Senior Scientist jobs at Planet Pharma

Pay Rate Range: $50.00/hr. - $55.24/hr. Target Pay Rate: $55.24/hr. Duration: 3 Months Onsite Shift (if applicable): M-F 8:00 AM - 5:00 PM JOB DESCRIPTION SUMMARY/JOB PURPOSE: The Scientist II will be joining the Biotherapeutics Translational Pharmacology team to support our research programs. This position is primarily responsible for developing, optimizing and reporting out data for Bioanalytical assays for Antibody Drug Conjugates (ADC) to include ELISA, LC-MS and hybrid LC-MS techniques. This job will require the candidate to have excellent organization, communication, and teamwork skills, as well as flexibility and versatility, to meet tight deadlines in a dynamic, fast-moving environment. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Responsible for running analytical samples from nonclinical PK studies using ELISA, LC-MS and hybrid LC-MS techniques * Operation and troubleshooting of automated instrumentation * Collaborates with Biotherapeutics team members to support project advancement. * Maintains electronic laboratory notebook in a complete, consistent, and timely manner in accordance with company intellectual property policies and practices. * Prepares and organizes data for presentation. May present data and status reports at individual, group, and departmental research meetings under general supervision. * Adherence to excellent health and safety practices and compliance with applicable EH&S safety rules and participates in mandatory safety training programs. * Other responsibilities as assigned SUPERVISORY RESPONSIBILITIES: * No supervisory responsibilities EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education: * Bachelor's degree in related discipline and a minimum of four years of related experience; or * Master's degree in related discipline and a minimum of two years of related experience; or, * Equivalent combination of education and experience. Experience: * Drug discovery experience is necessary with hands-on bioanalytical assay development with an excellent understanding of fundamental processes. * Experience with ELISA, LC-MS and Hybrid LC-MS is required * Experience using WinNonlin and PRISM applications are preferred. Knowledge/Skills: * Highly self-motivated with exceptional attention to detail is required. * Thorough knowledge of activities related to bioanalytical assay development and data generation * Excellent verbal and written communication skills with the ability to follow written instructions and SOPs. * Ability to multi-task and excellent time management skills. * Excellent work ethic, working effectively in both a team environment and independently. * Thorough proficiency in MS Word, MS PowerPoint and MS Excel is required. WORKING CONDITIONS: * Primarily working in laboratory and office environment. * Potential handling of hazardous materials, and brief periods of working in both 4°C and -20°C environments. * May be required to work weekends as needed. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

In Thousand Oaks, the Automated Screening Platforms/ High-Throughput Assays group in the Lead Discovery & Targeted Protein Degradation organization is seeking a temporary contract worker for a laboratory based on-site role to provide assay reagent preparation for screening assay delivery. The desired team member will primarily contribute to a high demand for routine cell culture (expansion, banking and quality-control) of various mammalian cell lines. Responsibilities will also include collaborating with robotic platform operators to execute high-throughput cell-based & biochemical assays, in support of small molecule therapeutic discovery research pipeline & platform projects. Additional tasks include general laboratory maintenance activities such as preparing media & buffers, ordering/ stocking reagents & consumables. Training will be provided to use assay information management software applications (electronic lab notebook) and as needed utilization of laboratory instrumentation to deliver on job responsibilities. Daily activity will vary day-to-day but in scope activities include: 1. Perform routine maintenance of mammalian cell lines (expansion, aliquoting, cryobanking) 2. Routine preparation of assay reagents to support screening on automated screening platforms 3. Order, prepare, and maintain laboratory reagents & consumables to perform assays 4. As needed, offline assay validation experiments in 384- and 1536-well plate format An ideal candidate will have experience with mammalian cell culture techniques. Additionally, candidates should be detail-orientated, highly motivated, team player and a quick learner with a strong background in life sciences, molecular & cellular biology, and/or biochemistry. Experience in a laboratory setting developing and performing microtiter plate based biochemical & cell-based assays, including familiarity with luminescence-based, TRF, ALPHA, &/or high-content imaging assays is preferred. Experience with software programming skills (Python), or using AI agents (Copilot, ChatGPT) are beneficial but not required. MS or Bachelor in biological sciences.

