Research Associate Jobs in Laguna Niguel, CA

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 *********************

The Center for Innovative Public Health Research is seeking a dynamic, experienced public health professional to fill the role of Research Associate on an adolescent centered, NIH-funded research study. About us: The Center for Innovative Public Health Research (CiPHR) has been quietly growing into one of the most innovative and progressive technology-focused organizations in the technology and public health space. We are a non-profit organization that primarily focuses on understanding how technology is affecting the health and well-being of youth, particularly LGBT+ youth, while also identifying ways we can harness the power of technology to promote healthy behaviors. We are looking for MPH-trained professionals who want to be part of something bigger. The office setting promotes healthy lifestyle choices: We have two walking desks that can be used by the team. Each researcher has a standing desk. We have an outdoor space with an ocean view for breaks and lunch time, and are a 15-minute walk to the beach. Benefits include generous health, dental and vision insurance coverage, and 403b matching. Research Associate Job Description This is an in-office position. The applicant must be local to Orange County and able to work in our San Clemente office Monday-Friday, 40 hours per week. Applicants who need to relocate for the position will not be considered. Some nights and weekends, based on study needs, will be necessary. The RA position provides a range of research/development activities, including the following: Leading a project, including ownership of milestones and deadlines Designing social media recruitment campaigns to engage young people in research Promoting participant retention through ongoing communication strategies Supporting and tracking IRB submissions to ensure ethical compliance Contributing to our organization's social media presence by creating professional posts Assisting with the finalization of research documents, including formatting the document for particular journal requirements, the insertion of references, etc. Proofreading research documents, including journal articles and grant proposals Other duties as assigned To perform the RA position successfully, an individual must be able to perform each duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required: Strong communication skills, both verbal and written; including the ability to speak clearly to different audiences (e.g., adolescents, parents) Ability to take ownership of tasks and take them from conception to completion, while communicating and coordinating with the larger research team Excellent prioritization skills Ability to complete tasks on time to meet articulated deadlines Demonstrate high productivity in a fast-paced work environment Ability to work independently and also cooperatively within a team Understand and adhere to standard concepts, practices, and procedures related to adolescent public health research and associated human subjects' research ethics. Strong attention to detail Excellent familiarity with Microsoft Word and Excel A certain degree of creativity and latitude Flexibility to work on nights and weekends as needed. Qualifications: Successful applicants will have a Master's degree in Public Health or a related field; or an undergraduate degree in Public Health or a related field and at least 2 years of post-graduate research experience. Experience working with LGBT+ populations is strongly desired. Applicants who are fluent in both Spanish and English are highly preferred. Applicants must currently live local to San Clemente and be able to commute to the office each work day. People who need to relocate or work remotely will not be considered. CiPHR is an equal opportunity employer. All applicants will be considered for employment without regard to age, race, ethnicity, religion, sex, sexual orientation, gender identity or expression, veteran or disability status. We are committed to fostering a supportive environment for our employees. Representation matters. Researchers who are part of the LGBT+ community are strongly encouraged to apply. Job Type: Full-time Compensation is dependent upon experience. Pay: $20.00 - $24.00 per hour COVID-19 considerations: CiPHR is a 100% vaccinated and boosted research team. Researchers are required to be fully vaccinated and boosted for COVID-19 unless they have a medical exemption. Please send both a cover letter & resume to ********************************* to apply to this position.

Responsibilities: Conduct antibody discovery campaigns from antigen design and library construction, through enrichment of candidate antibodies. Assist with recombinant protein production including antigen construct design, transient transfection, FPLC purification and initial QC and characterization. Use molecular biology techniques to assemble libraries and clone antigen and antibody expression constructs. Use experience with single domain, as well as conventional (sc Fv) formats to design and construct high-diversity synthetic antibody libraries as well as smaller, focused libraries used for optimization of therapeutic candidates. Assist with characterization assays to assess stability, specificity, solubility and other characteristics related to developability and manufacturability of lead molecules. Work closely with the Platform Development team to construct libraries suitable for screening on platform instruments. Contribute at the group level by using your experience in therapeutic antibody engineering to guide optimization and development of candidate molecules using thoughtful, well-researched technical approaches. Assist with the general operations of an antibody engineering lab including ordering, organization, stocking and maintenance of laboratory equipment. Required Techniques: Well versed in display technologies (phage, yeast and ribosome display) Library transformation into yeast and/or bacteria Flow cytometry and biosensor antibody binding assays (biacore, octet) Standard cloning techniques (PCR, ligation, Gibson assembly) General cell culture techniques for suspension cells (CHO and 293) including maintenance and transient transfection. Protein purification using FPLC or gravity column Preferred Techniques: FACS with yeast and mammalian cells NGS library prep NGS sequence analysis In vitro cell based assays for assessing biological activity of therapeutic antibodies. BLI (Octet) for measuring antibody binding kinetics and epitope binning. Ribosome display and/or IVTT Requirements: Bachelor's or master's degree in biology, chemical engineering or equivalent. At least 2 years antibody engineering experience. Ability and enthusiasm for working in a laboratory. Full-time, on-site in Carlsbad California.

