Analytical Research And Development Scientist Jobs

Participate laboratory organization activities (orders, management/maintenance of equipment, reception & verification of reagents and receipt of samples)

Participate in qualification and transferring of analytical methods

BS with 0-2 years of professional experience in the vaccine or pharmaceutical industry in the field of R&D, QC analytics

Excellent verbal and written communication skills

Participate in the selection, development of new analytical methods of mRNA products in collaboration with the scientists of the team

Develop and write work plans/protocols

Participate in cutting-edge technology development and establish internal and external partnerships to build Takeda's scientific capabilities.

Perform non-GMP method qualification for different biophysical assays and particulate characterization methods.

Lead the characterization of biologics including the qualification of reference standards, in-depth structure/function studies, product comparability and investigations.

Bachelor’s degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical sciences with 8+ years relevant industry experience.

Master’s degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical sciences with 6+ years relevant industry experience.

PhD in chemistry, biology, pharmacy, engineering, or related pharmaceutical sciences with 0+ years relevant industry experience.

Proven experience with assays, such as PCR, ELISA, and /or mammalian cell culture.

Positive, professional self-starter with a passion for science, innovative technical and analytical skills required to perform at the highest level

Excellent clear and concise writing skills for technical reports and documents along with strong verbal communication skills

Experience in analytical method development and assay transfer

Be BOLD (Find a Way)

Care Deeply – for our patients, each other and our work

The ideal candidate will have experience and understanding of qualification and validation of analytical methods.

Participates in testing to support method transfer, development, qualification, product characterization, routine GMP and non-GMP analysis, etc.

Excellent technical lab skills with attention to details and the ability to assume independent ownership of protocols/experiments.

Understands GDP and GMP regulatory requirements.

Excellent verbal and written communication skills with the ability to maintain formal recording.

Advance innovative science by pushing boundaries.

Good time and project management skills, ability to oversee several projects simultaneously.

Knowledge and skills in chemistry, biochemistry and microbiology.

Comply with institutional certifications and requirements in a BSL-2 environment.

Responsible for development, qualification, documentation, and transfer of assays.

Virology knowledge (especially flavivirology) is highly desirable.

Training and experience in Design of Experiments and other statistical methodologies.

2+ years of relevant experience in an analytical laboratory setting.

Previous experience with HPLC, LCMS, MALDI-TOF MS, and UV-Vis

Preferred - experience with oligonucleotides.

Experience working at a multi-site company and/or with CMOs is helpful.

Develope analytical methods of oligonucleotides, peptides, conjugates, and small molecules.

Analyze and trend stability data, archive data.

Manage laboratories including ordering lab supplies, chemicals, and gases

Mentor, train, and guide less experienced colleagues in the instrumental analysis

VOC analysis experiences by using GC and GC-MS with optimal sample preparation techniques

Standard testing (e.g. ASTM, ISO) experience

Programming and/or software skills for data analysis (e.g. curve fitting), statistical analysis, and automation.

Experience in GC, LC or GPC

Provide technical support and assistance to product managers, R&D chemists and engineers, production and warranty group.

Communicate and provide training on analytical group capabilities and techniques.

1+ years of minimum analytical experience in a relatable industry

Responsible for developing new and improved methods and techniques in chromatography, spectroscopy, microscopy, rheology, and physical and chemical separation techniques.

Responsible for identifying, developing and implementing analytical methods and techniques to better understand and predict formulation interactions and long-term performance.

Provide and maintain a safe and clean work environment.

Analysis and evaluation of material and products at all stages of development process under stringent quality and time requirements.

A minimum of 3-7 years of industrial experience with hands-on experience in analytical chemistry.

Experience with the development of bioanalytical methods is a plus.

Excellent written, reporting, and verbal communication skills.

Candidates with hands-on experience in the operation of Sciex LC/MS/MS are preferred.

Review of data for technical content and regulatory compliance.

A combination of education and demonstrated, related work experience will be considered in lieu of formal education.

Knowledge and experience with botanical ingredients are strongly preferred.

Research and manage claims substantiation files; oversee development of product monographs for new and existing products.

Create educational, scientifically driven content for internal and external trainings and administer trainings as assigned.

Demonstrated skills in critical analysis of scientific results, and translation of scientific results to claims.

