Scientist Ii Analytical Jobs

Experience, Education and Specialized Knowledge and Skills

Maintain knowledge of state-of-the-art principles and theories and apply this knowledge to the design, execution, and interpretation of experiments.

Expert in ion channel physiology who possesses knowledge and familiarity with high throughput ion channel screening platforms.

Experience using a range of data informatics tools.

Experience interacting with external vendors and with outsourced R&D models.

Possess a strong attention to detail, be highly organized, and have exceptional interpersonal, organizational and communication skills.

2-4 years of experience developing theory and applications to solve challenging real-life data science problems.

Experience with designing computational methods and tools.

Prior knowledge of neuroscience and/or neurodegenerateive disease biology is preferred, but not required.

Excellent oral and written English communication skills.

Develop, implement, and apply computational tools on genomic datasets.

Work closely with biologists to interpret and understand the data.

Chemical synthesis experience in an industrial, academic, or government research lab preferred

Minimum of a summer internship or equivalent research experience in a lab environment

Experience of characterization of chemical compounds via analytical techniques such as NMR, IR, GC, DSC, DMA, TGA, etc.

Knowledge of polymer chemistry and structure property relationships preferred.

Excellent interpersonal skills and ability to work in cross-functional teams.

Strong verbal and written communication skills.

Knowledge of inventory management/ERP systems and Microsoft Office products.

Minimum of 2-5 years of relevant work experience required.

1+ years regulated GMP environment experience required.

Experience in MDI/DPI analytical test methods (i.e. Andersen Cascade Impactor and Emitted Dose techniques) preferred.

Assure all Materials Control staff are current on existing compliance and training requirements, as well as industry best practices

Other duties, as assigned in accordance with company requirements.

Communicate toxicology study findings to Toxicology management and program teams in a timely manner

Additional responsibilities as assigned by the Toxicology supervisor

Strong scientific and leadership skills

Experience providing toxicology expertise on cross-functional development and discovery teams across different stages of development

Strong knowledge of GLP regulations

Current or previous Study Director experience

Experience in dietary supplements or pharmaceutical formulations or active ingredients

PLR is hiring for a biotech/ pharma, etc. company

Analyze and interpret the results of complex analytical data.

Develop CoA’s for agricultural and food-grade products.

Send raw materials and finished goods out for 3rd-party analyses or test in house.

Work with the product-development team to help create new products for dietary supplement industry.

Minimum Qualifications – Education And Experience

Preferred Qualifications – Education And Experience

Other projects or responsibilities as may be required.

M.S. with generally more than 8 yrs of relevant working experiences.

Ph.D. with generally 2-4 years of post-doctoral training or relevant working experiences

Experience in process development and optimization for stem cells and/or hybridoma cell culture

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

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.

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 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.

A leadership team that prioritizes your health and well-being; offering a remote work environment and flexible work hybrid situations

A clearly defined career framework to help you successfully manage your career

Competitive 401K and employee benefits

Leadership development and virtual training opportunities

Free financial counseling, health coaching and employee assistance program

Effective productivity/technology tools and training

Knowledge of current regulatory guidelines and cGMP requirements.

B.S. or Master degree from an accredited university is required. Working experience in the pharmaceutical or biotech industry is preferred.

Practical knowledge of method development and optimization for protein therapeutics is preferred.

High emotional intelligence, excellent interpersonal skills, and strong communication skills.

Follow and execute defined methods, SOPs. Under direct supervision, author SOPs, study plans, protocols, and method development reports.

Work with various Research and Development teams to support transfer of analytical test methods for development and clinical support.

Prepare and review technical reports, method validation protocols, and other documentation to support regulatory filings and client requirements.

Maintain and troubleshoot analytical instruments and equipment, ensuring their proper functioning and calibration to deliver accurate and precise analytical results.

Collaborate with external partners, including contract testing laboratories and clients, to coordinate analytical activities and address technical inquiries.

Familiarity with regulatory guidelines (e.g., FDA, ICH, USP) related to analytical method development, validation, and GMP compliance.

Prior experience binding adsorbents into structured forms/materials, such as integration of adsorbents into polymers, membranes, films, fibers, pellets, or extrudates

Minimum of 3 years of research experience post the PhD degree

Experience in synthesis and analysis of MOF and COF materials

Analyze and optimize the heat-transfer properties of different binder systems to achieve optimum MOF/COF system scale performance

Evaluate MOF/COF coatings and structured material stability to various process conditions (temperatures, flow rates, mechanical vibrations)

Quantify adsorption capacity and rates of MOF/COF coatings and structured materials as compared to pristine MOF/COF materials

Demonstrates effective project management skills.

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

Demonstrates broad technical program knowledge.

Develops and oversees novel scientific projects and will manage the work of others in a matrixed structure.

Independently manages workload and expectations.

Receives high level instructions on work; determines methods on new assignments; greater demonstrated independence; may manage junior staff

Demonstrates effective project management skills.

Demonstrates broad technical program knowledge.

Develops and oversees novel scientific projects and will manage the work of others in a matrixed structure.

Independently manages workload and expectations.

Receives high level instructions on work; determines methods on new assignments; greater demonstrated independence; may manage junior staff

A minimum of 3+ years of relevant pharmaceutical industry/academic experience is required after graduation.

Manage workload and time to perform multiple projects effectively, and ensure all necessary paperwork is completed on a timely basis

Minimum 9 years’ experience, including 2 years’ supervisory experience

Minimum 12 years’ relevant experience, including 2 years’ supervisory experience

Minimum 14 years’ relevant experience, including 2 years’ supervisory experience

Perform impurity identification and structure elucidation activities by High Resolution Accurate Mass LC-MS(MS) and GCMS.

Follow responsible actions regarding chemical disposal

Experience with IP-RP-UHPLC and AX-HPLC analytical techniques using Agilent, Waters and/or Thermo UHPLC’s and associated software

In depth knowledge of GLP/GMP’s in a pharmaceutical environment

The successful candidate must possess excellent writing and communication skills and a demonstrated ability to work independently and with cross-functional teams

Characterization of custom phosphoramidites and drug substance by UHPLC and/or LC-MS

Oversee implementation and validation of analytical methods related to starting materials and drug substances at CMOs

Oversee analytical work conducted at CMO’s including raw material suppliers and drug substance manufacturers