Read and interpret blueprints
• Attention to detail

Mechanical Assembler
Tustin, CA
6 Month Contract to Hire
$20-$21 an hour

Summary: 

Immediate hire at thriving company. Will be responsible for filling out the verification sheet for each job assigned. Reading and understanding assembly drawings. Read and understand assembly, test and packaging procedures. Complete necessary paperwork accurately for each Job order following GDP (Good Documentation Practices). Follow 5s processes. Package and label all products including batteries from cleanroom. Set up, Client out parts and maintain a clean working environment at all times . Performs a range of routine mechanical assembly of small parts or components in accordance with company instructions and procedures . Performs mechanical assemblies, subassemblies and potting. Visually inspect assemblies and subassemblies in progress to ensure compliance with assembly drawings and assembly procedures. Test air motor, medical devices following test established procedures. Reports on any unusual problems that occur during testing, packaging or assembling components. Notify assembly supervisor or manager of discrepancies. Identify non -conformance and initiate require documentation. Documentation may include (Non - conforming material report). Request parts from stockroom when needed. Sign and approve first articles.

Requirements:

• Understand Clock ON and Clock OFF Jobs.
• Strong attention to detail in every assembly, or task assigned.
• Able to read and understand work orders, interpret drawings and assembly procedures.
• Experience using hand tools and equipment to aid assembly.
• Ability to operate drill press, a variety air equipment, and electrical tools.

Welcome to ConsultNet, a premier national provider of technology talent and solutions. Our expertise spans across project services, contract-to-hire, direct search, and managed services onshore, nearshore, and hybrid. For over 25 years, we have connected thousands of consultants with meaningful roles through a personal, communication-driven approach, partnering with a diverse client base to build high-performing teams and create lasting impact. Our comprehensive service offerings cover a wide range of technology and engineering positions across key markets nationwide. Learn more at .

We champion equality and inclusivity, proudly supporting an Equal Opportunity Employer policy. We welcome applicants regardless of Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other status protected by law.

At Induce Biologics USA Inc., we are focused on developing and providing advanced technologies for bone regeneration. With a foundation based on science, clinical evidence, and clinical experience, our Natural Matrix Protein® (NMP®) products support healing across a wide range of spine, dental, and orthopedic procedures.

By joining Induce Biologics USA Inc., you’ll be part of a mission-driven team working with revolutionary technology that’s reshaping the future of bone regeneration—and making a real difference in patients’ lives.

The Sterile Processing and Materials Management Technician is responsible for the day-to-day operations of the sterile processing department, which includes processing, sterilization, and preparation of materials and components required for daily manufacturing activities. This role will also be responsible for management of manufacturing inventory and support manufacturing by coordinating the receipt, inspection, transfer of donor tissue, raw materials, supplies and finished products where needed.

Essential Functions & Responsibilities

Sterile Processing

• Responsible for the daily activities of sterile processing, ensuring compliance with all relevant policies, procedures, and regulations.
• Ensure the workflow processes of decontamination, cleaning, assembly, packaging, sterilization, storage, and distribution of tissue processing instrumentation and equipment.
• Ensure proper sterilization procedures and monitoring processes, including daily biological and chemical indicator verification.
• Maintain accurate and original records of sterilization procedures, equipment maintenance, and inventory levels.
• Operation and maintenance of reprocessing equipment, including ultrasonic baths, washer decontaminators, and autoclaves, ensuring proper function and maintenance.
• Promote and maintain a safe sterile environment, adhering to strict infection control protocols and procedures.
• Responsible for manufacturing support and controlled environment maintenance during routine production.

Material & Inventory Management

• Receive, inspect, and verify incoming donor tissue, reagents, and processing supplies to ensure compliance with tissue banking standards.
• Accurately log all incoming and outgoing materials using inventory management systems to maintain traceability.
• Monitor stock levels of critical materials such as cleanroom supplies, sterile packaging, and lab consumables and communicate with the Supply Chain Manager as needed.
• Conduct routine cycle counts and support physical audits to ensure inventory accuracy and regulatory compliance.

Logistics & Material Transfer Coordination

• Coordinate the timely transfer of raw materials, parts, and finished products between suppliers, warehouses, cleanrooms, laboratories, and production areas.
• Prepare materials for shipment, including labeling, packaging, and ensuring compliance with cold chain logistics or other storage conditions as needed.
• Arrange and track shipments with third-party logistics providers, ensuring timely and accurate delivery.

Warehouse and Storage Management

• Monitor and manage inventory levels of supplies, reagents and equipment, ensuring adequate stock and timely replenishment
• Organize and maintain warehouse and storage areas for efficient material retrieval and workflow.
• Operate pallet jacks, and other material handling equipment as needed.
• Ensure proper storage conditions (e.g., refrigerated or frozen storage) for temperature-sensitive materials.
• In collaboration with Manufacturing and Supply Chain Management, troubleshoot and resolve inventory discrepancies, material shortages, and storage capacity issues.

