Associate Scientist Jobs in Mississippi

**US** Posted: 11/20/2024 2024-11-20 2024-12-28 Employment Type: Contract Job Category: Job Number: 4148 **Job Description** **Responsibilities:** * Work in collaborative matrix environment including partner functional areas to support product and process characterization studies, data analysis and investigations. * Analyze late stage protein pharmaceutical products with advanced analytical methods including capillary electrophoresis, chromatography and mass spectrometry techniques to support product and process characterization * Lead or contribute to development, optimization and troubleshooting of analytical methods, participate in qualification, transfer and validation experiments with a focus on separation-based purity methods * Other duties include data analyses, maintenance of electronic notebook records of experimental data, participation in authoring of technical protocols and reports, and presentation of results in internal meetings **Requirements / Qualifications:** * Bachelor's degree and 3 years of Scientific experience OR Master's degree and 1 year of Scientific experience **Preferred Qualifications:** * Bachelor or Master in Biochemistry, Chemistry, Biophysics or closely related field * 2+ years of experience in industrial analytical laboratories supporting analysis and characterization of protein therapeutics * Advanced technical expertise in analytical methodologies used to characterize protein therapeutics including CE-SDS, cIEF/ic IEF, IEX, HIC, SEC, RP and HILIC * Experience with CE and LC instruments handling and troubleshooting * Experience with CE and LC operation and data analysis software * Previous experience in mass spectrometry (MS) will be a plus * Hands on experience with method qualification and transfer * Working knowledge of data processing and analysis tools in Excel and other statistical software * Ability to work in a matrix team environment and collaborate effectively * Ability to independently prioritize, manage and schedule multiple tasks in order to meet deliverables * Good written and verbal communication skills * Familiarity with electronic lab notebook (ELN) **Apply Now:** **Share This Job:** to save this search and get notified of similar positions.

By clicking the Accept button, you agree to us doing so. Learn more: Associate Scientist- Lab Sciences page is loaded **Associate Scientist- Lab Sciences** **Associate Scientist- Lab Sciences** remote type On-site locations Columbia, Missouri time type Full time posted on Posted 30+ Days Ago job requisition id R100487 **Your New Company!** At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences. **About the role:** **What You'll Do Here:** · Oversee and maintain study conduct according to GLP regulations and as described in the appropriate oversight documents (ex: SOPs, Study Protocol, and Analytical Study Plan). · Under supervision, critically analyze study or project data and compile into reports for internal and client sponsored GLP and non-GLP preclinical drug studies. · Collect and review molecular biology data according to the Contributing Scientist or Principal Investigator and the appropriate oversight documents (ex: Protocol, Analytical Study Plan, SOPs). · Write and peer review technical documents (ex: Protocols, SOP's, validation plans, study forms, and data reports). · Assist with the development and implementation of new assays and projects to support internal and client sponsored studies. · Assist with responding to inquiries from clients and other relevant parties regarding scientific aspects of projects. **What You'll Need to Succeed:** Education: BS, MS, or PhD in biological, pharmaceutical science or related field Work Experience: BS with 3 years or MS with 1 year of experience or PhD, or an equivalent combination of education and experience in performing laboratory-based assays related to immunology, molecular biology, and/or cell biology/ biochemistry/chemistry. Language(s) Skill: Ability to read and interpret documents such as safety rules, operating and maintenance instructions, software manuals, study documents, and procedure manuals. Advanced technical writing with the ability to write and present scientific articles and complex topics to people of different backgrounds and education levels. Ability to speak effectively before groups of customers or employees of the organization. Math Skills: Intermediate to Advanced Math Skills. Training Requirements: Attends scientific meetings as applicable. Continual GLP refresher training. Stays informed on current practices. Other Requirements: Advanced technical writing and good oral communication skills; the ability to learn and understand complex theories and applications; the ability to read, analyze, and interpret complex documents; and the ability to work independently with minimal supervision. Preferred Skills: Experience with GLP, knowledge of bioanalysis, and familiarity with analytical equipment e.g., chromatography, Luminex, RT-PCR equipment. **MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH** Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!

At RefinedScience, our mission is to advance care by bringing together the best science, data and minds - disease by disease, patient by patient, cell by cell to discover pathways to life beyond disease. WHAT WE ARE LOOKING FOR RefinedScience is seeking Scientist I to join an interdisciplinary team of computational biologists, data scientists, data engineers, cancer biologists, and clinicians who are seeking to develop new therapies, diagnostics, clinical decision support tools and optimize clinical trials for cancer and other diseases. KEY ACTIVITIES * The Scientist I will work directly with the Director, Translational Laboratory Research, CTO, CINO performing a wide range of cutting edge experiments to characterize specimens from patients to develop new therapies, diagnostics, clinical decision support tools and optimize clinical trials for cancer and other diseases. * Utilize a variety of laboratory techniques required for research projects to perform experiments and tabulate and analyze research with below techniques: + Isolation of rare blood and blood progenitor cells from bone marrow using magnetic bead separation and flow cytometry + In vitro functional assays on human cells; maintenance of cell cultures + Primer design and DNA/RNA manipulation + Quantitative PCR + Molecular cloning + High throughput DNA sequencing + Single cell technologies including library construction, quantification, and sequencing workflows + Gene expression studies, including RNAseq and RNAi technology * Provide laboratory science expertise and leadership in study design, study oversight, data management, data analysis and manuscript preparation to assist all levels of investigators, and researchers on new research activities across a wide range of disciplines * Teach staff as needed, review relevant scientific literature, and attend and present at lab meetings * Provide oversight on reagent purchases through management of budget and tracking of spending on specific projects, requiring in depth knowledge of nature of each individual project. Included in this duty is preparing a report of spending on projects and working with closely with administrative team to align budgets and spending. * Assist with identifying issues related to operational efficiency and shares results with leadership * Serve as a resource to PIs and other stakeholders * Independently and creatively identify laboratory solutions * Independently review, develop and implement new or modified laboratory techniques required for research projects * Assist management with creation and implementation of processes and procedures and quality improvement initiatives * Prepare lab for daily operations, including ordering, inventory, cleaning, and preparation of laboratory reagents * Pick up, transport, and maintain results, samples, documents, materials and other items as needed * The candidate will serve as lead on many of the above tasks including oversight and providing informal leadership to team members, including assistance in managing day-to-day priorities, and redistributing workloads, and mentoring staff. Will also lead in the identification of training and development opportunities for new and existing team members MUST HAVES * BS, MS, and/or PhD in Immunology, Molecular Biology, Cell Biology, or in a related discipline * BS with 7+ years experience in a lab setting, MS with 3+ years, or PhD with 1+ years experience in a lab setting, either within an industry and/or academic setting NICE TO HAVES * Prior experience with cancer therapeutics, drug and clinical trial development. * Prior experience with single cell technologies, flow cytometry, and working with human cells and tissues * Familiarity with bioinformatics (i.e., computational, molecular, and cellular biology). * Familiarity with quality assurance principles and activities (e.g. QMS), regulatory requirements (e.g., GDPR, HIPAA), and project management principles and tools (e.g., PMO, Slack, JIRA). WHY YOU'LL LOVE REFINED SCIENCE **Team + Values** At RefinedScience, we seamlessly integrate top-tier clinical and biological data with expert knowledge to provide unparalleled insights. We maximize patient impact with these unique insights by optimizing clinical trial probability of success and time to actionable results. We work across biopharma and we are a trusted partner in achieving better results, faster - working together to unlock strategic advantage. **Our Values** * Act with Purpose - We believe in rigor through deliberate and thoughtful actions * Be Curious - Curiosity is the spark that ignites innovation and growth * Take Ownership - True ownership leads to pride and commitment in the work we do * Invest in Relationships - Building strong connections is the foundation for effective collaboration and trust for long term success * Embrace Agility - We celebrate agile thinking, resilience, and adaptability WHAT WE OFFER * The target salary range is $75,000 - $90,000 per year * Base pay offered may vary within the posted range based on several factors, including but not limited to education, job-related knowledge, skills, experience, and location.

