Astrix jobs in Thousand Oaks, CA

Manufacturing LA, CA, US + Added - 01/12/2025 Apply for Job Pay Rate Low: 90,000 | Pay Rate High: 95,000 Our client is a growing cosmetic manufacturing company located in Los Angeles! They develop, manufacture and distribute their own full line of skin care and color cosmetic products. Title: Quality Assurance Manager Location: Los Angeles, CA 90045 Schedule: M-F; 6:30am-3pm (Onsite) Salary: $90,000-95,000 **Summary:** The Quality Assurance Manager is responsible for ensuring our manufactured products meet set standards of quality, reliability and performance. **Essential Duties and Responsibilities:** Collaborate with an organization's purchasing manager to ensure raw materials from external suppliers meet quality requirements Set and enforce standards for health and safety during work operations Carry out research to identify ways to reduce waste and maximize resources Ensure manufacturing processes are in compliance with both national and international standards of production Conduct surveys to identify customer requirements and ensure they are being met by established quality standards Supervise technicians, inspectors, and other company staff to ensure they perform their duties in line with established quality procedures **Qualifications:** BS or MS degree in scientific discipline with 2-3 years of management experience. 4-5 years of having direct reports (lead, supervisor or manager role) Minimum 2 years management experience. Experience drafting & rewriting SOPs, audits, FDA filings/docs, CAPAs, change controls, batch records, documentation. Knowledge of ISO 22716 & FDA regulations INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Manufacturing Los Angeles, CA, US + Added - 23/07/2025 Apply for Job Our client, a renowned leader in the field of biotechnology, is revolutionizing the use of living cells to create groundbreaking biologic medicines. As a guiding force in the biotech industry, they set the bar for innovation and advancement. We are excited to announce a fantastic opportunity to join the team! We are seeking a dynamic individual who is eager to contribute their expertise and drive their mission forward. **Title:** GMP Manufacturing Associate (Multiple openings!) **Location:** Thousand Oaks, CA **Schedule:** Multiple shifts available **Pay:** $22-30/hr Contract to hire (Benefits Included!) **Job Summary** : The Associate of Manufacturing will work in a dynamic production environment at the clients Thousand Oaks Drug Substance plant supporting development, clinical, and commercial activities. Under general supervision, employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs). Responsibilities include: - Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment - Preparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs) - Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance - Performing and monitoring critical processes with the ability to perform basic troubleshooting - Performing in-process sampling of equipment and operating analytical equipment - Performing washroom activities: clean small-scale and large-scale equipment used in production activities - Maintaining an organized and clean workspace - Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet, and gloves when performing all work - Initiating quality deviation records - Drafting and revising documents (SOPs, MPs) - Working around high-pressure systems and occasionally working around heavy equipment - Available to work various shifts (Days, Swings, Graves, Weekends, Holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) as dictated by the production schedule **Preferred Qualifications:** Bachelors Degree in Biology and/or Life Sciences Mechanically inclined Basic Qualifications: Bachelor degree OR Associate degree and 4 years of experience OR High school diploma / GED and 6 years of experience INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Manufacturing Thousand Oaks, CA, US + Added - 10/07/2025 Apply for Job **Onsite: Thousand Oaks, CA** **PR: $38.00-$40.00/hr.** **Join a team that powers innovation in clinical manufacturing.** We're seeking a skilled **Senior** **Maintenance Technician** to support our state-of-the-art manufacturing facility. You'll play a key role in ensuring equipment reliability and enabling new technologies that drive the production of life-changing therapies. If you're a hands-on problem solver with a passion for continuous improvement and GMP excellence, we'd love to hear from you. + Hands on maintenance tech experience + Experience performing advanced installation, troubleshooting, maintenance, repair, testing, and documentation/logs of a wide variety of office utility and facility equipment used in manufacturing, utility plants, analytical labs, and office areas + Develop, write, and complete a variety of technical and compliance documentation, including: + Standard Operating Procedures (SOPs) + Change Controls (CCMS) + Non-Conformances (NCs) + Work Orders (WOs) + Job Plans (JPs) + Hazard Risk Assessments (HRAs) + Job Hazard Assessments (JHAs) + Ensure all documentation meets applicable GMP, CFR, and internal Amgen standards. + Support operations of building, utility, and production systems/equipment with a focus on quality and efficiency. + Execute tasks safely and in accordance with applicable risk assessments (HRA, JHA), minimizing impact to