Associate Scientist Salary in USA

Associate Scientist, Biomarker ResearchJob LocationsUS-AZ-PhoenixReq No.2020-6329CategoryResearch & DevelopmentTypeRegular Full-TimeSummary of Major ResponsibilitiesThe Associate Scientist, Biomarker Research supports the day-to-day project development activity through interaction with scientists and/or contractors, while gathering, analyzing, and interpreting scientific data. The Associate Scientist, Biomarker Research evaluates literature research data, provides administrative support to the Director, Biomarker Research & Evidence, and self-manages projects as assigned. In particular, the Associate Scientist, Biomarker Research is responsible for the exploration and implementation of biomarker candidates that may be used to guide treatment selection and/or may become part of the Paradigm biomarker portfolio. This includes the fast track exploration of emerging clinical markers, the conceptualization of biomarker evaluation packages for the Evidence Review Committee, as well as the translation of approved target-drug associations into the Paradigm proprietary rules interface. As part of the biomarker research group, the Associate Scientist integrates basic and clinical science studies along with computational, statistical and epidemiologic approaches for a comprehensive understanding of biomarkers and their associations with disease processes. The ideal candidate has a good understanding of basic, translational and clinical research, as related to the treatment of cancer as well as proteomic and molecular profiling of cancer and molecular targets, pathways that may be targeted with relevant immunologic or molecular therapies, and the evolving role of biomarkers in precision oncology clinical trials.Essential Duties and ResponsibilitiesSupports quality assurance for outgoing patient reports; specifically related to the interpretation of evidence-based oncology biomarkers for therapeutic decision-making.Supports translation of novel biomarkers into clinical practice by surveying published literature, as well as clinical trial data from discovery to preclinical, clinical, and post-approval trials (real time evidence maintenance).Monitors validated target drug associations for personalized cancer diagnostics by providing cutting-edge knowledge transfer from bench to the bedside.Participates in the management of biomarker archives and biomarker-specific evidence dossiers, as well as updating the literature repository for continuous biomarker maintenance and exploration of novel targets.Supports efforts in technology transfer/convergence between the biomarker research group, lab personnel and IT.Reports surveillance and quality assurance for outgoing patient reports.Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.Support and comply with the company’s Quality Management System policies and procedures. Regular and reliable attendance. Ability to work independently and make decisions.Clear communication and ability to speak, read and write in English.Standing or sitting for long periods of time may be necessary.Some lifting (greater than 25 pounds) may be necessary.Use of computer and some time may be spent concentrating, reading, or analyzing data, or applying scientific rules.Manual dexterity, bend, reach, and stoop.Ability to coordinate information and activities.Ability to prioritize and manage multiple projects simultaneously.Ability to perform mathematical calculations.Ability to function in a fast-paced environment.Ability to meet critical deadlines.Teamwork oriented, and projects a positive interaction with outside agencies.QualificationsMinimum QualificationsPhD, MD, DO, or PharmD in Molecular and Cellular Biology, Biochemistry, Cancer Biology, or other related field.1+ years of experience in basic, translational, and clinical research related to proteomic and molecular profiling of cancer specimen, treatment of cancer patients and/or clinical trials.Ability to use literature review as a method to synthesize research in precision oncology.Authorization to work in the United States without sponsorship.Demonstrated ability to perform the Essential Duties of the position with or without accommodation.Preferred QualificationsPhD preferred.A background in clinical data interpretation and/or evidence-based medicine experience. We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. Applicable portions of the Company’s affirmative action program are available to any applicant or employee for inspection upon request.

