Scientific Associate Resume Samples

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RT
R Tremblay
Rosie
Tremblay
171 Lafayette Greens
Dallas
TX
+1 (555) 757 1947
171 Lafayette Greens
Dallas
TX
Phone
p +1 (555) 757 1947
Experience Experience
Boston, MA
Scientific Associate
Boston, MA
Auer-Murazik
Boston, MA
Scientific Associate
  • Provides work direction, training and advice to junior coworkers to enhance their work effectiveness in generating analytical data
  • Sample management duties involving submission/receipt of samples, outsourcing/shipping of samples for testing and management of sample documentation
  • Establish and use molecular and in vitro cellular methods to work with human healthy and disease samples (cells, blood, Tissue) and human cell lines
  • In vitro cell culture assay development including work with primary human and murine immune cells
  • Provide Support to reference standard program by aliquoting material for internal/external distribution, assisting in maintaining inventory and compiling data
  • Independently prepare method validation protocol/investigation plan, and execute validation work under cGMP practices
  • Conduct risk analysis in all aspects of method development to efficiently develop robust methods that are GMP friendly based on quality by design
Chicago, IL
Temporary Scientific Associate
Chicago, IL
Fisher-Armstrong
Chicago, IL
Temporary Scientific Associate
  • Independently carry out development and scale-up activities for synthetically derived compounds, including raw materials, intermediates, and drug substances in support of cGLP or cGMP studies
  • Analysis of chemical development and formulation samples using HPLC, Dissolution, and KF
  • Supporting PAT method (NIR, Raman, particle size) development and data collection for in-process control and real time release methods
  • Manage sample receipt, document experiments according to Vertex procedures and report results
  • Supporting PAT related cGMP manufacturing activities
  • Authoring and reviewing source documents for regulatory submissions
  • Participating in the planning of experiments
present
Los Angeles, CA
Senior Scientific Associate
Los Angeles, CA
McGlynn-Bednar
present
Los Angeles, CA
Senior Scientific Associate
present
  • Make conceptual contributions to development activities
  • Assist in the development of novel and creative solutions to overcome scale-up and manufacturing obstacles
  • Help design, plan, execute, and interpret laboratory experiments, with minimal supervision, to meet established project timelines
  • Assist other chemists in Process Chemistry and Development
  • Design and perform pharmacological studies to evaluate the efficacy of novel CNS drug candidates in labaratory animals
  • Assist in technical transfer to CMO partners for clinical trial manufacture
  • Selection, design and development of novel PET/SPECT radiotracers for pre-clinical imaging research programmes
Education Education
Bachelor’s Degree in Reliability
Bachelor’s Degree in Reliability
University of Kentucky
Bachelor’s Degree in Reliability
Skills Skills
  • Proficient in a Unix operating environment
  • Understanding of basic statistics
  • 1-3 years professional software development experience in a scientific environment
  • Ability to drive a fork truck and follow all safety related procedure
  • Knowledge of German
  • Good computer skills in commonly used scientific software tools
  • Good flexibility and adaptation to changes
  • Excellent team spirit
  • Good communication skills; used to effectively work in a well-organized manner in a team environment
  • Curiosity, initiative, commitment and good organization skills
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15 Scientific Associate resume templates

1

Scientific Associate Resume Examples & Samples

  • Bachelor’s degree in related field
  • Previous experience on ELISA and molecular biology techniques
  • Industry experience in a GxP environment preferred
2

Scientific Associate Resume Examples & Samples

  • Bachelor’s degree with 4+ years of laboratory experience in the biotech/pharmaceutical industry; OR Master’s degree with 1+ years of laboratory experience in the biotech/pharmaceutical industry
  • Direct experience with HPLC/UPLC, electrophoresis, immunoassay and other protein analysis methods
  • Excellent communication and presentation skills
3

Scientific Associate to the Director Resume Examples & Samples

  • Scientific writing in basic and clinical sciences
  • Identify, develop, facilitate, organize, write, and proofread large, multidisciplinary, and multi-collaborative grant proposals to a wide range of funding agencies and organizations, including both public and private external entities. Lead the effort in interpretation, collection, and assembly of scientific documents, as necessary (e.g., large institutional grants, annual/occasional reports, progress reports for grants administration, IND applications, etc.)
  • Search the internet and other sources for foundation and government grant opportunities
  • Translate scientific abstracts into lay terms
  • Perform other related duties as assigned or requested such as presentation of draft ideas and plan to investigators, coordination of meetings required to create collaborative interactions both within and outside UACC, and reporting of progress to PIs
  • Understand and create strategies to meet the Cancer Center Support Grant (CCSG), Program Leaders, UACC directors grant goals
  • Enhance the portfolio of CCSG related funding
  • Enhance scientific content of UACC website and other public materials
  • Master’s degree in a related field (Science, Business Administration, Communications or another related subject) and a minimum of five years of work experience in administrative analysis or program leadership; OR, An equivalent combination of education and experience
  • Ability to work weekends and evenings, on occasion, as needed to meet deadlines
  • PhD in a scientific field (life sciences)
4

Scientific Associate, / II, Liver Disease Resume Examples & Samples

  • The candidate needs to be a quick learner and work independently in experimental design, technology learning and trouble shooting
  • The candidate is expected to have the ability to handle multiple tasks simultaneously and works in a fast-paced environment
  • Oral and written reports in English are also required regularly
  • Candidates should hold an M.S. in Cell Biology, Molecular Biology, Biochemistry or related field and have at least two years of relevant bench experience
  • The ideal candidate should have skillful hands-on technology and in-depth knowledge in cell biology and molecular biology
  • Excellent oral and written communication in English
  • Ability to function in an interdisciplinary team setting
5