production operations. + Provide training to staff and stakeholders on documentation procedures, maintenance protocols, and safety practices. + Participate in audits and inspections, offering documentation support and technical guidance as needed. + Review and technically approve maintenance reports, forms, job plans, and records to ensure accuracy and compliance. + Develop, revise, and review technical documentation related to equipment and maintenance processes. **Qualifications:** + Strong working knowledge of GMP, CFR regulations, and quality systems in a pharmaceutical or life sciences environment. + Proven experience with documentation systems such as SOPs, CCMS, NCs, and work orders. + Technical expertise in utility, building, and production system maintenance. + Ability to read and interpret technical drawings and schematics. + Strong attention to detail and organizational skills. + Proficient in using CMMS or other electronic documentation platforms.INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Manufacturing Los Angeles, CA, US + Added - 28/07/2025 Apply for Job Our client, a renowned leader in the field of biotechnology, is revolutionizing the use of living cells to create groundbreaking biologic medicines. As a guiding force in the biotech industry, they set the bar for innovation and advancement. **Job Title:** GMP Manufacturing Process Technician (Contract-to-Hire) **Schedule:** Onsite | Monday-Friday, 8:00 AM - 5:00 PM **Pay Rate:** $24 - $26 per hour **Overview** A leading biotechnology organization is seeking a **GMP Manufacturing Process Technician** to join their Synthetic Manufacturing and Clinical Supply team. This role will be based onsite at their pilot-scale drug product manufacturing facility and formulation development lab in Thousand Oaks, CA. The technician will support both non-GMP and GMP manufacturing activities for early-phase clinical pipeline synthetic drug products, primarily solid dosage forms. **Key Responsibilities** + Execute manufacturing unit operations such as blending, granulation, roller compaction, drying, milling, compression, encapsulation, and film coating. + Support manufacturing process readiness activities and assist in preparing batch records for GMP campaigns. + Perform visual inspection of drug products and ensure adherence to quality standards. + Handle dispensing and management of hazardous raw materials while following safety protocols. + Conduct hands-on equipment cleaning, sanitization, and setup for manufacturing processes. + Maintain equipment and facility documentation, including logbooks and inventory of raw materials and consumables. + Collaborate closely with cross-functional teams including process development chemists, engineers, and analysts. + Recommend and implement process improvements to enhance efficiency and compliance. **Qualifications** **Basic Requirements:** + High school diploma/GED with 1+ year of relevant work or military experience, OR Associate degree. **Preferred Skills/Experience:** + Familiarity with GMP compliance, documentation practices, and manufacturing unit operations for synthetic drug products. + Experience with solid dosage drug product processes (granulation, blending, tablet compression, etc.). + Strong teamwork skills and ability to collaborate in a cross-functional environment. + Comfort working with complex machinery and hazardous materials while adhering to safety requirements. **Why Join?** + Opportunity to work with a dynamic team supporting innovative clinical drug development. + Hands-on experience in a pilot-scale drug manufacturing facility. + Potential for contract extension and growth within the organization.INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Clinical Pharmacology Los Angeles, CA, US + Added - 27/08/2025 Apply for Job _Our client has over 50 years of experience and expertise, provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services._ **Title:** Quality Assurance Document Control Specialist(Contract) **Location:** Fully Onsite - Torrance, CA **Schedule:** Mon - Fri 8-5pm **Pay rate:** $28-30/hr **Contract:** 3 months with potential for extension The QA Document Control Specialist will manage document control activities to ensure compliance with GMP and regulatory requirements. Responsibilities include reviewing, processing, and releasing controlled documents (SOPs, batch records, protocols, reports, specifications), maintaining records management systems, and supporting audits. This role requires collaboration across departments and contribution to process improvement initiatives. **Key Responsibilities:** + Review and process controlled documents via Master Control + Manage records, logbooks, certificates, and archival processes + Create/revise product labels and specifications + Support regulatory/customer audits and quality system improvements + Participate in cross-site process harmonization and system implementation **Qualifications:** + Bachelor's degree in Chemistry, Biology, or related field + 2+ years of QA document control experience in GMP biotech/pharma + Strong communication, organization, and multitasking skills + Proficiency with Microsoft Office; experience with Master Control preferred + Detail-oriented, proactive, and able to work independently or in teams INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

