Astrix jobs in Thousand Oaks, CA - 20 jobs

Manufacturing San Fernando Valley, California, US + Added - 27/01/2026 Apply for Job Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 Pay Rate Low: 28 | Pay Rate High: 30 _Pay Low: 28.00 | Pay High: 30.00_ _Our client, a leading food and beverage manufacturer, is looking for a skilled Production Planner to join their team in San Fernando Valley, CA!_ **Location:** San Fernando Valley, CA **Job type:** Contract- hire **Position Summary** The Production Planning Lead is responsible for leading production planning activities to ensure manufacturing goals are met efficiently and consistently. This role provides guidance to the planning team, coordinates closely with cross-functional departments, and proactively adjusts plans to meet changing production demands. The ideal candidate brings hands-on production planning experience, strong leadership skills, and a solid understanding of manufacturing operations, inventory flow, and materials management. **Location:** San Fernando Valley, CA **Schedule:** Monday-Friday 8-5pm, fully onsite **Job type** : 3 month contract- hire **Responsibilities:** + Lead and oversee daily production scheduling activities to ensure on-time execution. + Manage completion and accuracy of daily production schedules. + Proactively adjust production plans in response to equipment issues, material shortages, rework, or shifting priorities. + Collaborate with Production, Engineering, Quality, Warehouse, and Purchasing teams to meet daily output targets. + Provide leadership, training, and onboarding support for Production Planning team members. + Serve as backup coverage for all planning roles as needed. + Coordinate daily material pulls for production rooms. + Support forecasting and inventory management of raw materials and packaging components. + Assist with purchase order (PO) and transfer order (TO) postings and verify inventory transactions. + Perform minor inventory adjustments when necessary. + Process and close daily production batches. + Support month-end close activities and participate in physical inventory counts. + Maintain consistent and punctual attendance. + Perform additional duties as assigned. **Qualifications & Requirements** + Minimum of 2 years of production planning experience. + 1+ year of leadership experience as a Supervisor or Lead strongly preferred. + Bachelor's degree preferred. + Strong written and verbal communication skills. + Proficiency in Microsoft Excel. + Ability to work independently and collaboratively in a team environment. + Proven problem-solving skills with the ability to implement effective solutions. + Exceptional attention to detail and organizational skills. + Positive, self-motivated attitude with the ability to thrive in a fast-paced environment. + Strong multitasking and prioritization abilities. _*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- AH1 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 Los Angeles, California, US + Added - 07/01/2026 Apply for Job Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 Pay Rate Low: 120000 | Pay Rate High: 135000 _Our client, a growing health and wellness company, is looking for a skilled Senior Social Media Manager to join their team in Los Angeles, CA!_ **Location:** Los Angeles, CA **Salary** : $120K - $135K **Job type:** Direct- hire **Job Summary** We are seeking a Senior Social Media Manager to lead and evolve a global social media presence across bioscience, health, and wellness audiences. This senior-level role is responsible for developing and executing high-impact social media strategies that strengthen brand leadership, grow engaged communities, and drive measurable business outcomes. **Core Responsibilities** _Strategic Leadership_ + Develop and own the end-to-end social media and community strategy aligned with brand, product, and business objectives. + Establish a long-term vision for social platforms, identifying opportunities for innovation, investment, and differentiation. + Set annual and quarterly KPIs, lead reporting cadences and present insights, performance, and recommendations to senior leadership. + Monitor the competitive