Chemist jobs in La Mesa, CA

Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease. A Japan-based company, our goal is to translate science into smiles by delivering therapies where no adequate treatments currently exist, working from drug discovery to product development and commercialization. In North America, we are headquartered in Princeton, NJ, with offices in California, North Carolina, and Mississauga, Ontario. Summary: The Associate Scientist, Discovery Core Function will support Kyowa Kirin's cell therapy pipeline programs in a highly collaborative environment. This position will play a key role in developing next-generation cell and gene therapy programs by providing support to pipeline projects and evaluating and implementing new technologies. Essential Functions: • Support Cell and Gene Therapy pipeline projects by working with Project Leads to enable gene editing and generate new molecular workflows. • Serve as a Project Lead for technology themed projects if needed • Identify, evaluate, and implement new gene editing technologies • Contribute scientific and technical knowledge to project and support teams • Design, initiate, and optimize molecular, cell based, and analytical methods to support the Research, Technical Operations, and In Vivo Pharmacology teams • Maintain compliance with regulatory guidelines and internal standards, and prepare necessary documentation for project reviews (proposals, monthly, quarterly, annual, or study reports), patent applications, publications, and/or animal, biosafety, or human subject protocols. • Present research at project meetings and efficiently record experiments and data in laboratory notebooks, databases and monthly reports. Requirements: Education BS required, MA/MS preferred in a related scientific discipline. Knowledge and background in Molecular Biology, Bioengineering, Immunology, Hematology-Oncology is a plus. Experience 8 years of hands-on experience and in-depth knowledge of cell and gene therapy techniques and gene editing is required. Extensive experience in gene editing technologies, including CRISPR, base editing, prime editing, or transposase/recombinase-based editing is required. Strong background in molecular biology, with practical experience in NGS, molecular analytical development, gene editing design, and molecular cloning. Expertise in cell culture methodologies, development, and characterization of cell therapy products including HSCs, iPSCs, and/or CAR-T cells. Extensive experience in the molecular characterization of cell therapies, with a strong preference for expertise in NGS. Familiarity with CAR design, engineering, screening, and assay development is highly desirable. Experience in developing high-throughput screening platforms for cells, proteins, or antibodies is preferred. Background in antibody/protein engineering, protein production, and purification is highly preferred. Experience in virus production, transduction, and analytics is a valuable plus. Technical Skills Strong knowledge of industry standard gene editing techniques and analytics including CRISPR, guide RNA design and screens, indel analysis, knock-out and knock-in analysis, NGS, dd PCR. Solid understanding of cellular, molecular, and immunological techniques including cloning, ELISA, multi-color flow cytometry, in vitro functional assays, cell based assays, reporter assays. Experience in cell engineering processes including knowledge of cell line generation workflows and experience developing therapeutic engineered cells such as CAR-T. Expertise in cell culture techniques including culture of primary cells, iPSCs, HSCs, and cell lines from multiple species and cell manipulation techniques including transfection, nucleofection, and transduction. Experience with cell characterization including multicolor flow cytometry, FACS, MACS, and single cell isolation techniques. Experience in antibody or protein production, purification, and analysis is a plus. Proficient in MS Office Suite. The anticipated salary for this position will be $120,000 to $125,000. The actual salary offered for this role at commencement of employment may vary based on several factors including but not limited to relevant experience, skill set, qualifications, education (including applicable licenses and certifications, job-based knowledge, location, and other business and organizational needs. The listed salary is just one component of the overall compensation package. At Kyowa Kirin North America we provide a comprehensive range of benefits including: • 401K with company matching • Discretionary Profit Sharing • Annual Bonus Program (Sales Bonus for Sales Jobs) • Generous PTO and Holiday Schedule which includes a Summer and Winter Shut-Down, Sick Days and, Volunteer Days • Healthcare Benefits (Medical, Dental, Prescription Drugs and Vision) • HSA & FSA Programs • Well-Being and Work/Life Programs • Life & Disability Insurance • Concierge Service • Pet Insurance • Tuition Assistance • Employee Referral Awards The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. KKNA and all of its employees have an obligation to act in accordance with the law and with integrity in all our operations and interactions It is the policy of Kyowa Kirin North America, Inc. to provide equal employment opportunity to all qualified persons without regard to race, religion, creed, color, pregnancy, sex, age, national origin, disability, genetic trait or predisposition, veteran status, marital status, sexual orientation or affection preference or citizenship status or any other category protected by law. When you apply to a job on this site, the personal data contained in your application will be collected and stored by Kyowa Kirin, Inc. (“Controller”), which is located at 510 Carnegie Center Dr. Princeton, NJ 08540 USA and can be contacted by emailing ****************************************. Controller's data protection officer can be contacted at usprivacyoffice@kyowakirin.com. Your personal data will be processed for the purposes of managing Controller's recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes. Such processing is legally permissible under Art. 6(1)(f) of General Data Protection Regulation (EU) 2016/679 (“GDPR”) as necessary for the purposes of the legitimate interests pursued by the Controller, which are the solicitation, evaluation, and selection of applicants for employment. Your personal data will be shared with Greenhouse Software, Inc., a cloud services provider located in the United States of America and engaged by Controller to help manage its recruitment and hiring process on Controller's behalf. Accordingly, if you are located outside of the United States, your personal data will be transferred to the United States once you submit it through this site. The transfer will be made using appropriate additional safeguards under the standard contractual clauses approved by regulators for transfers of personal data outside the European Union. Your personal data will be retained by Controller as long as Controller determines it is necessary to evaluate your application for employment. Under the GDPR, if you are located in the European Union, you have the right to request access to your personal data, to request that your personal data be rectified or erased, and to request that processing of your personal data be restricted. You also have the right to data portability, and to lodge a complaint with an EU supervisory authority. If you have any questions about our use of your data, you may contact us by email at usprivacyoffice@kyowakirin.com. Recruitment & Staffing Agencies Kyowa Kirin does not accept agency resumes unless contacted directly by internal Kyowa Kirin Talent Acquisition. Please do not forward resumes to Kyowa Kirin employees or any other company location; Kyowa Kirin is not responsible for any fees related to unsolicited resumes. #LI-TT1 #La Jolla #On-Site

Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity. To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com Job Description As an Associate Scientist / Engineer 1 in Illumina's Array Development Group, you will play an integral role in developing next generation -omic Array based assays for diverse research and applied markets. You will work as part of a fast paced, multi-disciplinary team focused on the enhancement of current, and development of new biochemical assays to understand the presence of different -omic traits on Illumina's proprietary BeadArray technology Job Responsibilities: • Develop, characterize and optimize assay protocols and HW • Recognize potential problems, understand and troubleshoot assays and associated HW • Plan, conduct, analyze, interpret, and report recommendations based on tested experimental results. • Conduct experiments and analyze data to support a robust supply of key components of the Infinium Assay • Develop analytical test methods to QC and understand capability of assay HW, and consumable components accurately and precisely • Develop hypothesis and statistically relevant data sets to prove correlations between physical and biochemical metrics • Analyze large complex data sets with statistical methodology • Participate in fast paced multidisciplinary development and troubleshooting teams • Conduct focused research under general direction of supervisor and drive projects • Support the testing of new Array scanner and assay automation software • Keep a laboratory notebook, write reports and prepare presentations • Become an expert in Illumina's BeadArray assays including, but not limited to, Infinium Genotyping, Methylation, and Copy number variation. • Deliver results in a fast-paced, results orientated, product development environment • Perform other duties as assigned. Qualifications Required Skills and Experience: • MSc or BSc in Bioengineering, Chemistry (analytical /physical), Biochemistry, Mechanical Engineering or related field with a minimum 7 years' working experience in an industrial laboratory • PhD in Bioengineering, Chemistry (analytical /physical), Biochemistry, molecular biology or related field with an applied or application specific focus and a minimum 1 year of industrial experience • Demonstrated ability to develop analytical test methods to quantify inputs and outputs of key process steps • Hands-on experience with development and optimization of workflow / HW for biochemical assays. • Demonstrated ability to develop QC test methods to validate HW for genomic assays • Practical experience with design, planning and execution of system / workflow level verification and validation • Practical experienced with physical characterization metrology (topology, surface energy, fluid dynamics etc) • Proven record of troubleshooting assay processes to deliver root cause and robust fixes • Experienced in molecular biology methods for nucleic acid analysis and manipulation including purification, amplification, labeling, hybridization for both DNA and RNA. • Excellent verbal/written communication and interpersonal skills. • Flexible and adaptable. • Analytical, detail-oriented, organized, takes initiative, and self-motivated. • Record of process driven approach to experimental design and troubleshooting, including understanding of DOE and statistical analysis / scripting software such as JMP and R • Technical understanding of SNP genotyping analysis tools a benefit • Excellent lab notebook and documentation skills. Preferred Skills and Experience: • DNA Array experience preferred. Additional Information All your information will be kept confidential according to EEO guidelines. IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 619-727-5167 ASAP! I want to know more about your preferences. If in case you know someone who might be interested for this, feel free to pass it along. I look forward to hearing from you!

The Associate Scientist, Analytical Development will play a key role in developing and executing mass spectrometry methods to support research and clinical programs. This is a hands-on laboratory position involving experimental design, data analysis, and interpretation to guide decision-making across cross-functional teams. The individual will contribute to analytical method development, qualification, and troubleshooting, while maintaining a strong focus on data quality, innovation, and compliance. Key Responsibilities Design and perform experiments to develop, optimize, and qualify analytical methods for release, stability, and extended characterization testing. Analyze experimental data, interpret results, and propose next steps to improve methods or resolve analytical challenges. Implement novel analytical and mass spectrometry techniques for characterization of biologics and complex molecules. Document experiments in electronic laboratory notebooks and prepare detailed technical reports summarizing findings. Present data and updates regularly in team and project meetings. Ensure all work adheres to regulatory standards and internal policies, including FDA, EMA, ICH, and GMP requirements. Collaborate with cross-functional teams to support research, development, and technical operations initiatives. Contribute to a culture of innovation, teamwork, and scientific excellence. Qualifications Masters degree in Chemistry, Biology, or Pharmaceutical Sciences, or a Bachelors degree with at least 4 years of relevant experience in mass spectrometry analysis of biologics. Hands-on experience with LC-MS/MS, HPLC, CE, and related analytical techniques. Strong knowledge of antibody and/or oligonucleotide analytical characterization. Demonstrated ability to analyze complex data and solve technical problems independently. Excellent communication, organizational, and interpersonal skills. Ability to work collaboratively in a fast-paced, multidisciplinary environment while managing multiple priorities effectively. Working Place: San Diego, California, United States Company : 2025 Oct 16th Virtual - Avidity Biosciences