R&D Technical Services Scientist Full Time Professional Carlsbad-HQ, Carlsbad, CA, US Salary Range: $100,000.00 To $125,000.00 Annually Since 1980, NAI has been a leader in nutritional health, bringing whole food-based supplements to a global population. NAI is a leading expert and manufacturer of dietary supplements. We are involved in every facet of the industry, including research, development, manufacturing and marketing and advocacy. As a company, we continue to grow with manufacturing locations in Vista and Carlsbad, CA. We are looking for seasoned and entry level candidates that are interested in working for a great company with opportunities to grow, competitive pay and benefits. Benefits Free medical (one plan) and other medical plan options Dental, vision, life insurance and other voluntary benefit options. $1,000 Employee Referral Bonus 3 weeks' vacation and 11 paid holidays 401K including company matching and profit sharing Opportunities for advancement Comprehensive training Tuition Reimbursement and more! Summary Responsible for the successful technical transfer of product formulas from pilot lab to commercial equipment and through to cGMP production scale. Collaborate with R&D Team and Operations Team on formula development, providing technical expertise on reformulation needs through the product development process to achieve successful scale up. Create and maintain technical transfer documentation and history. Evaluate and refine product formulas as needed after commercial production, while maintaining customer requirements. Well versed on dietary supplement tablet, capsule and powder delivery formats. Essential Duties & Responsibilities Formulation: Provide technical expertise and support to ensure successful transfer of customer formulas from concept to pilot lab and on to commercial equipment and cGMP production. Collaborate with R&D Formulation Team and Technical Operations team on optimization of existing formulas to improve production efficiencies. Be readily available to perform quick and timely adjustments to optimize production runs at all stages of the production process Design and conduct appropriate formulation experiments to facilitate and ensure successful technical transfer of customer products to commercial production equipment, collaborating with R&D Formulation team, R&D Pilot Lab team and Director of Technical Operations. Present relevant findings following technical transfer trials and formula adjustments to provide guidance to R&D Formulation and R&D Pilot Lab team as needed. Provide technical expertise in review of initial formula concepts going through quoting process for any concerns around processability on commercial equipment Collaborate with R&D Formulation Team on development of new product concepts that would be suitable for commercialization Create and maintain relevant history and documentation on product formula transfer from pilot lab to commercial equipment: Pilot lab trial reports Commercial equipment trial reports First commercial production reports Modifications to equipment settings, blend instructions, and formulas during product trials Present technical transfer trial data/findings to senior management, Business Development and Client Management teams as needed Create and/or act as additional R&D reviewer as needed to ensure accuracy and/or maintain accurate records of technical documents for product development projects, including but not limited to: Draft formulas Final formulas Product specifications Product justifications Master batch records Testing requests for finished products Testing requests for prototypes Document change requests for formulas Pilot batch records Assist R&D Formulation team in evaluation of out-of-specification results on finished products Act as an additional reviewer and signoff of formula formula-related documents for others on the R&D team Maintain awareness of and update training as needed Proper use of laboratory and manufacturing equipment Development of new techniques, testing, and other areas related to product development Provide technical and scientific input, support and assistance to other technical disciplines Follow efficient operations in assigned project areas in accordance with NAI requirements, SOP's and GMP's Take leading role for projects as assigned Works independently while understanding the necessity for effective communication and coordination of work efforts with cross-functional team and external partners Participates in project meetings Support other projects as needed within the formulation team Raw Materials: Collaborate with and assist R&D Formulation Team, R&D Technical Services Team, Purchasing and Quality with qualification and replacement of new and alternate raw materials and suppliers. Collaborate with the R&D Formulation Team to identify raw material needs for prototypes and pilots for R&D Technical Services and Purchasing teams. Collaborate on specification development with R&D Technical Services and Formulation teams. Provide on-going internal and external technical support to ensure that production needs are met and customer requests are satisfied Manage and troubleshoot raw materials related products by understanding the potential ramifications caused by raw material and specification changes, such that appropriate actions are taken Build strategic relationships and maintain effective communications with vendors Foster professional knowledge of market and supplier information Collaborate with R&D Formulation Team and Purchasing as needed to help support a consistent supply of our raw materials, as well as avoid market price fluctuations Other Duties Maintain awareness of current developments within the functional discipline Develop a network of outside contacts such as vendors, consultants, educators, and attend appropriate continuing education courses Collaborate with and support cross-functional NAI teams Present ideas and suggestions for product or process improvements, and improvements to pilot laboratory operations Perform other related duties as assigned Qualifications Requires a four year college or university degree or its equivalent in Pharmacy, Chemistry, Food Science, Chemical Engineering or other science-related field In-depth knowledge of formula development in hard shell capsules, tablets, powder fills and/or other dietary supplement dosage forms Successful track record of developing/commercializing new products in manufacturing environment Requires a minimum of five years direct industry formulation development experience, ideally with an additional three years of related experience Possess comprehensive knowledge and practical experience with product/process development, and a firm foundation in chemistry, mathematics, pharmaceutics and/or food science Proficient in oral and written communication skills as well as effective organizational skills and the ability to make presentations and recommendations in the area of responsibility Must be able to communicate effectively in a cross functional team environment and have the ability to statistically analyze data Must have computer literacy, including word processing and spreadsheet software Must have strong critical thinking, sound judgment, planning, organizing and problem-solving skills Ability to work as a team member and interact at all levels Supervisory Responsibilities No direct supervisor responsibilities, but may guide and assign the work of others, such as technical support scientists, as well as provide technical guidance and support to formulation scientists. Physical Demands Manufacturing and general office environment Exposure to disagreeable elements is negligible Frequent work in pilot plant and production facilities Training The incumbent must be able to perform this job safely in accordance with standard operating procedures and good manufacturing practices, without endangering the health or safety of self or others. Work Environment General office, pilot plant and manufacturing environment A portion of the work will take place in the encapsulation, powder and/or tableting areas of the manufacturing facility, where one will be exposed to computerized equipment, moving mechanical parts, forklifts, heavy pallets, moderate to loud noise level, and air-borne dust and powders While working in the manufacturing area, one will be required to wear various personal protective equipment (e.g., clothing, hair net, face mask, gloves, goggles, etc NAI is an Affirmative Action/Equal Opportunity Employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, physical or mental disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.