R&D San Fernando , CA, US + Added - 26/11/2025 Apply for Job **Food Technologist** Join our dynamic product development team as a Food Technologist, where you'll craft the next generation of beverage experiences! This role combines scientific expertise with creative flair to develop cutting-edge concentrates and flavor systems that delight consumers and drive market success. Working alongside seasoned flavor chemists, you'll transform concepts into commercial realities while pushing the boundaries of taste innovation. **Location** : Onsite in San Fernando, CA **Type** : 3-month contract to hire **Compensation** : $29-$34/hour **Hours** : M-F 8-5 **What You'll Create & Accomplish** + Engineer sophisticated beverage concentrates and complex flavor profiles that capture market trends and exceed customer expectations. + Design robust shelf-life studies and accelerated stability protocols to guarantee product integrity throughout its lifecycle. + Pioneer testing methodologies that validate flavor performance under diverse storage and usage conditions. + Partner with Quality Assurance teams to establish new standards of excellence in flavor consistency and safety. + Work hand-in-hand with Manufacturing to optimize production processes and troubleshoot scale-up challenges. **Educational Expectations** + Bachelor's degree in Food Science, Chemistry, Chemical Engineering, or related STEM field with demonstrated analytical rigor. **Professional Experience** + 2+ years of applied R&D experience in food/beverage innovation or related product development environments. + Proven track record of successful formula development and product launch support. + Advanced mathematical proficiency including complex formula calculations, statistical analysis, and scaling algorithms. _This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_ _INDBH_ _\#LI-DNP_ We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Clinical Los Angeles, CA, US + Added - 04/04/2025 Apply for Job We're partnering with an innovative client in the biotechnology industry, and they're on the lookout for a talented **Clinical Compliance Auditor** to join their dynamic team! If you're passionate about ensuring the highest standards in clinical trials and want to make a real impact, this is the opportunity for you. Don't wait-apply today and take the next step in your career **Salary:** $100,000-$150,000 **Location:** Remote **Responsibilities:** + Oversee and regularly update the Clinical Trial Quality Management system to ensure alignment with current industry standards, guidelines, and best practices. + Assist in the creation and evaluation of standard operating procedures (SOPs) and other essential controlled documents, such as forms, templates, and work instructions. + Ensure adherence to SOPs and compliance with relevant standards, including ICH GCP E6 (R2). + Lead the incident management process by tracking and addressing complaints, deviations, and corrective actions (CAPAs). + Organize, coordinate, and execute audits of vendors, suppliers, clinical trial sites, as well as internal and compliance audits, including for-cause audits. + Prepare necessary documentation to support audit activities, including audit plans, reports, certificates, and corrective action plans. + Verify the accuracy of audit findings and follow-up activities, ensuring non-compliance issues are resolved appropriately. + Review and finalize audit reports for accuracy and completeness. + Examine trial-related documents such as protocols, amendments, informed consent forms (ICFs), pharmacy manuals, and clinical study reports (CSRs). **Requirements:** + Bachelor's or Master's degree in a life sciences or engineering discipline + 4-7 years of experience in a GCP-Biologics or pharmaceutical environment. + CQA or other audit certifications are desirable. + Previous experience with TMF or electronic document management systems is a plus. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Medical Communication Los Angeles , CA, US + Added - 11/09/2025 Apply for Job **We are seeking a dynamic PR Manager to spearhead strategic growth initiatives, cultivate high-impact partnerships, and expand our market presence across diverse channels. This role offers a unique opportunity to make a global impact while driving growth in a science-driven, mission-focused organization.** **Title: Associate Manager, Public Relations & Communications** **Location:** Los Angeles CA (Hybrid onsite 3x a week) **Salary Range:** $85,000 - $105,000 **Overview** The Associate Manager of Public Relations & Communications will lead initiatives that enhance brand visibility, support product communications, and position the organization as an industry thought leader. This role blends media relations, content development, and campaign management to drive meaningful engagement and positive reputation across multiple channels. **Key Responsibilities** + Develop and execute media outreach strategies for announcements, launches, and research milestones. + Build and maintain strong relationships with journalists, editors, and influencers. + Draft and edit press releases, media pitches, executive communications, and other content. + Lead PR campaigns from planning through execution and performance analysis. + Partner with cross-functional teams to ensure alignment with business priorities. + Manage external PR agencies and ensure effective campaign delivery. + Monitor media