Scientific Associate Resume Examples & Samples

  • Actively contribute to projects aiming at discovering new ways to modulate the immune system for the treatment of autoimmune diseases
  • Establish and use molecular and in vitro cellular methods to work with human healthy and disease samples (cells, blood, Tissue) and human cell lines
  • Combinatorial application of a variety of readouts, like multicolour flow cytometry, western blots, ELISA and the assessment of leukocyte differentiation for the characterization of novel immunomodulating substances and pathways
  • Use of human material for drug development and target / pathway validation
  • Interact in a cross-functional and cross-divisional project team active in drug development
  • Opportunity to work in teams with molecular histology and Omics technologies and bioinformatics experts
  • Immunology background and a theoretical knowledge of immunology and immunological methods
  • Experience in isolating and handling primary human leukocytes and human cell lines and human tissues
6

Scientific Associate Resume Examples & Samples

  • Establish and use molecular and in vitro cellular methods to work with preclinical and human samples (cells, blood, Tissue) and cell lines
  • Combinatorial application of a variety of techniques, like multicolour flow cytometry, western blot, ELISA and the assessment of leukocyte differentiation to characterize novel immunomodulatory substances and pathways
  • Presentation of your work in multidisciplinary project teams
  • Immunology background
  • Experience in isolating and handling primary leukocytes, cell lines and tissues
  • Animal experimentation license and experience in working with preclinical models
  • Knowledge of German
7

Temporary Senior Scientific Associate Resume Examples & Samples

  • Maintain accurate records of experiments and results in a laboratory notebook
  • Bachelor’s degree in the life or physical sciences with a
  • Experience with HPLC, GC, FT-IR, UV-VIS, KF, dissolution and
8

Scientific Associate Resume Examples & Samples

  • Supporting PAT method (NIR, Raman, particle size) development and data collection for in-process control and real time release methods
  • Supporting method transfer and validation of PAT methods/chemometric models for application in cGMP continuous manufacturing
  • Supporting the implementation of PAT methods/models for real time in-process controls and real time release testing
  • Presenting to cross functional teams and effectively communicate critical issues and proposed solutions
  • Supporting PAT related cGMP manufacturing activities
  • Authoring and reviewing source documents for regulatory submissions
  • A Bachelor’s degree in the physical sciences, mathematics or engineering
  • 0 - 3 years’ work experience
  • The ability to work successfully in both a team/matrix environment as well as independently
9

Scientific Associate, Immunology Resume Examples & Samples

  • Develop and run T cell and other immune cell assay to support SAR
  • Identify assays and determine target PD modulation
  • Run instruments such as flowcytometry, cell sorter and multiplex protein analyzer
  • Keep clear and detailed lab note, analyze and interpret data
  • Work smoothly and communicate effectively with other team members
  • Minimum of 1 years of work experience in Immunology or Immune Oncology post graduation
  • Experiences with immune cell assay, flowcytometry, bioplex and evision
  • Demonstrated record of delivering results in a fast paced environment
10

Scientific Associate Resume Examples & Samples

  • Develop assays and new technologies to study the efficacy, mechanism of action, and biomarker of the therapeutic agents
  • Conduct basic research on cancer and metabolic diseases
  • Ensure the integrity and preciseness of research data
  • Collaborate with colleagues cross functions and sites
  • Report research progress to lab head in regular basis
  • Fast learning capability in biological science and technology
  • Good experimental skills and knowledge in molecular and cellular biology
  • Sincere passion to experimental biology
  • Good flexibility and adaptation to changes
  • Excellent team spirit
11

Scientific Associate, / II, Genomics Resume Examples & Samples

  • Big data generation, the data are mostly generated by but not limited to next-generation sequencing (NGS) based technology
  • Perform the experiments in target/biomarker validation and disease mech-anism studies (molecular/cellular biology, e.g. cell culture, siRNA/plasmid transfection, RT-qPCR, IHC/IF staining, WB, ELISA, ChIP, etc)
  • New technology and assay development in the field of NGS, molecular bi-ology, and cellular biology
  • The candidate needs to deliver high quality and reproducible data within the timeline
  • The candidate is expected to have the ability to handle multiple tasks sim-ultaneously and works in a fast-paced environment
  • Self-motivation in science, quick-learning, fast-acting, and strong team work skills are highly preferred qualities
  • The candidate should hold an M.S. in Cellular Biology, Molecular Biology, Biochemistry or related field and have at least two years of relevant bench-work experience
  • The candidate should have skillful hands-on technology in cellular biology and molecular biology (e.g. cell culture, siRNA/plasmid transfection, RT-qPCR, IHC/IF staining, WB, ELISA, ChIP, etc)
  • Experience and knowledge in cancer biology, liver biology, immunotherapy, NGS or epigenomics is a plus
  • Proficient English skills in literature mining, oral and written communications
12

Scientific Associate, / II, Cancer Resume Examples & Samples

  • Apply cell biology, immunology, molecular biology and biochemistry expertise for assay development, target validation, mechanistic studies
  • Understand the concepts/ rationale behind the study
  • Design, perform, optimize assays with the relevant controls
  • Analyze and interpret results, and be able to troubleshoot
  • Execute independently but contribute as part of a team
  • Generate high quality, reliable data
  • Collaborate and communicate in professional English, both in oral and written formats
  • Quick learner, be well organized and be able to multi-task
  • Be self-motivated and have a strong desire to learn
  • Flexible, adaptable
  • M.Sc in Cell Biology, Cancer Biology, Immunology, Biochemistry or a related field
  • Require a minimum of 2 years industry (relevant bench) experience in a multi-national company
  • Minimal technical skills: Flow cytometry required, cell-based assays, transfections, western blotting, immunoprecipitation
  • Proficient with: Excel, Prism, FlowJo, Powerpoint, Spotfire
  • Strong work ethic, integrity and mutual respect in the workplace
  • High data quality and teamwork is a must
13