Sansum Diabetes Research Institute has an opportunity for a full-time, board certified, or board-eligible Endocrinologist to serve as a Clinical Research Physician Investigator. SDRI is a non-profit organization and center of excellence with a mission to improve the lives of people impacted by diabetes through research, education, and clinical care. We are a preferred site for industry sponsored clinical trials, a testament to our exceptional research capabilities. On average, SDRI conducts 25+ trials per year, engaging approximately 1,000 participants. Current industry partners include Abbott, Dexcom, Insulet, Eli Lilly, Mannkind, Medtronic Diabetes, Novo Nordisk, Sanofi, Tandem Diabetes Care, and more. We are experts with experience across all study phases, and a broad portfolio of trials and clinical work focused on diabetes and metabolic health. Diversity and inclusivity are prioritized in in our clinical trials---in 2023, 30% of our research participants were from underrepresented populations. We are currently renovating our 18,000 square foot research facility to create a state-of-the-art center where we will accelerate life-changing diabetes research. Position Details: Responsible for 12+ Industry Sponsored Trials Per Year Design, Fund, and Execute Investigator Initiated Trials Develop Strategies and Partnerships to Drive Innovation Across the Enterprise Opportunity to Maintain a Clinical Practice through our Clinics Standard Office Hours Salaried Position: $250,000 - $350,000 Annually NOTE: The listed range is solely a base compensation for experienced full-time physician researchers. It does not include incentives and benefits. The base compensation rate may be adjusted based on training, community need and other possible determining factors. We Offer: Medical/Dental/Vision CME Stipend Malpractice Insurance Disability Retirement 403 (b) Annual Leave and Sick Time Licensure/DEA/Board Exam Fees PSLF Eligibility Requirements: MD or DO with Directly Related Experience in Endocrinology Board Certified or Board Eligible in Endocrinology DEA Certificate Eligible to Work in the United States, Must be in or Relocate to Santa Barbara, CA CA Licensure or the Ability to Obtain CA Licensure Interest in Research, Experience with Research preferred Exceptional Communication and Interpersonal Skills About Santa Barbara: Santa Barbara is known as The American Riviera thanks to its Spanish Colonial Revival architecture, rich heritage, world-renowned food and wine scene, stunning natural beauty and near-perfect weather. We invite you to learn more and to consider joining us at SDRI where you will join an experienced cross-functional team focused on developing and executing trials targeting innovation and excellence crossing drugs, devices, and technology that will impact the health span and life span of people living with diabetes.

The Jackson Laboratory in Sacramento, CA has an excellent opportunity for a Scientist to join the Preclinical team! The Scientist may be responsible for designing, executing, and overseeing scientific research projects, applying advanced methodologies and techniques to explore and expand knowledge within a specific discipline. They lead experiments, analyze data, and interpret results while collaborating with interdisciplinary teams to achieve research goals. Key Responsibilities * May Design, plan, and execute experiments, applying advanced scientific principles and methodologies within the field. * Analyze and may interpret experimental data using statistical tools and software, drawing meaningful conclusions and identifying trends. * May prepare research findings for publication in scientific journals, present at conferences, and communicate discoveries to peers and stakeholders. * Lead research initiatives, setting objectives, timelines, and strategies to achieve project goals. * Collaborate with cross-functional teams, providing guidance and mentorship to junior researchers, fostering a collaborative research environment. * Contribute to grant proposals, securing funding for research projects, and managing budgets effectively. Minimum Qualifications * Master's Degree in oncology, immunology, animal pharmacology, or a relevant field required. Ph.D. preferred. * Four or more years of relevant experience in a contract research laboratory, pharmaceutical industry, 6 years preferred * May have a proven track record of conducting high-quality scientific research, evidenced by publications in reputable journals and successful project leadership. * Proficiency in specific methodologies, tools, and instrumentation pertinent to the research area. * Strong leadership, project management, and mentorship abilities to guide and inspire a team of researchers. * Excellent written and verbal communication skills for presenting findings, collaborating with peers, and writing grant proposals. * May have ability to innovate, propose novel approaches, and solve complex scientific problems. * Flexibility to adapt to changing research needs and technologies. * Strong networking skills to establish collaborations and partnerships within the scientific community. * Ability to develop long-term research strategies aligned with organizational goals. The salary range is $99,284-$129,069. Salary will be determined based on qualifications and experience. #CA-AM11 About JAX: The Jackson Laboratory is an independent, nonprofit biomedical research institution with a National Cancer Institute-designated Cancer Center and nearly 3,000 employees in locations across the United States (Maine, Connecticut, California), Japan and China. Its mission is to discover precise genomic solutions for disease and empower the global biomedical community in the shared quest to improve human health. Founded in 1929, JAX applies over nine decades of expertise in genetics to increase understanding of human disease, advancing treatments and cures for cancer, neurological and immune disorders, diabetes, aging and heart disease. It models and interprets genomic complexity, integrates basic research with clinical application, educates current and future scientists, and provides critical data, tools and services to the global biomedical community. For more information, please visit ************ EEO Statement: The Jackson Laboratory provides equal employment opportunities to all employees and applicants for employment in all job classifications without regard to race, color, religion, age, mental disability, physical disability, medical condition, gender, sexual orientation, genetic information, ancestry, marital status, national origin, veteran status, and other classifications protected by applicable state and local non-discrimination laws.

