Research Associate Jobs in Burbank, CA

Job Title: NDT Level III RT/DR, Quality Engineering Specialist Job Schedule: 9/80: Employees work 9 out of every 14 days - totaling 80 hours worked - and have every other Friday off Aerojet Rocketdyne, an L3Harris company, is seeking a NDT Level III RT/DR, Quality Engineering Specialist to join our team in Canoga Park, California. Essential Functions: Review supplier-submitted NDT technique sheets for compliance to AR-Los Angeles specifications and drawing requirements. Coordinate with suppliers on the development and approval of these technique sheets. Prepare necessary reports. Manage site NDT supply base by monitoring suppliers to ensure flow down of AR requirements to sub-tier suppliers, audit existing NDT suppliers and assess potential new NDT suppliers for their ability to meet site requirements. Review process specifications, in-house technique sheets, etc. as noted above under job responsibilities. Provide training and testing to L I and L II. Develop, review and approve NDT techniques with L II personnel. Write, review and approve specifications pertinent to NDT. Support review boards for inspectability of product. Prepare NDT for customer and internal audits. Develop and Lead Corrective action reviews on audit/NCR findings. Maintain own L III certifications. Participate in the direction of the NDT department. Audit and surveillance of quality systems and processes. Qualifications: Bachelor's Degree and minimum 9 years of prior relevant experience. Graduate Degree and a minimum of 7 years of prior related experience. In lieu of a degree, minimum of 13 years of prior related experience. Preferred Additional Skills: Requires NDT LVL III RT (Radiography) and DR (Digital Radiography) certifications. Needs to have direct experience with the testing of Aerospace Metallic products Must have experience with RT and DR inspection of welds along with defect recognition Must have both RT and DR Level 3 ASNT Certification and/ or currently active NAS410 Level III certifications. (May consider DR or RT with strong CT experience) Hands-on working experience in a manufacturing environment and a corresponding understanding of manufacturing processes is essential. Experience with auditing practices and Process Certification is desired. A demonstrated proficiency with a variety of NDT inspection techniques and equipment along with a working knowledge of blueprint reading and interpretation is required. Knowledge of industry NDT standards (ex. NAS410, ASTM 1742, ASTM 1417, ASTM 1444, AMS-STD-2154, etc...) is requisite. Candidate must meet requirements of NAS-410. Must have demonstrated excellent interpersonal, written and verbal communication skills, as well as the ability to work well in a team environment. Must possess strong computer skills and be well-organized. Position requires responding to customer needs and may include weekend work. Auditing experience/certification desired. In compliance with pay transparency requirements, the salary range for this role is $112,000 - $208,000. This is not a guarantee of compensation or salary, as final offer amount may vary based on factors including but not limited to experience and geographic location. L3Harris also offers a variety of benefits, including health and disability insurance, 401(k) match, flexible spending accounts, EAP, education assistance, parental leave, paid time off, and company-paid holidays. The specific programs and options available to an employee may vary depending on date of hire, schedule type, and the applicability of collective bargaining agreements.