Temporary Scientific Associate Resume Examples & Samples

  • Analysis of chemical development and formulation samples using HPLC, Dissolution, and KF
  • Participating in the planning of experiments
  • Maintains accurate records of experiments and results in a laboratory notebook and authors reports as assigned
  • Interpretation and communication of results
  • The ability to present results in both oral and written reports is required
  • Troubleshooting of instruments and experiments
  • Demonstrates responsible follow-up
  • Demonstrates knowledge of scientific principles and basic understanding of applicable drug development regulations
  • A Bachelor's degree in the physical sciences or engineering
  • 0-4 years of experience
14

Temporary Scientific Associate Resume Examples & Samples

  • Pharmaceutical Industry experience
  • The ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects
  • Good documentation practices and organizational skills
  • Understanding of NIR, Raman, particle size and other measurement techniques
15

Scientific Associate Resume Examples & Samples

  • Perform data review of analytical experiments and trending of results
  • Author laboratory investigations
  • Perform analytical testing using various techniques such as HPLC, GC, KF and dissolution
16

Scientific Associate Resume Examples & Samples

  • Perform routine analytical testing using various analytical techniques such as FTIR, KF and ROI
  • Sample management duties involving submission/receipt of samples, outsourcing/shipping of samples for testing and management of sample documentation
  • Provide Support to reference standard program by aliquoting material for internal/external distribution, assisting in maintaining inventory and compiling data
  • Familiar with FTIR, KF and ROI and
17

Scientific Associate Resume Examples & Samples

  • Contribute to the development of solid dosage forms for clinical and commercial use, generate data for project progression and regulatory filings, conduct optimization and scale up studies
  • Help design, plan, execute, and interpret laboratory experiments, with minimal supervision, to meet established project timelines
  • Initiate experimental troubleshooting on a routine basis, with minimal supervision
  • Contribute to drafting regulatory filing documentation
  • Perform QC checking of data that support regulatory filings
  • Sound knowledge of pharmaceutical and engineering principles in the solid dosage form development for both clinical and commercial scales
  • Hands on experience with formulation techniques, processing equipment, and unit operations at both the laboratory and clinical manufacturing scales
  • Strong math skills particularly as applied to material/energy balances, and intermediate applied statistical analysis
  • Successful and efficient multitasking and working on a few projects concurrently
18

Temp Scientific Associate Resume Examples & Samples

  • Provide basic data analysis and may provide assistance in design of next experiment
  • Implement new lab techniques according to literature
  • Document own experiment in lab notebook (including tables, graphs, etc.)
  • Present results to supervisor and may present to lab at project meetings
  • Maintain infrastructure of laboratory
  • Demonstrate ability to apply knowledge in discipline to complete work assignments
  • Maintain awareness of and provide recommendations on standard laboratory tools and procedures
  • Perform duties with appropriate knowledge of relevant laboratory tools and procedures
  • Operate and perform routine maintenance on instruments
  • Apply basic library research skills
  • Conduct activities according to the appropriate SOP, GLP, GMP and other guidelines
  • Conduct activities in compliance with Novartis safety, waste disposal and other regulatory guidelines
  • Demonstrate a working knowledge of relevant Novartis policies and procedures
  • Assist in the preparation of SOPs for department, where appropriate
  • Responsible to understand and follow established HSE policies and procedures applicable to particular function and consult with line manager if further guidance or assistance on performing tasks safely is needed
  • Identify and report unsafe equipment, conditions and practices so that they may be corrected prior to an incident
  • Complete training as required and use laboratory and personal protective equipment as required
  • May provide assistance in design of next experiment
  • Conducts experiments with input from supervisor
  • Participate constructively in working teams and at lab meetings
  • Offer assistance to co-workers
19

Senior Scientific Associate Resume Examples & Samples

  • Design, execute and interpret synthetic organic experiments with a high degree of reliability and independence
  • Hands on experience, capability and desire to scale-up and develop chemical processes
  • Make conceptual contributions to development activities
  • Contribute to the drafting of required documentation
  • Multitask to effectively manage multiple activities
  • Assist other chemists in Process Chemistry and Development
  • Ensure compliance with all applicable regulations and SOPs
  • Proven communication (verbal and written) and interpersonal skills
  • Experience interacting with CRO/CMO organizations would be beneficial
20

Scientific Associate Resume Examples & Samples

  • Interpretation and communication of results. The ability to present results in both oral and written reports is required
  • Maintains general lab equipment, including dissolution apparatus and HPLC
  • Strong, documented academic performance in Chemistry
  • The ability to work successfully in both a team/matrix environment as well as independently is required
21

Temporary Scientific Associate Resume Examples & Samples

  • 0-4 years of experience working in an analytical laboratory
  • The ability to work in a fast paced environment, manage priorities and maintain timelines for multiple projects is essential
  • The ability to maintain accurate records of test results in lab notebooks is essential. - Excellent written and verbal communication skills are essential
22