and cultural social landscape to identify trends, opportunities, and risks that inform content and channel strategy. _Content Strategy & Oversight_ + Oversee the creation of high-quality, scientifically accurate, and visually compelling content, including video, animation, graphics, stories, and integrated campaigns. + Lead content ideation and ensure all materials meet creative excellence and regulatory standards, including FDA and claims compliance where applicable. + Drive experimentation with emerging formats, platforms, and interactive content, with an emphasis on short-form video. _Team & Cross-Functional Collaboration_ + Partner closely with Marketing, Creative, Scientific Affairs, Research, Product Development, and Sales teams to ensure cohesive, accurate brand storytelling. + Provide clear direction and feedback to internal creators, agencies, freelancers, and production partners. + Mentor junior team members, supporting growth in strategic thinking, creativity, and platform best practices. _Performance Optimization & Analytics_ + Oversee platform analytics using tools such as Meltwater, Later, and other social and digital analytics solutions. + Analyze engagement, reach, traffic, conversions, and sentiment to inform optimization strategies. + Proactively manage crisis and reputation-related situations with strategic judgment and cross-functional alignment. **Qualifications** + Bachelor's degree in Marketing, Communications, Digital Media, or a related field; advanced degree preferred. + 7+ years of professional social media marketing experience, ideally within regulated, scientific, or highly competitive industries (e.g., bioscience, health, wellness, biotechnology, or technology). + Demonstrated experience leading channel strategy across Instagram, TikTok, LinkedIn, YouTube, Facebook, Reddit, and X (Twitter). + Proven ability to translate complex scientific or technical concepts into engaging, consumer-friendly content. + Strong experience with social media management platforms (e.g., Meltwater, Later) and digital analytics tools. + Working knowledge of SEO, content marketing, and paid social fundamentals. + Highly collaborative, proactive, and comfortable in a fast-paced, innovation-driven environment. + Strong project management skills with the ability to prioritize multiple initiatives and manage multiple social media accounts. + Curiosity and passion for science, biotechnology, and wellness 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! *_ \#LI- AH1 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, California, 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.

Quality Control Camarillo, California, US + Added - 22/01/2026 Apply for Job Pay Rate Low: 30 | Pay Rate High: 38 Our client is seeking a **QC Microbiologist** to support **environmental monitoring and routine microbiological testing** in a GMP manufacturing environment. This role is ideal for candidates with hands-on cleanroom or QC microbiology experience. **Key Responsibilities** + Perform **environmental monitoring** of cleanrooms (air, surface, and personnel swabbing) per **USP and EU** requirements. + Conduct microbiological testing including **endotoxin, bioburden, TOC, and conductivity** for water systems. + Test raw materials, in-process samples, and finished products for **endotoxin and bioburden** . + Trend, analyze, and report environmental and microbiological data. + Submit samples for **microbial identification** and maintain organism trending. + Support **media fills** , sample log-in, documentation, and OOS investigations. + Assist with general QC Micro lab activities, equipment upkeep, inventory, and housekeeping. **Qualifications** + Bachelor's degree in **Microbiology or related science** + **1-3 years** of experience in a **GMP or GLP** microbiology laboratory + Experience with **environmental monitoring, swabbing, endotoxin, and bioburden testing** + Knowledge of **FDA cGMPs (21 CFR 211)** ; cleanroom experience preferred + Proficient in **Microsoft Excel** **INDBH #LI-BH1** 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 El Segundo, California, 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.