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.

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Initially 6 month contract with high possibility of extension Top Skills, experience or education required Biologist II: BS or equivalent education with typically 3 or more years of experience or MS or equivalent education with typically 1 or more years of experience. Biologist III: BS or equivalent education with typically 5 or more years of experience or MS or equivalent education with typically 3 or more years Proficient and hands-on experience in cell culture, aseptic techniques, including cell passaging, and cell banking under GDP and GMP compliant conditions Experience in performing routine quality checks on cell cultures, including, qPCR, cell-based bioassays, sterility, and mycoplasma detection Excellent documentation and record-keeping abilities Job Description We have an exciting opportunity for a Biologist II/III position based in Irvine, CA. The candidate's primary responsibilities will include but are not limited to the production, testing, inventory, and supply of Master, Working, and development cell banks for clinical, and commercial production as well as analytical and bioassay testing. The candidate should be experienced in standard cell culture, biochemistry, and molecular biology techniques Key Responsibilities Execute production, testing, and release of Master, Working, development, and analytical cell banks and ensure the timely supply of customers Perform cell culture and cryopreservation of cells using aseptic techniques under GDP and GMP compliant conditions Performing routine quality checks on cell cultures, including sterility testing, mycoplasma detection, genetic stability analysis, and functional bioassay. Identifying and resolving issues related to cell culture, such as contamination, cell detachment, or abnormal growth patterns. Interface with internal and external customers to ship cell banks and supply critical information as per their requirements. Accurately document, critically analyze/interpret data and communicate the results promptly through various electronic means Understand and adhere to corporate standards regarding code of conduct, safety, and appropriate handling of materials Author, review, and approve technical documents, SOPs, and batch records. Availability to work occasional weekends as needed Must be comfortable with physical activities of constant standing, walking, and sitting with arm stretching into biosafety cabinets for cell culture work Proficient with but limited to the following key technical skills: mammalian cell culture, familiarity with cell culture instrumentation (cell counters, microscopes, centrifuges, cryopreservation systems), cell-based bioassays, qPCR, sterility testing, and mycoplasma detection. Additional Information This position requires the individual to work in areas requiring select agents and toxins access (i.e. Biosafety level 2 laboratories). Access to and use of select agents is regulated by federal policies. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Our client is a growing Food Manufacturer seeking a R&D Culinary Specialist to join their team in Orange, CA! Pay rate: $65- $85k annually Work Schedule: M - F, 40 hrs., with occasional evenings or Saturdays if necessary Key Responsibilities: Work closely with R&D, Production, and Sales teams to create and launch new products, transitioning them from concept to commercialization Continuously improve the quality, processes, and cost-efficiency of existing products Partner with R&D and Sales to generate innovative product ideas and develop samples that meet customer requests. Present samples to customers as needed Evaluate existing formulas and provide suggestions to enhance quality and cost Research market trends, ingredients, and new technologies to develop new product formulas and write white papers based on specific requests from the Director and Sales team Thoroughly document recipe development results, cooking yields, and descriptive qualities Ensure compliance with food safety standards, including Hazard Analysis Critical Control Points (HACCP) and Good Manufacturing Practices (GMP) Collaborate with technical and commercial teams across procurement, sales, quality, technical services, marketing, and distribution Qualifications: B.S in Food Science or Culinary paired with 2+ years of professional experience in the industry Looking for someone who is a "culinary creative" Experience in creating & documenting new recipes or formulas Strong understanding of food safety regulations, including HACCP and GMP Knowledge of food production, manufacturing, restaurant operations, and distribution Strong interpersonal skills, with the ability to maintain effective working relationships across all levels of management, employees, customers, and vendors Proficiency in Microsoft Excel, Word, PowerPoint, and Outlook INDBH #LI-DNP

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)