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. This is a fully onsite role based at our customer's site in San Diego, CA. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. We are seeking highly skilled and motivated Associate Scientist proficient in laboratory procedures, and cell culture to join our Discovery Core group. The successful candidate will work in a team setting and be responsible for large scale production of recombinant, primary human progenitors, stem cells, and 3D organoids. This will include utilization of automated systems to enable production of human cells to support drug discovery projects. A proven strong understanding of best practices to ensure reliability, efficiency, and quality control is required. Key responsibilities: Culture recombinant, primary human progenitors, stem cells and/or 3D organoids Completes experiments in a reliable, consistent manner Demonstrates high level of attention to detail Performs initial analysis of experimental data and interprets immediate experimental outcomes Records experiments and results in laboratory notebooks (including all electronic systems) in accordance with lab procedures Recognizes problems and suggests experiments to troubleshoot issues Implement new ideas to improve workflows, consistency and efficiency of the cell culture processes Clearly and optimally communicates (both written and verbal) results Education and Experience: Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 - 2 years') In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: Must have availability for over time on weekends and holidays when needed. Experience with advanced cell culture techniques to culture human cells Ability and willingness to work rotating weekend shifts according to business needs Adaptive to a time-line driven work environment Multitasking skills, attention to details and ability to work in a collaborative team environment Great interpersonal/collaboration skills and positive attitude Working Environment: Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary and/or standing for typical working hours. Able to lift and move objects up to 25 pounds Able to work in non-traditional work environments. Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! Compensation and Benefits The hourly pay range estimated for this position based in California is $30.00-$33.50. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. The Protein Homeostasis Thematic Research Center (TRC) at BMS is a fundamental Oncology research engine delivering oncology and hematology therapeutics to patients. The TRC has a major focus on exploiting BMS' expertise in protein degradation to discover and develop therapies aimed at tumor intrinsic vulnerabilities and mechanisms of resistance to existing cancer therapeutics. This focus on protein degradation allows us to attack protein classes that were previously deemed undruggable. The Pharmacology group within the Protein Homeostasis TRC at BMS San Diego provides in vivo pharmacology support to discovery teams focused on developing small molecules and biologics for oncology and immune-oncology. As an integral part of discovery programs, the group supports lead identification through in vivo model screening and mechanism-of-action studies, develops and validates animal disease models, identifies pathway biomarkers, and establishes clinically relevant endpoints to assess efficacy. Collaboration with DMPK, Exploratory Toxicology, and Translational Development is central to our work, and we contribute preclinical data to inform clinical development plans. Position Summary: We are seeking a motivated Associate Scientist with broad experience in pharmacology and drug discovery for both small and large molecules. The successful candidate will work collaboratively in a multidisciplinary environment, taking responsibility for experiment design, planning, and execution. Key duties include interpreting and presenting in vivo data, conducting sample and endpoint analyses (ELISA, Western blot, Jess, qPCR, IHC), and preparing protocols and reports. The role requires independent work, technical expertise, and contributions to project decisions. Strong communication, self-motivation, innovation, flexibility, and teamwork are essential. Position Responsibilities: In the role as an Associate Scientist within Pharmacology, the ideal candidate will be responsible for the following: Develop disease models for oncology and immune-oncology Independently design and execute in vivo efficacy and PK/PD experiments to identify drug candidates Analyze and interpret data accurately, reporting findings to supervisors and colleagues Troubleshoot routine issues and recommend solutions Evaluate endpoints from in vivo studies using Western blots, mesoscale, qPCR, etc. Write precise protocols and technical reports Present data to multidisciplinary discovery teams Collaborate with cross-functional team members Additional Qualifications/Responsibilities Basic Qualifications: Bachelor's Degree 2+ years of academic and / or industry experience Preferred Qualifications: Bachelor's Degree and 2+ years of academic and / or industry experience with oncology models Experience in mammalian cell culture Experience in the development of syngeneic and xenograft cancer models Proficient in animal handling, dosing (PO, IP, IV, and SC), tumor cell inoculation, data collection and analysis Hands-on experience in small animal surgeries, necropsy and tissue and blood collection Hands-on experience in evaluating small molecules in animal models Experience with small animal imaging modalities (e.g., Xenogen, ultrasound etc.) is a plus. Skilled in Western blots, ELISA, MesoScale, IHC, flow cytometry, RNA/DNA extraction, and PCR Proficient in Excel, Word, PowerPoint, FlowJo, GraphPad Prism, and Studylog Excellent interpersonal, communication, presentation, collaboration, and organizational skills Detail-oriented, focused, and able to deliver high-quality data efficiently Compensation Overview: San Diego - CA - US: $93,230 - $112,970 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.

Scientist, Protein Production and Characterization AlivaMab Biologics is a rapidly growing leader in the discovery of human antibody therapeutics, trusted by top-tier pharmaceutical and biotechnology companies to deliver panels of drug-quality human antibodies. We deliver on our partners' design goals, from simple to extraordinarily challenging, through collaborative access to our scientists' creativity and experience combined with proven technologies, including the AlivaMab Mouse suite of transgenic mice. Our organization is dedicated to creating a healthier world through partnerships that bring better medicines to patients faster, and we recognize our success starts with hiring people who share our passion for science. We are seeking a highly motivated and skilled Scientist to join our Protein Sciences team and contribute to both day-to-day operations and the advancement of Protein Science workflows. This position will focus on the design, optimization, and execution of transient transfection processes at various scales for antibody and protein production in mammalian expression systems. The successful candidate will leverage expertise in biophysical characterization and biochemical modification to evaluate key protein attributes. This position will report to the Associate Director of Protein Sciences and work closely with scientists in the Antibody Discovery, Antibody Engineering, Protein Sciences, and Project Management teams. The ideal candidate will drive innovation through process refinement, high-throughput automation, and growing proficiency of chemical conjugation techniques. This role offers the opportunity to work in a fast-paced, collaborative research environment, where creative solutions and a strong scientific approach are key to success. Responsibilities Responsibilities: Independently design, plan, and execute transient transfection workflows for antibody and protein production across various mammalian expression systems Develop, design, and optimize protein purification methods to enhance throughput, quality, and efficiency, as required Lead developability assessment studies by designing and conducting analytical experiments to evaluate protein stability, purity, and key biophysical characteristics Support production of complex construct design strategies (e.g VLPs, nanodiscs etc.), to enable immunization antibody discovery campaigns against challenging targets Drive implementation of automated high throughput processes to support protein production workflows using Bravo, and other robotic systems Maintain meticulous experimental records using electronic notebook (Benchling), and communicate results clearly through written reports and presentations to support project progression and scientific decision-making Contribute innovative ideas and collaborate effectively across teams to foster research excellence and ensure project success in a fast-paced environment Qualifications Qualifications: Ph.D. in Biochemistry, Chemistry, Molecular Biology, Protein Engineering, or a related field with a minimum of 2 years of industry experience or MS with minimum of 6 years of direct industry experience is required Proven hands-on experience with multiple mammalian expression platforms is required Proficiency with AKTA instrumentation, and a broad range of purification techniques, including affinity chromatography, ion exchange, HIC, and SEC, as well as standard protein QC methodologies is required Experience with therapeutic antibody developability assessment is highly desirable Strong analytical, troubleshooting, and communication skills with exceptional attention to detail Motivated self-starter with excellent organization, teamwork, and a passion for scientific innovation About AlivaMab Biologics AlivaMab Biologics sets its partners' antibody discovery programs on the fastest and most de-risked path through discovery and development. Trusted by top-tier pharmaceutical and biotechnology companies, AMB delivers drug-quality, fully human antibodies on exceptional timelines. AMB achieves its partners' design goals, from simple to extraordinarily challenging, through the generation and function-first screening of large, molecularly diverse panels of antibodies. AMB focuses on rapid and efficient delivery of antibodies, characterized for function, kinetics and developability, and engineering for alternative formats, including multi-specifics and CARs. The AMB team's experience and passion for antibody drug discovery and development combined with the use of trusted, proven technologies, including Ablexis' AlivaMab Mouse platforms, ensure the highest probability of success. The salary range for this position considers various factors, including skills, experience, training, certifications, and organizational needs. Note that this range does not reflect any geographic adjustments based on the location where the role will be based. At AlivaMab Biologics, it is uncommon for a new hire to start at or near the top of the salary range, as compensation is tailored to each individual's skills and breadth and depth of experience. The current estimated range is $98,500 - $140,000, plus a bonus target, benefits, and equity. AlivaMab Biologics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, gender identification, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. #LI-DNI