Scientific Associate Resume Examples & Samples

  • Independently carry out development and scale-up activities for synthetically derived compounds, including raw materials, intermediates, and drug substances in support of cGLP or cGMP studies
  • Safely and compliantly implement new synthetic routes and procedures on compressed timelines at both the bench and Kilo Lab scales
  • Generate effective scientific hypotheses to pursue desired synthesis or manufacturing goals and set new experimental direction based on results
  • Ensure compliance with all applicable regulations and SOPs and maintain excellent laboratory records and supporting documentation
  • Demonstrated understanding of common Kilo Lab equipment, processing methodologies and best practices
  • Working knowledge of modern analytical techniques used to support synthetic organic processing (HPLC, NMR, etc.)
  • Previous experience in a Kilo Lab or Pilot Plant environment
  • Ability to successfully interact and collaborate within an interdisciplinary scientific team environment. comprised of organic, physical, and analytical chemists; chemical engineers, project team members; and manufacturing personnel
23

Senior Scientific Associate Resume Examples & Samples

  • Design and perform pharmacological studies to evaluate the efficacy of novel CNS drug candidates in labaratory animals
  • Actively contribute to the set up of new animal models for neurological disorders, including literature search, biomarking technologies and big data analysis
  • Responsible for the efficient planning, detailed analysis and accurate documentation of experiments in a multidisciplinary environment
  • Lab technician in neurobiology, master’s or equivalent degree in pharmacology or related field
  • Strong experience in in vivo/ex vivo biology/neurobiology (behavioral pharmacology, general physiology and biomarkers)
  • Recognized as an animal experimenter (LTK1 or equivalent)
  • Disposition or readiness to use new software and data management resources
  • Scientifically curious, willingness to learn new techniques and skills
  • Flexible and motivated to work in a team
  • Excellent knowledge of English (verbal and written), additional knowledge of French or German is considered a plus
  • Good communication skills in a multicultural environment
24

Scientific Associate Resume Examples & Samples

  • Perform GMP analytical testing using various techniques such as HPLC, GC, KF and dissolution
  • Maintain accurate records of experiments and results in a laboratory notebooks
  • Bachelor’s degree in the life or physical sciences with a preference for a concentration in chemistry, analytical chemistry or pharmaceutical chemistry
  • 2-4 years of experience working in a GMP analytical laboratory
  • Experience with HPLC, GC, FT-IR, UV-VIS, KF, dissolution and other instruments. Strong expertise in HPLC is preferred
  • Familiarity with Empower and SLIM systems
  • The ability to conduct experiments independently following established methodology, procedures and SOPs with minimal supervision
  • The ability to work in a fast paced environment, manage priorities and maintain timelines for multiple projects
  • Strong attention to detail along with excellent written and verbal communication skills are essential
25

Scientific Associate, Embryology Resume Examples & Samples

  • Planning and execution of mouse embryology work; this includes e.g. cryopreservation and recovery, rederivation and in vitro fertilization
  • Planning and executing experiments to determine the genotype of genetically modified mice according to established or new developed protocols
  • Ensure accurate documentation and reporting of embryology and genotyping data
  • Lead a team ensuring highest performance and proper professional development of staff
  • Actively contribute to the future strategic direction of Transgenic Services
  • Build a strong network and relationship with scientists, identifying research needs and applying latest technologies to achieve best-in-class embryology & genotyping service globally
  • General organization and maintenance of the laboratory infrastructure; this includes e.g. ordering consumables and ensuring periodic maintenance of laboratory equipment
26

Scientific Associate Resume Examples & Samples

  • Bachelor's degree in virology, molecular biology, cell biology or other vaccinology related discipline
  • At least 2 years of experience in research and development, preferably including vaccines research in an industrial, academic or government laboratory setting
  • Experience in sterile techniques used for cell culture work
  • Basic experience with common bioanalytical assay execution (ELISA, SDS-PAGE, Western blot, PCR assays)
  • Good communication skills, positive attitude, ability to effectively collaborate with co-workers
  • Experience with FACS analysis and sorting
  • Knowledge of basic molecular biology methods, nucleic acid isolation and characterization
  • History of working in GLP or GMP laboratories
  • Fluency in English
  • Executes and documents experiments/technical studies/tasks with minimum supervision, maintaining good scientific practices
  • Participates in the experiment planning by applying critical thinking, experience and scientific knowledge to the data analysis
  • Interprets results and communicates to his/her supervisor
  • Operates designated laboratory equipment and trains other users as necessary
  • Participates in project meetings, prepares detailed oral or written summaries of results
  • Co-authors technical sections of internal and external reports
  • Maintains training requirements and applies laboratory procedures and SOPs applicable to vaccine development
27

Scientific Associate Resume Examples & Samples

  • Good knowledge and understanding of GSK Vaccines strategy and objectives, regulatory requirements, as well as competition intelligence and intellectual property aspects. Ability to integrate this knowledge in decisions and recommendations
  • Excellent communication skills, need to appropriately manage the interfaces with Project Teams
  • Able to efficiently manage uncertainty, changes in priority and timeline restrictions
  • Knowledge in several technologies and/or in several projects
  • Can read, understand scientific papers, extract technical protocols from literature
  • Possesses in-depth knowledge of how to analyze and interpret experimental data
  • Executes assigned tasks and activities with high quality and attention to own and other’s safety
  • Analyzes, interprets results, and proposes next steps
  • Able to operate with minimal supervision
  • Demonstrates basic management skills
  • Capable of independent decision-making
28

Senior Scientific Associate Resume Examples & Samples

  • Involvement in PET and SPECT studies including provision of radiochemical, scientific and technical input into the study design, results, interpretation and publications
  • Selection, design and development of novel PET/SPECT radiotracers for pre-clinical imaging research programmes
  • Training users to operate the radionuclide imaging instruments
  • Developing analytical methods
  • Promoting collaborations both within the CI and outside, including those with pharmaceutical companies
  • Radioprotection coverage in the pre-clinical imaging facilities in the CI
  • Advising users of the facility on appropriate methodology and use of radiotracers for new studies
  • Liaise with instrument manufacturers to ensure maintenance and prompt repair of faults of the radionuclide imaging and CT equipment in the CI
  • Constructing or purchasing equipment as required for new applications
  • Keep abreast of developments in the field
  • Provide written reports at the request of the head of the imaging core
29