**Key Responsibilities Include:** - Operate and maintain analytical and **preparative scale HPLC** instrumentation. - Support and troubleshoot walk-up analytical **LC-MS instrumentation** . - Purification of samples from **medicinal chemistry** projects on a milligram to gram scale by preparative HPLC. - Maintain and **troubleshoot NMR spectrometer** under the guidance of senior scientists. - Maintain a high level of productivity in the laboratory setting. - Demonstrate a high degree of responsibility in maintaining scientific standards and safe laboratory practices. - Keep accurate and current records of research and/or project related activities according to company policies. **Qualifications:** - Hands-on experience with **analytical HPLC, preparative HPLC** , mass spectrometry, and/or NMR. - Ability to operate and troubleshoot a variety of hardware/software platforms. - Proven effective written and verbal communication skills and ability to interact with scientists and engineers. - Knowledge of **synthetic organic chemistry** and the ability to communicate effectively with medicinal chemistry team. - Basic understanding of different organic functional groups and organic terminology including enantiomers and diastereomers. - Years of experience/education and/or certifications required: BS, or MS in Organic Chemistry ideal, Analytical Chemistry or closely related field would be ok , with typically 2+ (BS) or 0+ (MS) years of job-related experience **Top 3-5 skills requirements** 1: HPLC, and MS. 2: Analytical LC-MS instrumentation and analytical HPLC instrumentation. **Nice to have** Supercritical fluid chromatography (SFC) 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, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Biology Scientist - Must Have Flow cytometry Exp) Duration : 12 Months Total Hours/week : 40.00 1st Shift Client: Medical Device Company Job Category: Healthcare Level Of Experience: Mid-Level Employment Type: Contract on W2 (Need US Citizens or GC Holders Only) Work hours: 8 hours, ideally between 8:30-5:30pm 3 Must haves on the resume: Flow cytometry experience, min. 1-2+ years of hand-on research experience Job Description: Client, the leading provider of antibody reagents to the research immunology community, is seeking an outstanding Scientist II to join our highly motivated Research Development team. The Scientist II is responsible for the development and evaluation of new reagents and testing new antibodies for use in flow cytometry applications. The Associate is responsible for routine, accurate and timely testing of experimental samples according to standard protocols and operating procedures. The ability to execute scientific experiments of moderate scope is key. The successful candidate is expected to set up and execute these experiments, be detail oriented, skilled at data analysis and trouble shooting and will be accountable for preparing and presenting data at lab meetings. The Scientist II will prioritize daily workload and work with some supervision. The associate will participate in the analysis and review of data, report results, and complete all required documentation and database entries. In general, the Scientist II will receive specific instructions and ongoing guidance regarding required tasks and expected results. Duties and Responsibilities: Routine, accurate and timely completion of all assigned experimental tests. Will be expected to efficiently prioritize individual workload. Independently analyze research data, solve problems with appropriate guidance and effectively plan follow up experiments. Responsible for the execution of experiments with varying complexity using multi-color Flow Cytometry. Analyze data using FCS Express and FlowJo software, report test results including completion of all required documentation and database entries as required by protocols or operating procedures. Expected under supervision to develop skills and exercise judgment in troubleshooting routine assigned test procedures and in recommending appropriate corrective actions. Keeps abreast of the basic requirements for compliance in own area of work and complies with those requirements. Promotes a safe work environment. Participates in Environmental, Health and Safety programs. Addresses corrective actions whenever a hazard is identified. Performs other related duties and assignments as required. Knowledge and Skills: The ideal candidate has the following skills: Software: BD FACS Diva, FlowJo, FCS Express, and Microsoft Office Suite. Hands on experience: designing, performing, and analyzing flow cytometry experiments, preferably on client flow cytometers (LSRII, LSR Fortessa, Canto, Aria). Effective interpersonal skills must be able to work in a cross-functional team-oriented environment to achieve organizational goals. Effective written and oral communication skills. Demonstrated ability to follow established policies and procedures. Demonstrated ability to keep neat, accurate, and complete records. Effective analytical and problem-solving skills. Education and Experience: Requires a bachelor's degree in cell biology, immunology or related scientific discipline and a minimum of 2-4 years of laboratory experience.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Vaccine Immuno therapeutics (VITx) seeks to Client Client vaccines (prophylactic and therapeutic) for the prevention and treatment of significant human using a variety of vaccine technology platforms combined with immunomodulatory agents. A virus purification scientist is required to join Vaccine Immunotherapeutics in La Jolla, California, to develop and support vaccine platform production processes at the research scale. The candidate will have solid training and knowledge in virus/protein purification. The candidate will be able to independently and proactively apply this knowledge in the design and execution of experimental work, to enable progression of vaccine discovery projects. Experience in most or all of the following areas are desirable- protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. The candidate will be required to work semi-independently and, as a member of a team, be accountable for the critical appraisal of their results and present them for review, at specific project milestones. The role is laboratory based, and a major emphasis is placed upon laboratory training to increase the scope of practical abilities, as well as the theory behind such practical work. Position Comments visible to MSP and Supplier: Additional Skills: Protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. Expected qualifications/experience BSs or MSc in biological sciences or biochemical/chemical engineering At least 1-5 years working in a laboratory in an academic or industrial setting Qualifications BSs or MSc in biological sciences or biochemical/chemical engineering Additional Information For more information, Please contact Akriti Gupta ************** Morristown, NJ 07960