Abraxis Inc., a Eurofins Technologies company, is a member of the Eurofins Group with major offices and production facilities in the United States, Europe, and Asia, is an international provider of rapid test kits for regulatory agencies, academic and industrial research. The company's strengths are its strong customer orientation, fast service and high quality products. Abraxis, Inc. is searching for an Associate Scientist for Research & Development and Technical Manufacturing in Warminster, PA. Associate Scientist responsibilities include, but are not limited to, the following : • Perform method development, optimization, validation, and method transfer to manufacturing • Manufacturing support, including preparation of reagents, solutions and performance of all associated QA/QC testing • Perform feasibility studies • Perform validation protocols and reports The ideal candidate would possess : • Chemistry and biology courses including microbiology • Strong computer, scientific, and organizational skills • Excellent communication (oral and written) and attention to detail • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Basic Minimum Qualifications : • Bachelor's degree in biology, chemistry, or other related degree concentration • 0 - 3 years related laboratory experience • Authorization to work in the United States indefinitely without restriction or sponsorship Position is full-time, Monday-Friday, with overtime as needed. Candidates currently living within a commutable distance of Warminster, Pennsylvania are encouraged to apply. As a Eurofins/Abraxis employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. To learn more about Abraxis, please explore our website www.abraxiskits.com. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Eurofins is the world leader in the food, bio/pharmaceutical product testing. It is also number one in the field of environmental laboratory services and one of the global market leaders in agroscience, genomics, discovery pharmacology, and central laboratory services. With over $2 billion in annual revenues and 25,000 employees across 250 sites in 39 countries, Eurofins is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, biopharmaceutical, food, environmental, and consumer products industries and to governments. With over 25 years of experience in the crop protection industry, Eurofins Agroscience Services offers outstanding technical knowledge and project management skills. By acquiring a carefully selected range of CRO's, Eurofins Agroscience Services has created a unique portfolio of expertise that provides analytical, regulatory, and field support to plant breeders, agrochemical, biopesticide, biocide, and fine chemical manufacturers. Eurofins Agroscience Services is searching for an Associate Scientist I, Biodegradation & Metabolism to work in Hercules, CA. Associate Scientist I responsibilities include, but are not limited to, the following : Use a diverse range of analytical methods for investigation of a test substance in a test system Performs laboratory tasks including but not limited to use of analytical balances, measuring volumes, proficient at dispensing volumes with devices such as syringe, pipet, or graduated cylinder, preparation of buffer solutions, use of pH meter, sample processing/ homogenization, microbial analysis, total organic carbon measurement, wet/dry determinations, sample combustions, use of liquid scintillation counters and assist with experimental setup such as preparation of traps for volatile components Performs sample extractions, concentration of soluble fractions, partitioning of sample extracts, extract cleanup by solid phase extraction (SPE), calibrant preparations, chromatographic analysis using various techniques such as thin layer chromatography (TLC), or high-performance liquid chromatography (HPLC), preparation of derivatives of analytes/metabolites (chemical or enzyme) Documentation of work performed in laboratory notebooks, worksheets, instrument logbooks, or other printed documents as per applicable SOP and GLP guidelines Organization and maintenance of study raw data binders Helps with laboratory housekeeping maintaining and organizing the laboratory space to keep appearance clean and safe for laboratory personnel Maintain assigned laboratory instruments and equipment Review data entry and calculations associate with the above techniques and instrumentation. Organization and maintenance of study raw data binders Contribute to preparation of data summaries and draft reports. The ideal candidate would possess : Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Basic Minimum Qualifications : B achelor's degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas and three years of experience in a directly relevant setting. A Master's degree in a relevant field may be substituted for the bachelor's degree and experience. In rare cases, comparable demonstrated competence and experience in the relevant area may be used to substitute in whole or in part for the Bachelor's degree. Familiarity and/or experience in a laboratory setting is required. Professional experience under GLP regulations is preferred. Experience in a CRO environment is preferred. Authorization to work in the United States indefinitely without restriction or sponsorship Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime and some weekend shifts required as needed. Candidates currently living within a commutable distance of Hercules, CA are encouraged to apply. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. To learn more about Eurofins, please explore our website www.eurofinsus.com . Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Eurofins Lancaster Laboratories PSS is searching for a Associate Scientist to provide support in a Pilot Plant environment in Lincoln, Nebraska. Responsibilities include, but are not limited to, the following : • Clean, setup, perform minor maintenance, and operate equipment (such as autoclaves, ultrasonic washers, automated CIP/SIP stations, fermenters, filtration, centrifuges, chromatography, and filling/lyophilization,) in support of processes for bacterial and viral antigens and vaccine formulations • Operate automated process controllers • Manage samples including ensuring proper storage and handling of samples • Secondary gowning and aseptic technique in support of seed, antigen, and vaccine production • Demonstrate reliability in attendance and punctuality • Write, revise, and comply with SOP's and associated documentation • Perform data collection and analysis by using process controllers and office applications such as Word, PowerPoint, and Excel • Report writing • Complete documentation including GMP documentation, timecards, order requisitions, and charting. • Perform operations and maintain compliance with Good Manufacturing Practices (GMP's) • Clean areas according to specific SOP's • Assist in maintaining adequate supplies in the areas • Demonstrate safe work habits and maintain a safe work environment. Understand and comply with safety SOP's and procedures (Material Safety Data Sheet (MSDS) guidelines, Near Miss, Personal Protective Equipment (PPE), biohazard training, Monthly Safety training, etc.) • Demonstrate good interpersonal and communication skills within and outside the department using verbal, written, and non-verbal The ideal candidate would possess : • Self-starter, able to prioritize work and work efficiently with minimal supervision • Ability to handle change (changing workloads). • Good at multitasking with ability to work with deadlines. • Strong computer, scientific, and organizational skills • Excellent communication (oral and written) and attention to detail • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Physical Demands: • Manual dexterity using hands and fingers • Frequent twisting of wrists and forearms • Constant standing for extended periods • Ability to work flexible hours including work week, weekend, holiday, and overtime • Lifting: May include occasional lifting up to 50 pounds. Work environment: • The person filling this position works in a BSL-2 laboratory. There may be exposure to animal pathogens, chemicals, and bio hazardous materials. There may be handling of, and/or exposure to, zoonotic organisms • Work will be conducted in both lab and office facilities. Basic Minimum Qualifications : • Associate's degree in a scientific discipline with emphasis in microbiology, biochemistry, or related disciplines. • Authorization to work in the United States indefinitely without restriction or sponsorship Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed. Candidates currently living within a commutable distance of Lincoln, NE are encouraged to apply. As a Eurofins Lancaster Labs employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. To learn more about Eurofins, please explore our website www.eurofinsus.com . Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Eurofins Panlabs is committed to assisting clients achieve drug discovery success by providing comprehensive data. We are the most experienced pharmacology service company, in continuous operation for over 40 years, while setting the benchmarks for quality, convenience, and expertise. Our legacy includes: concurrent controls run with every experiment, a historical database on assay performance, industry experienced professionals that assist in study design and data interpretation, and eCTD compatible data reports. Eurofins Panlabs is searching for an Associate Scientist I to work in St. Charles, MO. Associate Scientist I responsibilities include, but are not limited to, the following : • Performs work in a laboratory setting, meeting the physical job requirements of a lab role • Prepares and manages inventory of buffers, reagents, media, semi-finished and finished goods • Maintains cell culture in a BSL2 laboratory, and adheres to cleanroom guidelines and aseptic technique, according to protocol • Conducts production assays in ADMET, Ion Channel, Immunosignaling, OncoPanel Services, and manufacturing, lot release assays and inventory management for Cell Products • Understands and complies with requirements for work performed at a GxP site • Completes required training and supports 100% of Employee Health and Safety requirements • Demonstrates proficiency with, care and maintenance of lab equipment and department assets • Conducts responsible use of confidential IT and business systems, as required • Adheres to department SOPs and documentation requirements, maintains accurate data management and reporting • Supports unit goals and demonstrates Eurofins' competencies, as defined in the job plan • Provides training to colleagues and external end users, when required • Contributes to scientific community, and site research and development objectives • Works effectively in a team environment, under minimum direction, to achieve business production, project timelines, and quality objectives • Adjusts work hours and provides cross-functional support to other departments, as required, and maintains accountability in delivering to client needs/timelines • Routinely communicates project updates to internal and external clients • Performs other duties, as