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We are seeking a Research & Clinical Investigator passionate about ensuring the sound science of our nutrition and personal care products, along with developing relevant and meaningful products that address key customer needs in the global health and wellness space. If you have a passion for health and wellness (nutrition and personal care), and would enjoy translating complex science into efficacious, experiential products, this would be a great role for you! Evaluate Scientific Evidence for Claim Substantiation Collaborate cross-functionally with marketing, safety, and regulatory teams to craft scientific stories and compelling substantiated claims for nutritional products. Translate complex scientific principles into consumer stories and education. Monitor policies, standards, and practices ensuring strong claim substantiation. Oversight of Clinical Trials & HUT Responsible for managing either in-house or outsourced clinical research to substantiate unique claims, uncover and generate intellectual property, and to develop research publications. Oversee study execution and results analysis and then translate the results into consumer-friendly and regulatory acceptable claims and stories which support the efficacy of our products. Oversee IRB, protocol, clinical execution & evaluate data on clinical trials. Responsible coordinating and evaluating results of Home Use Testing (HUT). Identify New Technology Responsible for front-end innovation with concept development using new ingredients. development and technologies scientific insights and executing innovative product concepts with unique technologies to meet consumer needs. Work on front end research, helping to identify relevant mechanisms of action and outcomes, and to partner with internal teams and/or external partners to advance ingredient and product technologies. Utilize qualitative and quantitative data to understand consumer needs, market landscape, and opportunities for innovation. What You Need: Advanced degree (MS or PhD) in Bioscience, Nutrition, Molecular Biology, Immunology, Microbiology or related discipline Minimum 2 -3 years background in scientific research, methods, analysis and data interpretation and publication Track record of scientific presentations and/or educating the public on health and wellness Ability to translate complex scientific and technical concepts into consumer appropriate language, to enable communication and understanding of the science underlying the product Interpersonal skills to influence and inspire both internal and external audiences Experience leading clinical studies in an industry setting is helpful RD (Registered Dietician) Certification, ACRP (Association of Clinical Research Professionals) Certification, or naturopathic background helpful. Ability to work on site up to 5 days a week. Commitment to model and live out our Core Values (Accountability, Community, Innovation and Courage) and a positive mindset are critical for success and should reflect in everything you do. The Arbonne Promise As a company, Arbonne has been driving the healthy living movement forward for over 40 years, creating positive change within the health & wellness industry, within our customers' and consultants' lives, and for the environment. We began by leading the clean beauty movement in 1980 and have continued to evolve and lead as healthy and wellness has become an integral part of our everyday lives. While some things change, our standards haven't. Throughout the years, Arbonne has been committed to sustainability, and we consider people and the planet in every decision we make. Arbonne is proud to be a Certified B Corporation. Our Culture We are a global family, united by a shared passion for excellence and a commitment to fostering a diverse, inclusive, and respectful environment where everyone feels valued and empowered to reach their full potential. We celebrate collaboration, knowledge sharing, and a sense of ownership. We believe that by learning from each other, supporting each other, and working together towards our shared goals, we can achieve extraordinary things. Join us on this journey of thriving together. Let's build a better future, for ourselves, for our planet, and for generations to come. Arbonne International is committed to employing a diverse workforce. Qualified applicants will receive consideration without regard to race, color, religion, sexual orientation, national origin/ancestry, age, sexual orientation, gender identity, gender expression, military/veteran status, marital status, disability status, or any other basis prohibited by law. At Arbonne International, it's about each person bringing passion and skills to a dynamic and inclusive workplace!

Research Associate - Biochemistry Duration: 3 year contract The ideal candidate would have 1+ year of industry (ideally) or academia in a lab setting with pipetting sample prep & handling, HPLC Chromatography, protein sample analysis (ideal) BS degree in pharmaceutics, biochemistry, chemistry, or related life sciences discipline a strong understanding of protein biochemistry and protein structure significant experience with basic laboratory skills and biophysical techniques related to protein analysis is essential Job description We are currently seeking a research associate for the Drug Product Technologies group in Thousand Oaks, CA. A fundamental understanding of protein chemistry, formulation, and biophysical characterization is desired. The successful candidate will perform experiments related to the development of formulations for therapeutic proteins, including stability testing and analytical characterization. The candidate will join a team of investigators using a variety of biochemical and biophysical techniques and will be involved in the design and execution of experiments. A background in protein solution manipulation (e.g. pipetting, dialysis, concentration) and HPLC analysis is expected. Experience with visible and sub-visible particle analysis and other analytical methods is desirable. Responsibilities will include detailed record keeping in electronic laboratory notebooks, analysis, and interpretation of experimental data. Basic qualifications BS degree in pharmaceutics, biochemistry, chemistry, or related life sciences discipline. A strong understanding of protein biochemistry and protein structure, as well as significant experience with basic laboratory skills and biophysical techniques related to protein analysis is essential. The applicants must be motivated, have good problem-solving skills, and an aptitude to learn and implement new techniques/skills. The candidate should be well organized and proficient in detailed record-keeping, have excellent written and oral communication skills, and be capable of working efficiently in teams and independently.