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Vaccine Immuno therapeutics (VITx) seeks to Client Client vaccines (prophylactic and therapeutic) for the prevention and treatment of significant human using a variety of vaccine technology platforms combined with immunomodulatory agents. A virus purification scientist is required to join Vaccine Immunotherapeutics in La Jolla, California, to develop and support vaccine platform production processes at the research scale. The candidate will have solid training and knowledge in virus/protein purification. The candidate will be able to independently and proactively apply this knowledge in the design and execution of experimental work, to enable progression of vaccine discovery projects. Experience in most or all of the following areas are desirable- protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. The candidate will be required to work semi-independently and, as a member of a team, be accountable for the critical appraisal of their results and present them for review, at specific project milestones. The role is laboratory based, and a major emphasis is placed upon laboratory training to increase the scope of practical abilities, as well as the theory behind such practical work. Position Comments visible to MSP and Supplier: Additional Skills: Protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. Expected qualifications/experience BSs or MSc in biological sciences or biochemical/chemical engineering At least 1-5 years working in a laboratory in an academic or industrial setting Qualifications BSs or MSc in biological sciences or biochemical/chemical engineering Additional Information For more information, Please contact Akriti Gupta ************** Morristown, NJ 07960

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Vaccine Immunotherapeutics (VITx) seeks to Client Client vaccines (prophylactic and therapeutic) for the prevention and treatment of significant human using a variety of vaccine technology platforms combined with immunomodulatory agents. • A virus purification scientist is required to join Vaccine Immunotherapeutics in La Jolla, California, to develop and support vaccine platform production processes at the research scale. • The candidate will have solid training and knowledge in virus/protein purification. • The candidate will be able to independently and proactively apply this knowledge in the design and execution of experimental work, to enable progression of vaccine discovery projects. • Experience in most or all of the following areas are desirable- protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. • Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. • The candidate will be required to work semi-independently and, as a member of a team, be accountable for the critical appraisal of their results and present them for review, at specific project milestones. • The role is laboratory based, and a major emphasis is placed upon laboratory training to increase the scope of practical abilities, as well as the theory behind such practical work. Additional Skills: protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. Expected qulaifications/experience BSs or MSc in biological sciences or biochemical/chemical engineering At least 1-5 years working in a laboratory in an academic or industrial setting Additional Information Best Regards, Anuj Mehta ************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Vaccine Immunotherapeutics (VITx) seeks to Client Client vaccines (prophylactic and therapeutic) for the prevention and treatment of significant human using a variety of vaccine technology platforms combined with immunomodulatory agents. • A virus purification scientist is required to join Vaccine Immunotherapeutics in La Jolla, California, to develop and support vaccine platform production processes at the research scale. • The candidate will have solid training and knowledge in virus/protein purification. • The candidate will be able to independently and proactively apply this knowledge in the design and execution of experimental work, to enable progression of vaccine discovery projects. • Experience in most or all of the following areas are desirable- protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. • Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. • The candidate will be required to work semi-independently and, as a member of a team, be accountable for the critical appraisal of their results and present them for review, at specific project milestones. • The role is laboratory based, and a major emphasis is placed upon laboratory training to increase the scope of practical abilities, as well as the theory behind such practical work. Additional Skills: protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. Expected qulaifications/experience BSs or MSc in biological sciences or biochemical/chemical engineering At least 1-5 years working in a laboratory in an academic or industrial setting Additional Information Best Regards, Anuj Mehta ************