assigned The ideal candidate would possess : • Ability to read, write, and interpret documents, such as standard operating procedures and technical reports • Ability to perform mathematical calculations, statistical analyses, and data interpretation • Ability to multitask with organization and manage time effectively • Ability to solve practical problems and troubleshooting skills • Ability to work in a laboratory setting, according to the physical requirements of a laboratory role • Lab equipment and office computer/software proficiency • Above average oral and written communication skills • Demonstrates a positive attitude, capacity for team environment, and exhibits a genuine interest in drug discovery in support of advancing human health • Strong computer, scientific, and organizational skills • Excellent communication (oral and written) and attention to detail • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Basic Minimum Qualifications : • Associate Degree with 1 year of relevant experience OR • B.A. or B.S. with 6 months of relevant experience • Experience in a contract research organization • Experience with cell-based assays • Work experience in laboratory setting • Authorization to work in the United States indefinitely without restriction or sponsorship Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed. Candidates currently living within a commutable distance of St. Charles, MO are encouraged to apply. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. To learn more about Eurofins, please explore our website www.eurofinsus.com . Eurofins is the world leader in the food, bio/pharmaceutical product testing. It is also number one in the field of environmental laboratory services and one of the global market leaders in agroscience, genomics, discovery pharmacology, and central laboratory services. With over $2 billion in annual revenues and 25,000 employees across 250 sites in 39 countries, Eurofins is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, biopharmaceutical, food, environmental, and consumer products industries and to governments. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Company Description Insmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most valuable resource is our employees, and everything we do is motivated by a patients-first mentality. We are dedicated to growing our team with talented individuals from around the world who are willing to challenge the status quo, solve problems, and work collaboratively with a sense of urgency and compassion. Guided by our core values of collaboration, accountability, passion, respect, and integrity, we aim to foster an inclusive, diverse, and flexible work environment, where our employees are recognized for leaning in and rolling up their sleeves. If you share our vision and want to work with the most dedicated people in the biopharma industry, come to Insmed to accelerate your career. Recognitions Named Science's Top Employer in 2021, 2022, and 2023 Insmed is dedicated to creating a collaborative environment where our team can thrive. Every day, our employees turn their passion for science and research into innovative solutions for patients. That's why we were named the No. 1 company to work for in the biopharma industry in Science's Top Employers Survey for two years in a row. A Certified Great Place to Work We believe our company is truly special, and our employees agree. In July 2023, we became Great Place to Work-certified in the U.S. for the third year in a row. We are also honored to have been listed on the Best Workplaces in Biopharma™, Best Workplaces in New York™, and Best Workplaces for Millennials™ lists. Overview Insmed is seeking a scientist with significant experience with mouse vivarium experiment management and execution. This scientist will be responsible for execution of preclinical mouse models of neuro and muscular genetic diseases with research preparations of therapeutic constructs, including mouse genotyping, dosing, functional analysis, and tissue collection. Additionally, the scientist will document his/her methods and studies, and participate in the technical transfer of assays to third party contractors. Depending on experience, the scientist will work with current team members to develop new animal models. Beyond vivarium expertise, this position will also be responsible for histology techniques related to the animal studies, including tissue collection, sectioning, and staining. Familiarity with the use of a cryostat, histological techniques, and immunostaining techniques are required. Experience with behavioral tests and electrophysiological readouts are desirable. Responsibilities Additional representative responsibilities will include, but not necessarily be limited to, the following: • Handle mouse genetic models of disease, including breeding pairs, ID-tagging, injections (ICV, facial vein and tail vein), weighing • Behavioral tests and physiological assessments • Tissue collection from mice on study and appropriate handling and storage of tissue • Use of cryostat to generate slides for histology • Staining protocols (eg. H&E) as well as immunohistochemistry • Documentation of results in appropriate formats provided by supervisor Qualifications Master's degree in biology or relevant discipline with a minimum of 3-4 years of relevant experience or Bachelor's degree in biology or relevant discipline with a minimum of 5 years of relevant experience. At least two years in vivo experience in mouse handling, tagging and weaning, demonstrating proficiency and ability to work with limited supervision. In vivo