Biotech/pharmaceutical jobs encompass a broad range of careers within the life sciences industry, dedicated to developing drugs, vaccines, and therapies that improve human health. People in this field work in various settings including laboratories, manufacturing facilities, and corporate offices. These roles often require a blend of scientific expertise and regulatory knowledge, as professionals must adhere to strict standards while innovating. Characteristically, these jobs demand a commitment to rigorous research, attention to detail, and a passion for advancing medical science to meet patient needs. As this sector thrives on cutting-edge technology and scientific breakthroughs, professionals frequently engage in lifelong learning to keep pace with rapid advancements.
Biotech/Pharmaceutical jobs involve roles in the development, manufacturing, and commercialization of medicinal products and innovative therapies. These positions often require a strong foundation in life sciences, and employees work in various settings, including laboratories, manufacturing facilities, and corporate offices. Characterized by rigorous research and adherence to strict regulatory standards, this sector offers roles ranging from research scientists and clinical trial managers to quality assurance specialists and regulatory affairs coordinators. Employees in this field contribute to advancing medical science and improving patient healthcare, often engaging in cross-disciplinary collaboration and operating at the forefront of technology and innovation.
Biotech/pharmaceutical jobs are positions within the sector that focuses on applying biological and chemical principles to the development of drugs, therapies, and medical technologies. These roles often entail conducting research, developing new medications, ensuring quality control, and overseeing clinical trials. The field is characterized by its innovative nature, adherence to stringent regulatory standards, and its critical role in advancing healthcare and patient outcomes. Careers in this industry often require specialized education and training in fields like biology, chemistry, pharmacology, and can range from laboratory scientists to regulatory affairs managers.
and post-analytic procedures on biological specimens to ais health care providers in the diagnosis, treatment, monitoring and prevention of disease. Job Description: JOB ACCOUNTABILITIES: PRE-ANALYTIC, ANALYTIC AND POST-ANALYTIC WORK: Under direct supervision of a Clinical Lab Scientist (CLS), performs procedures to complete test order entry, specimen collection and specimen processing/handling.
--- Performs analyses of biological specimens using automated and manual test methods of waived or moderate complexity (per CLIA definition), producing test results necessary for the diagnosis, treatment, monitoring and prevention of disease. --- Performs post-analytic procedures, including interpretation,
releasing, reporting results; amending/correcting results, responding to inquiries, and specimen storage and retrieval. Recognizes when patient results require additional action prior to reporting (e.
g. delta checks and critical values), taking action appropriately. EQUIPMENT: Calibrates and adjusts laboratory equipment according to requirements and manufacturer's guidelines, including providing regular preventive maintenance (where automated methods are used) of analytical equipment and performing minor adjustments and repairs. QUALITY ASSURANCE: Scope of Quality Assurance (QA) duties and tasks includes maintaining a safe and orderly work area, inventory management, quality control,
proficiency testing, record keeping, privacy, security and confidentiality, and continual process improvement.
Recognizes when test systems are not functioning within control, taking action appropriately. JOB KNOWLEDGE & CRITICAL THINKING: Maintains up-to-date operational information and job knowledge; effectively applies information, job knowledge and critical thinking to make sound decisions and solve problems within scope of job responsibilities; escalates problems appropriately if outside of job scope. Completes competency backssment activities as assigned. CUSTOMER SUPPORT: Contributes to the satisfaction of internal and external customers by responding to and resolving - inquiries, complaints, and problems; or by escalating appropriately if problem is outside of job scope.
TRANSFUSION SERVICE: If assigned to the Transfusion Service, performs various duties under direct supervision of a CLS. --- Manages blood product inventory, maintaining adequate working and safety stock. --- Performs pre-analytic, analytic and post-analytic procedures for moderate complexity testing. --- Prepares and issues blood products for transfusion. COMPLIANCE: Adheres to applicable laws, regulations, codes, accreditation standards, policies, processes and procedures EDUCATION: -Associate's Degree CERTIFICATION & LICENSURE: MLT-Medical Laboratory Technician Upon Hire SKILLS AND KNOWLEDGE: Demonstrated knowledge and technical competence in routine specimen collection, preparation, testing applications, laboratory operations, and quality assurance in one or more assigned clinical specialty areas; examples: Chemistry, Special Chemistry, Hematology (no microscopy), Urinalysis (no microscopy) and Coagulation.