coverage and track key metrics to evaluate PR impact. **Qualifications** + Bachelor's degree in PR, Communications, Journalism, Marketing, or related field. + 3-5 years of professional experience in public relations, communications, or media relations. + Proven ability to secure media coverage across traditional and digital platforms. + Strong writing, editing, and messaging skills with attention to detail. + Experience managing multiple projects in a fast-paced environment. + Familiarity with PR/monitoring tools such as Cision, Meltwater, or Muckrack. + Willingness to travel up to 25%. **Benefits** Comprehensive compensation package including competitive salary, health and wellness programs, life insurance, retirement savings with company match, paid time off, career growth opportunities, and a flexible hybrid work environment. INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Quality Assurance Gardena, CA, US + Added - 14/05/2025 Apply for Job Our Client, a fine chemical and laboratory products company, is seeking a QA Data Clerk to join their growing team. This is a great opportunity to work with a reputable organization, get the industry's best training, and work with state-of-the-art equipment, systems, and products. **Job Title:** QC Data Clerk (QA-Focused - Documentation Only) **Type:** 6-Month Contract (Potential for Hire) **Location:** On-Site Gardena, CA **Schedule:** Mon-Fri, 6:45am-3:15pm **Pay Rate:** $20-$24/hr **Objective:** Support QA by processing batch records, verifying documentation accuracy, and entering data into internal systems. No lab work. **Key Responsibilities:** + Review and process batch records (non-regulated to pharmaceutical-grade materials) + Transcribe data into internal databases + Ensure compliance with cGDP standards + Generate/review documents (e.g., Certificates of Analysis) + Coordinate with labs and departments for documentation needs + Monitor task queues and maintain organized workspace + Assist with QA projects as needed **Training:** Provided by internal team (James & Dylan) **Requirements:** + Bachelor's in a science field (new grads welcome) + Strong attention to detail, patience, and self-motivation + Familiarity with QA or GMP regulations a plus INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Science & Research Carson, CA, US + Added - 21/07/2025 Apply for Job _Our client is a global leader in chemical and ingredient distribution, serving industries such as paints, coatings, and lubricants._ **Job Title:** Lab Technician II (2nd Shift) **Pay:** $21.00 - $22.00 per hour **Job Type:** 6-Month Contract (with potential for hire) **Schedule:** 2nd Shift Monday-Friday, 2:00 PM - 10:30 PM **Position Type:** _Safety-Sensitive Position_ **Job Description:** We are seeking a detail-oriented and experienced **Lab Technician** to join our team in Carson, CA. This is a **6-month contract position** with the potential for permanent hire. The ideal candidate will have a strong foundation in laboratory practices, be knowledgeable in scientific terminology, and have hands-on experience supporting experiments and day-to-day lab operations. **Key Responsibilities:** + Perform standard laboratory procedures while strictly adhering to safety protocols + Label, track, and route specimens accurately + Conduct routine lab functions including solution preparation, equipment maintenance, and general support for experiments + Accurately perform specified tests and record findings in a detailed, organized manner + Compile data and assist with reporting of test results + Conduct QA/QC duties in alignment with lab standards and regulations + Calibrate, maintain, and perform minor repairs on laboratory equipment per manufacturer guidelines + Prepare mixtures and solutions in accordance with lab protocols + Support compliance with internal procedures and external regulatory standards **Requirements:** + 2-5 years of laboratory experience + Familiarity with lab techniques, scientific measurements, and terminology + Strong attention to detail and ability to follow specific protocols + Good organizational and communication skills + Ability to work independently and as part of a collaborative team + High school diploma or equivalent required; Associate's or Bachelor's degree in a scientific field preferred INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Existing Los Angeles , CA, US + Added - 05/12/2025 Apply for Job **About the Company** The company offers premium direct-to-consumer supplement brands that are clinically proven to support cellular health, as well as pharmaceutical-grade therapy products. As pioneers in their category, they continue to set the industry standard in scientific rigor, quality, safety, and transparency through their unwavering commitment to excellence, innovation, and integrity. **Location:** Hybrid (Los Angeles, CA) **Department:** Marketing & Digital Commerce **Reports to:** Chief Marketing Officer **Minimum Education:** Bachelor's degree from accredited university **Salary:** $185-270k (DOE) + Bonus potential and stock options **Position Overview** The Vice President of E-commerce Growth & Marketing will be responsible for developing and executing the end-to-end digital commerce and marketing strategy to drive growth, customer acquisition, retention, and brand equity. This leader will oversee performance marketing, DTC e-commerce, Amazon marketplaces, and