100% onsite - Oceanside, CA Hours: Mon-Fri business hours Reason for opening: continued/extra workload (projects) Role: Senior Research Associate - Biologics Drug Product Development (BDPD). Duration: 12 months, could possibly extend additional time, however that won't be know until closer to the end of the initial 12 months (this role has no opportunity for FTE conversion into this role, at this location, due to multi-year site closure plans) BDPD is responsible to develop and characterize formulations and processes for all biologic drug products in pivotal (P3) and commercial stages; also responsible for short / long term stability assessments, technology transfers to clinical and commercial sites, manufacturing support, in-use and compatibility to support clinical studies. Seeking motivated, team-oriented individuals with scientific experience in laboratory work related to biologics. Essential Duties and Job Functions: • Perform experiments pertaining to: o Protein formulation/stability of various dosage forms (liquid/lyophilized) and configurations (vial/syringe), employing a variety of biochemical and biophysical analytical techniques, such as HPLC, capillary electrophoresis, and/or spectroscopy methods o Scale-down/-up of biologics drug product processes o In-use stability and administration • Author protocols, technical summary reports/memos and tech transfer documentation defining the manufacturing process and parameters • Review Master Batch Records for accuracy and trend process data supporting process development or fill/finish manufacturing operations • Execute studies in support of drug product technology transfers to clinical and commercial manufacturing sites • Be an effective communicator of ideas, project goals and results at departments/meetings in both written and presentation format. • Be self-motivated, organized, thrive in team settings and enjoy scientific investigation and thinking, as well as be familiar with the relevant technical literature. Knowledge, Experience and Skills: • Degree in Chemical/Biochemical Engineering (or a related engineering discipline) or Pharmaceutical Sciences, and relevant industry experience that demonstrates expertise in drug product development as well as sustained excellence in performance and accomplishments that align to company goals. • Excellent communication (both verbal and technical) and interpersonal skills are required. • Demonstrates technical proficiency, scientific creativity, collaboration with others and independent thought in suggesting experimental design and research strategy. Minimum Qualifications: • A minimum of 5+ years of experience with BS degree or 3+ years of experience with MS degree in Pharmaceutical Sciences, Biology, Biochemistry, Biochemical Engineering, or a related scientific discipline. • A basic understanding of formulation and drug product process development for biologics (antibodies, fusion proteins, bi-specifics, vaccines, antibody drug conjugates, etc.). • Previous experience interfacing with biologics drug product manufacturing sites and providing technical support during engineering runs/GMP operations is a plus. Must Have Requirements/Skills: • Experience working with Biologics molecules (proteins, mAbs); experience working with ADC is a plus • Protein formulation/stability of various dosage forms (liquid/lyophilized) employing a variety of biochemical and biophysical analytical techniques, such as HPLC, capillary electrophoresis, and/or spectroscopy methods, analytical data analysis • Experience with some scale-down/-up of biologics drug product process development activities; buffer preparations, testing using compendial methods (osmo, protein conc., pH, etc.) and UF/DF is a plus Nice to Have Requirements/Skills • Presentation and Documentations (ELNs, technical reports, MEMO, etc) • good understanding / experience in biologics drug product process (freeze-thaw, filtration, mixing, filling, lyophilization) • some understanding of in-use stability and drug administration process and associated challenges (IV bags, subcutaneous injections) MISC Information: Team Size - 11 full time employees; approx 20 total in pivotal Biologics DP function

BDPD is responsible to develop and characterize formulations and processes for all biologic drug products in pivotal (P3) and commercial stages; also responsible for short / long term stability assessments, technology transfers to clinical and commercial sites, manufacturing support, in-use and compatibility to support clinical studies. Seeking motivated, team-oriented individuals with scientific experience in laboratory work related to biologics. Essential Duties and Job Functions: • Perform experiments pertaining to: o Protein formulation/stability of various dosage forms (liquid/lyophilized) and configurations (vial/syringe), employing a variety of biochemical and biophysical analytical techniques, such as HPLC, capillary electrophoresis, and/or spectroscopy methods o Scale-down/-up of biologics drug product processes o In-use stability and administration • Author protocols, technical summary reports/memos and tech transfer documentation defining the manufacturing process and parameters • Review Master Batch Records for accuracy and trend process data supporting process development or fill/finish manufacturing operations • Execute studies in support of drug product technology transfers to clinical and commercial manufacturing sites • Be an effective communicator of ideas, project goals and results at departments/meetings in both written and presentation format. • Be self-motivated, organized, thrive in team settings and enjoy scientific investigation and thinking, as well as be familiar with the relevant technical literature. Knowledge, Experience and Skills: • Degree in Chemical/Biochemical Engineering (or a related engineering discipline) or Pharmaceutical Sciences, and relevant industry experience that demonstrates expertise in drug product development as well as sustained excellence in performance and accomplishments that align to company goals. • Excellent communication (both verbal and technical) and interpersonal skills are required. • Demonstrates technical proficiency, scientific creativity, collaboration with others and independent thought in suggesting experimental design and research strategy. Minimum Qualifications: • A minimum of 5+ years of experience with BS degree or 3+ years of experience with MS degree in Pharmaceutical Sciences, Biology, Biochemistry, Biochemical Engineering or a related scientific discipline. • A basic understanding of formulation and drug product process development for biologics (antibodies, fusion proteins, bi-specifics, vaccines, antibody drug conjugates, etc.). • Previous experience interfacing with biologics drug product manufacturing sites and providing technical support during engineering runs/GMP operations is a plus. Must Have Requirements/Skills: • Experience working with Biologics molecules (proteins, mAbs); experience working with ADC is a plus • Protein formulation/stability of various dosage forms (liquid/lyophilized) employing a variety of biochemical and biophysical analytical techniques, such as HPLC, capillary electrophoresis, and/or spectroscopy methods, analytical data analysis • Experience with some scale-down/-up of biologics drug product process development activities; buffer preparations, testing using compendial methods (osmo, protein conc., pH, etc.) and UF/DF is a plus Nice to Have Requirements/Skills • Presentation and Documentations (ELNs, technical reports, MEMO, etc) • good understanding / experience in biologics drug product process (freeze-thaw, filtration, mixing, filling, lyophilization) • some understanding of in-use stability and drug administration process and associated challenges (IV bags, subcutaneous injections)

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.