Scientist, Protein Production and Characterization AlivaMab Biologics is a rapidly growing leader in the discovery of human antibody therapeutics, trusted by top-tier pharmaceutical and biotechnology companies to deliver panels of drug-quality human antibodies. We deliver on our partners' design goals, from simple to extraordinarily challenging, through collaborative access to our scientists' creativity and experience combined with proven technologies, including the AlivaMab Mouse suite of transgenic mice. Our organization is dedicated to creating a healthier world through partnerships that bring better medicines to patients faster, and we recognize our success starts with hiring people who share our passion for science. We are seeking a highly motivated and skilled Scientist to join our Protein Sciences team and contribute to both day-to-day operations and the advancement of Protein Science workflows. This position will focus on the design, optimization, and execution of transient transfection processes at various scales for antibody and protein production in mammalian expression systems. The successful candidate will leverage expertise in biophysical characterization and biochemical modification to evaluate key protein attributes. This position will report to the Associate Director of Protein Sciences and work closely with scientists in the Antibody Discovery, Antibody Engineering, Protein Sciences, and Project Management teams. The ideal candidate will drive innovation through process refinement, high-throughput automation, and growing proficiency of chemical conjugation techniques. This role offers the opportunity to work in a fast-paced, collaborative research environment, where creative solutions and a strong scientific approach are key to success. Responsibilities Responsibilities: Independently design, plan, and execute transient transfection workflows for antibody and protein production across various mammalian expression systems Develop, design, and optimize protein purification methods to enhance throughput, quality, and efficiency, as required Lead developability assessment studies by designing and conducting analytical experiments to evaluate protein stability, purity, and key biophysical characteristics Support production of complex construct design strategies (e.g VLPs, nanodiscs etc.), to enable immunization antibody discovery campaigns against challenging targets Drive implementation of automated high throughput processes to support protein production workflows using Bravo, and other robotic systems Maintain meticulous experimental records using electronic notebook (Benchling), and communicate results clearly through written reports and presentations to support project progression and scientific decision-making Contribute innovative ideas and collaborate effectively across teams to foster research excellence and ensure project success in a fast-paced environment Qualifications Qualifications: Ph.D. in Biochemistry, Chemistry, Molecular Biology, Protein Engineering, or a related field with a minimum of 2 years of industry experience or MS with minimum of 6 years of direct industry experience is required Proven hands-on experience with multiple mammalian expression platforms is required Proficiency with AKTA instrumentation, and a broad range of purification techniques, including affinity chromatography, ion exchange, HIC, and SEC, as well as standard protein QC methodologies is required Experience with therapeutic antibody developability assessment is highly desirable Strong analytical, troubleshooting, and communication skills with exceptional attention to detail Motivated self-starter with excellent organization, teamwork, and a passion for scientific innovation About AlivaMab Biologics AlivaMab Biologics sets its partners' antibody discovery programs on the fastest and most de-risked path through discovery and development. Trusted by top-tier pharmaceutical and biotechnology companies, AMB delivers drug-quality, fully human antibodies on exceptional timelines. AMB achieves its partners' design goals, from simple to extraordinarily challenging, through the generation and function-first screening of large, molecularly diverse panels of antibodies. AMB focuses on rapid and efficient delivery of antibodies, characterized for function, kinetics and developability, and engineering for alternative formats, including multi-specifics and CARs. The AMB team's experience and passion for antibody drug discovery and development combined with the use of trusted, proven technologies, including Ablexis' AlivaMab Mouse platforms, ensure the highest probability of success. The salary range for this position considers various factors, including skills, experience, training, certifications, and organizational needs. Note that this range does not reflect any geographic adjustments based on the location where the role will be based. At AlivaMab Biologics, it is uncommon for a new hire to start at or near the top of the salary range, as compensation is tailored to each individual's skills and breadth and depth of experience. The current estimated range is $98,500 - $140,000, plus a bonus target, benefits, and equity. AlivaMab Biologics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, gender identification, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. #LI-DNI

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. Job Description Responsibilities: Trains and becomes proficient in all the required techniques, operation of relevant equipment and software packages associated with testing, data analysis, and data reporting. This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues. Routine, accurate and timely completion of all assigned QC tests under supervision and according to standard protocols or operating procedures. Will prioritize daily workload and develop skills to work independently. Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures. Calibrate and maintain equipment. Report problems to QC Supervisor or Manager. Maintain logs and required documentation as necessary. Prepare supplies and reagents, and assist with laboratory maintenance as needed. Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participate in Environmental, Health & Safety programs. Address corrective actions whenever a hazard is identified. Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices. Keep abreast of the basic requirements for safety compliance in own area of work and complies with those requirements. Participate in assigned cross-training Perform other related duties and assignments as required. Qualifications BS degree, 1 year experience in a laboratory environment. The QC Temp is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures. The QC Temp will prioritize daily workload and work somewhat independently. They will perform testing, report results, and complete all required documentation. Additional Information Thanks!! With Regards, Sasha Sharma Clinical Recruiter Integrated Resources, Inc IT REHAB CLINICAL NURSING Direct: 732-662-7964 | (W) 732-549-2030 x 219 Inc. 5000 - 2007-2015 (9 Years in a row)