Manufacturing Cerritos, CA, US + Added - 02/12/2025 Apply for Job **Our client is a global biotechnology and aesthetics company specializing in skincare solutions. They are seeking a QC Lab Technician to join their growing team!** **Title:** QC Lab Technician (2 Openings!) **Location:** Los Angeles, CA 90701 **Pay:** $20-22/hr **Shift:** M-F 8am-4:30pm **Contract to hire** **Job Summary** We are seeking a full-time QC Laboratory Technician to join our team. This role is responsible for performing laboratory testing on raw materials, in-process samples, and finished products, as well as maintaining accurate documentation and supporting QC and Regulatory activities. Additional tasks may be assigned as needed. **Duties and Responsibilities** + Operate, calibrate, clean, and maintain laboratory instruments and equipment + Perform testing on raw materials, in-process batches, and finished products + Conduct stability testing on finished products + Monitor production batches to ensure quality standards + Verify pre-weighed raw material quantities prior to batch manufacturing + Prepare and submit samples to third-party laboratories + Organize and maintain inventory for raw materials, finished product components, lab supplies, and warehouse supplies + Record test results, organize data, perform basic calculations, and prepare reports using standard procedures + Inspect equipment, documentation, and finished products before and after filling **Requirements and Qualifications** + 1-2+ years of experience in an R&D, QC, or analytical laboratory + Familiarity with analytical techniques and instrumentation + Strong attention to detail, accuracy, and procedural compliance + Excellent documentation and organizational skills + Strong written and verbal communication abilities + Proficiency in MS Word, Excel, and Google Docs preferred + Ability to lift up to 20 lbs 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 Control Cerritos , California, US + Added - 13/01/2026 Apply for Job Pay Rate Low: 45 | Pay Rate High: 55 **Quality Control Manager** **Employment Type:** 6-month Contract to hire (40 hours per week) **Compensation** : $45-$55/hour **Hours** : M-F 8-5 **About the Role** We are seeking a seasoned Quality Control Manager to establish and maintain robust quality frameworks for cosmetic and over-the-counter skincare products. This facility-based position plays a central role in upholding regulatory compliance, ensuring inspection preparedness, and facilitating regulatory filings for OTC formulations including sun protection products. **Core Responsibilities** + Direct the quality assurance function ensuring adherence to federal regulations and organizational quality benchmarks. + Design, implement, and maintain quality management systems aligned with current regulatory frameworks. + Orchestrate preparation for and execution of regulatory inspections, serving as primary liaison with federal investigators. + Maintain state of readiness for unannounced regulatory visits. + Provide quality guidance for new drug application processes related to OTC products, with emphasis on topical sun protection formulations. + Collaborate on regulatory submission documentation ensuring quality data integrity. + Review and authorize batch production records, deviation investigations, corrective and preventive action plans, standard operating procedures, and change control documentation. **Required Experience & Credentials** **Education** + Bachelor's degree in Chemistry, Biological Sciences, Pharmaceutical Sciences, or related scientific discipline. **Professional Background** + Proven experience as a **QC Manager or Quality Manager** within a **cosmetic or OTC product company.** + Direct experience participating in and leading **FDA audits.** + Strong working knowledge of **21 CFR regulations.** + Hands-on experience with **MOCRA compliance.** + Experience supporting **NDA submissions** for OTC products, particularly sunscreens. _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.

Science & Research Pacoima, California, US + Added - 14/11/2025 Apply for Job _We are seeking a motivated Associate R&D Food Technologist to join our team! This contract-to-hire role is ideal for someone who is passionate about product development, enjoys hands-on formulation work, and thrives in a fast-paced, collaborative environment._ **Title:** Associate Food Technologist **Location:** North Los Angeles, CA **Job type:** Contract - hire **Pay Rate:** $25/hr. -$30/hr. (DOE) **Key Responsibilities** + Develop and improve new and existing products based on customer or internal requirements. + Demonstrate creativity and innovation in formulation development. + Taste, evaluate, and validate all developed products for quality and consistency. + Work independently with minimal supervision to meet project objectives. + Perform product costing calculations and maintain accurate cost data. + Create and maintain master formulas within company databases. + Draft product specifications for supervisor review and approval. + Conduct shelf-life and stability testing on finished products. + Establish and manage protocols for all outgoing product samples. **Requirements** + Bachelor's degree in Food Science, Food Technology, Chemistry, or a related scientific field. + Minimum 1 year of experience in the food industry or relevant field. + Strong mathematical skills, including working knowledge of algebra. + Excellent verbal and written communication skills. + Strong sensory acuity for taste and aroma evaluation. + Ability to occasionally lift and carry up to 15 lbs. \#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 Rancho Dominguez, California, US + Added - 19/01/2026 Apply for Job Pay Rate Low: 22 | Pay Rate High: 25 _Our client, a global life sciences and biotechnology company, is looking for a skilled QA Inspector to join their growing team in Los Angeles County, CA!