Rockville, Maryland Operations - Bioanalytical Sciences / Full Time / On-site + Develops, qualifies and/or validates robust bioanalytical methods per Health Authority Guidance Documents using Mass Spectrometry platforms to support the Company pipeline. + Promotes innovation and direct operational improvement and/or evaluation of new analytical techniques or technology. + Troubleshoots and resolves bioanalytical method issues to successful resolution. + Takes accountability and demonstrates responsibility regarding scientific study conduct. + Ensures analytical development/validation activities conducted internally and with contracted services lead to robust methods that support bioanalytical analysis. + Conducts technology transfer between research organization, in-house and contract laboratories. + Serves as the Responsible/lead Scientist for the bioanalytical portion of non-regulated as well as GLP and GCP studies. + Writes and reviews study protocols, analytical procedure, reports for regulatory submissions. + Performs technical reviews of analytical data and be responsible for data interpretation, analysis, and reporting of results for method development and validation. + Provides scientific and technical input to the study team and other departments. + Ensures that any circumstances that may affect the quality and integrity of the study are identified and documented as they occur and that appropriate corrective actions are taken. + Identifies process improvement opportunities, participates in execution of initiatives. + Coordinates parallel tasks across multiple projects and plans, prioritizes, and manages duties to meet departmental and organizational goals. + Mentors and/or trains new and less-experienced employees and develops training materials and schedules. + Reviews and participates in writing of departmental Standard Operating Procedures (SOPs). + Performs additional tasks or assist with special projects as assigned or needed. + The Scientist will be required to maintain familiarity with scientific literature and apply it appropriately to projects (such as evaluating new methodologies and techniques) **We set our employees up for success. To be successful in this role and help us achieve our goals, we are looking for someone with the following skills and qualifications:** + PhD in relevant scientific discipline with 2-5 years of industry or post-doctoral experience or Master's degree in relevant scientific discipline with 5+ years of relevant experience + Solid understanding of Mass Spectrometry platforms and working knowledge of Sciex instruments (7500 Triple Quad preferred).. + Knowledge/hands-on experience with LBA and/or qPCR/dd PCR methods is a plus + Working knowledge of relevant bioanalytical FDA guidance documents and health authorities expectations of bioanalytical assays. + Ability to independently plan experiments, willingness to solicit feedback and guidance to ensure proposals align with project needs + Ability to perform and execute experiments in a timely fashion to support scientific activities and project goals/deliverables + Ability to develop a wide range of methodologies/technologies and perform advanced data analysis + Ability to recommend alternatives as well as research new methods and techniques + Demonstrated ability to analyze and resolve problems, troubleshoot assay issues + Ability to interpret data, draw conclusions, and recommend next steps + Ability to effectively communicate information and results in the appropriate format (i.e. lab notebooks, presentations, reports, etc.) + Ability to lead internal and external functional projects + Must possess excellent oral and written communication skills. + Ability to present technical information to both technical and non-technical audience is required + Ability to effectively communicate information and results in the appropriate format (i.e. lab notebooks, presentations, etc.) + Must be able to work collaboratively and effectively as part of a team + Prior industry experience preferred + Familiarity with statistical analysis tools and able to apply the basic statistic tools desired. + Good computer skills and working knowledge of SoftMax or other data analysis software, MS word, Excel, Power Point are required. + Knowledge of gene therapy is a plus. By joining REGENXBIO, you will have the opportunity to be a part of a growing company and incredible team passionate about developing novel AAV gene therapy products to our patients. We offer a comprehensive and competitive benefit plan which includes market-competitive salaries, an annual bonus program, education assistance, retirement plan with employer match, stock options at all levels, summer hours and more! In addition, professional development is important to us. By joining our team, you'll have the opportunity to be exposed to challenging projects and development resources to help you grow personally and professionally.