Scientific Associate Resume Examples & Samples

  • Independently perform in vivo experiments in a wide range of rodent models. - Handling, surgery and necropsy of rodents
  • Perform functional tests and surgeries in rodents
  • Perform ex vivo analysis of tissues from rats and mice
  • Conduct biochemical, molecular biological and histology analysis
  • Demonstrate flexibility in adapting methods/skills according to evolving project priorities
  • Work collaboratively
  • Provide processed research data, evaluation and result interpretation
  • Optimize existing lab methods and develop new methods
  • General organization and maintenance of lab infrastructure, reporting and archiving of research data
30

Scientific Associate Resume Examples & Samples

  • Support data verification (QC checking) of data for regulatory filings
  • Sound k nowledge of pharmaceutical and engineering principles in the solid dosage form development for both clinical and commercial scales
  • Understanding of QbD and experience with regulatory filings is a plus
31

Temp Scientific Associate Resume Examples & Samples

  • Conducting ex vivo experiments in particular using primary human and animal cells
  • Lead and execute in vivo experiments investigating immunological questions
  • Development and execution of cell-based assays for compound characterization
  • Measurements of cell phenotypes (imaging, FACS, gene profiling) and cell activation (cytokines)
  • Independent planning and execution of experiments in a timely manner, pro-active data analysis and interpretation
  • Efficient management and maintenance of a functional laboratory, technical equipment and tools
  • Open mindset and ability to learn novel techniques based on project needs
  • Contribute to establish novel methods
  • Active contribution to lab and project teams, having tangible impact on the science and drug discovery (e.g. presentations at lab and project team level, discussion of literature data and contribution to internal/external scientific meetings)
32

Scientific Associate Resume Examples & Samples

  • 80% responsible for in vivo technical training
  • 5% responsible for ensuring compliance with all institutional and regulatory protocols, policies, and guidelines
  • 5% responsible for pursuing continuous learning/professional development opportunities and enhancing/expanding skill set
  • 5% responsible for drafting & periodic review of LAS Technical SOPs
  • Provide consistent and high quality technical training
  • Proactively meet and exceed customer service expectations
  • Continuously pursue educational and professional development opportunities to enhance and expand relevant skills and knowledge
  • Identify new/emerging techniques/refinements to expand the Research Support service portfolio
  • Identify process inefficiencies and streamline processes
33

Scientific Associate Protein Production Resume Examples & Samples

  • A scientific degree in a relevant Life Science discipline (BSc, MSc, but no PhD), or a successful completion of education as Lab Technician
  • Several years of experience in the context of recombinant protein production in mammalian cells, preferably in a pharma or biotech research environment
  • Proficiency with the maintenance of different mammalian cell lines
  • Proficiency with state-of-the-art transfection methods for mammalian cells
  • Proficiency with flow cytometric analysis of mammalian cells (FACS)
  • Proficiency with standard biochemical analytical methods for the detection of target proteins in cell culture supernatants (SDS-PAGE, WesternBlot, ELISA)
  • Additional experience with chromatographic protein purification systems (AKTA systems) is an advantage
  • Fluency in English is a prerequisite; fluency in German is an advantage
34

Parasitology Scientific Associate Nitd Resume Examples & Samples

  • Independently conduct and interpret routine phenotypic / biochemical assays to support drug discovery efforts with high reliability
  • Assist in troubleshooting and implementing new assays
  • Coordinate with various line-functions to ensure smooth running of assays
  • Ensure best practices by ensuring integrity and quality of data in a timely manner
  • Carry out innovative mechanism of action studies
  • Be self-driven and able to contribute significantly on experimental design
  • Comply with Novartis standards and practices for documenting and archiving research activities
  • Support scientific input for project presentations and progress reports
  • Maintain compliance with local and global standards in Health/Safety & Environment
  • Specific knowledge or expertise in working with Plasmodium, kinetoplastids or Cryptosporidium parasites will be an advantage
  • Knowledge in fluorescent microscopy, FAs analysis, high-content imaging and animal handling are a plus
35

Temporary Senior Scientific Associate Resume Examples & Samples

  • Conceive, execute and interpret synthetic organic and engineering-related laboratory experiments with a high degree of reliability and independence
  • Hands-on experience in a pharmaceutical development environment, as well as capability and desire to understand, develop, and scale-up chemical processes
  • Assist in the development of novel and creative solutions to overcome scale-up and manufacturing obstacles
  • Multitask to effectively manage multiple activities and projects
  • Assist other chemists and engineers in Chemical and Materials Engineering, Process Chemistry and the broader Pharmaceutical Sciences Department
  • Ensure compliance with all applicable safety regulations and standard operating procedures
  • MS in Chemical Engineering or Organic Chemistry with 0 – 4 years of relevant experience in a laboratory engineering or process chemistry environment
  • BS in Chemical Engineering or Organic Chemistry with 4+ years of relevant experience in a laboratory engineering or process chemistry environment
  • Working knowledge of common laboratory instrumentation (HPLC, GC, etc.)
  • Experience with statistical design of experiments desired
36