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $81,900.00 - $134,550.00 Cliniqa, a Bio-Techne brand, is seeking an outstanding Scientist with a PhD or equivalent professional experience to join our Manufacturing group charged with developing or optimizing procedures for both small- and large-scale processes. This role will lead product initiatives to enable novel products through integration of reagents, instrumentation, analysis algorithms and software. This position will support all stages of manufacturing, including activities such as prototype optimization, guard-banding, design lock, verification, validation, and design transfer. This position will lead key project deliverables (e.g. verification/validation plans, technical reports, design control documents, protocol guides), contribute to design control and technical risk analysis, and independently design, execute, and analyze complex experiments and large data sets to inform design decisions and risk mitigation. Independently design and carry out experiments leading to the development/ optimization of key biological intermediates and purifications. Gain understanding of various types of purification methods and support design and characterization of novel methods. Apply/ learn new characterization methods for the sensitive detection or quantification of multimodal biomarkers from clinical specimens or in process reagent qualification. Lead the creation of protocols, presentations, standard operating procedures, design verification and validation procedures, quality control procedures, and technical reports to support lab infrastructure, new product initiatives, and on-market product investigations. Contribute to design control and associated documentation for new product initiatives, including drafting of user needs, design inputs/outputs, risk analysis and mitigation, and design transfer. Train and mentor co-workers on equipment and procedures and lead data analysis and interpretation. Provide substantial, high-quality contributions to projects by working independently, communicating effectively within team and cross-functionally, and leveraging the active support of others. Organize, analyze, and/or visualize complex datasets using analytical software (JMP, R, or Python) and statistical comparisons and clearly communicate results or complex scientific topics to technical and non-technical audiences. Lead and contribute to design and execution of experimental plans or processes to support objectives within the organization. Apply scientific methods and process design principles to improve product development and manufacturing processes. Who You Are & What You Bring Required: A PhD in Chemistry, biomedical engineering, or related field or a Master's degree plus 6-8 years of relevant industry experience. Bachelor's degree is acceptable with 10+ years of related experience. Strong Chromatography knowledge. Prior demonstrated experience developing and validating/verifying purification procedures under design control using a requirements-driven, risk-based approach within the biotech industry or clinical laboratory. A strong track record of independence, productivity and creative problem-solving. Expertise in one or more technical areas and considered a resource by colleagues to develop similar skills. Demonstrated ability to independently design and implement experimental plans or processes to support objectives within the organization, including optimization and guard banding of product prototypes. Excellent written and verbal communication skills and attention to detail. A passion for improving patient care through diagnostic technologies. Preferred: Proficiency with Excel, JMP, Python and/or R. Experience with establishing DOE protocols and interpretation of the data Familiarity with standards and guidelines for validating critical procedures Ability to contribute to early-stage product prototype development where needed is a plus. Ability to apply statistical analysis to large data sets, especially with code, is a plus. Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. 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. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

How you will contribute: We are seeking a passionate and mission-driven Associate Scientist - Assay Development with passion for development, execution, and continuous improvement of the most critical assays and experimental methods in our drive towards producing the highest quality functional plant protein with exceptional yield and quality. This individual will lead efforts in our strain, nutrient, and environmental screens to optimize growth, protein production, and extraction while aiding in standardization of scale-down assay throughput & quality with fellow Scientists and Engineers. The individual will have the opportunity to make an immediate and sustainable impact in the development of the company. What you will be working on: Streamline assay development and assay throughput for key R&D projects related to plant strain screening, protein purification & extraction, odor and flavor modification, and protein functionality testing. Drive operational efficiency, precision, and scientific rigor to streamline bottlenecks in current experimental methods with a move towards standardization of methods and improved experimental outcomes. Leverage statistics and statistical design of experiments (DoE) to identify single and multi-factor variables that drive key metrics of interest as it relates to plant growth rate, protein production, protein extraction efficiency, and functional properties related to functionality, flavor, odor and color. Develop new and innovative experimental and scale-down assays to mimic plant growth and downstream processing. Implement improved analytical methods (chromatography, spectroscopy, etc.) to assess the effectiveness and robustness of extraction processes. Leverage these insights and in-process data to troubleshoot current processes and provide insights for the development of future research. What you bring to Plantible: B.S. or M.S in Biochemistry, Chemistry, Chemical Engineering or Bioengineering. 3 to 5+ years of industry experience in assay development in an industrial environment. Excellent laboratory skills and a passion for impacting R&D outcomes through experimentation where solid data is the ultimate influencer. Assay development experience in a diversity of applications where method improvement and standardization drove improved efficiency and outcomes. A willingness to solve problems using a combination of clever scientific approaches, rigorous and coordinated execution, and a bias to action. Relevant experience with screening photosynthetic organisms and/or protein production in varied organisms is preferred. Ability to learn quickly, solve complex problems and have excellent data analysis/interpretation skills. Excellent verbal and written communication and presentation skills. Being a self-starter and able to respond creatively and simply to continuous change and steady growth environment. Thrive in a fast-paced environment where the primary focus is on simplification and optimization. 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 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!

Job Description We are a growing pharmaceutical/medical device company specializing in polymer-based drug delivery systems actively seeking an experienced Analytical Chemist to join our Quality Control team. Key Responsibilities Independently perform analytical testing on polymers, monomers, raw materials, and finished drug products using HPLC, GPC/SEC, GC-MS, Karl-Fischer titration, and flow-through dissolution systems. Conduct incoming inspection of raw chemical materials per established specifications and procedures. Develop, validate, and execute test methods as needed. Manage and coordinate internal and external analytical testing, including stability studies for polymer devices and drug products. Generate Certificates of Analysis (CoA), product release documentation, and technical summary reports. Provide analytical support to Quality Assurance and Manufacturing teams. Maintain laboratory equipment, order supplies, ensure proper housekeeping, and oversee safe chemical waste disposal in compliance with safety standards. Perform additional tasks as required to support company objectives. Qualifications BS in Chemistry (or closely related field) with a minimum of 3 years (preferably 5+ years) of hands-on analytical experience in the pharmaceutical or medical device industry. An equivalent combination of education and experience will be considered. Proven expertise operating and interpreting data from HPLC, NMR, and Karl-Fischer instrumentation. Experience with GPC/SEC and GC-MS is highly desired. Familiarity with ChemStation, Empower, or OmniSec chromatography data systems is a strong plus. Working knowledge of cGMP, ISO 13485, and pharmaceutical analytical procedures. Prior experience analyzing polymers or macromolecules is highly advantageous. Excellent attention to detail, documentation practices (GLP/GMP), and technical writing skills. Strong teamwork and communication abilities. Ability to stand or sit for extended periods, lift up to 25 lbs, and perform close-vision/microscope work. We offer a competitive salary, comprehensive benefits package, and the opportunity to contribute to innovative drug-delivery technologies in a collaborative environment. If you thrive in a fast-paced, quality-driven lab and meet the above requirements, we'd love to hear from you!