customer retention strategies. **Key Responsibilities** + Own and optimize the end-to-end e-commerce ecosystem, including DTC channels and Amazon marketplaces. + Lead channel strategy to achieve revenue growth, margin expansion, and improved customer lifetime value (LTV). + Oversee DTC website operations (Shopify) and Amazon storefronts (Seller Central / Vendor Central), ensuring brand consistency and profitability across platforms. + Identify and capitalize on new revenue streams, subscription offerings, and international expansion opportunities. + Design and implement sophisticated marketing funnels encompassing brand awareness, customer acquisition, conversion optimization, and retention strategies. + Develop and execute data-driven retention strategies across DTC and Amazon channels, leveraging lifecycle marketing, loyalty programs, and personalized communications. + Partner with supply chain and operations teams to ensure best-in-class fulfillment, inventory management, and customer experience. + Build and mentor a high-performing team across e-commerce operations, digital marketing, creative development, and analytics. **Required Qualifications** + 10+ years of progressive leadership experience in DTC e-commerce, growth marketing, and performance strategy- **preferably in health, wellness, nutraceutical, consumer biotech, or regulated consumer products industries.** + Proven track record of owning and scaling an e-commerce P&L with strong financial discipline and LTV/CAC optimization expertise. + Advanced proficiency with major e-commerce platforms and marketplace management (Shopify, Amazon Seller Central/Vendor Central, etc.). + Exceptional strategic planning and cross-functional project management skills with the ability to manage through ambiguity in high-growth environments. + Strong leadership, communication, and team-building skills with the ability to inspire and influence across departments. + Passion for science-backed wellness, longevity, and cellular health innovation. _This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_ _\#INDBH_ _\#LI-DNP_ We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Engineering Thousand Oaks, CA, US + Added - 29/05/2025 Apply for Job _Our client is a premier biotechnology company at the forefront of discovering, developing, and delivering cutting-edge human therapeutics. They are currently seeking a_ **_Senior Software Engineer_** _with deep expertise in automation and control systems to drive software development and integration efforts within a highly regulated GMP manufacturing environment._ **Job Title:** Senior Software Engineer **Location:** Thousand Oaks, CA **Pay Rate:** $68-$72/hr **Contract Length:** (3-Year Contract) **Schedule:** Onsite | Mon-Fri, 8am-5pm | OT possible **Job Summary:** Seeking a Senior Software Engineer with strong automation and control systems experience to support software development and integration for manufacturing operations in a GMP-regulated environment. **Key Responsibilities:** + Develop and maintain automation applications (PLC, DCS, HMI, SCADA). + Support manufacturing through troubleshooting and ensuring system uptime. + Lead root cause analysis and resolution of control-related issues. + Prepare and manage system documentation (URS, SDS, IQ, OQ, SOPs). + Contribute to process improvements, product introductions, and tech integration. + Ensure compliance with cGMP, 21 CFR Part 11, and software development life cycle standards. **Required Qualifications:** + Engineering or software-related degree (or equivalent experience): + PhD or + MS + 2 yrs or + BS + 4 yrs or + AS + 8 yrs or + HS Diploma/GED + 10 yrs + 5+ years of experience with Rockwell Automation (FactoryTalk & ControlLogix). + Strong background in process control, validation, and regulated manufacturing. **Preferred Skills:** + Experience with batch processing, S88/S95 standards. + Familiarity with lyophilizers, filling systems, clean utilities, and BMS. + Skilled in creating technical documents and engineering packages. + Flexible to provide on-site and after-hours support as needed. + Strong communication, leadership, and cross-functional collaboration skills. **Why Join:** Join a high-impact team on a scenic campus and work with cutting-edge manufacturing technology in a collaborative, innovation-driven environment. INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Laboratory Los Angeles County, CA, US + Added - 15/10/2025 Apply for Job **Our client is a global biotechnology and aesthetics company specializing in skincare solutions. They are seeking a Compounder to join their growing team!