_ **Pay rate:** $22/hr. - $25/hr. **Location:** Los Angeles County, CA **Job type:** 6-month contract **Job Overview:** We are seeking a QA Inspector to provide quality support for a growing manufacturing team. This role will focus on processing backlogged documentation, prioritizing new inspections, and supporting electronics and finished goods releases. The QA Inspector will be responsible for daily quality inspection activities for finished products and sub-assemblies. **Responsibilities** + Perform in-process, finished goods, and final inspections, including visual inspections. + Verify components against engineering drawings, bills of materials, specifications, and purchase orders. + Prepare, print, and verify quality documentation and labels for manufacturing processes. + Review manufacturing batch records and document inspection results. + Identify and clearly communicate nonconformances to management in a timely manner. + Accurately document and maintain QA inspection records using applicable software systems. + Support batch record scanning and records retention activities. + Provide QA floor support, including NCMR investigations, deviations, and corrective actions. + Review Lot History Records (LHRs) for release of finished products and sub-assemblies in SAP. + Ensure compliance with all SOPs, Work Instructions, and Quality policies. + Support backlog reduction and prioritization of new inspections and releases. **Education & Experience Requirements** + High School Diploma, GED, or equivalent required with 1-3 years of Quality Inspection experience required. + Experience in a manufacturing or laboratory environment preferred. + Familiarity with ISO 9001, ISO 13485, 21 CFR 820, or equivalent QMS standards. + Knowledge of AQL inspection plans. + Experience working in a controlled Quality environment strongly preferred. + Strong attention to detail and organizational skills. + Effective written and verbal communication skills. + Ability to collaborate with multiple departments. + Positive, team-oriented attitude. **Physical Requirements** + Regularly required to stand, walk, use hands/fingers, and communicate verbally. + Frequently required to sit, reach, stoop, kneel, crouch, or crawl. + Must be able to lift and/or move up to 25 pounds. + Vision requirements include peripheral vision and depth perception. **_Note:_** _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 Pacoima, California, US + Added - 27/01/2026 Apply for Job Pay Rate Low: 35 | Pay Rate High: 38 _Our client is a global leader in food & beverage-specializes in quality fruit juices, concentrates, and flavor blends. We're seeking a Inventory Manager who brings a passion to help us deliver fresh, consistent, and unforgettable taste experiences every time._ **Title:** Inventory Control Manager **Location:** Los Angeles, CA 91331 **Schedule:** Monday-Friday 8-5pm, fully onsite. **Pay rate: $35-38/hr** **Contract to hire (Plus benefits)** The Inventory Control Manager will build and lead the inventory function in a fast-paced flavor manufacturing environment. This role is responsible for designing and implementing inventory control processes that ensure accuracy, efficiency, and compliance in a weight-based system (kilograms, pounds, and units). The ideal candidate is a hands-on leader with strong inventory expertise, team development experience, and the ability to collaborate cross-functionally to drive operational excellence. **Key Responsibilities** + Establish and lead the inventory control team, including hiring, training, and mentoring staff + Develop and implement scalable inventory control processes and SOPs for a weight-based manufacturing environment + Partner with purchasing, planning, production, warehousing, quality, and finance to ensure accurate inventory tracking and replenishment + Oversee cycle counts, physical inventories, reconciliations, and ERP inventory adjustments + Investigate and resolve inventory discrepancies and material variances + Analyze inventory data and trends to identify root causes and drive continuous improvement + Support month-end and year-end close activities, reporting, and audit readiness + Train cross-functional teams on proper inventory handling and system transactions + Promote a culture of accountability, accuracy, and continuous improvement **Qualifications** + Associate degree in Business, Supply Chain, Logistics, or related field (Bachelor's preferred) + 3+ years of inventory management experience in a supervisory role, preferably in food, flavor, or chemical manufacturing + Experience with weight-based inventory systems and ERP platforms (SAP preferred) + CPIM certification preferred (or willingness to obtain) + Strong Excel and reporting skills + Proven leadership, analytical, and problem-solving abilities + Highly organized, detail-oriented, and able to thrive in a fast-paced environment + Flexibility to report to any company facility as needed, sometimes on short notice INDBH \#LI-MG1 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 Torrance, California, 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.

