Senior Scientist Jobs At Boehringer Ingelheim

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Catalent Pharma Solutions in San Diego is a premier pharmaceutical chemistry development and manufacturing organization supporting the pharmaceutical and biotechnology industries. We focus on bringing client drug compounds from discovery to the clinic with services that include analytical development, pre-formulation testing, formulation development, Good Manufacturing Practices (GMP) manufacturing and stability storage and testing as well as Clinical Supply Services. Catalent Pharma Solutions is hiring a Principal Scientist for Product Development at our San Diego, CA site. An individual at the level of Principal Scientist, Product Development will lead projects as an individual or build a team focused on oral formulation development for small molecule or peptide drug products and amorphous intermediates. This individual may be required to have direct reports depending on growth and ability. The primary formulation platforms will include tablets, capsules, granules, beads, solutions, suspensions, immediate release and extended-release dosage forms, and amorphous intermediates. The individual will research and introduce new formulation technology to produce and characterize drug products and will be the primary point of customer contact for formulation strategy, compliance, and troubleshooting. All duties will be performed in compliance with company standard operating procedures (SOPs) and GMP regulations, as appropriate. This is a full-time position: Monday - Friday, 8am-5pm on-site with flexibility for periodic remote/hybrid work. The Role: Creates and develops innovative drug formulations and has depth of experience in one or more of the techniques described above. Performs and trains others on a variety of formulation techniques including, but not necessarily limited to: blending, encapsulation, suspensions, solutions, wet/dry/fluid bed granulation, tablet compression, coating, milling, spray drying. Responsible for the successful transfer of formulation projects to the GMP manufacturing team and for collaboration with process engineering team during technology transfer. Communicates results both internally and externally through oral and written updates and formal reports as necessary. Organize meetings and monitor all client interactions independently. Participate in and lead cross-functional teams. Individuals will stay abreast of current scientific technologies to maintain the state-of-the-art nature of Catalent's services and will evaluate new technologies to expand our technical service offering. Individuals will support the business aspects of their position by taking responsibility for the execution and billing communication for all work proposals under their supervision. Hire, train, and supervise formulation group members as necessary. Develop junior personnel for advancement within the team. Participate in business development and marketing activities by generating scientific expert content, hosting new client visits or teleconferences, and attending conferences or client visits to generate new leads. Other duties as assigned. The Candidate: 4-year degree (Bachelor's/B.S.) in a physical, chemical, biological, or pharmaceutical science required plus a minimum of eight years of oral formulation development experience. We will also consider candidates who have a Master of Science (M.S.) with six years' experience, or PhD with four years of experience in oral formulation development. Must have managed at least 1-2 people in the past. Must have oral formulation development experience (Tablets, capsules, granulation experience required). Strong preference for early phase development (preclinical, phase 1, and phase 2 with new chemicals/small molecules). Experience in a client-facing role is a plus, but not a must-have. Demonstrable leadership experience at Catalent may be considered in place of external experience. Physical Requirements: On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 25 pounds. Pay: The anticipated salary range for this role in San Diego, CA is $145,000 - $170,000 annually. Why you should join Catalent: Awesome employee activities. Environmentally friendly green initiatives. Defined career path and annual performance review. Several Employee Resource Groups focusing on Diversity and Inclusion. Competitive salary with bonus potential. 152 hours of PTO + 10 paid holidays. Positive and fast-paced working environment. Tuition Reimbursement. WellHub program to promote overall physical wellness. Perkspot - offers exclusive discounts. Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email. #J-18808-Ljbffr

Principal Scientist 1, In Vitro Pharmacology Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. Join our team as we transform the lives of others. Position Summary: We are seeking a highly motivated and collaborative Principal Scientist 1 with experience in GPCR pharmacology and drug discovery to join our growing and dynamic Biology team. A successful candidate will be responsible for providing in vitro pharmacology support for lead optimization campaigns, mechanism of action studies, and new target efforts in endocrinology. Essential Job Functions and Responsibilities: Lead and manage a small team of junior scientists, promoting collaboration, efficiency, and innovative science. Design, develop, validate, and execute in vitro assays that support drug discovery programs. Conduct critical analysis and interpret data into a meaningful understanding of small molecule ligand activity and mechanism of action. Demonstrate a high level of initiative to oversee, troubleshoot, and accurately perform data analysis in an environment that values scientific integrity and quality. Conduct resource management to deliver critical in vitro pharmacology data to support multiple programs simultaneously. Lead and/or provide in vitro pharmacology leadership role on cross-functional program teams. Interpret and demonstrate effective written and oral communication of results to interdisciplinary teams. Participate in the strategic planning of departmental growth and organization. Lead external collaborations and outsourced studies. Identify and evaluate new research targets within therapeutic areas of interest. Author scientific publications and prepare technical reports to support regulatory submissions. Ensure compliance with company-established practices and procedures, including laboratory notebooks, computer files, quality and regulatory guidelines, and safety standards. Education and Experience: Required: Ph.D. in Pharmacology, Biochemistry, Biology, or related discipline with at least 8 years of relevant experience. Applicants with a bachelor's degree must demonstrate a minimum of 15 years and those with a master's degree must demonstrate 13 years of significant and relevant experience. At least 7 years of experience with drug discovery and small molecule pharmacology in therapeutically relevant GPCRs or related fields. Demonstrated technical proficiency in biochemical, cellular, and/or radioligand binding assay systems. Ability to independently determine in vitro pharmacologic methods and procedures to achieve Program goals. Outstanding experimental design, problem-solving, and data analysis skills. Demonstrated practical experience and deep understanding of in vitro pharmacological theory, models, mechanisms, and experimental design, particularly with GPCRs. Must be independent and able to follow pre-established experimental designs, as well as develop new methods, protocols, and technologies based on existing literature. Strong work ethic and enthusiasm for a mix of laboratory work and management in a dynamic environment. Strong communication skills and the ability to work closely and effectively in a multidisciplinary team environment. Experience in management and daily supervision of scientific staff is highly preferred. Experience in program management/leadership desired. Strong written and verbal communication skills. Experience with writing reports and technical regulatory documents. Must be detail-oriented, punctual, and reliable. Ability to work in a fast-paced environment and adapt to change. Physical Demands and Work Environment: Physical Activities: On a continuous basis, sit at desk for a long period of time; intermittently answer telephone and write or use a keyboard to communicate through written means. Some walking and lifting up to 25 lbs. may be required. Laboratory Activities: Biology and chemical laboratory environment experience needed. Environmental health and safety requirements also apply. Travel: You may be required to travel for up to 5% of your time. The Anticipated Base Salary Range: $148,000 - $185,000 In addition to your base pay, our total rewards program consists of a discretionary annual target bonus, stock options, ESPP, and 401k match. Equal Opportunity Employer: Crinetics is proud to be an Equal Opportunity Employer. We provide equal employment opportunities to all employees and employment applicants without regard to unlawful considerations of sex, sexual orientation, gender, pregnancy, race, color, creed, national or ethnic origin, citizenship status, religion or similar philosophical beliefs, disability, marital and civil union status, age, genetic information, veteran status or any personal attribute or characteristic that is protected by applicable local, state or federal laws. Vaccination requirement: Crinetics requires that all employees and contractors be fully vaccinated and have received the COVID-19 vaccines as a condition of employment. #J-18808-Ljbffr