Cross-Functional Coordination

• Collaborate with Manufacturing, Quality, and Supply Chain teams to meet material demands and production schedules.
• Support product traceability efforts by ensuring accurate lot tracking and chain of custody documentation.
• Participate in process improvements to enhance material flow, inventory accuracy, and efficiency.

Education/Experience Required

• High school diploma or GED
• 2+ years of experience in material handling, warehouse/manufacturing operations, or inventory management in a hospital, surgery center, or regulated GMP biotech environment.
• Thorough knowledge of sterile processing principles, procedures, and regulations.

Education/Experience Preferred

• Associate’s or Bachelor’s degree in biotechnology, life sciences, supply chain, or logistics is a plus
• Certified in Sterile Processing, e.g., CST, CSPD, or RCST
• Prior experience in a biotech, pharmaceutical, tissue banking, or regenerative medicine company is highly preferred
• Ability to operate specialized material handling equipment (e.g., , biohazard containment units, cleanroom carts).
• Familiarity with handling biological materials, cryopreserved products, and controlled-temperature shipments (e.g., fresh/frozen tissues, stem cells, or other human-derived materials).
• Prior experience working under FDA 21 CFR Part 1271 regulations and AATB (American Association of Tissue Banks)
• Basic understanding of regulatory requirements, such as GMP, GDP, and other industry standards.

Skills, Knowledge, and Abilities

• Strong attention to detail for material tracking, documentation, and compliance reporting.
• Strong communication and teamwork skills to collaborate with manufacturing, purchasing, and customer service.
• Knowledge of ISO 13485 and FDA regulations preferred.
• Ability to work in a fast-paced, evolving environment, with flexibility to adapt to new processes.
• Must be able to adhere to Health, Safety and GMP requirements.
• Ability to work weekends, overtime and holidays, if required.
• Proficient in using MS Office suite.

For California, the base pay range for this position is $25.00 to $27.00 / hour. The pay for the successful candidate will depend on various factors (e.g., qualifications, skills, education, prior experience).

Equal Employment Opportunity Statement

Induce Biologics is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Third-Party Recruiters

Please note that Induce Biologics does not accept unsolicited resumes or inquiries from third-party recruiters or staffing agencies. Any resumes submitted to our team without a prior agreement will be considered the property of Induce Biologics, and we will not be obligated to pay any fees related to unsolicited submissions.

About The Position

If you thrive and excel at providing high-end experiences for clients and working in a creative space, then the Showroom Design Specialist position may be the perfect fit for you. We are looking for a people-person who is motivated by creating experiences to work with clients to design custom jewelry pieces that hold significant value in their lives. This is a client-forward role that primarily involves educating clients on our custom design process through in-person appointments, email inquiries, and virtual showings. We hold high value in our excellent client experience and encourage an educational approach to custom design, as opposed to an intimidating, pushy sales experience. A strong candidate for this role will have strong written and verbal communication skills and is motivated by providing excellent client experiences and working in a team-oriented, fashion-forward atmosphere.

*Please Note* - We are looking for candidates from all professional backgrounds, so no jewelry or design background is required!

About Us

East West Gem Co. is an e-commerce and by-appointment custom jewelry company with showroom locations in New York City, Charleston, Orange County. We are a female led and operated, growing company and this role takes place at our Orange County showroom! At East West, we believe in transparent and open communication within our team and with our clients. We're looking to build on our team of self-starters, who are motivated by an environment that fosters growth and rejects micro-management. At East West, we lead with and truly believe in work-life balance and stick to a schedule of 8:30-5pm, 5 days per week. We communicate with clients strictly via email and as-needed zoom calls. There is also opportunity to travel for cross-training at our locations in New York  and Charleston!

Check out our companies @createdrings and  @eastwestgemco on Instagram and TikTok!

Job Responsibilities

- Educating and assisting clients in designing and solidifying details for custom jewelry pieces via appointment and email inquiry

- Pricing custom rings based on pricing algorithm and sending invoices to clients

- Provide excellent customer service to pre-existing and new clients

- Assisting clients with initial custom design process

- Assistance with answering Instagram DM inquiries and comments via social media platforms

- Hosting by-appointment showings

- Provide consistent feedback to team to improve the custom order experience

- Day to day showroom management and upkeep alongside of colleagues

- Must host Saturday appointments 2x per month (with an alternate week day off)

Skills Desired

- Strong written and verbal communication skills

- People-motivated attitude

- Good work ethic

- Eagerness to learn

- Polished style and demeanor

- Understanding of Google products (sheets, slides and docs)

- Knowledge of Shopify (bonus, not required)

Job Perks

- Weekly pay

- Comprehensive health, dental, and vision insurance

- Comprehensive 401K program with match

- 50% employee discount

- 13 accrued PTO days per year with increases at 2 and 5 year anniversaries

- Maternity leave, sick time, and bereavement

- Opportunity to travel to other showrooms and locations

Full-Time, Direct-Hire, Onsite

Monday-Friday 9am-5:30pm

$85,000–$100,000

About The Job:

Quality Assurance & Regulatory Specialist ensures that products, processes, and documentation meet required quality standards and comply with all relevant regulatory frameworks. This role combines regulatory strategy/submissions with quality system implementation, audits, and continuous improvement to support product approval and patient safety.