Under general supervision, the candidate should work effectively in a team environment and have demonstrated high productivity and reproducible technical skills, including mouse physiological assessments, mouse surgery, cell culture techniques, Western Blotting, DNA / RNA extraction and PCR , gene transfection, protein purification, and Immunofluorescence/Immunohistochemistry. This person is also expected to be detail-oriented and self-motivated, and knowledge of computers is essential for high volume research and maintenance of the data records. The candidate will be expected to present data in the weekly laboratory seminars after independent analysis and write the methodology and results for the manuscript and grant preparation. This person also provides trainings to undergraduate students and oversees their research on the day-to-day basis. Responsibilities Conduct research experiments independently and in consultation with supervisor. Perform mouse handling, tattooing, tail sampling, and genotyping. Should be willing to work long hours for completion of long and time-consuming experiments. Determine mouse body temperature (rectal thermometry). Perform mouse blood collection, mouse behavior analysis, mouse organ dissection, thyroidectomy and mouse brain sectioning. Prepare technical reports, papers, graphs and/or records and provides interpretations. Perform PCR , Western blot, ELISA , immunostaining, immunohistochemistry, and other techniques of molecular biology as needed. Maintain mammalian cell lines, perform transfections, and collect samples. Maintain mamalian cell lines, perform transfections, and collect samples. Perform bacterial transformation and plasmid purification. Histology sample preparation, confocal microscopy, data analysis, and presentation. · Collaborate with other faculty with similar research interests on this topic. Maintains and updates record of all experimental studies. Stores all biochemical data in digital format on computers and backs up regularly. Consult and assist Principal Investigator Work alongside Principal Investigator to determine method, details, and means of performing the experiments. Furnish regular updates to Principal Investigator. Laboratory Ensure the facility is well equipped with all necessary tools to conduct research Place request orders for equipment and lab supplies Use equipment and laboratory space accordingly to work contract Contribute to the development of research documentation for publication and/or presentation. Perform other duties as assigned. Required Qualifications Ph.D in the field of Biomedical Sciences, Molecular Biology, Biochemistry, Cell Biology or Pharmacy with molecular biology emphasis or its equivalent in research skill and subject matter knowledge. Must be available to work extended hours to be able to complete time consuming experiments. Proven experience working with rodents, and genotyping rodents Proven practical experience with techniques of molecular biology. Working experience with cell lines and/or primary culture Proficient in research methods, testing and data collection, analysis, evaluation, report writing, independent discretion and judgment. Knowledge of research and experimental methods as issued by Institutional Research Boards. Good organizational skills and ability to prioritize and handle multiple complex tasks independently. Ability to operate laboratory equipment and maintain a safe working environment. Ability to conduct research in a timely manner and document all data. Strong writing skills and computational knowledge. Ability to establish and maintain cooperative working relationships with co-workers, investigators and other research staff. Ability to work alone and/or with student (or laboratory) assistants.

**Research Associate - Analytical Biochemistry/Physiology** *****Kindly be advised that we are handling the recruitment for this position internally and are not partnering with external recruiters.***** ****We are a Biology Company**** Plantible, backed by Astanor Ventures, Lerer Hippeau, Piva Capital, Kellogg's, and Vectr Ventures, is a vertically integrated biology company that is unlocking the power in plants in service of people & planet. Our mission is to create solutions that empower customers to make sustainable and regenerative choices without compromising on quality. We are beginning with the food industry. Please visit our website to learn more about our mission and continued success: ******************************* ****How you will contribute:**** We are seeking a passionate and mission-driven Research Associate (RA) in Analytical Biochemistry/Physiology with hands-on experience using basic lab techniques, data analytical skills and a problem-identifying/solving attitude. The individual will be responsible for ensuring biomass quality using biochemical assays and will design & execute experiments to improve our understanding of duckweed composition & changes in protein & carbohydrate content across different strains & environments. Through a focus on rapid experimentation, rigorous data analysis, and through working collaboratively with our team of RA's, Scientists, and Operators, the individual will have the opportunity to make an immediate and sustainable impact on the development of the company. ****What you will be working on:**** * Perform biochemical assays to ensure biomass quality using a host of QC assays including extraction of our flagship Rubi protein product using high throughput methods at small scale. * Operate, maintain and troubleshoot lab equipment focused on defining the carbohydrate & protein composition of biomass along with measurement of other small molecules of interest present in our culture media & in-process sample streams. * Design, execute, and analyze lab and field experiments to improve the quality and quantity of our plant protein and to increase biomass productivity. ****What you bring to Plantible:**** * B.S. in Biochemistry, Chemistry, or Plant Biology with 2+ years of industrial research experience or M.S. in assay development with 1+ year industrial experience. * Previous lab experience developing and executing methods of biochemical, analytical and/or physiological relevance with a passion for continuous improvement & an attention to detail in experimental execution. * Lab experience growing plants and/or using sterile technique as well as experience in protein purification or extraction is also highly desirable. * Excellent verbal/written communication, time management and organizational skills * Ability to thrive in a fast paced & dynamic startup environment as a self-starter * Ability to learn quickly, solve complex problems and have excellent data analysis skills including the recognition of proper controls & statistical analysis. * Creativity & a collaborative partner in teams focused on achieving company goals. * Willingness to travel up to 10-15% of the time to facilitate tech transfer with our commercial protein production facility. ****Choose Plantible Foods**** Joining Plantible means contributing to a sustainable future for all. We are a venture backed startup that is both spreading happiness amongst our employees and to current and future generations. We believe diversity creates uniqueness. Our team is composed of highly talented people with different interests and hobbies, which makes for a rich working environment. ****At Plantible we are continually working on our offerings to foster the best team. Check it out!**** * Competitive health and wellness benefits * Medical, Dental and Vision Insurance * Discretionary Unlimited PTO Program * Paid Holidays * 401k Program * Career Stipend * Career development and growth opportunities * Working in a rapidly growing, flexible and entrepreneurial environment * Team building and company-wide events * Financial support with your relocation, if necessary, ensuring a smooth transition * And of course, lots of beautiful land for outdoor activities! **Plantible Foods is an equal employment opportunity employer. Candidates are considered for employment without regard to race, creed, color, national origin, age, sex, religion, ancestry, veteran status, marital status, gender identity, sexual orientation, national origin, liability for military service, or any other characteristic protected by applicable federal, state, or local law. If you are interested in learning the status of your application, please note you will be contacted directly by the appropriate human resources contact person if you are selected for further consideration. Plantible Foods reserves the right to defer or close a vacancy at any time.** ****If you feel your skill set does not meet all listed qualifications for the role, we still encourage you to apply. As we continue to grow our company, we are seeking a range of candidates and would gladly consider you for other current or upcoming roles that may be a fit!**** The pay range for this role is: 65,000 - 82,000 USD per year (San Diego) Research San Marcos, CA Share on:

Company DescriptionJobs for Humanity is partnering with CEDARS-SINAI to build an inclusive and just employment ecosystem. Therefore, we prioritize individuals coming from the following communities: Refugee, Neurodivergent, Single Parent, Blind or Low Vision, Deaf or Hard of Hearing, Black, Hispanic, Asian, Military Veterans, the Elderly, the LGBTQ, and Justice Impacted individuals. This position is open to candidates who reside in and have the legal right to work in the country where the job is located. Company Name: CEDARS-SINAI Job Description Working under direct supervision, as a Research Associate II, you will perform routine and increasingly complex laboratory tasks and procedures and develops technical expertise in one or more areas relevant to research projects. You will participate in research activities involving all aspects of the research process, to include, but not limited to; investigation, technical, testing/validation of results, and report findings. Will perform a variety of routine experimental protocols and procedures to support the objectives of laboratory research projects. You will observe and comply with safety standards and procedures, assist in preparation of data for publication and/or presentation at scholarly meetings, and assist in general laboratory maintenance. This position does not have supervisory responsibilities. Essential Job Duties and Responsibilities: Performs a variety of increasingly complex experimental protocols and procedures and assist in the design of new complex or unusual protocols and techniques. Keeps accurate and detailed records of experiments and results, and assist in identifying and troubleshooting of unexpected results. Orders laboratory supplies and supports laboratory operations. Maintains lab equipment and related records and may coordinate use of lab equipment. Assists in the operation of specialized equipment, as required by the area of research. Assists in preparation of data for publication and/or presentation at scholarly meetings. Observes and complies with safety standards and procedures. Orients research laboratory assistants or lower level research associates and undergraduate student researchers on day-to-day lab operations and routine procedures. Department-Specific Responsibilities: Associate Investigates molecular mechanisms of lung fibrosis, and participates in research projects including the role of innate immune, stem cells, extracellular matrix, resident mesenchymal cells, and fibroblast lineages in lung injury and repair. Experimental approaches employed in our lab include molecular biology, genetically modified mice, lineage tracing, lung injury models, prospective isolation and organoid culture of lung stem cells, single cell RNA-sequence, immunology, and genomics studies. Under minimal supervision, s/he is expected to maintain and carry out mouse husbandry, perform in vivo experiments including mouse lung injury models and sample collections, and in vitro experiments including molecular sub-cloning, cell culture, flow cytometry, mRNA analysis, protein analysis and biochemical studies. Trains other lab technician on related lab procedures. Other lab duties include: ordering lab supplies, record keeping, lab maintenance, and other duties as assigned. #Jobs Education: Bachelor's Degree in a Science related field is required. Experience: One (1) year of laboratory experience. Understanding of general research objectives. Familiar with routine laboratory procedures, experimental protocols, and overall lab organization. Applicant must be highly motivated and able to work independently. Must have superior interpersonal, communication and organization skills and the ability to work across company disciplines and functional units, and computer application experience. Must possess computer skills to include, but not limited to, Excel and Word. Ability to simultaneously manage multiple clerical trials, and attention to details. Working Title: Research Associate II - Pulmonary - Jiang Lab Department: Home Dept - Pulmonary Business Entity: Cedars-Sinai Medical Center Job Category: Academic/Research Job Specialty: Research Studies/Clinical Trials Position Type: Full-time Shift Length: 8 hour shift Shift Type: Day Base Pay:$21.26 - $36.14