Join world-class R&D team as we work to reshape the future of health diagnostics. We are on a mission to extend and enhance life by developing non-invasive biometric testing, driven by groundbreaking AI technology. By joining us, you'll be at the forefront of healthcare technology, innovation and research. Your work will make a tangible difference to people's lives as we follow our journey from radical vision to transformative reality. ****What the role involves**** You will be working directly with our Chief Science Officer, helping to drive forward our efforts to identify and quantify compounds in breath and other biological materials. Key aspects of the role will include: * Develop, optimize and validate analytical methods using LC-MS, SESI-HRMS and other modes of sample delivery to identify and quantify metabolic compounds and exogenous compounds * Design and implement bench-scale experiments with multiple variables for small molecule compounds * Collaborate cross-functionally with others in the R&D team and wider company ****What we are looking for**** We are looking for a skilled researcher to join our growing team of scientists and engineers. The ideal candidate will display the following attributes: * Able to communicate clearly with people who have little or no knowledge of mass spectrometry and metabolomics * Able to maintain an excellent laboratory notebook * Able and willing to mentor junior team members * Prepared to voice ideas, discuss concerns, and offer solutions when engaging with others * Able to cope with the rapidly changing priorities that come with working in a startup environment * Being able to work in a startup environment which comes with shifting priorities. ****Required skills and experience**** We want candidates with the following experience: ****Essential**** * Ph.D. degree in Analytical Chemistry, Chemistry, Biochemistry or related fields * Experience using the Thermo Scientific Q-exactive platform, including data analysis using both Thermo software and open-source software * Experience with Fossilion Tech SESI devices * Proficiency in untargeted and targeted metabolomics and lipidomics data processing, statistical analysis and data interpretation * Ability to run LC-MS experiments without supervision * Knowledge of instrumentation hardware and software * Willing to relocate to San Francisco Bay Area ****Desirable**** * 5+ years of laboratory (academic and/or industrial) experience developing analytical methods for small molecule analysis (LC, MS, GC) * Proficiency using Python based analysis tools is desirable * Strong problem-solving skills and proven creativity * Strong oral and written communication skills * Proven ability to work effectively within a diverse and dynamic team * Start-up company experience is a plus ****What we offer**** The successful candidate will get * A good salary (range $120k-160k) * A competitive compensation package including medical/dental care, 401K, paid time off, holidays, and share options. * A generous relocation package where relevant. * The chance to work in a cutting edge lab in the heart of San Francisco's Bay Area We also offer assistance with visa applications and Physical Requirements ****Equal opportunities**** Diagnose Early is an equal opportunity employer. This role is FLSA exempt. ****Note**** This role involves the following physical activities: standing, sitting, walking, climbing stairs, light lifting, computer operation, operation of analytical equipment.

**Assessment Scientist, Clinical Surveillance & Training (CST)** Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** **Why Syneos Health** * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. **Job responsibilities** • Contributes to scale selection and draft protocol review • Participates in the development of endpoint review, rater qualification, training, and certification plans, documents, reports, etc. • Contributes to scales management and translations deliverables • Reviews case report forms and electronic clinical outcome assessment (eCOA) pages to ensure consistency between the database and original scale, and provides feedback to team • Works with vendors and/or Company staff involved in training regarding the use of clinical scales, diagnostic instruments, or provision of (eCOA) technology • Provides internal Syneos Health and site staff training on therapeutic indications, scale administration, and scale scoring • Performs clinical and statistical analysis of rating scale, and/or endpoint data • Provides professional, collaborative, and scientific feedback to investigators • Continuously improves clinical and scientific expertise through research and publication. Maintains familiarity with current relevant literature • Provides scientific and clinical expertise to Sponsors, study teams, and the Company. May serve as indication subject matter expert • May support business development activities by providing scientific proposal text, protocol considerations and/or slides. May participate in bid defense meetings **Qualifications** **What we're looking for** • Graduate (e.g., MA/MS) degree in psychology/behavioral sciences, or related field preferred • Knowledge of psychiatric and neuropsychiatric assessments, including patient reported outcome measures. Experience rating psychiatric and/or neuropsychiatric assessments preferred • Experience within the clinical research or pharmaceutical industry • Excellent planning/organizational skills and ability to prioritize and multitask • Proficiency in Microsoft Office Suite, specifically: Word, Excel, and PowerPoint • Ability to thrive in a fast-paced environment • Excellent interpersonal and communication skills, both written and spoken, with an ability to inform, influence, convince, and persuade • Strong presentation skills, with experience presenting in professional settings. • Ability to travel as necessary (approximately 20%). **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about . **Additional Information:** Tasks, duties, and responsibilities as listed in this are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Share this job At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. If your past experience doesn't align perfectly, we encourage you to apply anyway. At times, we take into consideration transferrable skills from previous roles. We also encourage you to to stay connected to additional career opportunities. **Inside Syneos Health** **Why Work Here** Discover what our 29,000 employees already know: work here matters everywhere. We work hard, and smart, all in the name of getting much-needed therapies to those who need them most. A career with Syneos Health means your everyday work improves patients' lives around the world. Selecting us as an employer secures a career in which you're guaranteed to: **Your Privacy**

**Our Company** Gentuity is an exciting and highly innovative medical technology firm, active in the research and development, clinical translation, and commercialization of vascular imaging devices. This opportunity provides the candidates the unique chance to work on innovative medical products, with the potential to significantly change the practice of medicine in the care of patients suffering from a wide range of highly debilitating vascular diseases. **SUMMARY OF PRIMARY DUTIES AND RESPONSIBILITIES:** * Experiment with state-of-the-art methods in camera-based 2D/3D segmentation, inter-modality co-registration, object detection and classification of key features within the IV-OCT imaging data. * Train neural networks on large-scale in-house OCT and X-ray Angiogram datasets. * Analyze experimental results and come up with ways to improve the accuracy and scalability of our models. * Help integrate models into the Gentuity system software, including profiling and optimization of both the model and the end-to-end AI pipeline. * Collaborate with researchers and engineers across several organizations within the company. **EXPERIENCE/SKILL REQUIREMENTS:** * 5+ years of relevant work experience with MS OR 2+ years of experience with PhD (postdoc included) * Extensive experience with Deep Learning, Computer Vision or a related field. * Advanced AI/ML experience in foundational models, generative AI, multi-modal models, multi-instance learning, semi/weakly/un-supervised learning and other cutting-edge ideas. * Experience with deep neural network training in leading frameworks such as TensorFlow and/or PyTorch. * Solid fundamentals in computer vision and ML theory. **EDUCATIONAL REQUIREMENTS:** * MS, or PhD degree in Engineering or Computer Science or equivalent experience. ** Machine Learning Scientist** **Department** Software **Employment Type** Full Time **Location** Sudbury