Scientific Associate Resume Examples & Samples

  • Independently perform a variety of project-oriented analytical work assignments (e.g., perform analytical experiments, organize data, and analyze/record/report results and conclusions of experiments) to support the development of drug substances and products. Design experiments with minimal supervision to meet the project objectives and timelines
  • If assigned, represent department in CMC teams, actively contribute to team strategies and collaborate with cross-functional groups to meet drug development milestones with guidance from supervisor
  • Develop and validate analytical methods with minimal supervision
  • Independently prepare method validation protocol/investigation plan, and execute validation work under cGMP practices
  • Analyze and troubleshoot results with minimal guidance
  • Ensures laboratory operational capability (for both cGMP and development laboratories) by following current SOPs, proper maintenance of laboratory equipment and instrumentation. Document all experiments, results, and conclusions promptly and accurately
  • Provide guidance and training to Scientific Associate I and II
  • Participate and contribute at group and project meetings as required. Contribute to publications such as department guidelines, technical reports, regulatory documents or scientific papers
  • Attend and present in seminars as required
  • Maintain and complete all required documentation including logbooks, lab notebooks, and analysis records in a timely manner
  • Prepare methods, qualification reports, investigational report, validation protocol / investigation plan, and validation report as required
  • Participate and contribute at group and project meetings as required (e.g., prepare and present results and conclusions to project sub-teams)
  • Contribute to publications such as department guidelines, technical reports, or scientific papers
  • Obtain necessary chemical reagents, reference standards and other components from appropriate sources
  • Maintain laboratory equipment and instrumentation
  • Perform all analytical activities per applicable safety guidelines, departmental guidelines, and cGMP requirements
  • Maintains knowledge of cGMP compliance through internal and external training
37

Scientific Associate Resume Examples & Samples

  • Bachelor’s Degree with 0-2 years of related work experience
  • Strong computer skills (Microsoft Suite - Word, Excel, PowerPoint)
  • Effective written and verbal communication
  • High productivity with minimal supervision – must be proactive and resourceful
  • Knowledge of drug development including pre-clinical and clinical
38

Scientific Associate Resume Examples & Samples

  • Understand drug substance and drug product in the context of chemical development and formulation development to identify and document critical factors that affect method performance
  • Conduct dissolution experiments, including sample preparation and data analysis, on development and commercially available test powders and solid oral dosage forms
  • Conduct risk analysis in all aspects of method development to efficiently develop robust methods that are GMP friendly based on quality by design
  • Design validation protocols that are in compliance with ICH and FDA guidelines; furthermore, identify critical factors that may not be mandated by the guidelines but are essential for validating the methods for their intended use
  • Present to cross functional teams and effectively communicate critical analytical issues and solutions
  • Help design validation protocols that are in compliance with ICH and FDA guidelines; furthermore, identify critical factors that may not be mandated by the guidelines but are essential for validating the methods for their intended use
  • Experience in analytical data review, analytical investigations, instrument and method troubleshooting is required
  • Bachelor’s degree in chemistry, analytical chemistry or pharmaceutical chemistry
  • Skilled in HPLC, GC, FT-IR, UV-VIS, KF, dissolution and other instruments is essential. Strong expertise in HPLC, GC, Dissolution and Dissolution method development is highly preferred
  • Good understanding of ICH and FDA method validation guideline
  • Previous experience in drug substance/drug product development is preferred
39

Scientific Associate Resume Examples & Samples

  • Minimum experience: 0-4 years of experience working in an analytical laboratory
  • Familiar with HPLC, GC, FT-IR, UV-VIS, KF, dissolution and other instruments. Strong expertise in HPLC and/or GC is preferred
  • The ability to conduct experiment independently following established methodology and procedures with minimal supervision is essential
40

Senior Scientific Associate Resume Examples & Samples

  • Tracking nonclinical timelines and deliverables (study- and program-related)
  • Quality control of routine documents including study protocols and study reports. Uploading final documents to internal EDMS and notification of all appropriate parties
  • Serves as coordinator on routine programs
  • Facilitation of project meetings and providing support for presentation materials
  • Maintenance of contracts and quotations, including requests for MSAs, CDAs, working in collaboration with Vertex outsourcing
  • Working with sub-functions in the department to schedule various study-related activities
  • Coordinating multi-site activities for study programs
  • May represent PSA in cross-functional initiatives
  • Demonstrates knowledge of the drug development process and GLP requirements for studies
  • Strong organizational skills and ability to maintain timelines
  • Demonstrates understanding of nonclinical protocols, and possesses a general understanding of study data
  • Possesses excellent written and oral communication skills
  • Demonstrates teamwork and collaboration skills
  • Proficient in MS Office applications, including Word, Powerpoint, and Project
  • M.S. (or equivalent degree) and 0-2 years of relevant work experience
  • B.S. (or equivalent degree) and 4+ years of relevant work experience
41

Scientific Associate Resume Examples & Samples

  • Generates accurate and precise data for samples used in stability, raw material, clinical and toxicological studies using a wide range of validated and compendial analytical procedures and analytical instrumentation
  • Executes laboratory experiments with independent planning, and critically evaluates and analyzes generated analytical data in support of Phase I / II /III drug development programs with limited supervision
  • Troubleshoots any poor quality data and instrument performance problems with minimum guidance from the supervisor
  • Evaluates analytical methods and provides critical feedback or proposes recommendations on method improvements, as required
  • Performs other laboratory procedures and special assignments as directed by the supervisor including, but not limited to, testing to support validation studies, investigative testing, and testing of raw materials, maintaining key infrastructure or key coordinator responsibilities, etc
  • Compiles, evaluates and statistically analyzes technical data and generates stability data tables and plots in support of specification development and regulatory submissions under limited supervision
  • Identifies any atypical data and reports to the supervisor with probable causes and suggestions for investigation
  • Works directly with manager/supervisor to maintain the integrity of the Laboratory Information Management System (LIMS) Stability Database. Performs requested data searches utilizing the LIMS
  • Maintains a broad knowledge of cGMP compliance through internal and external training
  • Working knowledge of cGMPs, FDA requirements, and a basic understanding of global regulatory requirements associated with stability studies is desired
  • M.S. in Analytical Chemistry or related discipline with 0-2 years of experience or B.S. in Analytical Chemistry or related discipline with 3-5 years of experience in analysis of pharmaceutical products or pharmaceutical method development and validation.Minimum 2 years of experience in the analysis of data and writing of technical protocols, reports, and submission ready documents
  • LI-DM3
42