Title: (Senior) Scientist, Cardiovascular Diseases Salary: $125,000-$145,000 EPM is currently partnered with clinical stage biopharmaceutical company with an exciting pipeline that shows preclinical promise in a broad range of clinical indications. Two lead assets are currently in early phase clinical developments, and on track for further clinical development this year. The leadership team brings over 25 years of success, with FDA-approved therapies, IPO launches, and multiple strategic biotech exits, along with deep connections across life sciences and venture ecosystems. Backed with resourceful funding and high-value partnerships in biotech and top-10 pharma, the company is well-positioned to reinvest into R&D, while advancing their current clinical pipeline in CNS and Fibrotic indications. They have identified that their platform naturally aligns with cardiovascular biology and are expanding into this area to drive the next wave of first-in-class therapies Key Responsibilities: Lead target discovery, identification, and validation efforts focused on cardiovascular and cardiometabolic diseases, leveraging a cutting-edge small molecule discovery platform. Design and execute in vitro and cell-based assays to interrogate target biology, disease-relevant pathways, and compound activity across cardiovascular indications (e.g., atherosclerosis, vascular remodeling, heart failure, and fibrosis). Collaborate cross-functionally with chemistry, translational, and clinical teams to ensure alignment between discovery biology and downstream development strategies. Apply deep knowledge of vascular biology, endothelial dysfunction, inflammation, and metabolic signaling to guide biological validation of new targets. Analyze and interpret complex data sets, integrating findings into broader disease biology and drug discovery programs. Contribute to the development of the cardiovascular research strategy, incorporating new technologies, disease models, and biomarker approaches to support target prioritization and lead optimization. Stay current with emerging science and competitive landscape in cardiovascular and cardiometabolic drug discovery, providing scientific insights to shape pipeline expansion. Key Skills & Qualifications: PhD in Cardiovascular Biology, Vascular Biology, Pharmacology, or a related discipline, with 3+ years of relevant industry experience(open to strong postdocs looking to transition). Deep expertise in cardiovascular disease biology, including knowledge of vascular dysfunction, endothelial biology, cardiomyocyte biology, cardiac fibrosis, and metabolic signaling. Hands-on experience with target discovery techniques such as: CRISPR screening RNA sequencing & omics data interpretation Biochemical and cellular assays to study target function (reporter assays, phenotypic screening, pathway modulation). Strong foundation in in vitro pharmacology- assay development, compound profiling, and mechanism-of-action studies for small molecules. Ability to work in a highly collaborative environment, communicating effectively with medicinal chemists, translational biologists, and external partners. Experience working within a small to mid-sized biotech environment is a plus - comfort operating in a fast-paced, evolving R&D setting. Passion for cardiovascular discovery and desire to play a hands-on role in shaping pipeline strategy in an innovative biotech setting.

What the Senior Scientist in Biomarker Analysis does at Worldwide As a Senior Scientist in Biomarker Analysis, you will be a key contributor to our bioanalytical team. Your role involves method development, validation, and sample analysis for ligand binding assays. You'll work closely with the supervisor to ensure accurate and efficient execution of bioanalytical processes. If you're passionate about advancing bioanalysis research and have a strong foundation in bioanalysis, this role is for you. What you will do Involve efficiently manage biomarker research projects from initiation to completion. Help project manager to ensure adherence to project timelines and budget constraints. Collaborate with cross-functional teams to achieve project goals. Engage with clients to understand their requirements, expectations, and feedback. Maintain effective communication channels throughout the project lifecycle. Provide troubleshoot for junior team member: troubleshoot experiments and address any technical challenges promptly. Optimize processes to enhance efficiency and data quality. Work closely with QA/QC teams to maintain high-quality standards. Ensure compliance with relevant regulations and guidelines. Manage project-related documentation. Review scientific literature to understand existing methods for detecting and quantifying biomarkers. Explore studies related to biomarker concentrations and their relevance in various diseases. Formulate a comprehensive strategy for biomarker testing across different platforms. Consider using techniques like MSD (Meso Scale Discovery) and PCR (Polymerase Chain Reaction). Ensures Inspection Readiness for risk assessment and centralized monitoring scope. What you will bring to the role Proficient in MSD, ELISA, and PCR is a plus. Experienced in LIM system is a plus. Strong analytical skills and attention to detail. Proficiency in general laboratory practices and techniques. Ability to work independently and as part of a team. Ability to read, execute, and understand complicated and detailed instruction and technical literature to plan, perform, and direct laboratory activities. Must be able to work well with a variety of laboratory personnel. Strong written and oral communication skills Basic computer knowledge Your experience Education: minimal request: bachelor's degree in a scientific discipline (Immunology, molecular biology, biochemistry, or related field). Master's degree and Ph.D. are plus. Experience: minimal request: bachelor's degree with a minimum of 10 years of direct laboratory experience. Master's degree with 5 year of direct laboratory experience. BSc/RN or equivalent combination of knowledge, skills and experience