Share **Scientist- Bioanalysis (LC-MS/MS)** Full-time Regular Dir= 100% / OH= 0% 30+ days ago Requisition ID: 1445 At ITR Laboratories Canada INC Our Mission is to bring new medicines to the world which relieve patients suffering from serious diseases. ITR Laboratories Canada has been servicing the pharmaceutical and biotechnology industries for over 30 years and has established itself as a trusted partner worldwide in Drug Safety Testing. We are actively seeking a **Scientist- Bioanalysis (LC-MS/MS)** to join our team as we continue to expand our reach and services. **Responsibilities:** The Scientist will be experienced in research and development for Bioanalytical LC-MS/MS assays. They will need to develop innovative solutions to mass spectrometry challenges. They will troubleshoot, optimize and develop assays to current GLP regulatory requirements. **Tasks Performed:** * Strong understanding of LC-MS/MS theory and applications. * Experienced in serum/plasma and tissue sample extraction techniques. * Research and development for LC-MS/MS assays including troubleshooting ongoing assays. * Conduct analytical pre-clinical and clinical studies in compliance with the Study Plan/Amendments, GLPs, SOPs, and current industry best practices. * Provide research project planning and deliver on time solutions. * Interpretation, analysis, documentation, and reporting of results on Analytical projects (validation and sample analysis). * Co-ordinate results with various Clients, Consultants and Toxicology Study Directors. * Generate reports, or reporting of results, within study timelines, and ensure any deviations/exception events are acceptable, including their impact on study data. * Keep up to date with respect to pertinent regulatory developments in the industry. * Write, review and apply all relevant SOPs. **Qualifications :** * Masters of Science (Chemistry, Biochemistry, Biotechnology, Pharmacology or related field). * Scientific industry experience of project management. * Excellent understanding of bioanalytical analysis and the associated regulations. * Experience and good hands on knowledge of analytical instrumentation (LC-MS/MS). * A strong team player with excellent oral and written communication skills. * Skilled in data interpretation and report writing. * Bilingual English /French; **This position offers:** * Permanent full-time position, * Group insurance plan and group RRSP. * A stimulating and friendly work environment. Start Date: ASAP

Company : Integrated Resources, Inc Role is reposted, previous JP 9175 We are seeking a highly motivated and creative scientist to join Client s Immunology and Inflammation Therapeutic Area (I&I TA) located in Cambridge, MA. This position will work with the Type 2 Inflammation research team towards increasing our biological understanding of the role of IL-4 and IL-13 and the mechanism of action of Dupixent in dermal and respiratory diseases. The successful candidate will be responsible for performing pre-clinical research that enhances our biological and therapeutic understanding of assets in clinical development and the life cycle management for multiple indications. The position requires an ability to work effectively both independently and in a collaborative team environment, as well as excellent technical/written/oral communication skills. The ideal candidate will be a driven bench scientist and excited to perform cutting edge research employing state-of-the-art technology. A strong working knowledge and demonstrated track record in immunology and cellular and molecular biology is highly preferred. The ideal candidate should possess strong laboratory experience and technical expertise in in vitro cellular immunology (including ELISA, MSD, assay development, tissue culture, flow cytometry, primary immune cell assays, cell isolation) and ex vivo tissue processing and analysis. Us02B Responsibilities: " Work within the project team to design, execute, troubleshoot, analyze and document in vitro and in vivo experiments to drive research data package generation to support clinical and commercial development plans. " Serve as an integral project team member, who is expected to communicate data updates and recommendations within project teams and I&I Therapeutic Area. " Understand and adhere to corporate standards regarding code of laboratory conduct, safety, and appropriate handling of materials " Proficiency with electronic notebooks. Qualifications: " BS in biology with 5+ years of research experience in laboratory setting/ MS/PhD in biology or Immunology with 3+ years of research experience in laboratory setting " Hands-on experience working with human and animal primary immune cells, such as PBMCs. " Experience with in vivo immunological experiments/techniques and ex vivo cultures. " Highly motivated, independent, collaborative and able to communicate effectively with a cross-functional team. " Possesses strong presentation skills and an exceptional work ethic. " Familiarity with technologies commonly used to assess immunological endpoints, including ELISA/MSD, western blot/JESS and multi-parameter flow cytometry. " Strong working knowledge and research experience in type 2 immunology (preferred). Education: " BS " MS/PhD in biological science or Immunology (Strongly Preferred) **Fast Four Quiz: Precision Medicine in Cancer** **Your one-stop resource for medical news and education.** Your one-stop resource for medical news and education.

**Job Type:** Full Time **Education:** B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences **Skills:** Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding ****Company Description**** **Katalyst Healthcares & Life Sciences** is hiring entry-level candidates for several positions in contract research focused on clinical trials for drugs, biologics, and medical devices. We are offering exciting job opportunities in **Drug Safety**, **Pharmacovigilance**, and **Clinical Research**, collaborating with university hospitals, pharmaceutical companies, and recruiting partners. ****Job Description**** **Position**: Regulatory Scientist As a **Regulatory Scientist**, you will play a key role in providing regulatory support throughout the lifecycle of clinical trials and product registration. You will assist in regulatory submissions, advise the team on regulatory requirements, and ensure compliance with applicable guidelines. ****Responsibilities**** * Participate in **global regulatory team meetings** and advise on regulatory requirements and project-specific issues. * Develop an understanding of the **regional regulatory environment**, competitor intelligence, and therapeutic areas. * Act as a **back-up contact** for regulatory agencies when needed. * Draft **cover letters** for regulatory communications and assist in **preparation for meetings** with regulatory agencies. * Liaise with **LOCs (Local Operating Companies)** to ensure timely responses to regulatory queries and maintain consistent content with the regulatory strategy. * Assist in **process development** and improvements related to regulatory submissions. * **Review clinical trial plans** and protocols to ensure alignment with regulatory requirements. * Provide regulatory support throughout the **registration process** and life-cycle management. * Advise on **required documents** and **submission strategies**, collaborating with LOCs as appropriate. * Ensure **timely availability** of submission documents, ensuring that all components are in place on time. * **Draft and review documents** related to regulatory submissions and compliance. * Assist in **submission** and **acceptance** of submission packages and ensure availability of **country-specific submission packages** for LOCs. * Provide regulatory input for **inspections, audits**, litigation support, and product complaints. * Stay updated on **current and pending approvals** in specific therapeutic areas and remain knowledgeable of related laws, guidances, and requirements. ****Requirements**** * An **advanced degree** (MS, Pharm D, PhD) is preferred; a minimum of a **Bachelor's Degree** is required. * 1+ year of relevant experience with an advanced degree **OR 4+ years** with a Bachelor's Degree is required. * **Pharmaceutical industry experience** is preferred, with a good understanding of the **drug development process**. * Knowledge of **regulatory submission** and **approval processes**, especially in the **US regulatory environment**, is required. * Direct experience in **regulatory affairs** is desirable. * Strong **project management**, **oral & written communication**, **organization**, and **multi-tasking skills**. ****Additional Information**** All your information will be kept confidential according to **EEO guidelines**.