** **Title:** Compounder (Cosmetics) - 2nd shift **Location:** Los Angeles County, CA **2nd Shift:** Monday-Friday 10am-6:30pm **Pay rate:** $25/hr-28/hr **Contract:** 6 months contract to potential hire **Position Overview:** We are seeking a skilled and detail-oriented Compounder to join our manufacturing team. The Compounder will be responsible for weighing, measuring, mixing, and preparing skincare product batches according to precise formulations and standard operating procedures. **Key Responsibilities:** + Accurately weigh, measure, and mix raw materials to create skincare product batches. + Follow detailed batch records, formulations, and SOPs to ensure consistency and compliance. + Operate and maintain mixing, heating, cooling, and related compounding equipment. + Monitor batch processing conditions (temperature, mixing speeds, time, etc.) and adjust as needed. + Document all production activities, including lot numbers, weights, and process parameters. + Clean and sanitize compounding equipment and work areas according to GMP and safety standards. + Collaborate with Quality Control to address deviations, perform in-process checks, and resolve issues. + Follow all safety, cGMP, and regulatory guidelines to ensure compliance with FDA and industry requirements. + Assist in inventory management by verifying raw material availability and reporting shortages. **Qualifications:** + High school diploma or equivalent required; technical or vocational training a plus. + 1-3 years of experience in compounding, cosmetics, skincare, pharmaceuticals, or related manufacturing preferred. + Knowledge of Good Manufacturing Practices (GMP) and safety protocols. + Ability to read and follow detailed batch records and written instructions. + Strong attention to detail and accuracy in measurements. + Physical ability to lift up to 50 lbs, stand for extended periods, and work in a fast-paced production environment. + Team-oriented with strong communication skills.INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Laboratory Los Angeles, CA, US + Added - 24/09/2025 Apply for Job _Our client is a global leader in the research and treatment of cancer, diabetes, and other serious diseases. They are seeking a Research Support Technician to join their expanding team and contribute to their mission of advancing innovative therapies and improving patient outcomes._ **Job Title:** Research Support Technician **Location:** Los Angeles County, CA **Pay:** $18-20.50/hr **Shift:** M-F 6:00am-2:30pm (Contract-to-Potential-Hire) **Position Summary:** The Research Support Technician assists in the management and production of research animal colonies, performing husbandry, breeding, and technical procedures while maintaining accurate records and supporting researchers. **Key Responsibilities:** + Monitor animal health and report any sick, injured, or distressed animals. + Perform routine husbandry: cage changes, feeding, watering, and maintaining clean housing. + Execute breeding plans, mating, weaning, and tissue sampling; document all activities accurately. + Respond to researcher requests and communicate colony status or issues effectively. + Maintain and monitor animal holding room environments; report equipment or environmental issues. + Restrain animals for procedures, assist with sample collection, and humanely euthanize as required. + Maintain equipment, including animal transfer stations, biosafety cabinets, and racks. + Participate in training, meetings, and continuing education. + Follow institutional and departmental policies, safety guidelines, and maintain confidentiality. **Qualifications:** + **Education:** High school diploma or equivalent. + **Experience:** 2+ years in laboratory animal care, veterinary technician work, or related field (no prior breeding experience required). + **Certification:** AALAS ALAT certification (or obtained within 12 months of hire). + **Skills:** Animal handling and restraint, record keeping, observation, teamwork, strong communication, organization, and ability to meet deadlines. + **Technical:** Basic computer skills (Mosaic, Microsoft Office), familiarity with lab equipment including barcode scanners and biosafety cabinets. **Working Conditions:** + Exposure to animal dander, odors, bites, infectious or biohazardous agents, and cleaning chemicals. + Use of PPE including gowns, gloves, masks, and face shields. + Physical demands include lifting up to 50 lbs., prolonged standing, bending, kneeling, and animal restraint. + Occasional weekend, holiday, or overtime work may be required.INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Regulatory Affairs Los Angeles County, CA, US + Added - 04/11/2025 Apply for Job _Our client, a leading manufacturer of food products, is looking for a skilled Regulatory Compliance Specialist to join their team in L.A County, CA!_ **Job type:** Direct - hire **Salary:** $75,000- $80,000 annually **Schedule** : Monday-Friday 12-8pm, with OT and weekends as necessary. **Location:** L. A County, CA **Overview:** The Regulatory Compliance Specialist supports the company's compliance with food regulations, labeling laws, and documentation control. This role ensures that all products meet regulatory, safety, and labeling standards while maintaining accurate and up-to-date records with suppliers and internal teams. **Key Responsibilities** + Develop and maintain ingredient and finished product specifications, including ingredient statements and nutritional information. + Review and proof labels to ensure compliance with FDA, USDA, and other applicable regulations. + Coordinate with suppliers to collect and update compliance documentation (GMO, Allergen, Organic, Kosher, etc.). + Manage and track supplier compliance and maintain the Supplier Approval Program. + Collaborate with Sales and Quality Assurance teams to meet customer and audit requirements. + Support and participate in Third-Party Audits. + Create and revise product labels for in-house printing. + Assist with investigations and customer complaint responses. + Ensure compliance with OSHA, GMP, Food Safety, Food Defense, and Food Quality regulations. + Perform additional duties and support projects as needed. **Qualifications** + Bachelor's degree in Food Science or related field (or equivalent experience). + 4-6 years Regulatory Experience in Food Industry/ Food Processing/Food Manufacturing. + **Experience working with Genesis and nutritional labels.