Company: Molecular Instruments, Inc. (molecularinstruments.com) is a biotechnology startup pioneering programmable molecular technologies for multiplexed quantitative bioimaging. We are looking for talented product-oriented people to help grow our company and develop next-generation capabilities using our state-of-the-art imaging reagents. Responsibilities Develop and maintain in-depth technical and strategic understanding of how products are planned, designed, validated, manufactured, and distributed at scale Assist in writing technical reports, protocol setup guides, and SOP for new products. Perform independent research on finding creative solutions to improve product performance, lower cost of production, and remove barriers toward product development goals. Lead exploration and evaluation of new tools, techniques, and materials, and engage with both external vendors and internal team members to improve company capabilities/efficiency and product performance Document thorough experimental findings and communicate them effectively in technical meetings. Perform on-site customer support on protocol setup and/or trouble-shooting when needed Provide support to all departments within the company through process capability analysis, troubleshooting, root cause analysis, and process changes Listed responsibilities are duties associated with the position. Changes to individual responsibilities may occur due to business needs. Preferred educational and experimental background: BS/MS or equivalent 3+ years of wet lab experience Strong familiarity with standard laboratory practices Experience in fluorescence microscopy, in situ hybridization, immunohistochemistry, blotting techniques, and quantitative analysis of experimental data Familiarity with histopathological auto-stainers such as Discovery Ultra, Oncore Pro X, and BOND RX is a plus Knowledge, Skills and Abilities: A successful applicant must be dedicated, responsible, detail-oriented, highly organized, proactive, efficient and capable of working closely and communicating with others in the multiple teams. Applicant must keep an accurate, detailed and neat lab notebook. Attention to detail in constructing grammatically correct emails is essential. The following wet lab skills are required: polyacrylamide and agarose gel electrophoresis and general molecular biology experience. The following wet lab skills are preferred but not required: in situ hybridization, immunohistochemistry, fluorescence microscopy. Previous wet lab experience, general technical dexterity, dedication, organization, and scientific curiosity are strongly valued. The following scripting languages are valued: MATLAB, Python, C/C++, or other equivalent. Must be authorized to work in the United States. EEO Statement Molecular Instruments is an equal opportunity employer and all qualified applicants will receive consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, religion, marital status, age, national origin, disability status, military or veteran status, or any other characteristic protected by law. To learn more about Equal Employment Opportunity (EEO), visit eeoc_self_print_poster.pdf.

The Research Associate, Analytical Sciences will be responsible for the execution of routine testing, including but not limited to cell-based cytotoxicity assays and molecular biology assays to characterize T cell therapy processes and products. Additionally, this role contributes to the daily operational tasks in the Analytical Sciences team. This role is based out of Santa Monica, CA and reports directly to the Senior Scientist, Analytical Science. Essential Functions and Responsibilities Perform routine analytical testing to characterize cell products or processes primarily using live cell imaging, luciferase assays, or qPCR/dPCR. Perform QC lot release testing of clinical batches, stability studies, and investigations for raw materials and drug products. Participate in writing and revising test methods, SOPs and/or other documents as appropriate. Participate in tracking assay results and test method performance parameters. Assist in everyday operation of analytical laboratories, including but not limited to equipment management, lab maintenance and restocking, and reagent inventory. Assist in building batch analysis dataset. Support cross-functional projects with process development, manufacturing, quality control, and quality assurance groups. Required Skills/Abilities Hands-on experience in performing and analyzing cell-based assays and/or qPCR/dPCR is preferred. Detail-oriented in both technical assay execution and data analysis. Must be eager to learn and willing to ask questions. Working knowledge in data visualization software (e.g. GraphPad Prism) is a plus. Experience in flow cytometry assays and equipment/software is a plus. Education and Experience BS degree in Biology, Chemistry, or related discipline with 0-2 years of relevant experience. Experience executing cell-based assays and molecular biology assays is preferred. Experience working in a regulated environment (e.g. GMP, GLP, or CLIA) is a plus.

Perform routine analytical testing to characterize cell products or processes primarily using live cell imaging, luciferase assays, or qPCR/dPCR. Perform QC lot release testing of clinical batches, stability studies, and investigations for raw materials and drug products. Participate in writing and revising test methods, SOPs and/or other documents as appropriate. Qualifications: BS degree in Biology, Chemistry, or related discipline with 0-2 years of relevant experience. Hands-on experience in performing and analyzing cell-based assays and/or qPCR/dPCR is preferred. Experience executing cell-based assays and molecular biology assays is preferred. Experience working in a regulated environment (e.g. GMP, GLP, or CLIA) is a plus.