Quantity of Work: Ability to organize and prioritize job duties and assigned tasks for completion within expected time-frames Proficiency: Quality of Work: Ability to accurately, precisely, and reliably perform job duties and assigned tasks.
Demonstrates sound judgment and problem solving relevant to assigned duties. Proficiency: Culturally Competent Communication: Ability to compassionately and effectively interact with patients of diverse ages, backgrounds, values, beliefs and behaviors Proficiency: Workflow Management Ability to appropriately respond to: 1) fluctuations in volume; 2) unexpected situations or problems such as equipment or information systems failure; 3) shift-to-shift hand-offs; 4) STAT test orders; 5) specimen integrity issues 6) regular review of pending logs, priority assignments, etc.
Proficiency: Adherence to Practices and Procedures: Ability to follow standard practices, processes, and procedures in sequence. Knowledge of applicable local/state/federal regulations, codes, policies, and procedures aimed at ensuring the privacy and safety of patients. Ability to use computers, including Microsoft Office suite, electronic mail, internet, etc. -Job Shift: Days Schedule: Per Diem/Casual Shift Hours:8Days of the Week: Variable Weekend Requirements: As Needed Benefits: No Unions: No Position Status: Non-Exempt Weekly Hours:0Employee Status: Per Diem/Casual Number of Openings:1Sutter Health is an equal opportunity employer EOE/M/F/Disability/Veterans.
Pay Range is $50.35 to $62.93 / hour The salary range for this role may vary above or below the posted range as determined by location. This range has not been adjusted for any specific geographic differential applicable by area where the position may be filled. Compensation takes into account several factors including but not limited to a candidate's experience, education, skills, licensure and certifications, department equity, training and organizational needs.
Base pay is just one piece of the total rewards program offered by Sutter Health. Eligible roles also qualify for a comprehensive benefits package. About Us Working at Sutter Health #J-18808-Ljbffr
studies using QBD principles to develop a thorough understanding of operation performance parameters for T cell manufacturing process. Lead from the lab to advance novel and differentiated cell therapy products toward clinical milestones, by working collaboratively with internal cross-functional teams and external partners.
Evaluate, develop and implement functionally closed systems for T manufacturing process. Oversee development activities for platform production processes and ensure processes are suitable for early-stage c GMP clinical development. Identify and evaluate new technologies to improve manufacturing outcomes such as: reduce costs, throughput, and quality. Perform in-vitro
cellular assays involving flow cytometry, cytotoxicity, and functional characterization of genetically engineered primary T cells. Contribute to regulatory filings as needed for IIT and IND submissions.
Support the technology transfer of the manufacturing process within Legend as assigned. Accurately capture data in a timely manner, ensuring data integrity and protocol compliance. Requirements Ph D or MS in Biological Sciences or related fields with 3 to 6 + years of experience working within biologics process development; Previous experience and working knowledge of T-cells or immunological cell therapies. Experience with cell therapy manufacturing scale up, process development and process
optimization are required. Create methods to monitor cellular immunophenotypes engaged in selection, activation, transduction, expansion and cryopreservation Develop methods to understand cellular impurities and impacts of cellular expansion, formulations/cryopreservation Experience with functionally closed systems or early technology evaluations for large-scale autologous or allogenic CAR-T cells processing are highly desirable.
Experience with cell-based functional assays using engineered and/or primary human cells are preferred. Good working knowledge in c GMP manufacturing of biological process and ICH regulations #LI-RT1 #LI-Onsite #J-18808-Ljbffr
emissions from fermentation in ruminants and promoting effective digestion. This position provides a unique opportunity to contribute to cutting-edge research and deepen our understanding of antigen design, immune responses, and vaccinology in the veterinary field.