** + Knowledge of FDA, USDA, AIB, HACCP, GMP, and Allergen Programs. + Strong understanding of Labeling Regulations, including COOL, Prop 65, and Nutritional/Health Claims. + Experience with NLEA guidelines and ESHA Genesis for nutrition data. + Excellent written and verbal communication skills in English. + Proficient in Microsoft Office (Word, Excel, Outlook). **Preferred:** + Bilingual in Spanish. _*This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! *_ \#INDBH \#LI-DNP We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Manufacturing Los Angeles, CA, US + Added - 14/08/2025 Apply for Job _Our client is a leading global specialist for high-quality plastic films, sheets and other plastic products. They are a stable, growing global organization with 30+ production sites and over 5,000 employees._ **Job Title:** Quality Validation Engineer **Location:** Los Angeles County, CA **Salary:** $90k-110k **Direct Hire** **Position Overview:** The Quality Validation Engineer ensures the quality of product design and manufacturing processes. This role combines quality engineering, validation, and compliance responsibilities in a customer-facing capacity, without hands-on manufacturing or bench work. **Key Responsibilities:** + Apply statistical tools for design verification and test method validation. + Lead FMEA and risk analysis meetings; document results and action items. + Investigate material failures, determine root causes, and implement corrective actions. + Support new product transfers and participate in qualification/validation of products, equipment, and processes. + Review and approve process and design document changes. + Assist R&D with test method development and validation. + Participate in internal quality audits and contribute to ISO-compliant quality systems. + Review and approve receiving inspection requirements and sampling plans; improve QC inspection methods. + Provide backfill support for QC testing, receiving inspection, and product release activities. + Support implementation of the company's overall validation strategy. **Training:** + 1-2 months of initial training with hiring manager, then transition to independent projects. **Required Qualifications:** + Bachelor's degree in Engineering or related discipline. + 1-3 years of validation experience (IQ/OQ/PQ, test method validation). + Experience in quality engineering: risk analysis, CAPA, root cause analysis, FMEA, lean six sigma, audits, corrective actions. + GMP and ISO 13485 quality systems experience; medical instrumentation preferred. + Familiarity with testing equipment (Instrons, pin gages, snap gages, micrometers, calipers, etc.). + Working knowledge of SPC, DOE, Six Sigma, and other fundamental quality/statistical tools. + ASQ Certified Quality Engineer (preferred). + Systems experience: MS Office (Excel, Access, PowerPoint); LIMS or PM tools a plus. **Preferred Experience:** + Plastics industry strongly preferred; medical device, aerospace, or food & beverage experience considered. **Company Highlights:** + Stable, growing global organization with 30+ production sites and over 5,000 employees. + Leading plastics manufacturer. + Ideal role for engineers or material scientists seeking customer-facing responsibilities.INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Manufacturing Gardena, CA, US + Added - 17/01/2025 Apply for Job _Our Client, a fine chemical and laboratory products company, is seeking a Quality Inspector to join their growing team. This is a great opportunity to work with a reputable organization, get industry best training, and work with state of the art equipment, systems and products._ **Title:** QA Inspector **Location:** Gardena, CA **Pay:** $25-28/hr **Schedule:** M-F 7am-3:30pm **Contract to hire** QA Inspectors play a key role in ensuring materials and components meet quality standards and verifying the final release of finished goods according to specifications and regulations. They utilize approved methods, statistical sampling, and process audits to uphold compliance and exceed customer expectations. **Responsibilities:** + Inspect, approve, or reject materials and finished products based on documented criteria. + Follow sampling plans and perform inspections or measurements as specified. + Review and approve labeling, routers, and other documentation for product release. + Record inspection results in forms, checklists, and databases. + Inspect packing, sampling, QC lab, and warehouse areas to ensure compliance with standards. + Verify calibration of inspection and measurement equipment. + Compare products against specifications, drawings, and documentation at various stages. + Isolate defective or nonconforming materials to prevent mix-ups. + Initiate deviations, nonconformance reports (NCMRs), or reject reports. **Qualifications:** + High school diploma or GED. + Minimum 2 years of experience in a regulated manufacturing environment (FDA, DEA, ISO). + Familiarity with cGMP processes and sampling plan tools preferred. + Proficiency in using PPE and Microsoft/ERP systems. INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Laboratory