Beloteca, Inc. is a generic pharmaceutical development company specializing in the development of injectable products. It is desirable that the candidate have past practical experience and education in handling chemicals, operating laboratory equipment, generating and manipulating data, as well as computer database and word-processing skills. Job Description: Independent execution of various standard laboratory techniques, including but not limited to H/UPLC, GC, water content analysis per USP, appearance assessment, water activity per USP May participate in qualification/verification of assays Assay and documentation review and report writing Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company's policies and practices. Execution of more advanced analytical techniques with assistance such as LC/MS, DSC, and TGA Independent preparation of samples, solutions, instrument set-up and breakdown Independent preparation of data packets and creation of stability data sheets and Certificates of Analysis to summarize analytical testing Assisted participation in Out of Specification investigations and the documentation of analytical deviations along with Qualified Investigators and management Understand and apply ICH and FDA guidance Basic Qualifications: BS in Biology, Chemistry and/or related science discipline. Computer literacy in Windows applications and the MS Office. Excellent oral and written communication skills are essential. Minimum of 3 years experience with HPLC, UPLC, GC, Karl Fisher, pH Maintain a safe working environment for all employees, ensuring compliance to all local, state, and federal codes and regulations. Preferred Qualifications: Ability and willingness to work flexible hours. Great attention to detail, quality, and a desire for success. Self-motivated individual with the ability to learn, lead and strengthen the Beloteca, Inc. team.

Job DescriptionSalary: $70K-$80K, depending upon experience Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to build lasting partnerships that enable the life sciences industry to accelerate discovery and innovation in research and manufacturing. We can offer you the chance to build on your skills and knowledge while working among experts in their fieldsand with cutting-edge instrumentation. Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment.We aim to recruit the best people who stand out among their peers and embody our Core Values: C lient Focused: We only succeed when our clients succeed. O utstanding: We deliver meticulous results through outstanding performance. G ood: We act ethically and morally. E mployee-Centric: We honor and support our employees. N imble: We are prepared to adapt in an ever-changing industry. T eam-Oriented: We collaborate with each other and with our clients. We currently have a role available for an Experienced Pharma Biochemist. Job duties include, but are not limited to: Designing and executing biophysical assays (such as SPR, BLI, etc.) to support hit validation and characterization for project teams. Accurately preparing test materials, including serial dilutions, and following established protocols for assay execution. Analyzing data using Excel and/or custom analysis software. Presenting project data at meetings as needed. Job requirements include, but are not limited to: BS degree in Biology or relevant field with 5+ years of laboratory experience or MS degree with 2-5 years of laboratory experience (biotech or pharma experience preferred). Prior experience in assay development with peptides and small molecules is a plus Prior biophysical assay experience (SPR, BLI, etc.) is preferred. Basic knowledge laboratory liquid handling equipment is required (i.e Tecan, Hamilton, etc.); advanced robotic liquid handling experience is preferred. Excellent communication skills verbal and written. Works well both as a team and as an individual. Demonstration of excellent team player skills, very strong attention to detail, very strong problem-solving skills, a high level of learning agility, and the ability to work across functions. The ideal candidate will be enthusiastic and self-motivated, with the leadership and communication skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery. This job posting will close by 3/1/2026 or when a candidate is identified, whichever comes first.