Essential Duties and Responsibilities:

• Develop, implement, and maintain Quality Management Systems (QMS).

• Conduct or coordinate internal audits, supplier audits to ensure compliance with regulatory standards (e.g., CLIA, CAP)

• Oversee document control, change control, CAPA (Corrective and Preventive Actions), nonconformance management, complaint handling, and Medical Device Reporting (MDR)/Vigilance.

• Coordinate proficiency testing programs and analyze results to identify areas for improvement.

• Maintain quality documentation, SOPs, and testing procedures.

• Prepare and present quality metrics and reports for management review.

• Be familiar with laboratory protocols and procedures for specimen processing, operating equipment and instruments, maintenance of designated laboratory environment and instruments, and data analysis.

• Review and approve product labeling, packaging, promotional materials, and technical documentation for regulatory compliance.

Education and Experience:

• A minimum of 2 to 3 years of laboratory experience.

• Strong knowledge of key regulations and standards: CAP/CLIA, FDA QSR (21 CFR Part 820/211), ISO 13485/9001, MolDx, etc.

• Understanding of regulatory frameworks relevant to the industry.

• Experience with audits, compliance systems, and regulatory submissions.

• Bachelor's degree (required) in life sciences, biology, chemistry, engineering, pharmacy, or related field; advanced degree (Master's/PhD) preferred.

Preferred Experience:

• Professional certification is a plus (e.g., Regulatory Affairs Certification – RAC, ASQ Certified Quality Auditor – CQA).

• A Valid and active CLS (Generalist) or CGMBS license

A pharmaceutical contract clinical testing company that partners with biotech and pharmaceutical companies to develop and test injectable drug products is looking to hire a Quality Assurance Associate III on a contract basis filling in for an employee that is out on leave. The Quality Assurance Associate must have experience working in a laboratory setting.

The Quality Assurance Associate will responsible for:

• US FDA 21CFR210, 211, 11 and applicable ICH guidance documents. Develop and revise QA procedures to strengthen cGMP compliance.
• Reviewing test results and supporting technical documentation. Work directly with operations management to resolve findings noted during the review process.
• Performing release of raw materials and consumables.
• Reviewing and approving Certificate of Analysis for raw materials, drug substance and drug products.
• Collaborating effectively with operations management to review and approve: SOPs, protocols, reports, equipment qualifications and calibrations, change controls, specifications trend reports and other quality documentation.
• Responsible for writing/revising Quality Assurance procedures to strengthen compliance with cGMPs.
• Reviewing and approving deviations and gather/issue quality metrics reports to QA management.
• Providing QA support during cGMP compliance inspections of the facility by clients, the FDA and/or other regulatory bodies.
• Acting as a co-auditor during supplier/internal quality audits.
• Providing subject matter expertise for the supplier assurance program at the site.
• Providing QA management with the support needed for compliance training.
• Maintaining workspace cleanliness by adhering to the 5S method of organization.
• Abiding by safe work practices and adhere to general safety rules, performing all duties in a safe manner and never placing yourself or those around you in an unsafe condition. Reporting all unsafe conditions to your supervisor.
• his list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary.

Requirements:

• Bachelor's degree with 3-5+ years in scientific discipline, or a minimum of 5+ years with lab & QA related work experience.
• Advance experience and knowledge of cGMP regulations, and FDA and ICH guidelines as they pertain to contract laboratory and/or aseptic manufacturing operations.
• Advance experience and knowledge of USP, Pharm. Eur. (EudraLex) and other applicable standards.
• Advance knowledge of root cause investigation and problem solving; experience in the use of 5 Whys and/or other appropriate root cause investigation tools.
• Advance experience and knowledge in the use of LIMS and electronic documentation systems.
• Strong interpersonal skills. Must be able to express oral and written communication in a clear and concise manner and effectively present information and respond to questions from managers, customers and employees.
• Effective organizational and time management skills with the ability to multi-task and prioritize assignments as needed.
• Works on complex issues; exercises good judgement in selecting methods, techniques and evaluation criteria for obtaining results while handling Quality Assurance tasks.
• Ability to perform routine work with minimal instructions, determines methods and procedures on new assignments.
• May coordinate activities of other personnel.
• Ability to work effectively under pressure in a rapidly changing environment.
• Ability to work well independently and effectively with a wide variety of colleagues both inter- and intra- departmentally.
• Ability to seek critical information from key resources to assist in problem solving.
• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Project, etc.).