Responsibilities Design and engineer novel antigens based on an understanding of immunological principles and vaccine targets. Synthesize m RNA using in vitro transcription methods to generate RNA transcripts for various applications such as in vitro translation, transfection, and functional studies. Primer designing, cloning, expressing, and purifying recombinant proteins and antigens using molecular biology techniques. Develop
and optimize expression systems for high-yield production of antigens. Conduct molecular characterization and validation of expressed antigens. Develop and perform immunological assays to evaluate antigen-antibody interactions, such as ELISA, SPR, and FACS.
Culture and isolate microorganisms ( e. g. bacteria and archaea) to identify them and run tests to determine how they function. Prepare and dispense solutions and chemicals for lab needs, including reagents, acids, bases, buffers, and stains. Design and execute immunization schedules in animal experimental models to evaluate antigen immunogenicity, vaccine efficacy, and in vivo immune responses. Hands-on tissue homogenization, dissociation,
and preparation techniques for DNA, RNA, protein extraction, and cell harvesting.
DNA (Sanger) and RNA sequencing including an understanding of sample preparation and sequencing platforms for accurate mutation identification and gene expression analysis. Visualizing specific proteins within tissues with techniques like immunohistochemistry (IHC) and immunofluorescence (IF). Collaborate with cross-functional teams to integrate antigen design and characterization into broader research and development projects. Work closely with bioinformaticians, immunologists, and other scientists to analyze data and derive meaningful insights. Maintain detailed records of experiments, protocols, and results.
Prepare and present scientific findings internally and, when necessary, externally at conferences, scientific meetings, peer-reviewing manuscripts, and patent applications. Data Interpretation, analyze complex data sets, generate reports, and present findings to internal stakeholders and external partners. Contribute with management and collaborations with external resources CRO and research partners. Qualifications Ph. D. in Molecular Biology, Veterinary Research, Immunology, Biochemistry, or related field, with a focus on antigen design and protein sciences with 2-3 years experience.
Expertise and hands-on experience in antigen design, precision RNA synthesis, innovative transfection techniques, and quality control Proficiency in molecular biology techniques including hands-on protein expression, m RNA development, DS-PAGE, analytical SEC, western blot, q PCR, RT-PCR and purification methods. Hands-on experience in immunological assays and protein characterization techniques, such as ELISA, ELISpot SPR, Luminex, MSD, and multicolor flow cytometry. Cultivate and propagate viable pathogenic and nonpathogenic stock cultures of bacteria, viruses, and fungi.
Excellent data analysis, presentation, problem-solving skills, and written and oral communication skills Ability to work collaboratively in a team-oriented environment and cross-functionally Experience using Excel and Graphpad Prism and Knowledge of statistics methods. Good to Have Familiarity with methane-producing microorganisms and their metabolic pathways, and methods to quantify methane emission by ruminants in vivo and in vitro. We offer competitive compensation, excellent benefits, and opportunities for career advancement. Join us in our mission to make significant contributions to the field of vaccine development to mitigate methane emissions in ruminants.
The candidate should be authorized to work in the United States without visa sponsorship. Equal Employment Opportunity Pasture Biosciences is committed to providing equal opportunity and a work environment free of discrimination. All qualified applicants will receive consideration for employment without regard to race, color, religion, marital status, national origin, ancestry, interaction, interactionual orientation, gender identity, disability, medical condition, pregnancy, protected veteran status, age, citizenship, or any other characteristic protected by applicable laws. #J-18808-Ljbffr
a group of esteemed, world-class scientists from the University of California, San Francisco: Nevan Krogan, Kevan Shokat, Sourav Bandyopadhyay, Natalia Jura, as well as renowned biotech executives George Scangos and Norbert Bischofberger. These leaders bring with them a strong track record of amazing discoveries and scientific breakthroughs, leading to very successful companies and many FDA approved drugs.