- Job Description **Research Associate - III** Contract: Oceanside, California, US Salary: $48.00 Per Hour Job Status: Expired **This Job is no longer accepting applications** **Pay range: $44 to $48/hr. (Negotiable) Education & Experience Requirements:** * BS or MS degree in a relevant scientific discipline (no PhD candidates) * Minimum 3 years experience **Essential Duties:** * Perform cell-based and flow Cytometry analysis to support late-stage biologics projects. * Plans and executes assigned experiments that support assay development activities and project goals. * Proactively seeks out senior personnel to discuss potential solutions to problems. Participates in group meetings to share test results. * Demonstrates ability to recognize anomalous and inconsistent results and interpret experimental outcomes. * Develops skills in data analysis and the ability to evaluate the quality of data. * Operates scientific equipment, selects appropriate methods and techniques to perform experiments, and prepares related reports. * Plan and organize details of experiments with guidance. * Basic understanding of cell-based methods. * Experience with cell-based assays and flow Cytometry analysis and perform routine maintenance of these instruments. * Develop flow Cytometry, flow imaging assays, and explore new technologies and methodology for viral vector characterization, and help develop a robust process for vector production. * Responsible for data analysis using Softmax Pro software and graphic display of data using Excel and PowerPoint presentation formats. * Demonstrate good verbal communication skills and interpersonal skills to provide insight into the processes used to achieve the results of assigned tasks. * Be able to work in a fast-paced and highly collaborative working environment. **Must have requirements/skills:** * Experience with performing cell culture * Experience working with biologics (proteins, fusion proteins, mAbs) * Experience with analytical methods such as ELISA, cell binding assay, or reporter assay **Nice to Have Requirements/skills:** * Experience working with antibody-drug conjugate (ADC) * Experience working with virus generation or virus neutralization assay * Good presentation and documentation (electronic notebook-ELN, testing methods, etc.). **Privacy Overview** CookieDurationDescription

** |** **Posting Details** About WesternU As you take your first step onto a Western University of Health Sciences campus, each path, each person, each structure comes with a transformative story. WesternU is more than the practice of medicine. We are defined by character and culture. At WesternU, you will discover humanism at the heart of every interaction: a warm welcome, a sincere smile, a positive word, a kind deed, a thoughtful gesture. You will see students work together on case studies; a parade of pets in campus parks; student clubs offering opportunities for career growth and community involvement; and faculty, staff and students designing their future and the future of WesternU. We display a collaborative mindset in how we operate, educate, and serve others. Although, geographically, we are two campuses - as humanists, we are one: to enhance and extend the quality of life in our communities and achieve excellence in everything we do. We attract diverse, professional faculty, staff and students that thrive in an environment of humanistic health care education. Join our team of faculty and staff and make a difference. Posting Details Position Title Research Associate Position Control Number S04172 Type of Position Staff Position Status Full-time Campus Western University Campus-Pomona, CA Position Location California Department 1504-Biotechnology & Pharmaceutical Sci Job Summary Developing and applying molecular simulation and machine-learning approaches to facilitate biomedical research and drug discovery. Knowledge, Skills and Abilities Desirable skills include a good understanding of molecular structures and force field methods, molecular dynamics simulations, basic programming skills, solid doctoral publication record, good verbal and written communication skills, and an ability to work effectively in a teamwork environment with collaborators from different disciplines. Prior experience with machine learning or Python programming is required. Required Qualifications Applicants should have a Ph.D. in Computational Chemistry, Biochemistry, Biophysics, Computer Science, and related fields. Preferred Qualifications Essential Job Duties Key Responsibilities Develop and conduct multiscale molecular dynamics simulation, enhanced sampling, AI-guided virtual screening, free energy calculations. Key Responsibilities Conduct data curation and data analysis. Key Responsibilities Prepare manuscripts and conference presentations under the supervisor of Dr. Lyna Luo. Posting Details Continued Work Schedule Non-Exempt position Working at WesternU We believe in making an impact in the lives of our employees, personally, and professionally. Every employee has different individual and/or family needs. We offer benefits that are both comprehensive and flexible to address your unique needs. We believe work-life harmony is positive and achievable. We offer competitive salaries, generous paid time off, insurance plans, reimbursements, and retirement benefits. Additionally, • Our faculty, staff, and administrators are 100% focused on student success. • Our University culture creates the context for a nurturing and supportive environment. • Faculty, staff, and students can expect to make deep, personal relationships within the University community. • As a Faculty, Staff, or Student at WesternU, you can focus on work that you love, be your authentic self, and lead to the future with innovation in health sciences. • WesternU's core value of humanism encourages all to bring their whole self in all that they do. • We are committed to fostering a culture of respect, equity, collaboration, and fun at all levels for all people! Expected Pay Scale Minimum $27.35 Maximum $27.35 **Physical Demands** Physical Demands Yes If yes, list maximum weight and duration The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be available to enable individuals with disabilities to perform essential functions. While performing the duties of this job, the employee is frequently required to use hands to operate a PC in the performance of job duties and talk or hear. The employee is regularly required to sit, and reach with hands and arms, and occasionally required to stand, walk, stoop, and smell. The employee must occasionally lift and/or move up to 25-30 pounds. Specific vision abilities required by this job include close, distance, and peripheral vision, depth perception, and the ability to focus. Describe Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be available to enable individuals with disabilities to perform essential functions. Duties are routinely performed in a typical laboratory setting. While performing duties in this setting the employee may be exposed to fumes or airborne particles, toxic or caustic chemicals, extreme cold (non-weather), and risk of electric shock. The employee is regularly exposed to wet humid conditions (non-weather), moving mechanical parts, and highly precarious places. The employee is occasionally exposed to outdoor weather conditions, extreme heat (non-weather), and risk of radiation. The noise level in this setting may be loud due to the noise of the ventilation system and hydraulic body hoist. Posting Information Posting Number S01542 Posting Date 11/16/2024 Close Date Open Until Filled No Conditions of Employment - Background Check To secure employment, successful fulfillment of a background check, including a criminal records check, may be required. Western University of Health Sciences will extend a conditional offer of employment, subject to rescission if the background check unveils disqualifying information or if it is found that the candidate deliberately withheld or misrepresented information. Non-completion of the background check to satisfaction may impact the ongoing employment of a current Western University of Health Sciences employee who received a conditional offer for the position. Pay Transparency Act Pay Transparency Act- Western University of Health Sciences is required to provide a reasonable estimate of the compensation range for this role. This range considers various factors in making compensation decisions, including but not limited to experience, skills, knowledge, abilities, education, licensure and certifications, and other business and organizational needs. It is not typical for an individual to be offered a salary at or near the top of the range for a position. Salary offers are determined based on final candidate qualifications and experience. The Expected Pay Scale is defined as the budgeted salary or hourly range that the University reasonably expects to pay for this position. Placement within the Expected Pay Scale is determined by internal equity and relevant qualifications. Equal Opportunity Statement (EEO) It is the policy of Western University to provide equal employment opportunity to all employees and applicants for employment as required by law without regard to age, race, color, national origin ancestry, citizenship, ethnicity, creed, religion or religious creed, sex or gender (including gender identity), marital status, sexual orientation, disability (both physical and mental) including HIV and AIDS, medical condition (cancer and genetic characteristics), pregnancy (which includes childbirth, breastfeeding and medical conditions related to pregnancy, childbirth or breastfeeding), age, genetic information, military and veteran status, or any other applicable protected characteristic as outlined by federal, state, or local laws.This policy

