Analytical Scientist Jobs

Developing benchscale techniques to enhance Magrathea's analytical capabilities.

Experience with analytical techniques such as ICP-OES, titrations, TGA, dissolved organic measurements, calibrations, and other aqueous measurements

Leading analytical chemistry experiments and workstreams in support of Magrathea's engineering team.

Supervising elemental analysis of lab samples, conducting QAQC on data collection, and analyzing experimental results to accelerate development of our technology

Contributing actively to a safety culture that puts physical wellbeing ahead of all other company priorities

Occasional travel to off-site locations where the company is developing commercial smelter operations

Bachelor/Master of Science in Biology, Molecular Biology, or Biochemistry, with a minimum of 5 years’ industry GLP/GMP experience.

Experience in running stability protocols with associated experimental planning and data collection and analysis.

Strong written and oral communication skills.

Develop, qualify, and implement biophysical assays to support early and late-stage vaccine development programs.

Author, review, and approve SOPs, study protocols, reports, and other scientific and quality documents.

Thorough and accurate documentation of work

You need skills and experiences that enable you to:

Lead aspects of capability development within the Personal Health Care Analytical Chemistry organization

Lead characterization strategies for critical materials used for manufacture of our products

Or a closely related field

Your Technical Background/training Should Include

Starting Pay / Salary Range

Perform other duties as needed or directed by direct manager/supervisor and/or the leadership team

Degree in ecology, biology, or marine related field or 1+ years of experience in aquaculture, lab, or other scientific setting

Ability to learn and use various digital systems (e.g. Excel, Google Suite, remote sensor monitoring systems)

Ability to use math skills in performing duties

Daily microscopy, documentation, and assessment reporting of algal cultures with respect to biosecurity and production targets.

Perform duties accurately and according to protocols, providing optimal care to the algae independently and with minimal supervision, once trained

4. Technical project management experience is a must.

3. Strong organizational and analytical skills required.

5. Exceptional computer and spread sheet skills required.

6. Three to five years’ experience in food and drug cGMPs.

Columbus, GA 31907: Reliably commute or planning to relocate before starting work (Required)

7. Advanced understanding of experimental design, chemical theory and analytical instrumentation like HPLC, GC, ICP-MS, ICP-OES etc

* 8+ years of BioPharma, BioPharmaceutical, Pharmaceutical or Biotechnology industry experience.

* Experience contributing to CMC sections of regulatory filings including IND, NDA, and BLA submissions desired.

* Experience working on technology transfer and validation activities within cGMP compliance.

* Leading technology transfer processes and working cross functionally with Quality Control departments.

* Designing and conducting stability, impurity and degradation studies.

* Leading analytical related process characterization studies.

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 working as an Analytical Chemist, preferably in a production setting.

Strong knowledge of analytical techniques such as chromatography and spectroscopy.

Experience in method development, validation, and troubleshooting of analytical instruments.

Excellent analytical and problem-solving skills, with the ability to interpret complex data and draw meaningful conclusions.

Effective communication skills, both written and verbal, to convey technical information to diverse audiences.

Develop and validate analytical methods to ensure accuracy, precision, and reliability of results.

Analytical testing experience with analytical instruments

Experience complying with FDA, EPA, and OSHA regulations and policies

At least 1 year of work experience in pharmaceutical or chemical industry

Excellent full time benefits including comprehensive medical coverage, dental, and vision options

BS/MS degree in Chemistry or related fields

Yearly goal-based bonus & eligibility for merit-based increases

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.

Analytical testing experience with analytical instruments

Experience complying with FDA, EPA, and OSHA regulations and policies

At least 1 year of work experience in pharmaceutical or chemical industry

Excellent full time benefits including comprehensive medical coverage, dental, and vision options

BS/MS degree in Chemistry or related fields

Yearly goal-based bonus & eligibility for merit-based increases

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.

Analyze and communicate experimental results both orally and in written reports to colleagues and management.

BS degree with 6 or MS degree with 4 years relevant experience

Strong verbal and written communication skills are required

Working knowledge of applicable industry test standards, relevant regulatory guidance, Design Controls and Product Development Process

Effective verbal and written communication skills

Experience in using Mass spectrometry (LC/MS) for large biomolecules and MS related software (Xcalibur, BioPharma Finder, MassLynx, Protein Metrics)

Perform sample management, laboratory testing, analysis and utilize standard procedures.

Experience and skill in following directions and instructions

Experience and skill in general laboratory practices and maintaining an organized workspace

General knowledge of scientific equipment and capabilities in laboratories is useful

Strong interpersonal, verbal, and written communication skills

Ensure sample analyses are done per standard operating procedures and done in a timely manner

Iii. Minimum Education, Experience, Skills

Responsible for generating management review metrics and KPIs.

Provides mentoring and Conducts Performance Management of direct reports.

Performs managerial duties, as assigned, in support of QC operations such as resource management, routine data and investigation review.

Must possess skills and knowledge of implementing and managing a compliant stability program.

Manage the Biochemistry Group operations in support of production by ensuring the timely execution of QC testing.

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.