Practice/Department: Habitat Restoration Internal Title: As-Needed Coastal Scientist Work Environment: Hybrid Compensation: $30-$40 hourly* Dudek's journey began in 1980 with a vision to serve Southern California's water and wastewater agencies. Today, we are a 100% employee-owned firm supporting clients nationwide and delivering projects that improve and protect the built and natural environments of communities throughout the United States. Our work has been recognized by leading industry organizations, and we've been honored with multiple national Top Workplace Awards. Our employees are unified by a singular commitment to supporting projects that address key societal issues, such as the transition to renewable energy, infrastructure hardening and repair, environmental protection, and community resilience. Learn more about our award-winning culture, the benefits and perks of being a Dudekian, and the projects you will have the opportunity to shape.Who You AreAs an employee you embrace accountability, working safely, and collaboration while thinking resourcefully and independently. Like all Dudekians, you are curious and solution-oriented, with the ability to adapt quickly to changes and approach challenges with a spirit of innovation.How You'll Make an ImpactWe are currently seeking a self-motivated individual with proven experience in coastal science to join our Habitat Restoration Team. This position will have professional growth and career advancement opportunities as well as expanded responsibilities consistent with the recipient's skills and motivations. This is a variable-hour role.Duties and Responsibilities Support the planning and design of a wide range of coastal projects, including ecosystem restoration, coastal flood and erosion management, and sea level rise adaptation planning. Provide quality work products ensuring high standards in design and documentation. Collaborate with multidisciplinary teams-geotechnical, structural, hydraulic engineers, landscape architects, biologists, and more-to advance integrated, nature-based solutions from concept through construction. Thrive in a fast-paced consulting environment managing multiple priorities and deadlines independently or as part of a team. Prepare written technical reports including site assessments and monitoring reports for coastal projects. Perform observations of project implementation/construction and prepare punch list field reports for projects. Minimum Qualifications B.A. or B.S. in Environmental Science, Earth System Science, Biology, Coastal Engineering, or other applicable environmental field with strong coastal background. 2+ years of professional experience in coastal science and habitat restoration Excellent verbal and written communication skills and ability to draft and edit technical documents. Able to conduct strenuous field work in hot weather (over 100 F) and in steep terrain conditions. Work may involve assignments in remote locations with overnight stays and working individually. License to legally operate a motor vehicle in the State of California. Must possess a valid driver's license and have active personal automobile liability insurance by first day of employment Preferred Qualifications Ability to support the development of new projects and/or lead business development efforts in collaboration with the Habitat Restoration Practice Director. Experience with Resource Agency coordination related to coastal projects. Fluency in coastal physical and ecological processes. Experience and knowledge of the environmental policies and regulations which may require coastal nature-based work to be performed, and that may constrain various approaches to project design and implementation. Excellent technical writing skills. Compensation: $30-$40 hourly* *Final agreed-upon compensation will be based on a variety of factors including, but not limited to, an individual's related experience, education, certifications, skills, and work location. Successful candidates must pass a pre-employment drug test and background check prior to beginning employment. Working Conditions Environment This job operates in an outdoor or office-based environment and this role routinely uses standard office equipment such as computers, phones, printers, etc. Outdoor activity may involve walking/trekking in uneven terrain over long distances in extreme weather conditions for extended periods of time. This job requires project site visits, based outdoors which can include excessive noise, uneven walking surfaces, extreme weather, and moving vehicles and equipment. Physical RequirementsThe physical demands described here are representative of those that must be met to successfully perform the essential functions of the job. This job requires the following: Working on a computer, sitting, or standing for long periods of time in an office or remote office setting. Employees must be capable of bending, squatting, climbing ladders, and lifting up to 35 lbs. unassisted; 50lbs in a team lift (two or more employees). Attending meetings, both in person and virtually, and speaking on the phone with peers, clients, etc. Specific vision abilities, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. Dudek is committed to creating a workplace where all employees, regardless of their background, feel valued, respected, and have equal opportunities to succeed. We believe that a diverse and inclusive workforce is essential to our business success, and we are dedicated to fostering a culture where everyone can thrive. We are committed to fair and equitable processes, based on merit, free from any discrimination. Dudek is genuinely committed to equal employment opportunities within our company and on our project teams. Dudek is also committed to compliance with all applicable laws providing equal employment opportunities. This commitment applies to all persons involved in Dudek's operations and prohibits unlawful discrimination by any employee of Dudek, including supervisors and coworkers. Equal employment opportunities will be extended to all persons (including those with disability and veteran status) in all aspects of the employment relationship, including recruitment, hiring, training, promotion, transfer, compensation, benefits, discipline, layoff, recall, and termination. Any employee who violates this policy and Dudek's commitment to equal employment opportunities will be subject to disciplinary action. *As-needed and part-time employees are eligible for our 401(k) plan, sick leave, and our Employee Assistance Program (EAP). As-needed and part-time employees have the option of additional benefits like medical benefits and ESOP participation provided they meet minimum hours worked during the 12-month look back measurement period. Speak with your recruiter to learn more. Dudek is a U.S.-based employer. All positions are based in the United States and require U.S. work authorization.