Research Scientist- Simply Biotech Are you looking for a new career opportunity with an exciting biotech company?! Then we've got the right team for you! In this role, you're responsible for the duties listed below. Immediate opening for a Research Scientist with a biotech company in Irvine, CA who possesses: Ph.D. or Masters in Chemistry, Biology, or related field 3+ years' experience performing R&D functions in IVD industry (reagents/assays) Proficiency with protein characterization, purification, and extraction techniques Experience with immunoassay development Email resumes to ************************* or call ************ FULL DESCRIPTION : Our client is currently looking for a Research Scientist to develop reagents and assays to enable new capabilities for biological workflows, and transfer technology from R&D to manufacturing. Be challenged and inspired, be a part of the team that makes an impact. The selected candidate will be responsible for: Lead R&D efforts to develop reagents to enable new Biomarker/IVD assays. Examples of reagents include, but not limited to, surface chemistry reagents, critical raw materials (e.g., antibody, antigen, protein, peptides, DNA, RNA) and functionalized microparticles. Design experiments and research studies to test hypotheses and gather data that will inform the development of new products. Ensure the experiments are well-designed, controlled, and reproducible. Collect data from experiments and other sources and analyze the data to draw meaningful conclusions. Use statistical and analytical tools to interpret the results. Conduct thorough literature reviews to understand the state of art in the field and identify gaps that the research can address. Identify potential areas of innovation and improvement. Create prototypes of proof-of-concept models to demonstrate the feasibility of new product concepts. Collaborate closely with cross-functional teams to ensure that the research aligns with the overall product development goals. Ensure that the work complies with relevant regulations and standards. Troubleshoot and solve technical challenges that arise during the development process. Keep detailed records of experiments, results, and research findings for future reference and for meeting regulatory requirements. Communicate the findings and insights effectively to both technical and non-technical stakeholders. Oversee the transfer of new reagents from R&D to Manufacturing. This includes relevant documentation and appropriate quality control (QC) procedures. Support the scale-up of reagent manufacturing. Provide technical guidance to research associates. Act as a mentor to team members. Collaborate with suppliers to synthesize custom reagents and characterize reagents using appropriate analytical techniques, as needed. Be responsible for completing projects and other assignments from upper management on time. The selected candidate will also possess: Ph.D. or MS in Chemical Engineering, Chemistry, Bioengineering, or related disciplines. Minimum 1-3 years of related industrial experience in IVD R&D for PhD Minimum 8 years of related industrial experience in IVD R&D for MS Must be willing to handle human whole-blood, plasma and/or serum samples. Experience developing IVD and life science reagents. Bio-conjugation experience - involving the chemical modification and conjugation of proteins, peptides, and nucleic acids. Experience with protein extraction and isolation a plus. Proficiency in protein characterization (SDS-PAGE, Western blot, HPLC, etc.) Proficiency in purification techniques for both macromolecules and small molecules, such as chromatography (IEX, SEC, and affinity). Fundamental understanding of physical, chemical, and biological phenomena which govern biological assays. Experience with immunoassay assays and related techniques is a plus. Rigorous scientist with a record of developing robust, transferrable processes. Data-driven, proficient with the design of experiments (DOE), and statistical analysis. Ability to thrive in a dynamic company with demanding schedules and deliverables. Outstanding collaborative, interpersonal, verbal, and written communication skills to clearly articulate ideas, problems, and solutions within a highly interdisciplinary environment. Salary Range: $90k-140k/yr For immediate and confidential consideration, please email your resume to ************************* or call ************. More information can be found at *********************