expertise in colony management, breeding and weighing. Daily colony maintenance for multiple mouse models is required. Experience with in vivo injections including p1 ICV and facial vein injections and p28 tail veins injections demonstrating proficiency. Histology proficiency required for sectioning and staining various in vivo samples for biodistribution. Analyze functionality and survival data for ongoing experiments. Development of survival study graphs and survival curves. Organization of experiments and protocol writeups for developing R&D experiments. Knowledge of Good Documentation Practices and Good Laboratory Practices (GxP) is a plus. Proficiency in following protocols and working in a fast-paced, high-energy environment. Willingness to learn new techniques and train other laboratory staff in technical matters. Entrepreneurial spirit, with strong willingness to take on new challenges required to bring novel medicines to the clinic. Strict adherence to environmental, health, and safety guidelines. #LI-KM #LI-Onsite Travel Requirements Minimal Salary Range Insmed takes into consideration a combination of candidate's education, training, and experience as well as the position's scope and complexity, the discretion and latitude required in the role, and external market and internal value when determining a salary level for potential new employees. The base salary range for this job is from $86,000.00 to $115,333.00 per year Compensation & Benefits We're committed to investing in every team member's total well-being, now and in the future. We offer a competitive total-rewards package to all employees around the world, including: Flexible approach to where and how we work Competitive compensation package including bonus. Stock options and RSU awards Employee stock purchase plan 401(k) plan with company match Professional Judgment Vacation Policy 11 paid holidays per year and Winter Break (typically between Christmas and New Year's Day). ADDITIONAL U.S. BENEFITS: Medical, dental, and vision plans Company-provided short- and long-term disability plans Company-provided life insurance Unique offerings of pet, legal, and supplemental life insurance Flexible spending accounts for medical and dependent care Accident and Hospital Indemnity plans Supplemental AD&D Employee Assistance Program (EAP) Mental Health on-line digital resource On-site, no-cost fitness center at our U.S. headquarters Paid time off to volunteer Additional Information Insmed Incorporated is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.Unsolicited resumes from agencies should not be forwarded to Insmed. Insmed will not be responsible for any fees arising from the use of resumes through this source. Insmed will only pay a fee to agencies if a formal agreement between Insmed and the agency has been established. The Human Resources department is responsible for all recruitment activities; please contact us directly to be considered for a formal agreement.Applications are accepted until the position is filled.

Associate Scientist, Biotech Eurofins BioPharma Product Testing has delivered expert scientific support to companies working to improve human and animal health. As a member of the Eurofins BPT team, you'll work alongside respected technical experts dedicated to scientific excellence in a process driven regulatory compliant environment. Eurofins BPT-Columbia is looking for an Associate Scientist to join our Biotech team located in Columbia, Missouri . Employee Responsibilities: The Associate Scientist position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. Working with increasing independence on studies and assignments. The Ideal Candidate would possess: Experience with GLP and/or GMP and hands-on experience with HPLC and/or GC. Experience with LIMS system desirable. Familiarity and/or experience in a laboratory setting is required. A highly motivated staff member that is not afraid to make mistakes but must learn from them, be willing to work on a team, and be willing to work with others to teach and learn new skills. Good organizational skills; ability to follow direction and good communication skills are required. Minimum Qualifications: Bachelor's degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas and a minimum of two years of experience in a directly relevant or demonstrated comparable competency and skill attainment is required. A Master's degree in a relevant field may be substituted for the bachelor's degree and experience. In rare cases, comparable demonstrated competence and experience in the relevant area may be used to substitute in whole or in part for the bachelor's degree. Authorization to work in the United States indefinitely without restriction or sponsorship. What we offer: As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, and dental and vision options. To learn more about Eurofins, please explore our website www.eurofinsus.com . Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. As a part of Eurofins BioPharma Product Testing - the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide - Eurofins BPT provides comprehensive laboratory services for the world's largest pharmaceutical, biopharmaceutical and medical device companies. Our service offering includes comprehensive chemistry, biochemistry, microbiology, molecular and cell biology and biosafety testing of drug substances, final products, intermediates, and starting materials for both small and large molecule drug products. We are looking forward to receiving your application including your expected salary and possible start date via our career website.