* Full-time * Department: Scientific / Technical Science ** Axolabs specialises in a new class of drugs whose active ingredients are chemically derived from DNA or RNA. They are called oligonucleotide or nucleic acid therapeutics. We use our many years of expertise to help our clients make them a success. Some of these drugs have already been approved and are being used successfully against diseases that were previously untreatable in some cases. New drugs from this class are added every year. We believe in Science for a Safer World and are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organization. LGC Axolabs is located in Petaluma, US, Kulmbach and Berlin, Germany. **Job Description** **Join Our Innovative R&D Team in Oligonucleotide Chemistry!** **Your Key Responsibilities** * Develop innovative synthetic and downstream processing routes for complex oligonucleotide formats, including conjugates with fatty acids, peptides, and antibodies * Collaborate with the team to design and execute experiments that optimize lead oligonucleotide drug candidates, focusing on potency, selectivity, stability, and pharmacokinetic properties * Take on responsibility for customer order projects after a thorough training period * Support the Department Head in project planning, client communication, and report writing * Analyze experimental data, interpret results, and present findings internally, to customers, or at international conferences. Contribute to technical reports and manuscripts for publication in peer-reviewed journals * Guide and coach junior staff members in the oligonucleotide synthesis laboratory **Qualifications** **Education & Preferred Qualifications** * Hands-on experience in oligonucleotide synthesis via automated solid-phase methodologies, complemented by a Ph.D. in Chemistry or Biochemistry, or equivalent experience * Prior experience in ligation chemistry (enzymatic and/or chemical) is required * Proficient in conjugation and purification technologies, with expertise in HPLC, LC-MS, UV spectroscopy, and endotoxin measurement and control * Strong oral and written communication skills in English, ideally also in German, with a keen ability to maintain detailed lab notebooks and reports * A reliable, dedicated working style characterized by a focus on quality, dedication, and excellent communication skills **Your benefits** * Comprehensive onboarding and mentoring for a successful start * Permanent employment contract * Responsible tasks and individual development and career opportunities in an innovative, international company * An open corporate culture that values integrity, respect, and a passion for forward-thinking, creative solutions * Company pension scheme and attractive employer subsidies, such as JobRad, as well as corporate benefits * Extensive employee offerings related to health management, as well as online options for childcare and educational support * 30 days of annual leave * Relocation assistance for candidates from outside the region * 100% coverage of the Jobticket (Deutschlandticket) or a free parking space in the adjacent parking garage Join our innovative team and be part of the exciting future of oligonucleotide research! We look forward to receiving your application **in English**. **Additional Information** **ABOUT LGC:** LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers' products and workflows and are valued for their performance, quality, and range. **OUR VALUES** **Passion** for our work makes the world a safer place. We are inspired by our purpose. It drives us forward to deliver the best we can every day. **Curiosity** makes tomorrow's innovations possible. We challenge and question to discover creative and innovative solutions, enabling our customers and LGC to grow and evolve. **Integrity** is embedded in LGC and our 180+ year heritage. We hold ourselves to the highest standards and trust our colleagues to do the right thing. **Brilliance** is in everything we do. Our remarkable colleagues are experts in their field. They collaborate to deliver brilliant science to exceed our customers' expectations. **Respect** for individuality and diversity is our strength. We respect and value our colleagues, our customers, our environment and our science. **EQUAL OPPORTUNITIES** LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership. For more information about LGC, please visit our website **#scienceforasaferworld** **Job Location** Scientist - DNA-, RNA- Oligonucleotide Synthesis (x/f/m) * Fritz-Hornschuch-Straße 9, 95326 Kulmbach, Germany * Full-time

convergentresearch.org **Parallel Squared Technology Institute** (PTI) is a non-profit research institute aiming to catalyze a leap in protein analysis technology and use it to explore new biological frontiers. PTI supports open research and educational opportunities supporting rapid career development for scientists, engineers, and mathematicians. Protein dysfunctions directly cause many diseases, such as Alzheimer's disease. Yet, proteins remain understudied because of technological hurdles. To resolve these limitations, PTI will develop mass tags enabling a new framework for multiplexed protein analysis by mass spectrometry towards achieving 100-fold increase in throughput. Scientists at and collaborating with the institute will use these gains to directly investigate disease mechanisms and resolve problems that have proven intractable for decades. Our proof of principle technology and strategies are outlined at: parallelsq.org . **New career opportunities**Members of PTI will be supported with industry-level resources to lead research projects and disseminate their discoveries and innovations to the broader biomedical community through frequent publications, presentations, and submissions to public data portals. **Summary Of Position**We are looking for an Immunopeptidomics Scientist who has done research in the field of mass spectrometry-based proteomics. This position will focus on using bulk and single-cell analysis to increase the throughput of HLA and/or MHC peptide identification. The idea candidate has an in-depth understanding of instrumentation in addition to sample processing and data analysis. In this role, the successful applicant will have the opportunity to work closely with co-founders and an interdisciplinary group of researchers to help achieve PTI's milestones. ***In order to be seriously considered for this position, we require a cover letter as part of the candidate's application.*****Responsibilities** * Develop highly-sensitive immunopeptidomics workflows for data acquisition by LC-MS/MS pipelines. * Collaborate with biologists, chemists, research associates, computational scientists, and mass spectrometrists to leverage PTI's multiplexing platform. * Collaborate with external labs as needed. * Mentor scientists and research associates. Prepare internal reports and manuscripts, and present results at internal or external scientific meetings as appropriate. * Demonstrate a commitment to diversity, inclusion, and cultural awareness through actions, interactions, and communications with others. * Other duties as assigned. **Qualifications** * Ph.D. degree in Immunology, Biochemistry, Molecular Biology, or a related field. * Experience in immunopeptidomics, in particular: optimization of protocols for extraction and isolation of immunopeptides from biological samples. * Excellent communication and interpersonal skills, record keeping ability, attention to detail. **Preferred Qualifications** * Experience with LC-MS/MS. * Experience with mass spectrometry proteomics. * Experience with bioinformatics tools and software used for mass spectrometry data analysis. * Experience using R, Python, or similar computational language/software. **We Offer** * An opportunity to change the world and work with some of the smartest and the most talented experts from different fields. * Excellent medical, dental, and vision insurance with many $0 premium options for you and your family with several national and regional providers. Most employees have more than 20 plan options to choose from. * Company-paid group life, AD&D, long- and short-term disability insurance * 15 days PTO + 10 sick days per year * 18 company holidays + your birthday off * $5,000 per year educational reimbursement * Up to 16 weeks paid parental leave We aim to help fill a structural gap in today's R&D system. We enable fundamental research that requires unusual levels of scale and coordination yet is not rapidly monetizable by industry. We're bringing together top talent from academia, industry, and startups to build a new model for innovative R&D. As an incubator within the Schmidt Futures Network, we identify high-impact scientific or technical research and development opportunities, ultimately defining and launching these projects as Focused Research Organizations. We are an Equal Employment Opportunity employer that proudly pursues and hires a diverse workforce. We do not make hiring or employment decisions on the basis of race, color, religion or religious belief, ethnic or national origin, nationality, sex, gender, gender-identity, sexual orientation, disability, age, military or veteran status, or any other characteristic protected by applicable local, state, or federal law or company policy. We strive for a healthy and safe workplace and strictly prohibit harassment of any kind.