Scientist/Senior Scientist - In Vitro Diagnostics (IVD) Test Development Reports To: Senior Director, IVD Test Development A growing team is looking for a Scientist/Senior Scientist with expertise in in vitro diagnostic (IVD) assay development to lead research projects, contribute to scientific innovation, and oversee Validation & Verification studies supporting PMA, 510K, and IVDR approvals. This position requires working within a regulated environment under design control, managing project timelines, analyzing data, and mentoring junior scientists. Additionally, the role may involve handling human biological specimens (blood, plasma, urine, and other bodily fluids) while ensuring compliance with safety regulations and organizational policies. Key Responsibilities: Oversee project studies that contribute to regulatory filings while effectively managing multiple unrelated projects. Design and refine study protocols, ensuring scientific rigor and compliance with CLSI guidelines and regulatory standards. Execute and document product development activities in alignment with design control procedures and quality management systems. Independently perform statistical analyses or collaborate with statisticians to evaluate data. Analyze and interpret experimental results, providing insights and determining next steps for project advancement. Ensure data accuracy and validity for internal reports, regulatory submissions, and scientific publications. Prepare comprehensive and well-structured study reports for regulatory documentation. Develop and deliver data-driven presentations to internal teams and external stakeholders. Lead technical discussions, drive project meetings, and ensure strategic alignment with company goals. Supervise and mentor junior scientists, fostering a culture of innovation and scientific excellence. Maintain compliance with safety guidelines, including biosafety and hazardous material handling protocols. Perform other duties as required. Required Qualifications & Experience: Education & Experience: Ph.D. in Biology, Biochemistry, Molecular Biology, Biomedical Engineering, or a related field with 7-12 years of industry experience. Master's degree with 10-15 years of relevant experience. Bachelor's degree with 16-20 years of experience. Technical Expertise: Extensive experience in IVD product development, with strong knowledge of FDA and global regulatory requirements. Hands-on experience creating protocols and reports suitable for regulatory submission. Proficiency in statistical analysis software (Analyze-It, JMP). Experience in commercial IVD product development is preferred. Leadership & Analytical Abilities: Demonstrated ability to lead research teams and effectively manage multiple projects. Strong analytical and problem-solving skills, with expertise in data interpretation and statistical analysis. Ability to troubleshoot complex technical challenges and drive research forward. Communication & Collaboration: Proven experience in developing high-quality scientific reports, publications, and presentations. Excellent verbal and written communication skills, with confidence in presenting findings to diverse audiences. Strong interpersonal skills for mentorship and cross-functional collaboration.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $69,000 - $179,300. Overview: At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism. Position Summary: Lilly Oncology's Large Molecule Discovery team is looking for a Principal Scientist in Chemistry/Biochemistry to support our growing biologics portfolio. This role will support Antibody-drug conjugates (ADCs) linker and payload design, develop conjugation technologies, and downstream biochemical assays to enhance ADC biological and pharmacologic properties. We are looking for a strong scientist with good knowledge and hands-on experience in designing, preparing, and characterizing ADCs. This individual will be a self-motivated, responsible, and productive scientist who enjoys collaborating. He/she will be responsible for rigorous experimental design, data analysis, and data interpretation. This position requires excellent people skills, a positive can-do attitude, and the ability to thrive in a highly interactive, fast-paced, team environment. Responsibilities: Prepare, purify, and characterize the high-quality antibody-conjugates (ADCs, ARCs, DACs etc.) with a high degree of independence in support of discovery and development of programs. Implement state of the art bioconjugation technologies (cysteine, lysine, site-specific and other) and utilizing novel chemistries to generate bioconjugates. Experienced in development of purification strategies (up to 200 mg) with affinity, ion-exchange, hydrophobic interaction, size exclusion, and tangential flow filtration. Experienced in ADC characterization methods, including UV-Vis, SEC, HIC, RP, IEX, cIEF, and LC-MS. Maintain thorough documentation of experimental procedures in electronic notebook or database, writing of reports and technical documents. Maintain scientific and technical expertise through familiarity with scientific literature and attending conferences. Engagement with multidisciplinary project teams to design, execute, and interpret experiments. Demonstrated record of scientific accomplishments and publications. Participate and present periodic updates and reports to management team. Participate in long-term strategies for creation of innovative solutions and intellectual property for securing FTO for Lilly. Maintain a safe, pleasant, and efficient working environment. Basic Requirements: A minimum of a bachelor's degree in chemistry, Biochemistry, or other related scientific discipline with a record of minimum 4 years lab-based independent research experience is required. Advanced degree (Master's, Ph.D.) with 2+ years of relevant experience is preferred. Deep expertise in using state-of-the-art conjugation methods and handling of highly potency cytotoxic payloads. Additional Preferences: Strong hands-on experience producing and characterizing antibody and protein drug conjugates using HIC, SEC, LC-MS, IEX, and RP-HPLC. Experience with protein purification systems is preferred with hands-on experience and proficiency working with AKTA FPLCs. Must be highly collaborative and able to effectively engage small-molecule research project teams to make rapid progress. Demonstrated ability to work well with other accomplished professionals within and across functions/teams. Ability to multi-task and shift priorities rapidly to meet tight deadlines. Excellent written and verbal communicator. Detail oriented and well organized. Enthusiastic, self-motivated, and keen to improve processes. Additional Information: Physical Demands/Travel: The physical demands of this job are consistent with a laboratory/bench environment. Some light lifting, and maneuvering may be required. Work Environment: This position's work environment is in a laboratory/bench environment. #J-18808-Ljbffr