Quality Control Chemist Location: San Diego, CA | Employment Type: Full-Time Help ensure the quality behind life-changing peptide therapeutics. PolyPeptide Laboratories is seeking a Quality Control Chemist to join our dynamic analytical team. In this role, you'll perform essential testing that ensures the purity, safety, and consistency of our peptide products - directly supporting global customers and advancing breakthrough therapies. If you're detail-oriented, science-driven, and excited to grow in a fast-paced GMP environment, this role is for you. What You'll Be Doing Perform analytical testing on raw materials, intermediates, in-process samples, and finished products Work with key instruments including HPLC/UPLC, GC, MS, FTIR, Karl Fischer, elemental analysis, polarimetry, and more Prepare samples and solutions following established methodologies and validated protocols Calibrate lab equipment and perform basic troubleshooting Document all testing in accordance with GMP and data-integrity requirements Identify potential quality issues and support corrective actions Contribute to SOP updates and improvements in QC workflows Maintain a clean, organized, and audit-ready laboratory What You Bring Education & Experience Bachelor's degree in Chemistry, Biochemistry, or closely related field 1+ year of experience in a GMP pharmaceutical or biotechnology laboratory Technical Strengths Hands-on experience with analytical instrumentation (HPLC/UPLC required; GC, MS, FTIR, KF, and others preferred) Strong documentation skills and Microsoft Office proficiency Soft Skills Exceptional attention to detail and strong technical writing ability Ability to multitask and adapt to shifting priorities Strong communication skills and the ability to work both independently and collaboratively Why PolyPeptide? At PolyPeptide, your precision powers progress. You'll join a collaborative, science-driven team that values expertise, integrity, and continuous improvement. Every measurement you make helps ensure the quality and safety of products that improve lives around the world. Ready to make an impact? Join us and help drive quality at the heart of peptide innovation. Salary: $26-$29/hr We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Quality Control Chemist Location: San Diego, CA | Employment Type:Full-Time Help ensure the quality behind life-changing peptide therapeutics. PolyPeptide Laboratories is seeking a Quality Control Chemist to join our dynamic analytical team. In this role, you'll perform essential testing that ensures the purity, safety, and consistency of our peptide products - directly supporting global customers and advancing breakthrough therapies. If you're detail-oriented, science-driven, and excited to grow in a fast-paced GMP environment, this role is for you. What You'll Be Doing * Perform analytical testing on raw materials, intermediates, in-process samples, and finished products * Work with key instruments including HPLC/UPLC, GC, MS, FTIR, Karl Fischer, elemental analysis, polarimetry, and more * Prepare samples and solutions following established methodologies and validated protocols * Calibrate lab equipment and perform basic troubleshooting * Document all testing in accordance with GMP and data-integrity requirements * Identify potential quality issues and support corrective actions * Contribute to SOP updates and improvements in QC workflows * Maintain a clean, organized, and audit-ready laboratory What You Bring Education & Experience * Bachelor's degree in Chemistry, Biochemistry, or closely related field * 1+ year of experience in a GMP pharmaceutical or biotechnology laboratory Technical Strengths * Hands-on experience with analytical instrumentation (HPLC/UPLC required; GC, MS, FTIR, KF, and others preferred) * Strong documentation skills and Microsoft Office proficiency Soft Skills * Exceptional attention to detail and strong technical writing ability * Ability to multitask and adapt to shifting priorities * Strong communication skills and the ability to work both independently and collaboratively Why PolyPeptide? At PolyPeptide, your precision powers progress. You'll join a collaborative, science-driven team that values expertise, integrity, and continuous improvement. Every measurement you make helps ensure the quality and safety of products that improve lives around the world. Ready to make an impact? Join us and help drive quality at the heart of peptide innovation. Salary: $26-$29/hr We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Job TitleBiochemist I - Recombinant Protein Manufacturing About Us Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world's greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we're able to push boundaries in pursuit of better human health. Find your future at Revvity Job Summary BioLegend is seeking a Biochemist I join our recombinant protein manufacturing team. The Biochemist I is responsible for producing recombinant protein products using bacterial cell culture systems. This role involves multiple stages of production, including protein expression, purification, and quality support. Key responsibilities include preparing buffer solutions, culture media, and dilution reagents; performing bacterial cell cultures; purifying recombinant proteins via affinity methods; and conducting DNA isolations following standard operating procedures. Additional duties may involve transferring products for downstream testing, maintaining production records and inventory, and preparing documentation related to products and projects. The ideal candidate is an organized, collaborative team player with strong verbal and written communication skills and a solid understanding of recombinant protein manufacturing methodologies. Essential Functions Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Perform DNA isolation, prepare various buffers and reagents for experiment of recombinant protein projects. Perform transformation, culture and harvest culture of bacterial cells. Clarify and process the culture supernatant/cell pellet/inclusion body to capture, extract, or denature/refold recombinant proteins. Purify of recombinant proteins & antibodies by affinity chromatography. Monitor protein processing by SDS-PAGE for various protein production stages. Perform protein bulk processing (concentration, dilution, buffer change), purity analysis and endotoxin removal Support inventory management of raw material and plasmid constructions for protein production Assist in transferring products across different departments for QC or other inventory-related activities. Maintain batch records and other documentations that are essential to be in compliance with ISO13485:2016 Support the preparation of material and checking for documents or historical records are available for incoming tissue and insect culture work orders. Support bottling of recombinant protein products Maintain general upkeep of the lab. Other projects or responsibilities may be required. Minimum Qualifications - Education and Experience Bachelor of Science in in Life Science or related area with 6 months of working experience in related biotech manufacturing environment. Preferred Qualifications - Education and Experience Bachelor of Science in in Life Science or related area with at least 12 months of working experience in related biotech manufacturing environment. Experience in DNA isolation and bacterial culture. Experienced in purification and formulation of recombinant protein. Applicants must be currently authorized to work in the United States on a full-time basis for any employer. Work Environment & Physical Demands Lab While performing the duties of this job, the employee regularly works in a laboratory environment with occasional data entry on a computer. Occasional exposure to a warehouse environment. 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. While performing the duties of this job, the employee is regularly required to use hands and fingers to handle, feel, or operate objects, tools or controls, and reach with hands and arms. The employee is frequently required to stand, talk and hear. The base salary range for this full-time position is $22.80 - $27.00/hr . This range reflects the minimum and maximum target for a new hire in this position. The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Please note that base pay is only one part of our total compensation package and is determined within a range. This range allows for the successful candidate to have an opportunity to progress within the position and develop at our company. This base pay range does not take into account bonuses, equity, or other benefits which may be applicable and are dependent on the level and position offered. What do we offer? We provide competitive and comprehensive benefits to our employees. Below are some highlights of our benefits: Medical, Dental, and Vision Insurance Options Life and Disability Insurance Paid Time-Off Parental Benefits Compassionate Care Leave 401k with Company Match Employee Stock Purchase Plan Learn more about Revvity's benefits by visiting our Bswift page. Log-In instructions are provided towards the bottom of the Bswift page. *For benefit-eligible roles only. Part-time and temporary roles may not be eligible for all benefits listed. Please reach out to your recruiter for more information. Revvity is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to any characteristic or status protected by applicable federal, state, and/or local laws. If you are an applicant with a disability that requires reasonable accommodation to complete any part of the application process or are limited in the ability-or unable to use-the online application system and need an alternative method for applying, you may contact ********************.

Job DescriptionRare opportunity to learn and grow with our company! Liberty EnviroLab is currently seeking Full Time Experienced Laboratory Analysts specializing in wildfire, structure fire, asbestos, and mold analysis. Liberty EnviroLab is located in San Marcos in the northern San Diego County. Liberty offers a variety of analytical testing services to support environmental investigations focused on wildfire, structure fire, asbestos, mold (microbiology). Our management team has over 71 years of combined experience in particulate analysis and trace evidence examination. We believe in empowering our customers with accurate and defensible analytical results. Some Responsibilities Include: Safely perform analyses on samples according to Libertys Standard Operating Procedures (SOPs) using advanced instruments. Follow all laboratory QA/QC requirements Record data using computer software and programs. Maintain equipment according to manufacturer guidelines and company procedures. Perform other assigned duties, as requested by supervisor. Requirements: Associates or Bachelors Degree in a life science (biology, chemistry, environmental science, etc.) preferred. 1-2 years of Polarized light microscopy (PLM) experience required. 1 year of Phase contrast microscopy (PCM) experience required. Self-motivated, independent, and team oriented. Must be able to work in a fast-paced setting, multi-task, and prioritize assignments. Good communication, computer, typing, and organizational skills. Liberty EnviroLab offers full time benefits: medical, 401k, sick pay, paid time off, and holiday pay. Pay range for this position is $22.00-$29.00 per hour. The work schedule is flexible. Visit our website for more information about our company. ************************ Please submit your resume, or call us at ************ for assistance!