Capitalizing on our Series A of $78M from top-tier investors, we are leveraging a unique integrated approach, combining capabilities in genetics, proteomics, structural biology and AI to generate deep biological insights and novel therapeutic approaches. Located in San Francisco's vibrant
Mission Bay neighborhood, Rezo is in close proximity to UCSF, numerous urban amenities, and outdoor recreational opportunities. We recognize that realizing our mission depends as much on our people as it does on our science and are building a workplace that fosters collaboration, respect, and diversity where contributing to your team's success is valued as highly as individual achievements.
If you're passionate about team science and breaking down barriers to progress in drug development, please consider joining us! The Opportunity We are seeking a highly enthusiastic and motivated Scientist to join our R&D team. In this role you will contribute to a breadth of activities that span both
our Platform and Discovery Biology functions to help advance drug development programs.
Becoming a member of Rezo at an early stage is a great opportunity to help build our company from the ground up. What You'll Do: Implement cutting-edge molecular and cellular techniques to determine target function in cell-based 2D/3D tumor models Work in a team to interpret high-throughput datasets to prioritize target lists and create target validation plans/packages Dissect mechanisms of target biology to translate into new and better therapeutics Help develop platform datasets and support data generation Support preclinical translational efforts for discovery and IND-enabling studies Design, execute, and analyze key biological experimental strategies to define drug MOA, develop novel disease models and biomarkers for target engagement and patient selection Communicate and collaborate across diverse interdisciplinary research teams Contribute to and balance multiple projects in parallel in a fast-paced environment About You: Ph D with a focus on cellular/molecular biology, biochemistry, or related field with 0-2 years of industry or relevant post-graduate experience or BS with 8+ years of experience Expertise in oncogene/tumor suppressor pathways and/or drugs resistance a plus Hands-on experience with in vitro 2D/3D tumor models Proficient in molecular biology techniques, including genetic manipulation in mammalian cells, immunoblotting, and proliferation and apoptosis assays Excellent communication, organizational, and interpersonal skills Ability to work independently while maintaining a collaborative attitude in a team setting Compensation at Rezo The expected starting salary range for this position based in San Francisco, California is $104,000-$145,000.
Actual starting salary will be determined based on multiple job-related factors including a candidate's skills, education, and experience, the level at which they are hired, market demand, business needs, and internal parity.
This role is eligible for participation in our Annual Discretionary Bonus Plan (based on individual and company performance) and our Equity Incentive Plan, subject to the terms of those plans and associated policies. This position is also eligible for the benefits detailed below. Benefits at Rezo Medical (HMO or PPO), dental, and vision insurance Discretionary time off policy Company holidays (including summer and winter shutdown)401(k) retirement savings program Commuter / Mass Transit Benefit Program Healthcare Flexible Spending Account (FSA)Dependent care Flexible Spending Account (FSA)Parental leave Competitive compensation Flexible work schedule EEOCAt Rezo we value a diverse, equitable, inclusive workplace and provide equal employment opportunity to all persons without regard to race, color, interaction, gender identity, gender expression, religion, age, national origin, ancestry, citizenship, physical or mental disability, medical condition, family care status, marital status, domestic partner status, interactionual orientation, genetic information, military or veteran status, or any other basis protected by federal, state or local laws.
This statement covers all facets of employment and is especially important when it comes to growing our team. If you are wondering if you'll belong at Rezo, or are worried that you don't meet 100% of the qualifications for this role, take a chance on us and yourself - please apply! SF Fair Chance Ordinance Pursuant to the San Francisco Fair Chance Ordinance, Rezo considers qualified applicants with arrest and conviction records for employment. #J-18808-Ljbffr
Biotech / Pharmaceutical jobs encompass a range of roles within the industries dedicated to researching, developing, and producing drugs, vaccines, and other medical products. These positions often involve scientific experimentation, clinical trials, regulatory compliance, and product commercialization. A hallmark of such jobs is the emphasis on innovation and the use of cutting-edge technology to combat diseases and improve health outcomes. Workers in this field typically have a strong background in life sciences and must keep abreast of rapid advancements. The sector is known for its stringent ethical and quality standards, as well as its potential for high-reward outcomes both in terms of career satisfaction and the positive impact on public health.