Strong knowledge in physiology and nutrition science.

4.Knowledge of protein purification methods and chromatography techniques (e.g., Ni-NTA sepharose, Protein A/G resin, spin columns).

6.Experience with data analysis and scientific software tools, such as Snapgene, Prism.

7.Excellent organizational, communication, and problem-solving skills.

Research Associate/Scientist Molecular biology and protein purification

Multiverse Pharma, San Diego, CA

Send your letter of interest with credentials to:

Clean data, prepare data documentation, manage, and analyze data files

Manage field activities, including the implementation of quality control procedures

Independent thinking, a strong understanding of social sciences, an ability to manage workflows on multiple projects, and self-motivation are highly valued.

Knowledge of statistical software, specifically R or Python (Stata is a plus).

Self-directed, intrinsically motivated; capacity to manage work independently and organize workflows across multiple projects.

Previous experience as a research analyst or conducting independent research.

Executes on strategy, vision, and direction set by line management

Master's/PhD in relevant discipline and Some similar experience as noted above

Knowledge of protein and gene therapy biology with a good understanding of testing/characterization methods required

Some experience with novel methods in AAV characterization (e.g. ddPCR, DLS, AUC, NGS, CE-SDS) preferred

Good knowledge of cell-based methods associated with bioanalytical analytical method development (e.g. TCID50, Potency assay, viral transduction, and ELISA methods) preferred

Familiar level knowledge of the biologics drug development process is recommended

Possess knowledge of, and experience with ELISA, Capillary Western, ddPCR/RT-ddPCR, and qPCR.

The ideal candidate will have experience and understanding of qualification and validation of analytical methods.

Participates in testing to support method transfer, development, qualification, product characterization, routine GMP and non-GMP analysis, etc.

Excellent technical lab skills with attention to details and the ability to assume independent ownership of protocols/experiments.

Understands GDP and GMP regulatory requirements.

Excellent verbal and written communication skills with the ability to maintain formal recording.

Experience with High Performance Liquid Chromatography, Gas Chromatography, and Liquid Chromatography-Mass Spectrometry, Ion Chromatography, spectroscopy, and wet chemistry;

Experience in method development and validation for Active Pharmaceutical Ingredients (APIs); and

Experience with Karl Fisher, Nuclear Magnetic Resonance, UltaViolet-Visible Spectroscopy, Fourier Transform Infrared Spectroscopy, Differential Scanning Calorimetry and Thermogravimetric Analysis.

A Manager with broad experience, passionate about the science, with an extensive research and development portfolio

Perform routine and novel testing to support biological therapeutic products from early-stage development through late-stage/commercialization and their lifecycle management.

A team with broad experience and passion for science

Excellent verbal and written communications skills

Experience troubleshooting and developing analytical methods.

Experience in analytical method troubleshooting, optimization, and validation.

BS with 3+ years of experience in analytical development

MS with 2+ years of experience in analytical development

PhD with 0+ years of experience in analytical development

Demonstrated experience in physical characterization techniques such as TGA, DSC, PXRD, GVS, and SEM.

Must demonstrate excellent communication, critical thinking, and organizational skills.

Physical requirements: must be able to lift up to 25lbs, walk/sit/stand on regular basis, and regular use of computers

Experience with matrix management and peer to peer coaching

B.S. in Chemistry, Biochemistry, Engineering, Pharmaceuticals or related field with ten (10) years of relevant experience

M.S. in Chemistry, Biochemistry, Engineering, Pharmaceuticals or related field with seven (7) years of relevant experience

Ph.D. in Chemistry, Biochemistry, Engineering, Pharmaceuticals, or related field with three (3) years of relevant experience

Strong background and experience in separations science

Experience with complex glycan analysis and link to mechanisms of actions and various Biologic modalities (e.g., mAb, antibody-drug conjugate, fusion protein)

Experience working with Python/R in bioinformatics data analysis, SQL data management, and data visualization tools such as Power BI or Tableau.

Improve the data management of analytical laboratories, ex. automation, digitalization, and data visualization.

Experience in statistical analysis to analyze complex biological datasets.

Experience working with lab automation systems, including scripting, operating, and maintenance.

Hands-on experience in nucleotide extraction, PCR and library preparation.

Hands-on experience in Bioinformatic data analysis.