Senior Scientist - Protein & IVD R&D We are seeking an experienced Senior Scientist to lead R&D efforts for reagent development and IVD assay innovations, ensuring seamless technology transfer from R&D to manufacturing. Responsibilities: Develop reagents (e.g., antibodies, proteins) for Biomarker/IVD assays. Conduct experiments, analyze data, and contribute to product innovation. Collaborate with cross-functional teams to meet product development goals. Oversee the transition of reagents to manufacturing, including QC procedures. Mentor team members and troubleshoot challenges in reagent development. Qualifications: Ph.D. (1-3 years) or M.S. (8+ years) in Chemistry, Bioengineering, or related fields. Expertise in protein modification, purification, and stability studies. Familiarity with GMP/GDP standards and IVD assay development preferred. Experience with immunoassays, chromatography, and bio-conjugation is a plus. Why Join Us? Competitive salary ($90-150k), benefits, 401(k), and PTO. Strong training programs, team-building events, and career growth opportunities. Work in a research-driven, GMP-compliant organization. Relocation considered for exceptional candidates.

Mantell Associates is partnered with an innovative Biotech in their search for a Battery Scientist III as a key position within Research & Development. Battery Scientist III - Responsibilities: Lead projects that stretch the bounds of what was previously thought possible in batteries Responsible for developing areas of research that coincide with technical roadmap Coordinate external and internal resources to study areas of research Research activities related to all cell components - anode, cathode, electrolyte, design, and ancillaries Battery Scientist III - Requirements: PhD in Chemical, Mechanical, Materials, Electrical Engineering, Chemistry, or Physics An additional 5+ years of post-graduate work in the battery industry, with preference for startups Direct experience working on battery cells and battery cell materials Creative thinker and strong a faculty for learning Ability to advance multiple projects in a fast-paced and multidisciplinary environment Verifiable track record of discovery and development in next-generation Lithium-ion batteries Deep knowledge of fundamental electrochemistry and understanding of critical battery tradeoffs Strong and verifiable written/verbal communication skills Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at *****************.

100% ONSITE IRVINE CA PAY: $45 - $50/hr Required: BS in Biochemistry or related science discipline and 3-5 years biochemistry or immunology lab experience Primary cell isolation and culture, sterile technique, pipetting samples, generating titrations/dilutions, dealing with cells, making buffers ELISA, or other ligand binding assay basics In vitro cell assays Luminex, MSD or Gyros Flow cytometry Assay development experience Job Description: Isolation & characterization of human blood cells and in vitro cell assays- Contractor will request donor samples, isolate cells from human or monkey peripheral blood, set up cultures with isolated cells, perform cell stimulation or differentiation by test compounds, harvest cells and supernatants, prepare these samples for further analysis; run ELISA, Luminex or MSD tests to study immunosafety of compounds; analyze and present the data generated by these experiments.

Isolation & characterization of human blood cells and in vitro cell assays- Contractor will request donor samples, isolate cells from human or monkey peripheral blood, set up cultures with isolated cells, perform cell stimulation or differentiation by test compounds, harvest cells and supernatants, prepare these samples for further analysis; run ELISA, Luminex or MSD tests to study immunosafety of compounds; analyze and present the data generated by these experiments. What are the top 3-5 skills, experience or education required for this position? • BS or MS & 3-5 years biochemistry or immunology lab experience • Primary cell isolation and culture • Sterile technique, pipetting samples, generating titrations/dilutions, dealing with cells, making buffers • ELISA, or other ligand binding assay basics • In vitro cell assays • Enthusiastic, organized What is a nice to have (but not required) skill, experience, education, or certification? • Luminex, MSD or Gyros • Flow cytometry • Assay development experience In what type of environment would this individual be working (i.e.: Team; Individual; type of office, etc.) ? • 100 % Lab, benchwork, team and individual work Daily Work Schedule Expectations: M-F regular business hours US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: Rahul Lahiri Email: ***********************************