**Company Overview:** Terray Therapeutics is a venture-backed biotechnology company led by pioneers and long-time leaders in artificial intelligence, synthetic chemistry, automation, and nanotechnology. We're generating chemical data purpose-built to propel drug discovery into the information age - and we're doing it on a larger scale and faster than has ever before been possible. Our closed loop system generates precise chemical datasets at unrivaled scale that work seamlessly with AI to systematically map biochemical interactions between small molecules and causes of disease. Iterative cycles of virtual molecular design and experimentation power AI and machine learning models, which in turn guide the next cycle of design. With a chemistry engine that measures billions of interactions daily and becomes increasingly precise with every cycle, we can answer an unprecedented array of questions - deriving insights that enable us to predictably create drugs for patients in need. Position Summary: Terray is currently seeking a motivated, creative, and experienced scientist to join our Molecular Design group within the Computational and Data Sciences (CDS) team. The candidate will design combinatorial libraries for our platform and contribute to hit-to-lead and lead optimization efforts across multiple drug discovery programs. In this interdisciplinary role, the candidate will work closely with the chemistry and biology functions at Terray, as well as the machine learning, data science, and software teams within CDS. The core responsibilities of this position are: * Design focus libraries and productionize library design methods that use our proprietary ML models and other computational tools * Develop metrics to assess and improve library designs * Extract insights from our ultra-large proprietary screening datasets in collaboration with data scientists and cheminformaticians * Contribute to the design of small molecules with in-house, high-throughput computational tools using both structure-based and ligand-based models * Communicate molecular design strategy and outcomes to teams across the company Experience and Qualifications: Part of Terray's success is nurtured by a hands-on work environment where everyone is accountable, vested in a vision of excellence, and actively taking part in the success of the business. Terray supports a positive work environment where employees can feel engaged, recognized and empowered to be creative. Required Qualifications: * BS/MS/Ph.D in computational, organic, or medicinal chemistry, or a related field * Experience designing small-molecule libraries for virtual screens, DEL screens, and/or HTS * Experience triaging large data sets from virtual screens, DEL screens, and/or HTS * Proficient in Python and the PyData stack (numpy, pandas, scipy, scikit-learn, etc.) * Familiar with ligand-based and structure-based methods to designing small molecules for drug discovery projects * Experience with RDKit, and familiarity with molecular simulation suites (Schrodinger, MOE, etc.) and docking programs (AutoDock Vina, rDock, etc.) **Compensation Details:** $ 132,000 - $198,000 (annually) depending on seniority; participation in the Company's option plan; 3% retirement safe harbor contribution; full y - paid medical, dental, vision, life and disability benefits . Computational & Data Sciences Remote (United States) Share on:

PhD in Chemistry, Bio Chemistry , Biophysics , Chemical engineering, or relevant field with 0-2 years of relevant experience , a MS with 6 + years or BS with 8 + years of relevant experience . Extensive experience on developing phase appropriate formulations and fill finish processes . Working experience on various injectable dosage forms in vials, prefilled syringes/ cartridges . Ability to work in a collaborative setting and adhere to timelines. Demonstrated ability to work effectively in a cross -functional settings. Hands-on experience with liquid chromatography methods ( e. g. , SEC, RP, IEX, HIC) and capillary methods ( e. g. iCE , LabChip GXII Touch) . Strong knowledge of analytical software ( e. g. Empower). Ability to interpret raw data, organize results and communicate findings to project team and management The duties of this role are generally conducted in an lab environment . As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious, and hazardous materials; gown/ degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours. Experience with electronic record keeping and data software, like electronic lab notebooks, EndNote, as well as MS Word, PowerPoint, Excel/GraphPad, Visio, JMP/Minitab, and Adobe Pro, would be an advantage. Excellent interpersonnel and communication skills . Knowledge of cGMP and quality guidelines.