Summary: The R&D Formulator develops and optimizes formulations, conducts testing, and ensures accurate documentation. Supports technology transfer, collaborates cross-functionally, and stays updated on industry trends. Maintains lab safety, mentors staff and participates in management meetings. Evaluates raw materials, improves formulations, and oversees special projects as assigned. Essential Duties and Responsibilities Formulation creation (bench mix, formulation sheet, product description sheet, sample measurement, color verification, etc.) Writes and/or reviews procedures, purchase orders, quotes, and specifications needed to support product development activities Develops and/or performs all formulation requirements on new formulas Documents test results, specifications, and final formula procedures in a standard format for inclusion in the master file Participates in the technology transfer from pilot scale to manufacturing Communicates, in a timely fashion, all information regarding formulation, project status, raw material research, results, etc. to all appropriate individuals in Purchasing, Sales, Customer Services, and Quality departments Conducts intellectual searches for technical information through a variety of resources Keeps abreast of current trends, practices, developments, and regulatory changes, which would impact products, procedures, or formulation Ensures the maintenance and/or adherence to good laboratory practices and all safety regulations both in laboratory and manufacturing areas Provides technical knowledge in guiding other assistants/technicians in the R&D Lab Develops and presents to the R&D Manager or Director, R&D matters requiring his/her decision Participates in scheduled Management and Sales meetings in the absence of the R&D Manager/Director Evaluate new and alternative raw materials for functionality and stability Assist in verification studies as required Reformulate to improve existing products as needed Special projects as needed and any other tasks assigned by the R&D Director or Manager. Qualifications/Education/Experience: Minimum Bachelor of Science in Chemistry or related field 2+ years' Experience in R&D, Quality Assurance, Quality Control or Manufacturing is required; nutritional, pharmaceutical or biotechnology experience preferred; Have strong eye for color, finish, and detail Must have proficient math skills; weights and volumes experience a plus Excellent communications (verbal/written) Excellent organizational and multi-tasking skills Proficient with MS Word, Excel, Teams, and Outlook Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to work near moving mechanical parts, fumes, or airborne particles and risk of electrical shock. The noise level in the work environment is usually moderate. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Physical demands require sitting for extended periods of time, walking, bending, reaching, carrying, and occasionally lifting and/or moving objects up to 25 pounds. Specific vision abilities required by this job include Close vision, Peripheral vision, and the ability to adjust focus. While performing the duties of this job, the employee is occasionally required to use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and talk or hear.

Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. What will you do? Responsible for developing innovation technologies and Taste solutions in the area of reaction flavors (Maillard reaction), contributing to the growth objectives of the Global Taste Innovation Platforms. Expertise in Maillard reactions, with focus on thermal generation of flavors, comprehensive understanding of interactions between reducing sugars with amino acids. Research experience of reaction chemistry within the flavor categories of: savory, dairy, brown tonalities and taste modulation. Work on global projects, delivering results against technology gaps and needs in Kerry by collaborating closely with key stakeholders and partnering departments including regional Flavorist technology champions, RD&A Scientists and Technologists, Portfolio Manager, Marketing, Sensory, End use market business teams, Operation, and Regulatory. What will you need to be successful? Bachelor's of Science with 10+ years of experience, Master of Science with 6+ years of experience or Ph.D. with 4+ years in organic chemistry or analytical chemistry or food chemistry, chemical Engineering or related science. Strong research track record in reaction flavors, Maillard chemistry, and relevant analytical skills. Analytical skills for gas chromatographic systems with several detectors as FID, pFPD, MSD, and MSMS; GCO for characterization of key Savoury and smoke aroma components and off notes. Expertise in Maillard chemistry, ability to explain mechanisms; Need for skills that can decipher competitive complex flavors, reaction notes, characterize top notes, as well as work closely with flavorist and culinary teams. Create methods that are more sensitive Development of methods for the generation and detection of important intermediates using Py/GC/MS, HPLC, FTIR and other analytical techniques. Structural elucidation of reaction mechanisms using 13C- and 15N-labeled reactants is one of the main objectives of the research program. Compensation Data The typical hiring range for this role is $91,311 to $134,638 annually and is based on several factors including but not limited to education, work experience, certifications, location, etc. In addition to your pay, Kerry offers benefits such as a comprehensive benefits package, incentive and recognition programs, equity stock purchase and retirement contribution (all benefits and incentives are subject to eligibility requirements). Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at: Know Your Rights: Workplace Discrimination is Illegal (dol.gov). Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a “starter kit,” investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.

Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. About the role Plays a key role in the profit enhancement and business growth of Kettle. Supports RD&A with analyses, tests, and experimental designs at the manufacturing level. Will be based in Ft. Worth (manufacturing facility),and work closely with production and corporate R&D teams to scale up items. Responsible for implementing trials successfully to drive business growth through formulation and process improvements. What will you do? Work with team to design and conduct research including new product research and the development of foods. Work with Sales, RD&A and Culinary teams to field customer requests both internal and external to satisfy project needs from a conceptual phase through troubleshooting and commercialization. Work with cross functional groups to optimize the strengths of Kerry and deliver the best Taste and Nutrition experience for our customers What will you need to be successful? BS/MS/PhD in Food Science/related science field. Strong background in food chemistry, sensory, microbiology, food packaging systems. Food engineering or product development expertise in related field. Core understanding of food safety and quality Demonstrated ability to work well on team projects Compensation Data The typical hiring range for this role is $75,602 to $111,475 annually and is based on several factors including but not limited to education, work experience, certifications, location, etc. In addition to your pay, Kerry offers benefits such as a comprehensive benefits package, incentive and recognition programs, equity stock purchase and retirement contribution (all benefits and incentives are subject to eligibility of the requirements). Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at: Know Your Rights: Workplace Discrimination is Illegal (dol.gov).

Title: Analytical Scientist About the Company Are you passionate about groundbreaking science and innovative healthcare solutions? We are a rapidly growing, well-funded biotech company with a hybrid platform that combines both innovative and specialty products. Our mission is to revolutionize the biotech industry by developing cutting-edge therapies and specialty products that address unmet medical needs. Job Description As an Analytical Scientist, you will play a crucial role in our research and development efforts. You will be responsible for developing and validating analytical methods from scratch, ensuring compliance with Good Manufacturing Practices (GMP), and utilizing advanced analytical techniques to support our projects. Key Responsibilities Develop and validate analytical methods independently. Perform routine and non-routine analysis using techniques such as High-Performance Liquid Chromatography (HPLC), Mass Spectrometry (MS), and UV-Visible Spectroscopy (UV-Vis). Ensure all work complies with GMP regulations and standards. Troubleshoot and optimize analytical methods and instrumentation. Document and report analytical data accurately and promptly. Collaborate with cross-functional teams to support product development and quality control. Maintain and calibrate analytical instruments and equipment. Qualifications Bachelor's, Master's, or Ph.D. in Chemistry, Analytical Chemistry, or a related field with minimum 2 years GMP industry experience. Proven experience in developing analytical methods from scratch. Strong knowledge of GMP regulations and practices. Proficiency in using HPLC, MS, and UV-Vis techniques. Excellent problem-solving skills and attention to detail. Strong communication and teamwork abilities. Ability to work independently and manage multiple projects simultaneously. Benefits Competitive salary and benefits package. Opportunities for professional growth and development. Collaborative and inclusive enviornment

What the Research Associate 1 does at Worldwide The Research Associate 1, has have familiarity with processing and reviewing clinical documentation, interacting with participants, and accommodating competing priorities in a dynamic clinical research environment. What you will do Conducts screening visits for participant recruitment into clinical trials under the supervision of the Screening Supervisor. Reviews study protocol and informed consent form for studies they are assigned to. Ensures electronic and paper source documents for the trial are accurate according to study specific protocol. Prepares and maintains study-specific screening documents and study folders. Responsible for reviewing the informed consent form, medical history, inclusion/exclusion criteria, and other study documents as required with participants to determine eligibility. Serves as primary contact for participants from screening through check-in for studies. Addresses all questions from participants related to study eligibility, study participation, and/or concerns What you will bring to the role Excellent written and oral communication skills. Ability to understand complex written and oral instructions. Excellent attention to detail resulting in high-quality work. Exceptional organizational skills. Ability to set and meet deadlines. Your experience Bachelor's Degree (preferably in the field of Life Sciences or Health). Six months or more experience in health care.

Florida Job Description: As an Analytical Scientist, you will play a crucial role in our research and development efforts. You will be responsible for developing and validating analytical methods from scratch, ensuring compliance with Good Manufacturing Practices (GMP), and utilizing advanced analytical techniques to support our projects. Key Responsibilities: Develop and validate analytical methods independently. Perform routine and non-routine analysis using techniques such as High-Performance Liquid Chromatography (HPLC), Mass Spectrometry (MS), and UV-Visible Spectroscopy (UV-Vis). Ensure all work complies with GMP regulations and standards. Troubleshoot and optimize analytical methods and instrumentation. Document and report analytical data accurately and promptly. Collaborate with cross-functional teams to support product development and quality control. Maintain and calibrate analytical instruments and equipment. Qualifications: Bachelor's, Master's, or Ph.D. in Chemistry, Analytical Chemistry, or a related field with minimum 2 years GMP industry experience. Proven experience in developing analytical methods from scratch. Strong knowledge of GMP regulations and practices. Proficiency in using HPLC, MS, and UV-Vis techniques. Excellent problem-solving skills and attention to detail. Strong communication and teamwork abilities. Ability to work independently and manage multiple projects simultaneously. Benefits: Competitive salary and benefits package. Opportunities for professional growth and development. Collaborative and inclusive work environment. Cutting-edge laboratory facilities and resources.