Temporary Scientific Associate Resume Examples & Samples

  • Conduct in vivo experimental models of diseases on rodents, including
  • Apprenticeship as laboratory technician with additional BSc of a Swiss “Fachhochschule” or BSc / bac +3 from a University in Pharmacology/Biology/Immunology
  • Working experience in the field of Biology/Immunology
  • Show technical expertise in all aspects of in vivo pharmacology (animal handling, immunization, body fluid sampling, isolation and further ex vivo characterization of different cell types), working experience with EAE models would be an asset
  • Practical background in different in vitro techniques (ELISA, primary cell culture handling, FACS, cytokine detection assays)
  • Good knowledge of English, French and/or German proficiency would be an asset
  • Well trained in computer programs: Excel, Power Point, GraphPad Prism
  • Ability to plan, perform, analyze and accurately document experiments independently
  • Capable to work independently with minimum supervision
  • Dynamic, flexible and scientifically curious, willingness to learn
  • The candidate must also be willing and able to share weekend work duties with others members of the team
43

Senior Scientific Associate Resume Examples & Samples

  • Perform high-throughput in vitro and in vivo study sample analysis using LC/MS/MS methods. This responsibility will include duties such as biological sample preparation and extraction using protein precipitation, solid phase extraction, liquid-liquid extraction and relevant techniques
  • Bioanalytical method development for high throughput sample analysis
  • Data processing from bioanalytical runs and study report generation
  • To review and interpret scientific results for communication among appropriate stakeholders
  • Work in a collaborative team environment
  • Assist other scientists in a team based environment in the execution of LC/MS/MS experiments by performing supportive tasks such as preparation of study materials, sample processing, instrument tuning and maintenance, and troubleshooting
  • Work with other DMPK scientists on bioanalytical method development and validation
  • Laboratory experience with chemical, biological, and/or analytical techniques
  • Candidates should have hands-on experience with HPLC and LC/MS/MS analytical instrumentation, sample preparation techniques and sample analysis
  • Hands-on familiarity with Analyst software to control AB Sciex LC-MS systems for quantitative analysis
  • Familiarity with laboratory information management systems (LIMS)
  • Capacity to work independently with minimal supervision in executing outlined studies as well as collaboratively in a team environment
  • BS (or equivalent degree) and 4+ years of relevant employment experience, or
  • MS (or equivalent degree) and 0-2 years of relevant employment experience
44

Scientific Associate Resume Examples & Samples

  • BA/BS in engineering technology, materials science, chemistry, physics, or electron microscopy, or the equivalent combination of education and related experience
  • Experience conducting complex experimental activities with a solid scientific background
  • Significant experience designing, fabricating, and modifying laboratory equipment and mechanical systems, such as vacuum systems
  • Knowledge of engineering designs and drawings, including geometric tolerancing and dimensioning
  • Experience in machining processes, mechanical fabrication, and assembly
  • Significant experience in materials properties and materials characterization
  • Advanced verbal and written communication skills necessary to effectively collaborate with other scientific and technical staff members, present research results, and deliver scientific presentations
  • Ability to work on complex projects with a high consequence of error
  • Significant experience working with radioactive materials
  • Experience working in an inert atmosphere glovebox
45

Scientific Associate Resume Examples & Samples

  • Perform GMP analytical data review for various techniques such as HPLC, GC, KF, TOC, IR and dissolution
  • Compile and summarize analytical raw data in various report formats
  • Coordinate and track the outsourcing of testing to CROs with attention to project timelines
  • Track and manage the release of raw materials
  • Perform review of laboratory equipment logbooks and daily check logbooks
  • Data entry and various administrative functions for laboratory systems and GxP training software
  • Generate and compile metrics reports to track group functions and identify areas for improvement
  • Strong attention to detail along with excellent written and verbal communication skills is essential
  • Familiarity with Waters Empower chromatography software, SLIM data management system, Oracle applications
46

Scientific Associate Resume Examples & Samples

  • Degree in Science, B.Sc.(E.g.Toxicology or related field) (0-1 years’ experience)
  • Critically evaluatescientific papers
  • Strong writing skills andcommunications skills (discuss project versatility)
  • Ability to handlemany different tasks simultaneously
  • Familiarity with softwarepackages&#96
  • Ability to prioritize andmanage time effectively
  • Ability to processinformation, follow directions
  • Create/edit reports withguidance
47

Senior Scientific Associate Resume Examples & Samples

  • Develop solid dosage forms for clinical and commercial use, generate data for project progression and regulatory filings, conduct optimization and scale up studies
  • Maintain accurate and complete laboratory notebook capturing protocols, results and observations. Interpret data to form sound conclusions
  • Timely document integrated experimental outcomes in presentations and research reports
  • Perform basic statistical analysis of experimental data
  • Assist in technical transfer to CMO partners for clinical trial manufacture
  • Comply with all relevant Safety and GMP procedures
  • Direct experience working with CMOs is a plus
  • Understanding of QbD and experience with Regulatory filings is a plus
48