🌟 Join Our Growing Team as a Scientist 3 at Apex Companies! 🌟 Are you a driven, hard-working professional eager to make an impact in the environmental consulting and engineering field? Do you want to work for a company that values your growth, invests in your future, and celebrates your success? If so, Apex Companies might be the perfect place for you! 🚀 Why Apex? As one of the fastest-growing environmental consulting and engineering firms in the US, we're powered by record sales, exceptional client retention, strategic acquisitions, and an entrepreneurial spirit. At Apex, we don't just do work; we create award-winning solutions and lasting relationships. We're growing-and we want YOU to grow with us. 💼 Your Role as Scientist 3: Provide senior technical oversight and hands-on project work. Write and review technical reports and proposals. Take part in project management activities. Mentor and train scientific staff while supervising their work. Actively invest in your own career growth and development. 🎉 What You'll Love About Apex: Comprehensive Benefits: Company-subsidized medical and dental, plus company-paid life, short, and long-term disability insurance. Financial Perks: 401k match, tuition assistance, performance-based bonuses, and more. Professional Growth: Cross-training opportunities and exposure to a variety of projects. Award-Winning Culture: Work alongside the best and brightest in the industry at a 1,500+ employee firm with 50+ locations nationwide. Room to Shine: Be part of a company recognized for project excellence and client satisfaction. 📋 What We're Looking For: BS in Geology, Hydrogeology, Environmental Science, or a related field. 4-6 years of experience in environmental services, including technical writing and oversight. Ability to mentor and train staff with strong communication and technical writing skills. 40-hour HAZWOPER certification (or willingness to obtain). Hands-on experience in light construction a plus. Proficiency in Microsoft Office suite. Valid driver's license, good driving record, and reliable transportation. 💰 Salary Range: $75,000-$90,000 Ready to join a team that values your expertise and rewards your hard work? Apply today and discover what it means to thrive at Apex Companies!

Company is seeking a highly motivated Senior Associate to join the bioanalytical Sciences group of TS&BA department in Thousand Oaks to perform experiments, organize data and analyze results. Specific responsibilities include planning and performing immunoassays/ELISAs, participating in method validations, preparing and analyzing biological samples, analyzing own data, interpreting and developing solutions to technical problems under GxP regulations with some supervision, and documenting and communicating results. Excellent inter-personal skills and verbal and written communications skills are also required. Basic Qualifications: A Bachelor's degree in Life Sciences Minimum 3 years laboratory-based research experience in academic or industrial labs under GxP regulations. Knowledge and experience in performing immunoassay especially ELISA Good computer skills Good documentation skills Preferred Qualifications: Hands on experience and knowledge in ELISA/immunoassays. Ability to operate specialized laboratory equipment and good computer skills. Strong organizational and record keeping skills. Highly motivated, creative, collaborative and detail-oriented. Effective verbal and written English communication skills Work effectively in a highly collaborative research and develop environment.

The Mogharebi Group is an investment advisory firm specializing in the multifamily property sector throughout the Western United States. We are seeking a full-time Junior Research Analyst. The hybrid role (1 day remote, 4 days in-office) is an integral part of The Mogharebi Group platform. This opportunity will put you at the forefront of critical market information, industry analytics, and transaction velocity reporting. You will be providing the data and the market knowledge that fuels one of the top multifamily brokerage firms in Southern California. Responsibilities Research ownership of multifamily commercial real estate properties and gather client information Research established as well as emerging commercial real estate markets, trends, and economic indicators Compile (and maintain as necessary) the client, property, and transaction information our internal database and advisor dashboard Synthesize market data (internal and external) into digital collateral that can be easily processed by investment advisors, real estate professionals, and colleagues Perform regular/semiregular quality control checks on the work produced by Interns or other Research personnel Qualifications 4-year college or university graduate Proficiency using the Microsoft Office suite (primarily Excel and Word) Previous experience using, or exposure to, commonly used real estate tools (primarily CoStar, Yardi Matrix, and LandVision)