Vertex is seeking an experienced scientist eager to help develop both cutting-edge small molecule as well as synthetic peptide and oligonucleotide-based pharmaceuticals and the science underpinning the analytical control of their syntheses. As a member of the Analytical Development team, this role will support drug development programs at Vertex with a focus on drug substance process and control strategy development for both small molecules and oligonucleotide-based therapies. Specifically, the individual will help design the tests and control strategy for novel drug substances, collaborate closely with associated CM&C functions, and act as a subject matter expert liaison with our global network of external drug substance manufacturing and development vendors. The ability to develop novel and creative solutions to overcome project obstacles and make significant conceptual contributions to project teams are criteria for success. Key Duties and Responsibilities: Collaboratively design and oversee drug substance process development analytical activities across all phases of development, including late phase development following Quality by Design (QbD) principles. Serves as subject matter expert for setting and justifying drug substance, intermediates, and starting materials specifications with the understanding of clinical study design, supporting toxicology studies, and CMC processes. Identify critical in-process-control issues and develop appropriate IPC methods. Serve as the subject matter expert for drug substance analytical development with contract manufacturing and testing labs. Develop analytical methods, suitable for progressive stages of pharmaceutical development and/or supervise activities. Justify and set retest period, storage, and shipping conditions for starting materials and intermediates. Understand chemical development and solid-state development to identify and document critical factors that impact method performance and/or analytical development activities. Develop and review source documents for regulatory submissions. Present to cross functional teams and effectively communicate critical analytical issues and solutions. Knowledge and Skills: Excellent verbal and written communication skills are essential. Experience and/or working knowledge of control strategy development, spike/purge studies, drug substance QbD process development. Good understanding of cGMP, ICH, FDA, and USP guidelines, including ICH guidelines on the control of impurities (organic, residual solvents, and elemental, DNA reactive (including ICH M7 option 4 / in silico control), and nitrosamines). Skilled in modern analyses for peptides, oligonucleotides, and/or small molecule pharmaceuticals, particularly chromatography. The ability to work successfully in both a team/matrix environment as well as independently. The ability to work in a fast-paced environment, manage priorities, communicate outcomes and maintain timelines for multiple projects. Education and Experience: Ph.D. with 4-7 years of relevant analytical development experience, particularly focused on development of novel drug substances. Exceptional candidates with MS or BS degrees and extensive high-level experience will also be considered. Background in, or good understanding of modern synthetic organic chemistry, as well as of the drug substance development process, process chemistry, and pharmaceutical manufacturing, and their interrelationship with analytical development. Hands-on experience in the analysis and familiarity with the control strategy of synthetic peptide and oligonucleotide-based pharmaceuticals. Flex Designation: On-Site Designated Flex Eligibility Status: In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility. Company Information Vertex is a global biotechnology company that invests in scientific innovation. Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. #J-18808-Ljbffr

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at *************** Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description We are seeking a highly motivated and creative Scientist with a scientific background in immunology or immuno-oncology to join Precision Medicine Translational Research Immunology Group as Principal Scientist at AbbVie. The candidate will provide leadership in clinical biomarker strategy and assay development in inflammatory/autoimmune disease areas, including Dermatology, Gastroenterology, Rheumatology and Fibrosis for AbbVie's drug development programs from late discovery to clinical trials. The successful candidate will be part of a growing translational research group working with cross-disciplinary teams both internally and externally. Key Responsibilities: Lead biomarker strategies through cross-functional teams in a matrix environment to identify gaps and develop fit-for-purpose clinical TE/PD biomarker, predictive and exploratory biomarker assays to support human dose projection and establish early signs of efficacy in clinical trials and patient selection strategies. Collaborate with Data Science team and Precision Medicine lead to analyze internal and external omics data, understand heterogeneity of diseases, identify disease endotypes, support disease strategy and generate patient selection and combination hypotheses for further testing with preclinical studies. Develop preclinical patient derived disease models, design studies with appropriate controls and endpoints to understand drug target mechanisms for PD biomarker development and evaluate biomarker hypotheses and combination strategies. Serve as a subject matter expertise in analytical methodologies/technologies for translational research including single cell and spatial omics, proteomics, methylomics, metabolomics, genomics, NGS, MSD, ELISA, Luminex, flow cytometry, ex vivo primary cell culture and organoid-immune cell culture. Manage external CROs and academic collaborations including study proposal, budget, timeline, and data review. Manage and coach a team of translational scientists, ensuring the successful execution of translational research plans across multiple projects. Keep abreast of latest research & development in inflammatory and immune diseases through critically reviewing literature, attending conferences, and seeking advice from KOLs. Qualifications Major or advanced degree in Immunology, cell & molecular biology, pharmacology, pathology, bioinformatics or other relevant biological sciences. B.S. & typically 14+ years, M.S. & typically 12+ years, Ph.D., or equivalent & typically 8+ years of relevant industrial biotechnology experience. Experience in leading translational medicine in Rheumatological diseases (RA, SLE, SSc) is a plus. Expertise in a broad range of translational technologies, data analytics and computational tools. Proficient in multi-parameter flow cytometry, including spectral flow cytometry and analytical software (e.g., BD FACSDiva, Flowjo, OMIQ) to analyze different immune cell types and cell states from mice, human and cynomolgus monkey. Experienced in designing and conducting single cell omics, spatial omics, genomic-based assays and developing analytical workflow to generate or validate biomarker hypotheses. Knowledgeable with integrative analysis of multi-dimensional datasets using bioinformatics tools and methods (e.g., R, Python, SQL, AI/ML, HPC and cloud environments) Strong project leadership and organizational skills to prioritize tasks and allocate resources to meet projects' goals in a tight timeline. Experienced in managing CROs and collaborators, facilitating meetings, and working independently and collaboratively with multi-functional teams in a dynamic and fast paced environment. Demonstrated ability to supervise and coach direct reports. Excellent communication, presentation, organizational and people management skills Strong track-record of scientific publications from peer reviewed journals and presentations in major conferences Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit ************************************************************************* US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: ************************************************************* #J-18808-Ljbffr