Hi, My name is Gaurav and I am a recruiter with Net2Source Inc. Our direct client is looking to hire a Research Associate - II* in their growing team. Please find below the job description. Job Title: Research Associate - Protein Purification Location: Oceanside, CA 92056 Duration: 12 months (Possible Extension) Payrate: $35/hr - 42/hr on W2 Role: Sr Research Associate with experience in protein purification process development and process characterization to support client's biologics development group (early and late stage development of our protein molecules). Focus: Downstream Process Development. Top 3 Must Have: Skills in data analysis and interpreting experiment outcomes including the ability to evaluate data quality and recognize anomalous results Demonstrate strong verbal communication and interpersonal skills including the ability to explain processes used to achieve results of assigned tasks. Working understanding of downstream process development including centrifugation, normal and tangential flow filtration, chromatography operations, and virus clearance. The ability to demonstrate hands on experience in several of these areas is expected. Ideal Requirements (in addition to Must Have's): Experience in biologics purification, with an emphasis on conjugation, tangential flow filtration (UF/DF), and filtration. Knowledge of cGMPs, technology transfer, and scaling up bioprocesses Experience with multiple modalities - specifically mAbs and antibody drug conjugates Essential Duties and Job Functions: Plan and execute assigned experiments on-site that support Process Development activities and project goals. Select appropriate methods and techniques for performing experiments. Recommend alternatives, research new methods and techniques and proactively seek out senior personnel to discuss potential solutions to problems. Participate in group meetings and present results, data interpretation and conclusions. Work with team oriented, collaborative and problem-solving mindset. Always work with safety in mind. Able to work with highly potent compounds upon training. Knowledge, Experience and Skills: Experience in analytical operations: SEC/HPLC, CE (R/NR), HCP testing is beneficial, but not required. Must be able to work effectively in cross-functional teams. Must demonstrate excellent technical writing skills. Experience with multiple modalities (mAbs, bispecifics, fusion and antibody drug conjugates, virus particles) produced in microbial and mammalian expression systems is a plus. Ability to work effectively within the purification team to help design and execute experiments supporting process definition, optimization, and characterization with an increasing level of independence. Ability to collaborate with Technical Operations during technology transfer from process development to GMP manufacturing, including serving as a process development representative during purification operations, providing technical troubleshooting and identifying opportunities for future process and equipment improvements. The candidate will also contribute to the preparation of regulatory filings and process validation and characterization reports. Ability to effectively communicate ideas, project goals and results and should have the ability to proactively identify issues and suggest solutions in a collaborative, multidisciplinary environment. This is a highly collaborative environment where willingness and ability to communicate and work effectively with individuals across various teams is essential. Self-motivated, organized, and enjoy scientific investigation and thinking. The candidate will monitor and contribute to external literature and scientific conferences. Education/Qualifications - preferred degree in Chemical/Biochemical Engineering, Biochemistry, Chemistry or a related scientific discipline. BS degree in a relevant scientific discipline and 2+ years of relevant experience; OR MS degree in a relevant scientific discipline and 1-2+ years of relevant experience Thanks Gaurav Gupta Sr. Pharma Recruiter *************************** **************

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