Scientific Associate Resume Examples & Samples

  • Demonstrate excellent understanding of cGMPs requirements and other relevant regulations (e.g. environmental etc.)
  • Be responsible for strict adherance to SOPs, policies and other necessary procedures to ensure successful operation of the drug product facility and GMP warehouse
  • Responsible for assuring materials are stored in the proper conditions per specification and reflect accurate location and quantities within the material management system
  • Interface with cleaning staff, and Facilities/Operations to make sure the facility meets its intended use requirements as well as to schedule routine cleaning and all the necessary calibration and preventive maintenance activities
  • Interface with all appropriate key stakeholders, such as Quality and EH&S to ensure appropriate procedures are followed to ensure successful operation of the drug product facility and Materials Management areas
  • Be responsible for batch record execution under supervision
  • Effectively multitask and demonstrate resourcefulness in running multiple activities concurrently
  • Ability to drive a fork truck and follow all safety related procedure
  • Minimum education/experience includes, a Bachelor’s degree or 3 years relevant GMP experience
  • Ability to build excellent understanding and application of cGMPs and other appropriate regulations to ensure success in the GMP Operations group
  • Inventive and innovative, self-starter who is comfortable and successful working in a multi-disciplinary team under defined timelines
  • Teamwork, leadership and collaboration skills
  • Excellent basic computer skills and ability to learn new systems
49

Scientific Associate Resume Examples & Samples

  • Collection and analysis of cleaning verification samples using TOC and HPLC
  • Perform GMP analytical testing using various techniques such as HPLC, GC and dissolution
  • Experience with cleaning verification and TOC analysis
  • Experience with HPLC, GC and dissolution and other instruments. Strong expertise in HPLC is preferred
  • Familiarity with Empower software
  • Schedule and hours for this role are Sunday - Thursday 3-11pm**
50

Scientific Associate Resume Examples & Samples

  • Strong oral and written communication skills in English and German is mandatory
  • Good knowledge of cellular biology, biochemistry/molecular biology and immunological techniques
  • Experience with isolation and culture of human and rodent immune cells
  • Experience with Prism, Spotfire and FloJo would be advantageous
  • Showing initiative, commitment, independence and willingness to learn new techniques is required as is the ability to work in multidisciplinary team
  • Must possess excellent record keeping and be detail oriented
51

Scientific Associate Resume Examples & Samples

  • Proficiency with dosing via multiple routes – IP, PO, IV, SC
  • Hands on in vivo skills necessary to validate and implement rodent models
  • Demonstrated ability to quickly learn and perform in new areas, implement new techniques and instrumentation
  • Meticulous laboratory approach, careful adherence to protocol and excellent lab notebook documentation
  • Strong analytical and computer skills
52

Scientific Associate Resume Examples & Samples

  • Independently generates accurate and precise data for samples used in stability, raw material, clinical and toxicological studies using a wide range of validated and compendial analytical procedures and analytical instrumentation
  • Executes laboratory experiments with independent planning, and critically evaluates and analyzes generated analytical data in support of Phase I / II /III drug development programs
  • Demonstrates strong planning, initiative, efficiency and timeliness in performing experiments and generates error free data
  • Independently troubleshoots any poor-quality data and instrument performance problems
  • Provides work direction, training and advice to junior coworkers to enhance their work effectiveness in generating analytical data
  • Independently identifies technical issues and proposes solutions or troubleshooting techniques and implements with minimal supervisor input
  • Maintains a broad knowledge and understanding of global regulatory requirements and expectations related to stability studies, special studies and stability testing
  • Independently compiles, evaluates and statistically analyzes technical data. Critically analyzes all analytical data generated from studies, interprets the significance and reports any atypical data with likely causes to the supervisor and plans for investigation
  • Under supervisor’s guidance, prepares critical technical memos, protocols and reports
  • Interacts with contract laboratories, as needed, to troubleshoot analytical issues and/or address lab incidents and investigations. Reviews, evaluates and archives contract laboratory generated documentation and keeps supervisor and/or stability lead informed of data/quality issues. May perform other activities as directed by supervisor to support analytical activities at contract laboratories
  • Maintains strong working knowledge of cGMP compliance through internal and external training, literature and other sources. With limited supervisor input, identify and train on laboratory instrumentation and techniques requiring additional trained resources to meet current business needs
  • Independently identifies SOP document issues or cGMP gaps and takes proactive measures to address issues, by writing or revising pertinent SOPs to meet cGMP requirements. Trains and assists peers on more complex analytical techniques where appropriate and as assigned
  • Independently interfaces with method development/validation staff to learn new techniques and troubleshoot analytical issues
53

Scientific Associate Resume Examples & Samples

  • In vivo development and validation of syngeneic and tumor models
  • Ex vivo FACS data acquisition and analysis to allow the determination of PD markers for novel immune modulators
  • In vitro cell culture assay development including work with primary human and murine immune cells
54

Scientific Associate Resume Examples & Samples

  • Perform mechanistic and disease studies in rodents
  • Establish and use molecular and in vitro cellular methods (e.g. assessment of different activation parameters of leukocytes) to investigate the function of primary human and mouse leukocytes
  • Combinatorial application of a variety of readouts, like multicolor flow cytometry, western blots, ELISA and the assessment of leukocyte differentiation for the characterization of novel immunomodulating substances and pathways
  • Expertise in cellular and biochemical methods to determine activation of complement pathways in primary cells and organs (blood, urine, tissue) derived from rodents or humans
  • Use of human and rodent material for drug development and target validation
  • Implement new in vitro and in vivo lab techniques according to literature, and explore new approaches
  • Present results at project team meetings and engage in scientific discussions with the team members