Laboratory Pacoima, California, US + Added - 17/06/2025 Apply for Job _Our client, a growing innovative food & beverage manufacturer, is experiencing significant growth, and with that comes exciting opportunities. We're seeking an R&D Manager to join their dynamic team!_ **Job Title** : R&D Product Development Manager **Location:** Los Angeles County , CA **Job type:** Contract-hire **Pay rate:** $45- $56/ hr. **Position Summary:** We are seeking a dynamic and experienced R&D Product Development Manager to lead our product development efforts from concept to commercialization. This role is ideal for a critical thinker with a strong background in food science and a passion for developing innovative flavor and beverage solutions. The ideal candidate will supervise a team of chemists and lab technicians while ensuring all products meet customer requirements, cost targets, and regulatory standards. **Key Responsibilities:** + Oversee and manage all product development projects within the R&D department. + Lead the formulation and development of products according to customer or internal specifications. + Supervise, mentor, and provide technical guidance to R&D chemists and lab technicians. + Collaborate with cross-functional teams including Quality Control, Analytical, Production, and Sales. + Evaluate the technical feasibility of new products based on equipment, technology, and production capabilities. + Conduct cost analysis and determine suggested selling prices for developed products. + Ensure thorough documentation of master formulas and compounding instructions. + Approve product specifications and ensure compliance with SQF (Safe Quality Food) standards. + Communicate directly with customers to gather requirements, present prototypes, and provide technical support. + Support scale-up processes and monitor initial production runs to ensure consistency and quality. + Participate in special projects and other duties as assigned. **Qualifications:** + Bachelor's degree in Food Science, Nutrition, or a related field. + Minimum of 4 years of supervisory or management experience in an R&D environment. + Strong taste and aroma acuity for product evaluation and formulation. + Proficient in Microsoft Office Suite; solid math skills (algebra level). + Strong written and verbal communication skills in English. _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!_ 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 Rancho Dominguez, California, US + Added - 17/10/2025 Apply for Job _Our client, a global leader in bioprocessing, is looking for a skilled assembler to join their team in L.A County, CA! This is a great opportunity for a more entry-level candidate looking to gain assembly experience with a leading life science company._ **Pay rate:** $20 - 21/hr. **Job type:** 6-month contract **Schedule:** 2 nd shift **Location:** Los Angeles County, California **Overview:** This is a hands-on manufacturing role focused on assembling fiber and filtration components for medical or industrial devices. The assembler must follow detailed instructions to ensure high product quality and compliance with manufacturing standards. This role is entry-level and works under the guidance of more experienced assemblers and supervisors. **Key Responsibilities:** + Assemble fiber, filtration, and plastic components manually and with tools. + Follow work instructions, blueprints, and manufacturing procedures. + Conduct visual inspections and routine testing for quality assurance. + Operate and maintain small hand tools and some automated equipment. + Clean workstations and follow Good Manufacturing and Documentation Practices (GMP/GDP). + Package finished goods and kits per Bill of Materials (BOM). + Work across multiple product lines as needed. + Identify and report quality issues promptly. **Qualifications:** + High school diploma or equivalent required. + 0-1 year of manufacturing experience