** Permanent employee, Full or part-time · Martinsried (BY)** **Purpose of your Job** We are seeking a highly skilled and motivated Scientist specializing in LC-MS (Liquid chromatography-mass spectrometry) to join our analytical team. In this role, you will contribute to the characterization of biopharmaceutical molecules, supporting client projects through advanced analytical techniques. This is an opportunity to work in a dynamic, innovative environment and play a key role in advancing therapeutic development. **Your Responsibility** * Perform LC-MS analyses to characterize biopharmaceutical molecules, ensuring accuracy and compliance with project goals. * Act as a subject matter expert in LC-MS during client projects, providing technical guidance, insights, and solutions tailored to specific needs. * Develop, implement, and validate analytical methods to meet client-specific requirements and regulatory standards. * Collaborate closely with clients and internal teams to ensure seamless execution of projects and alignment with client expectations. * Analyze, interpret, and report complex LC-MS data in a clear and actionable format for clients and project stakeholders. * Optimize and maintain LC-MS equipment, including troubleshooting and calibration. * Stay abreast of advancements in LC-MS technologies and methodologies to drive innovation and improve operational efficiency. * Ensure compliance with quality standards, including documentation and reporting in accordance with regulatory guidelines. **What you need to succeed** * Advanced degree (Ph.D./M.Sc.) in pharmacy, pharmaceutical sciences, (bio)chemistry, chemical engineering, or a related field. * Minimum of 3-5 years of hands-on experience in LC-MS for biopharmaceutical characterization. * Proficiency in operating and maintaining high-resolution mass spectrometers such as Xevo G2-XS QTOF and related software (e.g., UNIFI, Connect, PEAKS Studio, Byos). * Strong analytical skills with a proven ability to handle complex datasets and deliver high-quality reports. * Experience with method development and troubleshooting in a regulated environment (e.g., GMP/GLP). * Effective communication skills in English (German is a plus) with the ability to work collaboratively across teams. * Self-motivated with a proactive approach to problem-solving and innovation. ***Let's formulate innovation together…*** *Our success & development is created by the people working together @Coriolis. We put People first! That's why we have a growth mindset, and value personality, collaboration and community to create an empowering and inspiring working space with focus on quality and customers.* ***We would like to grow together with you!*** *Let's continue building and creating the future now! Join our Team of currently around 200 employees. In a highly motivated and interdisciplinary team, we provide you with a great chance to increase your experience. We offer an attractive work space at the Martinsried site. Let's make a difference together!* *Coriolis Pharma is an equal opportunity employer and welcomes applications from all qualified individuals regardless of ethnicity, sex, citizenship or gender identity, color, disability, religion/belief, sexual orientation, marital status, age or individual preferences. Different backgrounds, experiences and ideas push us further and raise the bar.* **Thank you for your interest! We look forward to receiving your application documents. **Please use our career portal exclusively for this purpose.** We would like to support you from the very beginning to shape your development possibilities here at Coriolis. For questions or further information, please visit our website or contact us directly. **We are looking forward to your application!**** **Your Contact** *****Dominik Schwemmer**** *Senior Business Partner - Talent & Development* People, Organization & Culture Unit Coriolis Pharma Research GmbH Phone: +49 (0) 89 - 417760 - 0 Fraunhoferstraße 18 b, 82152 Martinsried ************************ **Coriolis Pharma** , is a globally operating service provider and one of the world leaders in formulation research and development of (bio)pharmaceutical drugs and vaccines. We revolutionize the development process of biopharmaceutical drugs by integrating innovative digital formulation approaches from drug development to commercial products. As a people and team-oriented company with an interdisciplinary team of highly skilled scientists and an expert scientific advisory board, we provide cutting-edge services and tailor-made solutions for our clients. Our company culture is based on diversity, teamwork and open and appreciative communication. That's why wonderful people from over 35 nations around the world work together successfully at Coriolis. Our motivation is to enable the development of innovative drugs by performing outstanding biopharmaceutical research to improve the quality of life for humankind. **Your application!** We appreciate your interest in Coriolis Pharma Research GmbH. Please fill in the following short form. Should you have any difficulties in uploading your files, please contact us by mail at ************************** .

Basic properties of the chemical should be known. Should be able to setup R & D trials independently. Should be able to best lab practices. Should be able to work in shifts. Should be able to execute the instructions received from manager. Good communication skills. Should be able to follow confidentially. Ensure safety at work place. Collect the literature for relevant step Establish product specifications and procedures as required for R & D projects. Education Qualifications * B.Sc/Chemistry * MS/M.Sc(Science)/Chemistry Behavioural Profile 1.good communication skills 2.well behave with seniors and colleague 3.Know the basis concept of R & D. Desired Skills Computer Skills **Company Profile** Established in 1984, Finor is a specialty chemicals manufacturing company. We pioneered the production of slimicides for the Indian paper industry and offer an even wider range of paper chemicals to the industry today. Finor also manufactures biocides, defoamers, dispersants and water soluble polymers catering to a wide array of industries like paints, inks and coatings, construction chemicals, water treatment chemicals and the textile industry. Our corporate office and R&D facilities are located in Navi Mumbai where our qualified personnel run product application tests. Our manufacturing plant is situated in Ankleshwar, Gujarat attached to which we also have a pilot plant and product development laboratory. We operate across India and have personnel stationed in close proximity of customer locations. Our personnel possess several years of rich experience and share their knowledge with customers in order to serve them better. We are a family owned, professionally managed company and constantly seek opportunities for growth. We would be glad to get an opportunity of serving you!

**Your role** * Method development for (radio) HPLC, ICP-MS, IC * Development of separation methods for rare earth elements and actinides * Development of manufacturing processes of novel radionuclides * Gamma spectrometry, alpha spectrometry, liquid scintillation counting * Equipment qualification and maintenance * Writing SOPs for devices and methods * Creation of scientific reports and development plans * Supporting technology transfers **Your profile** * Higher education in Chemistry, Chemical engineering or Radiochemistry * Strong experience and knowledge in radioactive material handling * Experience and knowledge in radioanalytical methods (e.g. gamma spectrometry) * Strong experience and knowledge in radiochemical separation methods, such as liquid/liquid extraction, solid phase extraction, cation- and anion chromatography. * “Fachkunde im Strahlenschutz” preferred * Ability to work both independent and in a team * “Hands-on” mentality * Creativity, problem solving skills * Good English skills, both spoken and written * Exciting challenges in an up-and-coming and fast-growing company with a high degree of creative freedom * An open working atmosphere in an international corporate culture with short communication channels * Comprehensive onboarding programme * Flexible working hours with home office options * Attractive special payments + Employee participation programme + Job bike or subsidised job ticket + Above-average contribution to the company pension scheme + Individually tailored further training programme (including German and English courses) + Health promotion programmes (e.g. subsidy for local fitness studio, sponsorship of sporting events, various lifestyle coaching sessions) When you apply, please let us know your earliest possible starting date and your salary expectations. You can submit your CV in German and English in docx or pdf format. **Contact** Deborah Angelè ************************** ITM Isotope Technologies Munich SE Human Resources Walther-von-Dyck-Str. 4 85748 Garching/München, Deutschland **Note for recruitment agencies** Please note that we do not accept unsolicited applications or offers of assistance. The telephone number given in the advertisement is intended exclusively for applicants and should not be contacted for any other purpose. Thank you very much! **More about ITM** With us, you will have the opportunity to work in an international environment on ground-breaking projects that can have a significant impact on cancer care worldwide. We are looking for dedicated, talented and passionate professionals who share our vision and want to help shape the future of oncology. If this exciting challenge appeals to you and you would like to contribute to realising our common goal, please do not hesitate to send us your application. We look forward to hearing from you! For more information please visit: *********************** ITM is a privately owned biotechnology and radiopharmaceutical group of companies dedicated to the development, production and global supply of targeted diagnostic and therapeutic radiopharmaceuticals and radioisotopes for use in cancer treatment. We are developing a proprietary portfolio and growing pipeline of targeted treatments in various stages of clinical development addressing cancers such as neuroendocrine cancers or bone metastases. Our main objectives are to significantly improve treatment outcomes and quality of life for cancer patients through a new generation of Targeted Radionuclide Therapies in Precision Oncology. The headquarters are located in the heart of the research center of the Technical University of Munich (TUM). We would like to fill the following permanent vacancy in Garching as soon as possible **Radiochemist R&D (f/m/d)** **Your role** * Method development for (radio) HPLC, ICP-MS, IC * Development of separation methods for rare earth elements and actinides * Development of manufacturing processes of novel radionuclides * Gamma spectrometry, alpha spectrometry, liquid scintillation counting * Equipment qualification and maintenance * Writing SOPs for devices and methods * Creation of scientific reports and development plans * Supporting technology transfers **Your profile** * Higher education in Chemistry, Chemical engineering or Radiochemistry * Strong experience and knowledge in radioactive material handling * Experience and knowledge in radioanalytical methods (e.g. gamma spectrometry) * Strong experience and knowledge in radiochemical separation methods, such as liquid/liquid extraction, solid phase extraction, cation- and anion chromatography. * “Fachkunde im Strahlenschutz” preferred * Ability to work both independent and in a team * “Hands-on” mentality * Creativity, problem solving skills * Good English skills, both spoken and written * Exciting challenges in an up-and-coming and fast-growing company with a high degree of creative freedom * An open working atmosphere in an international corporate culture with short communication channels * Comprehensive onboarding programme * Flexible working hours with home office options * Attractive special payments + Employee participation programme + Job bike or subsidised job ticket + Above-average contribution to the company pension scheme + Individually tailored further training programme (including German and English courses) + Health promotion programmes (e.g. subsidy for local fitness studio, sponsorship of sporting events, various lifestyle coaching sessions) When you apply, please let us know your earliest possible starting date and your salary expectations. You can submit your CV in German and English in docx or pdf format. Deborah Angelè ************************** ITM Isotope Technologies Munich SE Human Resources Walther-von-Dyck-Str. 4 85748 Garching/München, Deutschland **Note for recruitment agencies** Please note that we do not accept unsolicited applications or offers of assistance. The telephone number given in the advertisement is intended exclusively for applicants and should not be contacted for any other purpose. Thank you very much! **More about ITM** With us, you will have the opportunity to work in an international environment on ground-breaking projects that can have a significant impact on cancer care worldwide. We are looking for dedicated, talented and passionate professionals who share our vision and want to help shape the future of oncology. If this exciting challenge appeals to you and you would like to contribute to realising our common goal, please do not hesitate to send us your application. We look forward to hearing from you! For more information please visit: ***********************