Who We Are: At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs. What We Do: Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis* and uterine fibroids,* as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X and Facebook. ( *in collaboration with AbbVie ) About the Role:Performs research and/or development in collaboration with others on in-vivo and in-vitro pharmacokinetics, pharmacodynamics and drug metabolism studies working with clinical pharmacology, drug metabolism and therapeutics areas. Assists in the outsourcing and conduct of in vitro drug metabolism and permeability assessments to support early drug discovery efforts. Provides support as the point of contact for study coordination, initiation, distribution of data and management of blanket work orders. Responsibilities also include tracking of invoices against services performed. _ Your Contributions (include, but are not limited to): Manage or conduct in vitro experiments to characterize PK properties of new investigational drugs Collect, analyze, communicate results, and assist in preparing reports in a timely manner Work collaboratively with other scientists, technicians and colleagues as part of multidisciplinary project teams Understand and interpret study protocols/SOP's to ensure that the tasks are conducted accurately Other duties may be assigned as necessary Requirements: BS/BA degree and some relevant experience preferred Able to manage or execute experiments efficiently and suggest small process improvements Able to recognize patterns or inconsistencies in data results Able to deduce meaningful results while conducting routine analyses or troubleshoot minor issues. Good knowledge of one scientific discipline Developing knowledge of scientific principles, methods and techniques Good knowledge and some experience working with DMPK specific laboratory equipment/tools such as LC-MS, laboratory automation platforms, etc Ability to work as part of a team Good computer skill Developing communications, problem-solving, analytical thinking, planning and organization skills Detail oriented #LI-OB1 Neurocrine Biosciences is an EEO/Disability/Vets employer. We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.

At Devon, we will offer you a career full of energy and unmatched opportunities to solve today's greatest challenges. Innovation, creative problem-solving and positive change happen when people step out of their comfort zone and think differently. Our values, workplace practices, wellness programs, benefits and compensation are aimed at helping employees manage their unique personal life and care for their families so they can focus on contributing to the fullest. The Chemical Technologist, working under limited supervision, is responsible for leading production chemical support, corrosion strategies, risk assessment, failure analysis, and integrity management support to the production operations group. The role drives project prioritization and cost monitoring, and maintains regulatory, environmental, and safety compliance. The role directs monthly chemical review with vendors and Devon staff, leads failure review analysis for corrosion induced failures, and presents review results. The role leads cost/benefit analysis of individual chemicals, supports and facilitates field equipment installs and upgrades, conducts data analysis to enable equipment reliability improvement, repairs cathodic protection equipment, ensuring a cost effective approach to asset longevity. The role supports the vendor selection and qualification process, prioritizes, organizes, and completes basic assignments on time with some direction, frequently seeking guidance from experienced peers when faced with routine problems in chemical processes. * Leads production chemical support, corrosion strategies, risk assessment, failure analysis, and integrity management support to the production operations group, ensuring optimal performance and safety of production assets. * Drives project prioritization and cost monitoring, prepares recommendations to optimize chemical treating processes, and leads implementation of SOPs and technical documents. * Maintains regulatory, environmental, and safety compliance in conjunction with and through close coordination with the Operations Foreman, Superintendents, and Environmental Health and Safety Department. * Participates in monthly chemical review with vendors and Devon staff, leads failure review analysis for corrosion induced failures, and presents results of review reports during monthly chemical reviews. * Analyzes technical data to optimize chemical program with the goal to minimize chemical cost and asset failures, evaluates effectiveness of chemical treatment, improves process related to drilling, completions, and production, and analyzes data through SAP. * Leads cost/benefit analysis of individual chemicals along with each area's chemical program, educates lease operators on chemicals, injection rates, and chemical injection/storage equipment used in their area through training sessions. * Supports and facilitates field equipment installs and upgrades, reviews surface equipment failure database, conducts data analysis to enable equipment reliability improvement, and repairs cathodic protection equipment, ensuring a cost effective approach to asset longevity. * Implements modifications to routine tasks related to production chemical support, supports vendor selection and qualification process, and actively participates in proactive safety and continuous improvement activities, demonstrating a visible commitment to EHS. * Prioritizes, organizes, and completes basic assignments on time with some direction, frequently seeking guidance from experienced peers when faced with routine problems in chemical processes. * Possesses the right and obligation to stop work in unsafe conditions, contributing to a safe and secure working environment for all personnel. Education: * High School Diploma/General Education Diploma (GED)/Higher Secondary education and/or commensurate work experience is required. Associate's Degree in Engineering, Business Administration or any other related discipline is preferred. Experience: * 0-3 years of relevant experience with an Associate's Degree in Engineering, Business Administration or any other related discipline, otherwise 9+ years of relevant production operations experience, preferably in E&P Operations specializing in areas Chemical Treatment Processes, Equipment Maintenance, Process Optimization or a related field. Industry experience is preferred. Certifications: * Certified Chemical Technician (CCT) (preferred) Competencies: * Oral & Written Communication * Results Oriented * Active Learning * Digital Literacy * Business Acumen Skills: * Root Cause Analysis (RCA) * Corrosion Mitigation * Process Improvements * Failure Analysis * SAP ERP System * Risk Analysis * Data Analysis & Reporting * Equipment Maintenance Qualified applicants are considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, status as a protected veteran or other characteristics protected by law. For more information on Equal Employment Opportunity, please follow these links: EEO is the Law EEO is the Law Supplement Pay Transparency Provision