Los Angeles County, CA, US + Added - 01/12/2025 Apply for Job Pay Rate Low: 20 | Pay Rate High: 22 We are seeking a reliable, detail-oriented **Materials Preparation Technician** to support production operations by accurately locating, measuring, and documenting raw materials used in manufacturing. This role is critical to ensuring batches are made correctly, efficiently, and in compliance with standard operating procedures. **Location:** Los Angeles County, CA **Schedule:** Monday-Friday, 8:00 AM-4:30 PM **Employment Type:** Contract-to-Hire **Pay Rate:** $20-$22/hr **Start Date:** ASAP **Key Responsibilities** + Locate required raw materials in the warehouse for upcoming production batches. + Weigh raw materials accurately using appropriate scales and equipment. + Record all weights clearly and legibly for each batch. + Perform basic math calculations and conversions as needed. + Assist with raw material inventory counts and stock rotation. + Ensure all materials are returned to the correct storage location. + Maintain a tidy, clean, and organized pre-weigh and warehouse area. + Maintain detailed, accurate records of all materials weighed. + Follow established procedures to ensure compliance and traceability. + Communicate any discrepancies or low-stock items to the appropriate team member. + Assist other departments when needed during high-volume periods. + Perform additional tasks as assigned to support production and warehouse operations. **Requirements & Qualifications** **Must Haves:** + 1+ year of experience in a pre-weigh, production, or manufacturing environment. + Experience in **personal care, cosmetics, or nutraceutical** industries preferred. + Strong attention to detail and accuracy. + Reliable, self-directed, and punctual. + Strong basic math skills, including weight conversions. + Ability to lift up to 50 lbs. + Proficiency with Microsoft Office (Excel, Word). + High school diploma or equivalent. **Preferred:** + Familiarity with warehouse operations and material handling. + Comfort working in a start-up environment where processes are evolving. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Clinical Los Angeles County, CA, US + Added - 24/07/2025 Apply for Job Pharmaceutical Company in Los Angeles, CA is seeking a Production Chemist to join their Production team! This is a direct hire opportunity! Eagerly hiring! **Shift:** Monday-Friday 8-5pm, with occasional shift to 2nd (2pm-10pm) **Must have** : 1 year of HPLC **Responsibilities:** + Perform purification process by chromatography, crystallization and other techniques, and in-process test method + Follow approved GMP manufacture directions such as Master Batch Records, Standard Operation Procedures, Standard Test Procedures and other procedures to manufacture GMP materials, perform in-process test, package the product including other related activities + Perform project-planning and initiate raw material order-request. Receive raw materials, coordinate with QA/QC and Material Management for material release and monitor raw material inventories + Install, test equipment, operate and maintain equipment for manufacturing and in-process testing. The equipment includes analytical HPLC and prep HPLC system, Lyophilizes, balances, reactors, HF cleavage equipment, diafiltration systems, water purification systems, oven, washing systems and others used in manufacture + Develop processes for purification of chemicals other than peptides + Follow and maintain GMP Documentation System. Investigate any process deviation and write process deviation report. Initiate document change request. Help quality control and assurance unit to maintain equipment calibration program + Routinely maintain/organize work areas (Hood, bench, floor, wall, etc.) and other designated areas at the manufacturing facility + Develop peptide-manufacturing processes including peptide/protein purification by chromatography, crystallization, and other techniques, and in process test methods + Assist QA/QC for monitoring raw material inventories + Write Standard Operation Procedures, Standard Test Procedures, Master Batch Records and other related GMP documents + Follow SOPs and approved directions to clean equipment used in GMP processes, maintain cleaning log for each equipment, assist in equipment calibration program, and dispose chemical waste generated in the manufacture + Monitor compliance of Maintenance and Cleaning procedures of equipment and instruments used in GMP processes by periodically reviewing and signing off on maintenance and cleaning log for each equipment **Requirements:** + BS degree in Chemistry or related field + 1-5 years' work experience + Experience with HPLC and chromatography + May work with hazardous materials and chemicals + Excellent written and oral communication skills + Basic computer knowledge, including Microsoft Word, Excel and PowerPoint + Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment + Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues. + Detail oriented with the ability to troubleshoot and resolve problems + Ability to work independently and manage one's time + Communicate effectively and ability to function well in a team environment + Flexibility of working hours based on business needs, may include some nights and occasional weekends We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.