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Atlas Holdings LLC
Formulation Scientist
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What they do
A Process Development Scientist researches and develops methods for creating and improving chemical manufacturing processes. They may work in a range of industrial sectors, including manufacturing, biotech, and pharmaceuticals. They design experiments, analyze data, and optimize procedures to enhance efficiency, quality, and cost-effectiveness.
$75,777 / year median in South Carolina
Job Description
Formulation Scientist Atlas Holdings
LLC - 2.0
Columbia, SC Job Details Full-time $75,000 - $85,000 a year 1 hour ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance Life insurance Qualifications Protein analysis (analytical chemistry specialty) Biochemical laboratory techniques Chemical separation processes Pharmaceutical analysis Mass spectrometryFull Job Description About COMPANY:
Atlas Holdings is a growing life sciences company that oversees a portfolio of research- use-only (RUO) and physician-use-only (PUO) brands specializing in peptides and related laboratory products. Our company supports researchers, laboratories, healthcare professionals, and industry partners by delivering high-quality products manufactured under rigorous quality standards. We are committed to innovation, operational excellence, and continuous growth while fostering a collaborative, fast-paced work environment. As we expand, we are seeking talented individuals who are passionate about quality, problem-solving, and helping build industry-leading organizations.Job Summary:
We're looking for a hands-on Formulation Scientist with an interest in developing formulation for peptides and small molecules to create innovative consumer health products. In this role, you'll work both in the lab and closely with our manufacturing team members to transform raw materials (peptides and small biomolecules) into viable, freeze dried products. You'll develop and optimize formulations across a range of dosage forms, troubleshoot technical challenges, and support products throughout the entire development lifecycle from concept and prototyping through scale-up, validation, and commercial launch. This role is ideal for someone who enjoys hands-on bench work, thrives in a collaborative cross-functional environment, and is excited about bringing high-quality consumer health products to market that people will use every day. Responsibilities (may include but not limited to):- Plan and execute independent research work at the project level, including, but not limited to, project planning, execution, analysis, data compilation, data interpretation, presentation and reporting.
- Report status of assigned projects through the preparation of detailed reports and documentation that summarize experiment results. Interprets results of experiments and makes recommendations for improvements.
- Contribute to intellectual property by developing new products and/or processes.
- Independent time management and prompt completion of multiple projects.
- Familiarity with programming on various lyophilizers.
- Characterization and analysis of peptides and small biomolecules in liquid and dried formats using various analytical tools ranging from
HPLC, LC-MS/MS, CD
spectroscopy, NMR spectroscopy, DLS, SLS, Tm/Tg and DSC.- Peptide and biomolecule stability testing (melting temperature, aggregation temperature, particle sizing) and optimizations of formulations and lyophilization.
- Working with other department representatives to deliver cross-departmental objectives.
- All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodation for additional tasks and responsibilities. Required Qualifications (knowledge AND experience):
- Ph.D. (preferred) in Chemistry, Biochemistry, or related field and 0+ years combined postdoctoral and relevant work experience; or
- M.Sc. in Microbiology, Chemistry, Biochemistry, or related field and 3+ years relevant work experience;
- Hands-on experience in peptide and biomolecule characterizations using a range of different spectroscopic techniques.
- Working knowledge of different types of chromatography and associated resins as well as relevant buffer systems used for size exclusion, ion-exchange, reverse and normal phase chromatography.
- Knowledge of bioanalytical methods and standard biomolecule quality assays is required.
- Ability to prioritize and work quickly to identify key reagents in FDA approved GRAS components for formulations.
- Interpret CoAs, identify key ingredients based on analytical results and achieve appropriate formulations for bulk and vial lyophilization
- Excellent organizational and verbal/written communication skills.
- Must be resourceful and self-motivated. Preferred Qualifications (knowledge OR experience):
- Exceptional candidates will demonstrate proficiency in the latest technologies used in downstream processing (i.e. membrane chromatography or monoliths).
- Experience with high-throughput protein purification workflows starting from cell lysis, clarification, filtration, and chromatography, followed by buffer exchange and subsequent analytical processes.
- Demonstrated ability to work in team setting as well as independently on multiple projects in parallel on strict deadlines.
- Demonstrate a firm understanding of the protein purification processes, theory, and practical workflows from R&D (micro and milligram scales) and larger scale manufacturing (grams to kilograms).