AbbVie Parenteral Product Development Science & Technology (PDS&T) is a global organization responsible for all CMC activities related to the development and commercialization of AbbVie's parenteral products. Our scope includes AbbVie's diverse pipeline of innovative therapeutic biologics medicines, including monoclonal antibodies, antibody drug conjugates (ADC), and other novel modalities, and spans from clinical proof of concept through commercial product launch. We are a world-class team of scientists and leaders driving the advancement of industry-leading analytical capabilities and AbbVie's pipeline of innovative medicines. Careers in AbbVie Parenteral PDS&T provide opportunities to work with global and cross-functional teams to develop innovative products and drive exceptional science. Job Description The Analytical Development group within Parenteral PDS&T is responsible for biologics programs that are transitioning from development stage to optimization and commercialization. We lead final method development, optimization, and validation, ensuring all analytical methods are fit for use in commercial QC laboratories. Key deliverables include product control strategies informed by analytical data and method understanding; robust analytical methods suitable for commercial QC labs; comprehensive data packages that drive product and process understanding; stability studies to establish commercial product dating; and approvable marketing application submission content. We are looking for a highly motivated person with experience in analytical development for biologics products who can oversee laboratory activities supporting analytical method development, optimization, and validation. Key Responsibilities Provide leadership and talent development for a team of scientists responsible for a suite of late-stage biologics products including monoclonal antibodies, antibody drug conjugates, bispecific antibodies, etc. Lead the design and execution of experiments for method robustness and method validation studies. Demonstrate a critical mindset for method troubleshooting, examining data holistically, and guiding and advising scientists through protocol execution. Independently responsible for project activities within area of expertise while also contributing within the project team to the overall progress of the program. Deliver results in a team-oriented setting and willing to work across scientific disciplines to drive programs through critical milestones. Effectively organize and present scientific plans and data. Author, review, and/or approve technical documents (e.g., methods, protocols, reports, etc.), scientific publications, presentations, and regulatory documents. Qualifications PhD (8+ years), Master's Degree (14+ years), or Bachelor's Degree (16+ years) in scientific discipline (e.g., Analytical Chemistry, Biochemistry, or Biology) with previous laboratory experience. Previous supervisory experience managing teams required. Practical experience and strong knowledge of protein HPLC (e.g., SEC, IEX, HIC), capillary electrophoresis (e.g., ic IEF, CE-SDS), and/or other separation techniques as applied to protein analysis is required. Practical experience with method validation and working in a GMP environment is required including designing studies, authoring protocols and reports, laboratory notebook documentation, etc. Experience with investigations, validation events, out of specification, or out of trend evaluations preferred. Familiarity with analytical Quality by Design (AQbD) preferred. Solid understanding of protein chemistry and biochemistry, particularly as related to biologics drug development, is preferred. Ability to multitask and work within timelines. Demonstrated scientific writing skills and strong verbal communication skills. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit ************************************************************************* US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: ************************************************************* #J-18808-Ljbffr

Who we are We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! What the Senior Scientific Associate, Biomarker Analysis does at Worldwide As a Senior Scientific Associate in Biomarker Analysis, you will be a key contributor to our bioanalytical team. Your role involves method development, validation, and sample analysis for ligand binding assays. You'll work closely with the supervisor to ensure accurate and efficient execution of bioanalytical processes. If you're passionate about advancing bioanalysis research and have a strong foundation in bioanalysis, this role is for you. What you will do * Conduct bioanalytical assays such as Ligand Binding Assays for example MSD (Meso Scale Discovery) singleplex and multiplex assays and ELISA assays. * Draft work-related document such as working instructions, analytical methods. * Properly handle and store biological samples in freezers and maintain accurate records of sample locations and conditions. * Prepare stocks, standards, quality controls, reagents and buffers required for ligand binding assays and other bioanalytical assays. Follow precise protocols to ensure consistency and reliability. Perform mathematic calculations. * Apply GCLP principles to maintain high-quality data and documentation. Ensure compliance with relevant regulations and guidelines. What you will bring to the role * Proficient in MSD, ELISA, and PCR is a plus. * Experienced in LIM system is a plus. * Strong analytical skills and attention to detail. * Proficiency in general laboratory practices and techniques. * Strong written and oral communication skills * Basic computer knowledge Your experience * Education: minimal request: bachelor's degree in a scientific discipline (Immunology, molecular biology, biochemistry, or related field). * Experience: minimal request: bachelor's degree with a minimum of 1 years of direct laboratory experience. Master's degree with 0-1 year of direct laboratory experience. University/college degree (life science preferred) or certification in a related allied health We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit ***************** or connect with us on LinkedIn. Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We're on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

Who we are We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! What the Senior Scientific Associate, Biomarker Analysis does at Worldwide As a Senior Scientific Associate in Biomarker Analysis, you will be a key contributor to our bioanalytical team. Your role involves method development, validation, and sample analysis for ligand binding assays. You'll work closely with the supervisor to ensure accurate and efficient execution of bioanalytical processes. If you're passionate about advancing bioanalysis research and have a strong foundation in bioanalysis, this role is for you. What you will do Conduct bioanalytical assays such as Ligand Binding Assays for example MSD (Meso Scale Discovery) singleplex and multiplex assays and ELISA assays. Draft work-related document such as working instructions, analytical methods. Properly handle and store biological samples in freezers and maintain accurate records of sample locations and conditions. Prepare stocks, standards, quality controls, reagents and buffers required for ligand binding assays and other bioanalytical assays. Follow precise protocols to ensure consistency and reliability. Perform mathematic calculations. Apply GCLP principles to maintain high-quality data and documentation. Ensure compliance with relevant regulations and guidelines. What you will bring to the role Proficient in MSD, ELISA, and PCR is a plus. Experienced in LIM system is a plus. Strong analytical skills and attention to detail. Proficiency in general laboratory practices and techniques. Strong written and oral communication skills Basic computer knowledge Your experience Education: minimal request: bachelor's degree in a scientific discipline (Immunology, molecular biology, biochemistry, or related field). Experience: minimal request: bachelor's degree with a minimum of 1 years of direct laboratory experience. Master's degree with 0-1 year of direct laboratory experience. University/college degree (life science preferred) or certification in a related allied health We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit ***************** or connect with us on LinkedIn. Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We're on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