preferred (medical device industry is a plus). + Ability to read blueprints and work instructions. + Comfortable with repetitive tasks and working in a cleanroom environment. **Physical & Work Environment Requirements:** + Regular standing, walking, reaching, bending, and lifting (up to 50 lbs occasionally). + Good hand-eye coordination and visual acuity (depth perception and peripheral vision). + Exposure to moving machinery, vibration, and occasionally chemicals or airborne particles. + Work is done in a cleanroom environment with loud noise levels. _Note: 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 Thousand Oaks, California, US + Added - 13/10/2025 Apply for Job **Job Opportunity: Senior Maintenance Technician** **About the Opportunity** Our client, a leader in biotechnology, is revolutionizing the use of living cells to create groundbreaking biologic medicines. We are excited to announce a fantastic opportunity to join their team as a **Senior Maintenance Technician** ! **Shift Details** + **Standard:** Thursday-Saturday, 6:30 PM - 7:30 AM, alternating Wednesdays + **Onboarding (2-6 weeks):** Monday-Friday, 8 AM - 5 PM **Role Overview** Perform advanced installation, troubleshooting, maintenance, repair, testing, and documentation of facility and utility equipment in manufacturing, labs, and office areas. Ensure all work is safe, timely, and compliant with GMP and SOPs. **Key Responsibilities** + Maintain, repair, and troubleshoot building, utility, and production systems + Develop and complete quality and safety documentation (SOPs, WOs, JHAs, HRAs) + Train staff and provide audit support + Review and approve maintenance reports and procedures + Interpret electrical schematics, P&IDs, loop sheets, and wiring diagrams + Reconcile components and calculate product exposure to room temperatures **Required Skills** + Hands-on maintenance experience in manufacturing or lab settings + Knowledge of GMP and batch record documentation + Filling/finishing manufacturing experience, preferably vial inspection **Qualifications** + Associate degree + 4 years experience **or** High school/GED + 6 years experience **Top Skills** 1. Facility/utility equipment maintenance and troubleshooting 2. Batch record documentation and packaging knowledge 3. Electrical schematics and P&ID interpretation \#LIDNP \#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 Pacoima, California, US + Added - 24/07/2025 Apply for Job _Our client, global leader in food & beverages, specializes in quality fruit juices, concentrations, and flavor blends. We're seeking a R&D Lab Technician who brings a passion to help us deliver fresh, consistent, and unforgettable taste experiences every time._ _Are you excited to blend craftsmanship with creativity to shape flavors enjoyed around the world?_ **Location:** L.A County, CA **Pay rate:** $29- $30/ hr. **Jo type:** Contract-hire **Schedule:** M-F:8-5pm, fully onsite **Responsibilities:** + Assist in the preparation of flavor samples and prototypes. + Perform basic laboratory tasks, including weighing, measuring, and mixing ingredients. + Maintain accurate records of experiments and observations. + Clean and maintain laboratory equipment and workspaces. + Assist in the evaluation of flavor samples using sensory analysis techniques. + Follow established safety protocols and procedures. + Order and maintain inventory of lab supplies. + Support senior scientists and flavorists in research and development projects. **Qualifications:** + Associate's or Bachelor's degree in Chemistry, Food Science, or a related field (or equivalent experience). + Basic understanding of laboratory procedures and techniques. + Strong attention to detail and organizational skills. + Ability to follow instructions and work independently. + Excellent communication and teamwork skills. + A passion for food and flavor. _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.