About Varda Low Earth orbit is open for business. Varda is accelerating the development of commercial space infrastructure, from in-orbit pharmaceutical processing to reliable and economical reentry capsules. From life-saving pharmaceuticals to more powerful fiber optics, there is a world of products used on Earth today that can only be manufactured in space. Varda is accelerating innovation in the orbital economy by creating both the products and infrastructure needed so space can directly benefit life on Earth. Our mission is to expand the economic bounds of humankind. Our team is uniquely suited to accomplishing this goal, with leadership and staff comprised of veterans from SpaceX, Blue Origin, major pharmaceutical companies and Silicon Valley. Varda was founded in January 2021 by Will Bruey and Delian Asparouhov with significant backing from world class investors including Khosla Ventures, Lux Capital, Founders Fund, Caffeinated Capital, General Catalyst, and Also Capital. Varda is headquartered in El Segundo, California, where we have offices and a production facility where our vehicles, equipment, and materials are built, integrated, and tested. Varda also has offices in Washington, DC and Huntsville, AL (coming soon). Join Varda, and work to create a bustling in-space ecosystem. About This Role Our pharmaceutical team is looking for a highly motivated and creative Formulation Scientist who will lead our biologics efforts in improving therapeutics with microgravity. This is an opportunity in an exciting area of growth for Varda, where you will get to shape Varda's product culture and will play a significant role in establishing the low Earth orbit economy. Responsibilities Develop formulations of biologic drug products Carry out hands-on experiments in the lab and work with external testing sites Collaborate closely with product development, process engineering, analytical development, and broader engineering groups to drive drug development activities Basic Qualifications PhD degree in Chemistry, Biochemistry, Chemical Engineering, Materials Science or related fields with 3+ years of relevant industry experience Experience as technical lead driving end-to-end development of biologics formulations Knowledgeable on formulation development across a range of dosage forms, spanning development, characterization, and scale-up Understanding of physical/chemical stability of proteins, and product quality considerations Preferred Skills And Experience PhD in pharmaceutics, biochemical engineering, chemical engineering, materials science, organic chemistry, or related fields with 5+ years of relevant industry experience Experience with regulatory submissions and regulatory questions Track record of biologics formulation development as demonstrated by publications in peer-reviewed journals and presentations at scientific conferences Pay Range Salary Range: $120,000.00 - $180,000.00/per year This role is on-site in El Segundo, CA Leveling and base salary is determined by job-related skills, education level, experience level, and job performance You will be eligible for long-term incentives in the form of stock options and/or long-term cash awards ITAR Requirements Varda, like all employers, must ensure that its employees working in the United States are lawfully authorized to work in the U.S. Additionally, our employees are exposed to and have access to certain export-controlled items. At present, some of our technology to which employees have access requires a license to be exported to individuals other than “U.S. Persons” as defined in U.S. export regulations. Because our employees are provided access to export-controlled items, our current policy is to only hire “U.S. persons” who are permitted to have access to our technology without an export license. “US person” means: U.S. citizen, U.S. lawful permanent resident, or protected individual as defined by 8 U.S.C. 1324b(a)(3) (i.e., individual admitted to the U.S. as a refugee or granted asylum in the U.S.) Learn more about the ITAR here. Benefits Exciting team of professionals at the top of their field working by your side Equity in a fully funded space startup with potential for significant growth (interns excluded) 401(k) matching (interns excluded) Unlimited PTO (interns excluded) Health insurance, including Vision and Dental Lunch and snacks provided on site every day. Dinners provided twice a week. Maternity / Paternity leave (interns excluded) Varda Space Industries is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Candidates and employees are always evaluated based on merit, qualifications, and performance. We will never discriminate on the basis of race, color, gender, national origin, ethnicity, veteran status, disability status, age, sexual orientation, gender identity, martial status, mental or physical disability, or any other legally protected status. E-Verify Statement Varda Space Industries, Inc. participates in the U.S. Department of Homeland Security E-Verify program. The E-Verify program is an Internet-based employment eligibility verification system operated by the U.S. Citizenship and Immigration Services. Learn more about the E-Verify program. E-Verify Notice Right To Work Notice Read more Read more

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Candidate will provide support on analytical projects of varying size and demonstrate awareness of broader project objectives. • The fundamental analytical techniques to support vaccines and other biological products should be understood and practiced in an education setting, along with basic understanding of method development, qualification and validation. • The successful applicant will be able to analyze information and standard practices using existing procedures to solve routine problems, and be accountable for self-development to enhance contribution. Major Accountabilities: • Analytical assay execution in support of vaccine process and product development programs, e.g. HPLC/UPLC, gel electrophoresis, ELISA etc. • Data collection and reporting with knowledge of GLP/GMP environments. • Perform tasks under limited supervision and able to execute experiments independently. • Able to work under tight deadlines. • Understand business drivers and be able to work under tight deadlines. • Reviews laboratory documentation • Partner with diverse team members from various functions, countries and members at various levels in the organization. • Solve complex problems using analytical thinking gained through formal education, experience and sound judgment. • Self-development to enhance contribution Skills: • Hands on experience on HPLC/UPLC, electrophoresis, immunoassay and other protein analysis methods are required for the position. • Ability to work under limited supervision and take scientific direction from scientists. • Excellent communication and presentation skills. Qualifications Education: BS degree in a scientific discipline. Internship or Academic experience preferred. Additional Information For more information, Please contact Akriti Gupta ************** Morristown, NJ 07960

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Candidate will provide support on analytical projects of varying size and demonstrate awareness of broader project objectives. • The fundamental analytical techniques to support vaccines and other biological products should be understood and practiced in an education setting, along with basic understanding of method development, qualification and validation. • The successful applicant will be able to analyze information and standard practices using existing procedures to solve routine problems, and be accountable for self-development to enhance contribution. Major Accountabilities: • Analytical assay execution in support of vaccine process and product development programs, e.g. HPLC/UPLC, gel electrophoresis, ELISA etc. • Data collection and reporting with knowledge of GLP/GMP environments. • Perform tasks under limited supervision and able to execute experiments independently. • Able to work under tight deadlines. • Understand business drivers and be able to work under tight deadlines. • Reviews laboratory documentation • Partner with diverse team members from various functions, countries and members at various levels in the organization. • Solve complex problems using analytical thinking gained through formal education, experience and sound judgment. • Self-development to enhance contribution Skills: • Hands on experience on HPLC/UPLC, electrophoresis, immunoassay and other protein analysis methods are required for the position. • Ability to work under limited supervision and take scientific direction from scientists. • Excellent communication and presentation skills. Qualifications Education: BS degree in a scientific discipline. Internship or Academic experience preferred. Additional Information For more information, Please contact Akriti Gupta ************** Morristown, NJ 07960