Clinical Diagnostic Solutions, Inc. (CDS) is a company that provides total hematology solutions for the physician office laboratory, clinic, small hospital, and veterinary office markets. At CDS, our mission is to provide the highest quality experience to our valued customers. Our employees achieve this through our cultural goals of working together through Teamwork, high Quality in the work we do, being Innovative and Courageous, always Results Oriented, and most importantly - being Customer Oriented. Under supervision, uses fundamental concepts, practices, and procedures of particular field of specialization to perform scientific, R&D tasks of some complexity requiring application and adaptation of established techniques, procedures, and criteria. Participates in new product development, optimization, validation, and transfer into production. Prioritizes work schedules to support team objectives. Job Responsibilities: Participates in method development and technical innovation within the research team and supports project timelines Performs method optimizations, validations and participates in technology transfer to production Performs routine operation, maintenance, calibration and troubleshooting of laboratory instruments such as pH, conductivity meters, osmometers, spectrnphotometers, hematology analyzers and nucroscopes Evaluates and selects methods, applies protocols and scientific techniques to accomplish study objectives Drafts and updates protocols, test methods and standard operating procedures as applicable Proactively collaborates and supports the team, communicates problems as they arise Provides solution/s to problem/ s of limited complexity, exercises judgment within defined policies to determine appropriate action Collects, analyzes and compiles data. Summarizes for interpretation and discussion Drafts statistical and narrative reports as applicable Recognizes and reports experimental variances Is able to coordinate a small project or a small component of a larger project according to set deliverables Maintains good laboratory records and documentation for experimental work and results Maintains workplace safety and environmental practices Maintains clean workplace including laboratory bench and glassware Supports the department with QC technical investigation activities as needed Works in the spirit of continuous improvement Engages in inter and intra-departmental activities/studies Performs other related duties as required or as directed. The omission of specific duties does not preclude the supervisor from assigning duties that are logically related to the position. Qualifications: Knowledge of scientific approach and methodologies. Ability to design small studies, gather, organize and analyze statistical data and generate reports Excellent oral and written communication skills Ability to investigate and analyze information and to draw conclusions Skill in the use of personal computers and related software applications such as Word/Excel/Powerpoint/Teams Knowledge of current technological developments/trends in area of expertise is desirable but not required Capable of adjusting to dynamic work environment and changing priorities Willing to take on new challenges and implement new ideas Must be Comfortable handling blood products Willing to embrace a learning environment, is open to suggestions, new ideas and innovation Ability to grasp methods fast and willingness to change course as applicable Familiar with GLP, GMP practices and capable of working in a regulated medical device company (ISO and FDA) Must have strong analytical skills Must be a team player and driven individual Must value innovation, accuracy and accountability Minimum Requirements: Bachelor's degree with 2-5 years or Associates degree with 5-8 years' experience that is directly related to the duties and responsibilities specified. EOE

Role Description Zoetis is seeking a highly motivated and skilled Immunologist with expertise in Next-Generation Sequencing (NGS) and multi-omics technologies to join our team in Veterinary Medical Research and Development (VMRD). The successful candidate will play a pivotal role in advancing our understanding of immune system mechanisms by integrating and analyzing complex datasets. The ideal candidate should have experience in immunology with non-model species or demonstrate translational insights from model to non-model systems. Key Responsibilities: * Design research studies and analyze high-dimensional data. * Collaborate with interdisciplinary teams to drive innovative discoveries and translational applications that align with our portfolio. * Stay current with the latest advancements in immunology, NGS technologies, sequencing methodologies, statistical approaches, and data integration techniques. * Embrace a systems biology framework and demonstrate excellent communication skills. * Collaborate with internal and external stakeholders, including researchers and clinicians, to translate findings into actionable outcomes. Education and Qualifications: * Ph.D. in Immunology, Molecular Biology, or a related discipline with coursework and doctoral research in immunology. Post-doctoral experience preferred but not essential. Required Experience and Skills: * Expertise in integrating DNA, RNA, protein, single cell data using multi-omics approaches (e.g., DNA-Seq, RNA-Seq, proteomics, single-cell, spatial single-cell technologies). * Proven ability to derive meaningful biological conclusions from the integration of multiple omics datasets. * Proficiency in designing and applying computational, statistical, and visualization methods to extract actionable insights from diverse omics data types, including animal, human, and pathogen sources, within a systems biology framework. * Experience with pathway analysis workflows and the development of robust frameworks for understanding disease biology. * Collaboration with stakeholders to design experiments, provide strategic methodologies, and validate hypotheses effectively. * Proficiency in at least one programming language (e.g., Python, BASH, C, C++, R, Ruby). * Exceptional verbal and written communication skills for effective interaction with experimental biologists, clinicians, and non-specialists. * Demonstrated ability to work independently and collaboratively in a multidisciplinary environment. * Experience working in a high-performance computing (HPC) environment and managing large and complex biological data is required. * Conceptual knowledge of GWAS, microbiomes, metagenomics, variant detection (e.g., SNPs), and CNV analysis is advantageous but not required. Full time Regular Colleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.