Science & Research Los Angeles County , CA, US + Added - 28/01/2026 Apply for Job Pay Rate Low: 26 | Pay Rate High: 28 _Our client, a leading cosmetics manufacturer, is looking for a skilled QC Chemist to join their team in Los Angeles County, CA!_ **Job type:** Contract- hire **Location:** L.A County, CA **Responsibilities** + Perform stability testing on new and existing products to determine shelf life + Pull and test raw materials, in-process samples, and finished goods to ensure compliance with specifications + Collect, prepare, and ship samples for third-party laboratory testing + Generate Certificates of Analysis (COAs) for finished goods + Maintain, calibrate, and ensure proper operation of laboratory instruments and equipment + Assist R&D with formulation development, testing, and optimization + Prepare, review, and organize quality documentation for QA review + Support inventory management of laboratory supplies, samples, and materials + Follow SOPs, GMPs, and internal quality procedures + Assist with continuous improvement of QC and laboratory processes **Requirements** + B.S degree with prior experience performing QC testing in a laboratory setting + Background in Chemistry or a related scientific field + Strong attention to detail and accuracy in testing and documentation + Ability to manage multiple priorities and wear multiple hats + Comfortable working in a fast-paced, startup environment + Strong organizational and time management skills + Ability to work independently as well as collaboratively across teams + Willingness to follow safety protocols and quality standards \#LI-AH1 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 Thousand Oaks, California, US + Added - 14/01/2026 Apply for Job Pay Rate Low: 25 | Pay Rate High: 30 Our client is a global, research-driven biotechnology company focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for additional Manufacturing Associates to join their different departmental teams. This is an amazing opportunity to work on cutting edge treatments and make a difference! Located in Simi Valley, CA **Type:** Contract **Pay:** $25-30/hr **All shifts available** **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 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 reports- Drafting and revising documents (SOPs, MPs) **Requirements:** + BS degree from an accredited institution in a relevant scientific discipline + Laboratory experience from previous employment/academic programs "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 Rancho Dominguez, California, US + Added - 16/01/2026 Apply for Job Pay Rate Low: 22 | Pay Rate High: 25 **Our client is a biotech research and bioprocessing company that develops tools and technologies used to manufacture biologic drugs-especially antibody-based therapies** **Title: QA Inspector I** **Location: Los Angeles County, CA** **Pay:** $22-25/hr **Shift:** M-F 8am-5pm **Contract:** 6 months to potential hire (plus benefits) **Role Summary** Reports to the QA Supervisor or QA Manager and supports daily quality inspection activities for finished products and sub-assemblies. Responsible for in-process and final inspections, documentation review, and ensuring compliance with quality systems and procedures. **Key Responsibilities** + Perform in-process, finished goods, and final visual inspections. + Verify components against engineering drawings, BOMs, specifications, and purchase orders. + Review manufacturing batch records and Lot History Records (LHRs) for product release in SAP. + Prepare, verify, and maintain quality documentation, labels, and inspection records. + Identify, document, and communicate nonconformances; support NCMRs, deviations, and corrective actions. + Provide QA floor support and assist with batch record scanning and records retention. + Ensure compliance with SOPs, Work Instructions, and company Quality policies. + Accurately document inspection activities using applicable software tools. **Qualifications** + High School Diploma or GED required; 1-3 years of quality inspection experience. + Experience in manufacturing or laboratory environments, preferably in regulated or controlled settings. + Working knowledge of ISO 9001, ISO 13485, 21 CFR 820, or equivalent QMS standards. + Familiarity with AQL inspection plans. + Strong attention to detail, organizational skills, and ability to work independently after training. 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 Control Cerritos, CA, US + Added - 28/01/2026 Apply for Job Pay Rate Low: 26 | Pay Rate High: 28 Our client is a fast-growing skincare company rooted in over 30 years of regenerative medicine research. Using proprietary DNA-based technology, they develop advanced products for both professional clinical use and daily skincare. This role offers the opportunity to help build a company from the ground up, with strong growth potential as the organization scales **Schedule -** Monday-Friday, 8:00 AM-5:00 PM **Key Responsibilities** + Perform stability testing to determine product shelf life + Test raw materials, in-process samples, and finished goods + Collect and prepare samples for third-party testing + Maintain laboratory instruments and equipment + Support R&D with formulations + Generate Certificates of Analysis + Prepare QC documentation for QA review + Manage laboratory inventory **Qualifications** + 1-2+ years of QC testing experience + Bachelor's degree preferred + Chemistry background + Experience in personal care, cosmetics, or nutraceuticals preferred + Strong attention to detail + Comfortable wearing multiple hats + Proficient in Microsoft Office **Why Join** + Early-stage company with room for growth and advancement + Hands-on role with visibility across QC, R&D, and operations + Expanding product portfolio following recent regulatory approval INDBH #LI-BH1 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.