Biology Scientist Duration : 12 Months Total Hours/week : 40.00 1st Shift Client: Medical Device Company Job Category: Research & Development Level Of Experience: Mid-Level Employment Type: Contract on W2 (Need US Citizens or GC Holders Only) Job Description: This position works as a member of the biology group and is responsible for biocompatibility testing on medical devices and materials. Testing is performed in a corporate lab that performs biocompatibility and chemical testing as required by FDA for medical devices and/or therapeutics and in compliance with ISO 10993. This position participates in /support the conduct of nonclinical laboratory testing of medical devices and materials in accordance with GLP regulations and the BD CPDT Quality System. Conducts the appropriate biological testing in accordance with ISO 10993 guidelines, FDA regulations, GLP regulations, and/or other applicable international standards. Perform sample preparation and sample extraction. Prepare reagents and solutions needed for testing. Maintain a safe laboratory environment. A bachelor's degree in biology. At least 3-5 years biocompatibility work experience, preferably including work in a GLP or GMP environment. The individual should be well-organized and detail-oriented, proficient with MS Office applications, including Word and Excel, be able to multitask and operate effectively within a diverse work environment, e team oriented and have strong interpersonal skills, and have excellent written and verbal communication skills.

Biology Scientist Duration : 6 Months Total Hours/week : 40.00 1 st Shift Client: Medical Device Company Job Category: Healthcare Level of Experience: Mid-Level Employment Type: Contract on W2 (Need US Citizens or GC Holders Only) Workdays/hours: M - F 8am - 5pm Job Description: The Life Science Innovation group at client Technologies and Innovation is seeking a highly talented associate to join our team for a 6-month contingent position. The associate will join a multi-disciplinary team developing molecular diagnostic solutions to address current and future healthcare needs in the infectious disease space. The associate will be responsible for the formulation, organization, and quality control of assay raw materials, amplification master mixes, buffers, and consumables. The associate will apply good laboratory practice and analytical skills to lead the overall reagent inventory, and material output and works with other team members to resolve technical challenges during assay development. Duties and Responsibilities Supports the management of reagent and material inventory, and initiates resupply orders as needed. Receives, aliquots, and labels incoming raw materials and processes CoA's in accordance with Quality Policy. Monitors freezers and refrigerators to ensure proper storage conditions are maintained. Prepares various molecular biology reaction buffers and assists in optimization and re-formulation of buffers to meet product development requirements. Formulates and lyophilizes master mixes for Nucleic Acid Amplification Tests (NAATs). Utilizes a broad range of practical techniques in molecular biology and chemistry for material formulation. Supports the development and/or adaptation of relevant Standard Operating Procedures (SOPs). Maintains familiarity of molecular diagnostics methodologies and demonstrates this knowledge within responsibility areas. Provides technical input based on experience to colleagues and provides support to other functional groups. May assist with product quality investigations. Knowledge and Skills Skilled with a variety of complex laboratory procedures and instruments. Proven ability to formulate Master mixes for DNA/RNA amplification methodologies Skilled in Microsoft Excel to aid in generating various formulations. Proven ability to work effectively within a team, under direction, and independently. Excellent oral and written communication skills. Experience working in BSL-2 environment is highly desired. Experience in execution of molecular biology methods including qPCR, DNA quantitation/characterization, DNA extraction and purification is preferred Job Requirements and Experience B.A./B.S. in Chemistry, Biology, Biochemistry, Microbiology, Biotechnology, or related field Minimum of 2 years of relevant academic, clinical, or industry lab work required. Work experience in a laboratory requiring meticulous technique in the formulation of contamination-free, molecular grade buffers and amplification master mixes. Learning agility and timely execution of tasks is required Experiences with GLP/GMP standards are a plus Familiarity of lyophilization processes, and the application of lyophilization to molecular biology reagents are a plus

Biology Scientist - Expertise in primary lab-developed PCR assay design Duration : 6 Months Total Hours/week : 40.00 1 st Shift Client: Medical Device Company Job Category: Research & Development Level of Experience: Mid-Level Employment Type: Contract on W2 (Need US Citizens or GC Holders Only) Workdays/hours: M - F 8am - 5pm NOTE: Explicitly demonstrated expertise in primary lab-developed PCR assay design and optimization is an absolute requirement. Job Description: The associate will join a multi-disciplinary team developing innovative diagnostic solutions to meet healthcare needs in the infectious disease space. Substantial experience with molecular methods is required. The associate will be responsible for performing molecular assay work with a primary focus on nucleic acid quantitation and PCR, but also including DNA extraction from microorganisms and isothermal nucleic acid amplification. The associate will analyze and interpret results to guide experimental design with minimal oversight. An ideal candidate demonstrates the ability to adapt to the rapidly changing requirements in a dynamic work environment and works effectively in a multi-disciplinary team environment. Previous experience in microbiology and infectious disease is a strong plus. Job Responsibilities Design, execution, and troubleshooting of nucleic acid amplification assays (e.g., qPCR, isothermal) using lab-scale, non-automated instrumentation Execution of standard molecular biology techniques like nucleic acid extraction, purification and quantitation (e.g., electrophoresis, TapeStation, Nanodrop, Qubit) Analysis, interpretation, and presentation of results Accurate and comprehensive documentation in an electronic lab notebook (ELN) environment Adherence to all laboratory SOPs, including handling infectious agents under BSL-2 containment practices Requirements Explicitly demonstrated expertise in primary lab-developed PCR assay design and optimization B.A./B.S. in Chemistry, Biology, Biochemistry, Microbiology, Biotechnology, or related field 2+ years' experience in a university or industry micro/molecular biology lab setting Fluency with standard molecular biology methods and ability to swiftly learn new techniques Excellent attention to detail with an understanding of laboratory practices Strong ability to meet goals under tight timelines and adapt to changing priorities Willingness and ability to work with infectious agents in BSL-2 environment, with prior experience in bacterial or viral culture being a strong plus.