Associate Scientist/Data Review-QA Eurofins BPT-Columbia is looking for an Associate Scientist/Data Review in our Quality Assurance team located in Columbia, Missouri . The Associate Scientist/Data Review position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. Working with increasing independence on studies and assignments. Employee Responsibilities: Reviews and approves/rejects completed client laboratory reports and manufacturing records for accuracy (of entry provided, e.g. lot numbers, calculations, etc.), traceability, and completeness. Evaluates addressed deficiencies for clarity and for potential impact on compliance status. Works with staff to correct any noted deficiencies and/or inconsistencies. Assists with development, implementation, and monitoring of quality systems and procedures (e.g. CAPA, Change Control, Training, etc.). Reviews and approves equipment calibrations, qualifications, and validations for adherence to company procedures and federal guidelines. Performs internal, external, and quality audits (CGMP, GLP, and DEA, etc.). Develops content and format of training materials for GCMP and/or GLP and QA. Executes training for new and existing employees. Organizes and presents training sessions to groups or individuals. Reviews protocols, procedures, data, reports, and other documents to ensure accordance with specified regulatory requirements, protocol, and/or project plan, methods and SOPs. Works with study directors, principal investigators, and study owners to detect and resolve any quality issues. Reviews standard operating procedures for accuracy and consistency to ensure agreement with regulations. Updates the Master Schedule in accordance with specified regulations and standard operating procedures. Files protocols, amendments, deviations, inspections, and other quality documents appropriately. Keeps supervisor informed of significant issues or developments identified during quality assurance activities. Performs other related duties as required and directed. The Ideal Candidate would possess: Experience with GLP and/or GMP and hands-on experience with HPLC and/or GC. Experience with LIMS system desirable. Experience reviewing Empower. Familiarity and/or experience in a laboratory setting is required. A highly motivated staff member that is not afraid to make mistakes but must learn from them, be willing to work on a team, and be willing to work with others to teach and learn new skills. Good organizational skills; ability to follow direction and good communication skills are required. Strong computer, scientific, and organizational skills. Excellent communication (oral and written) and attention to detail. Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude. Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies. Minimum Qualifications: Bachelor's degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas and a minimum of two years of experience in a directly relevant or demonstrated comparable competency and skill attainment is required. A Master's degree in a relevant field may be substituted for the bachelor's degree and experience. One year bio/pharmaceutical experience with knowledge of regulatory requirements preferred. Authorization to work in the United States indefinitely without restriction or sponsorship. What we offer: Position is full-time, Monday-Friday, 8 a.m.-4:30 p.m., with overtime as needed. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, and dental and vision options. To learn more about Eurofins, please explore our website www.eurofinsus.com . Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. As a part of Eurofins BioPharma Product Testing - the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide - Eurofins BPT provides comprehensive laboratory services for the world's largest pharmaceutical, biopharmaceutical and medical device companies. Our service offering includes comprehensive chemistry, biochemistry, microbiology, molecular and cell biology and biosafety testing of drug substances, final products, intermediates, and starting materials for both small and large molecule drug products. We are looking forward to receiving your application including your expected salary and possible start date via our career website.