Previous Pharmaceutical experience is mandatory for this role. MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and other Consulting services. MMR's Engineering expertise includes Process, Automation, Facilities engineering. Pharmaceutical expertise includes Oral Solid Dosage, Semi-Solids, Liquid-Dosage (TS and Aseptic), API manufacturing, Biotechnology (Vaccines, Blood Plasma Fractions, Monoclonal Antibodies). This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers and specialists involved in project management, commissioning and qualification, of equipment, systems and facilities. This role is for Pharma Lab Scientist to work with one of our clients in Los Angeles area, California. The ideal candidate will execute process development projects, process improvement, scale down, technology transfer, and support of manufacturing operations. Responsibilities: Performs experiments in small scale to assess process changes/improvements. Evaluates performance and suitability of new technologies and process changes by testing and reporting different critical parameters. Performs trials and experiments, participate into the design and scale-up of new technologies. Conducts routine bases analytical tests to evaluate and control product yield, purity and impurity profiles. Works closely with other Lab team members to support the upkeep, maintenance, and efficient utilization of the lab. Write SOPs, batch records, and develop research outlines for development projects. Utilize robust statistical analysis to draw appropriate conclusions from the data. Qualifications: Bachelor's degree in a scientific discipline with at least 2+ year's relevant experience. Knowledge of protein purification techniques. Experience in protein process development. Knowledge of analytical tools for analysis of proteins. Experience with DOE (design of experiments), six sigma, and lean manufacturing a plus. Knowledge of GMPs. Able to work in cold, wet environment. Must be able to work in controlled environments requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body. No make-up, jewelry, contact lenses, nail polish or artificial fingernails may be worn in the manufacturing environment. Good interpersonal skills, good verbal and written communication skills. Must be able to work multiple shifts, including weekends. Equal Employment Opportunity and Reasonable Accommodations MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.

Avery Products Corporation is looking for a R&D Lab Technician to join our Research & Development team. You will prepare test samples and materials, measure performance, and record and analyze data. This role is an essential part of the team to ensure accurate and timely testing and will focus on evaluating the physical properties of various products. Primary Responsibilities: Perform activities in support of various lab operations with minimal supervision. Must be familiar with analytical equipment and solvents. Primary activities involve focus on evaluating the physical properties of print quality of various products; including quality of construction and performance. Self-motivated team player who enjoys working with others. Problem solver with a "can do" attitude who can overcome obstacles in order to get the work done in an efficient and accurate manner. Must pay attention to detail, follow written and verbal procedures and protocols. Experience in preparing reports summarizing data, technical findings and making recommendations. Work in a cross-functional team environment with Product Development, Product Technology, Supply Chain, Quality and Marketing to deliver against set project deliverables and timelines. Work with print trade associations (e.g. IDC, PIA, and Photizo) to identify trends, upcoming product launches. Visiting tradeshows and Printer OEMs Quarterly Printer OEM Trends Report Mine Industry portals to get trends on latest print technologies that need to be tested. Minimum Qualifications: Minimum of 2 years' experience in a similar position. Undergraduate degree preferred. Good oral and written communication skills. Intermediate knowledge of Microsoft Office including Word, Excel and Outlook. A self-motivated, detail oriented individual who is comfortable providing feedback and observation of test results to team members. Ability to manage multiples activities and prioritize simultaneously. Works well in and enjoys team environment. About Us: Avery Products Corporation, is a wholly owned subsidiary of CCL Industries, is one of the world's leading manufacturers of self-adhesive labels, labeling software, binders, dividers and other products. Founded in 1935, Avery has built a solid reputation as the trusted brand and leading resource for organization and identification solutions. Combining dynamic capabilities in technology with groundbreaking ideas, Avery offers innovative products to make life easier-at work, home, school, and small business. Avery also offers free software, design templates and mobile apps. The consumer can now access the Avery experience anywhere, anytime and create customized projects that are uniquely their own. We Offer: Temporary to Hire position. After approximately 90 day evaluation period you will considered for permanent hire and eligible for Avery full benefit programs.

12 Month Contract (May extend or convert to permanent) $30/hour W2 Top 3 Must Have Skill Sets: BS or MS in Pharmaceutical Sciences, Material Sciences, Chemistry, Chemical Engineering, or other relevant field Strong drug development experience (hands-on involvement in drug discovery, formulation, or clinical development). Day to Day Responsibilities: The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to work group. In addition, this individual will ensure that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. The Pivotal Synthetic Drug Product group of the Drug Product Technologies (DPT) department at Thousand Oaks, CA is seeking for an enthusiastic, highly motivated, and team-oriented scientist for the position of Associate Scientist. In this role, the scientist will serve as member of Drug Product development teams, providing hands-on formulation and process expertise during the development of clinical and commercial formulations for solid oral dosage forms. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to work group. In addition, this individual will ensure that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.

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