Biology Scientist Duration : 6 Months Total Hours/week : 40.00 1 st Shift Client: Medical Device Company Job Category: Research & Development Level of Experience: Mid-Level Employment Type: Contract on W2 (Need US Citizens or GC Holders Only) Work days/hours: M - F 8am - 5pm Job Description: The Life Science Innovation group at client Technologies and Innovation is seeking a highly talented associate to join our team for a 6-month contingent position. The associate will join a multi-disciplinary team developing innovative diagnostic solutions to address current and future healthcare needs in the infectious disease space. Substantial experience with molecular methods is required. The associate will be responsible for performing molecular assay work primarily focused on nucleic acid quantitation and PCR, but also potentially including DNA extraction from microorganisms and isothermal nucleic acid amplification. The associate will be expected to analyze and interpret results to guide experimental design with minimal oversight. An ideal candidate can demonstrate ability to adapt to the rapidly changing requirements of a dynamic work environment and to work effectively in a multi-disciplinary team environment. Previous experience in microbiology and infectious disease is a plus. Job Responsibilities: Execution of molecular biology methods including qPCR, DNA quantitation and characterization (Electrophoresis, Nanodrop, Qubit, etc), DNA extraction and purification Analysis, interpretation, and presentation of results Accurate and comprehensive documentation in an electronic lab notebook (ELN) environment Adherence to all laboratory SOPs, including BSL-2 practices for handling infectious agents. Job Requirements and Experience: B.A./B.S. in Chemistry, Biology, Biochemistry, Microbiology, Biotechnology, or related field 2+ years' experience in molecular biology laboratory environment (university or industry) Demonstrated expertise in molecular biology methods Excellent attention to detail with an understanding of laboratory practices Learning agility and timely execution of tasks is required Candidate must be comfortable working in BSL-2 environment Experience with bacterial and/or viral culture and enumeration is a plus

Biology Scientist Duration : 6 Months Total Hours/week : 40.00 1 st shift Client: Medical Device Company Job Category: Healthcare Level Of Experience: Mid-Level Employment Type: Contract on W2 (Need US Citizens, GC Holders Only) Workdays/hours: M - F 8am - 5pm NOTE: Explicitly demonstrated expertise in primary lab-developed PCR assay design and optimization is an absolute requirement. Job Description: The Life Science Innovation group at client Technologies and Innovation (BDTI) is seeking a highly talented associate to join our team for a 6-month contingent position. The associate will join a multi-disciplinary team developing innovative diagnostic solutions to meet healthcare needs in the infectious disease space. Substantial experience with molecular methods is required. The associate will be responsible for performing molecular assay work primarily focused on nucleic acid quantitation and PCR, but also potentially including DNA extraction from microorganisms and isothermal nucleic acid amplification. The associate will be expected to analyze and interpret results to guide experimental design with minimal oversight. An ideal candidate can demonstrate ability to adapt to the rapidly changing requirements of a dynamic work environment and to work effectively in a multi-disciplinary team environment. Previous experience in microbiology and infectious disease is a strong plus. Job Responsibilities Design, execution, and troubleshooting of nucleic acid amplification assays (e.g., qPCR, isothermal) using lab-scale, non-automated instrumentation Execution of standard molecular biology techniques like nucleic acid extraction, purification, and quantitation (e.g., electrophoresis, TapeStation, Nanodrop, Qubit) Analysis, interpretation, and presentation of results Accurate and comprehensive documentation in an electronic lab notebook (ELN) environment Adherence to all laboratory SOPs, including handling infectious agents under BSL-2 containment practices. Requirements Explicitly demonstrated expertise in primary lab-developed PCR assay design and optimization B.A./B.S. in Chemistry, Biology, Biochemistry, Microbiology, Biotechnology, or related field 2+ years' experience in a university or industry micro/molecular biology lab setting Fluency with standard molecular biology methods and ability to swiftly learn new techniques Excellent attention to detail with an understanding of laboratory practices Strong ability to meet goals under tight timelines and adapt to changing priorities Willingness and ability to work with infectious agents in BSL-2 environment, with prior experience in bacterial or vira lculture being a strong plus.