Responsible for translating biochemistry workflows into laboratory automation processes. Develop and execute automated strain construction, cultivation, and assay protocols for high-throughput construction and screening of microbial libraries using laboratory automation robotics. Use laboratory data information systems, such as Benchling, to capture and track lab processes and experimental data. Use and write methods for automated capture, processing, and analysis of laboratory datasets. Work within an agile team to design and conduct scientific experiments to support multiple research projects. Interpret experimental results, and contribute to writing reports and presentations. Engage in troubleshooting, ideation, and collaborative problem solving of automation and experimental challenges. Ensure timely delivery of results to internal and external customers.2 years of experience in the job offered or as a research associate/scientist in a laboratory environment. Requires knowledge of carbohydrate-active enzymes (CAZyme), enzymology, protein biochemistry, biological lab techniques, analytical instrumentation, statistical packages (JMP or R studio), and assay development (UV-VIS, fluorescent assays, or analytical chromatography) on liquid and solid substrates. Requires 2 years of hands-on laboratory experience to develop new chemical and biological assays to assess microbial phenotypes and enzyme performance, or characterize proteins from industrial host strains. Requires 1 year of hands-on experience writing new automation methods for liquid handling on Beckman Biomek or Hamilton systems.$91,810 - $113,500 per yearPlease copy and paste your resume in the email body do not send attachments, we cannot open them and email them at candidates at placementservicesusa.com with reference #2312084 in the subject line.Thank you.

CambrexAssociate Scientist - AnalyticalUS-MA-WalthamJob ID: 2024-3679Type: Regular Full-TimeCategory: AnalyticalCambrex - WalthamOverviewAssociate Scientist – Job Description About the Company Snapdragon Chemistry, Inc. is a leader in continuous flow services and solutions. Our company is catalyzing the transformation of research, development, and manufacturing across industries where organic chemistry underpins product development. We rely on our most valuable resource – our people – to maintain a leadership position in this market. As part of our dynamic team, you will have the opportunity to collaborate with world-class leaders in flow chemistry and product development, as well as with dedicated colleagues while also cultivating and furthering your career. At Snapdragon Chemistry, we strive to create an environment of innovation and excellence where mutual respect and teamwork underpin our culture. ResponsibilitiesJob Description Snapdragon Chemistry is currently seeking exceptional candidates for the position of Associate Scientist in analytical sciences. A successful candidate will be joining a group of innovative and entrepreneurial scientists, with broad deliverables including the design of synthetic routes amenable to continuous flow processing, the development of reactor systems incorporating cutting­-edge flow technology, and delivering intermediates, APIs and high value specialty chemicals to our clients. We are looking for a candidate who has a passion for working in a fast­-paced, dynamic environment. The ideal candidate will have a BS in chemistry with 1+ years’ experience or MS in analytical chemistry. The candidate should have experience in the development of (U)HPLC and GC methods for synthetic molecules. Experience in pharmaceutical development and modern process analytical technologies is preferred. Candidates must possess strong written and oral communication skills. Responsibilities Leverage scientific knowledge and develop technology to solve analytical challenges in pharmaceutical process development.Contribute to day-to-day analytical laboratory operations and assist in equipment management, method setup and troubleshooting. Contribute to GMP manufacturing related analytical activities such as method qualification, validation, day-to-day QC activities.Contribute to activities that build upon Snapdragon Chemistry’s proprietary knowledge and technology fulfill their value creation potential.Participate in project teams to complete complex deliverables within stringent timeline and communicate results to key stake-holders.Ensure up­-to-­date knowledge of continuous flow technology, process analytical technologies and process development principles.Ensure that the integrity and profile of Snapdragon Chemistry within the scientific community are maintained at a high level, consistent with the requirements of the business. Qualifications Education:A BS or MS in chemistry or related field. GMP experience is preferred but not required. Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.PI239477449