Scientist – Analytical Chemist 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

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.

In addition to competitive compensation, we offer a comprehensive benefits package including:

Manage investigations and troubleshoot existing methods to assess impact of out of specification materials of finished product.

5+ years of experience working as a leader in a GMP laboratory.

Outstanding verbal and written communication skills.

Intermediate to expert level administrative knowledge of MS Office applications; proven ability to leverage digital technology and resources.

Proven ability to successfully manage projects and timelines, organize/track information, prioritize accordingly.

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.

Maintain appropriate training/certification including GLP and GMP

Excellent communication and interpersonal skills

Level of Experience: Entry Level

Maintain and implement efforts in housekeeping, and safety programs.

Maintain the cleanliness and orderliness of the laboratory.

Prepare solutions and diluents used in the QC Laboratory.

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.

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)

Interpret data and make recommendations to management for improvement or potential concerns

Assist laboratory management with the preparation and execution of laboratory investigations/deviations and CAPA.

Strong analytical skills with experience using HPLC, GC and other lab equipment

Compare laboratory data against specifications, prepare reports, and trend data where applicable to determine if results meet requirements

Experience with Medical Devices and/or OTC consumer products

Independently perform method evaluation/development/validation/verification and troubleshooting instruments and improvement of processes

Assisting sales and product managers with technical support.

Monitoring of specification conformance of assigned products in conjunction with Quality Assurance Manager.

Minimum of three years' experience or equivalent with concrete and concrete products evaluation and development of additives, coatings or related products

Working knowledge of MRP systems

Formulations and specification conformance of coatings, additives and other products in the Specialty Products group.

Issuing and updating raw material specifications, production formulations, manufacturing instructions for assigned products and all checklist documentation.

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.