Biotech/pharmaceutical jobs encompass a broad range of careers within the life sciences industry, dedicated to developing drugs, vaccines, and therapies that improve human health. People in this field work in various settings including laboratories, manufacturing facilities, and corporate offices. These roles often require a blend of scientific expertise and regulatory knowledge, as professionals must adhere to strict standards while innovating. Characteristically, these jobs demand a commitment to rigorous research, attention to detail, and a passion for advancing medical science to meet patient needs. As this sector thrives on cutting-edge technology and scientific breakthroughs, professionals frequently engage in lifelong learning to keep pace with rapid advancements.
Biotech/pharmaceutical jobs encompass a broad range of careers within the life sciences industry, dedicated to developing drugs, vaccines, and therapies that improve human health. People in this field work in various settings including laboratories, manufacturing facilities, and corporate offices. These roles often require a blend of scientific expertise and regulatory knowledge, as professionals must adhere to strict standards while innovating. Characteristically, these jobs demand a commitment to rigorous research, attention to detail, and a passion for advancing medical science to meet patient needs. As this sector thrives on cutting-edge technology and scientific breakthroughs, professionals frequently engage in lifelong learning to keep pace with rapid advancements.
Biotech/Pharmaceutical jobs refer to careers within companies that research, develop, produce, and market drugs and therapies based on biological and chemical sciences. These positions are characterized by a strong focus on innovation, as professionals work to create solutions for medical conditions. Typical roles include research scientists, laboratory technicians, clinical trial managers, regulatory affairs specialists, and pharmaceutical sales representatives. This field demands a high degree of technical expertise, strict adherence to regulatory standards, and a commitment to ethical considerations, as the products directly impact human health.
Biotech/pharmaceutical jobs encompass roles in companies that develop drugs, vaccines, and medical technologies to improve health and treat diseases. These jobs can range from research and development, clinical trials, regulatory affairs, quality control to production and marketing. Key features of these roles include a rigorous focus on scientific innovation, adherence to strict regulatory standards, and often a collaborative environment aimed at advancing medical science and patient care. Careers in this field typically demand specialization, a strong educational background in life sciences or related disciplines, and a commitment to ongoing learning due to the fast-paced nature of biotechnological advancements.
Biotech/Pharmaceutical jobs refer to careers within companies that research, develop, produce, and market drugs and therapies based on biological and chemical sciences. These positions are characterized by a strong focus on innovation, as professionals work to create solutions for medical conditions. Typical roles include research scientists, laboratory technicians, clinical trial managers, regulatory affairs specialists, and pharmaceutical sales representatives. This field demands a high degree of technical expertise, strict adherence to regulatory standards, and a commitment to ethical considerations, as the products directly impact human health.
Biotech/Pharmaceutical jobs involve roles in the development, manufacturing, and commercialization of medicinal products and innovative therapies. These positions often require a strong foundation in life sciences, and employees work in various settings, including laboratories, manufacturing facilities, and corporate offices. Characterized by rigorous research and adherence to strict regulatory standards, this sector offers roles ranging from research scientists and clinical trial managers to quality assurance specialists and regulatory affairs coordinators. Employees in this field contribute to advancing medical science and improving patient healthcare, often engaging in cross-disciplinary collaboration and operating at the forefront of technology and innovation.
Biotech/Pharmaceutical jobs encompass a range of careers involved in the development, production, and marketing of drugs and therapies derived from biological sources. These roles typically require a strong foundation in life sciences and may include research scientists working on new drug discovery, quality control specialists ensuring product safety, clinical trial managers overseeing tests on human subjects, regulatory affairs professionals navigating complex legal and ethical standards, and sales representatives educating healthcare providers on the latest treatments. These jobs are characterized by a blend of cutting-edge science, strict regulatory oversight, and the potential for significant impact on patient health and well-being.