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, but few options. **Who We Are:** **What We Do:** Neurocrine Biosciences is a neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, endocrine and psychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson's disease, endometriosis* and uterine fibroids*, as well as clinical programs in multiple 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. **in collaboration with AbbVie* **About the Role:** Supports In Vitro Pharmacology drug discovery efforts across multiple projects. Provides consistent bioanalytical support, utilizing LC-MS/MS technology. Works and learns analytical instrumentation, regularly performs bioanalytical assays, and conducts assay optimization tests. Responsible for documenting protocols, maintaining attention to detail, and presenting clear written and verbal data summaries at meetings.\_ ******Must be local - no relocation will be offered****** **Your Contributions (include, but are not limited to):** * Performs routine bioanalytical assays to support in vitro and/or in vivo efforts * Supports a range of activities, including LC-MS instrument operation, maintenance and troubleshooting * Assists in assay development, optimization, and exploratory studies * Interacts with in vitro/in vivo team to learn various aspects of drug discovery and provide bioanalytical support * Tracks and documents instrument and assay performance * Provide accurate documentation of protocols with clear presented written summaries in addition to frequent verbal data summaries * Other duties as assigned **Requirements:** * BS/BA degree in biological sciences preferably related to behavioral neuroscience, pharmacology or biopsychology neuroscience and some relevant industry experience * Experience operating and troubleshooting UPLC-MS systems (Chromeleon preferred) * Familiarity with High Resolution, qTime of Flight, and/or Triple Quad MS systems * Ability to interpret chromatographic and mass spectrometry data (small molecule focus) * Competency to perform assays consistently, efficiently and identify issues if presented * Ability to recognize patterns or inconsistencies in data and instrumentation * Ability to work individually and as part of a team * Good computer skills, knowledge of Excel, Powerpoint * Developing communications, problem-solving, analytical thinking, planning and organization skills * Understands importance of meeting deadlines * Collaborative and highly motivated * Ability to keep accurate records * Academic and working knowledge of analytical chemistry, chromatography, mass spectrometry, molecular biology, in vitro biological assays #LI-OB1 Neurocrine Biosciences is an EEO/AA/Disability/Vets employer. We are committed to building a diverse, equitable, and inclusive workplace, 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.

The successful and highly motivated candidate will evaluat e the activity of small molecule inhibitors in cell-based assays for oncology drug discovery. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will actively contribute to develop cell-based functional assays and problem resol ving , reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet deadlines. **ESSENTIAL DUTIES AND RESPONSIBILITIES:** May d evelop new methodologies and laboratory protocols in conducting general research duties within assigned area of responsibility. Maintains familiarity with current scientific literature relevant to the research experiments or program. **SUPERVISORY RESPONSIBILITIES:** **EDUCATION/EXPERIENCE/SKILLS:** **Education:** BS/BA degree in related discipline and a minimum of two years of related experience; or, MS/MA d egree in related discipline and a minimum of one year of related experience; or, Equivalent combination of education and experience. **Experience:** **Knowledge/Skills/Abilities:** General knowledge of cellular, biochemical and molecular techniques, theories and practices. Ability to effectively capture data and results. Familiarity with genomic databases is a plus. Strong communication skills , excellent work ethics, self- motivated and work effectively both in a team environment and independently. Computer proficiency including MS Word, MS PowerPoint and MS Excel required . Every Exelixis employee is united in an ambitious cause: to launch innovative medicines that give patients and their families hope for the future. In this pursuit, we know our employees are our most valuable asset. After operating in the challenging biotech sector for 25 years, we have a proven track record of resiliency in the face of adversity. The success of our lead product has provided a solid commercial foundation allowing us to reinvigorate our research efforts, and grow our team in areas such as Drug Discovery, Clinical Development and Commercial. As we expand our global partnerships and further reinvest in R&D to help us discover the next breakthrough for difficult-to-treat cancers, we're seeking to add talented, dedicated employees to power our mission. Cancer is our cause. Make it yours, too.