QC Chemist

QC Chemist - Kennesaw, GA
This is a full-time, non-exempt position.

Nature & Scope:
QC Chemist will perform, under the direct supervision of the Director of QA/QC, inspection and analysis on raw materials, in-process samples, and finished goods to ensure compliance with cGMP/GLP/ISO standard operating procedures. The scope of responsibility for this position crosses multiple departments within Deerland Enzymes (e.g. Quality Assurance, Production, Sales, etc.); therefore the incumbent needs to collaborate with various departments and institutions. A successful candidate will be expected to maintain accurate and legible laboratory logbooks and testing documentation in accordance with SOP's

Responsibilities:

The responsibilities of a QC Chemist I include, but are not limited to the following:

• Perform laboratory tests in a manner such that results are accurate, precise, and reproducible
• Inspect and analyze raw materials, in-process samples, and finished goods in accordance with cGMP/GLP standard operating procedures
• Identify imperfections of samples with mechanical/electronic equipment and chemical analysis
• Test chemical and physical samples
• Document data, report results, perform equipment verification and calibration, and laboratory cleaning in accordance with Deerland Enzymes' SOP's
• Perform a variety of QC assays with established procedures and SOP's
• Preparation of wet and dry samples for laboratory analysis
• Maintain familiarity with current scientific literature and technologies
• Carry out routine tasks and follow strict methodologies to carry out analyses
• Identify opportunities for method or SOP improvement
• Ensure a well-stocked and resourced laboratory
• Local travel (between sites): Occasional ( less than 25%)

Requirements

Education

• Minimum - Bachelor of Science in Biochemistry, Biology, Chemistry, or equivalent

Experience

Required

• Proficient in MS Word, Excel, and PowerPoint
• Basic mathematical and statistical skills
• Basic laboratory skills (e.g. pipetting, weighing, dilutions, etc.)
• Experience with any of the following: standard assay procedures, IR, HPLC, PCR, Real-Time PCR,

Preferred

• 0-3 years of previous laboratory experience
• Quality Control and knowledge of cGMP / ISO 17025

Specific Skills

• Strong attention to detail in order to produce accurate, precise, and reproducible data
• Strong analytical, organizational, and time management skills
• Task-oriented and results-driven
• Strong work ethic and prioritization skills
• Work collaboratively with various departments to compile, analyze, and interpret data
• Manual dexterity
• Ability to follow written protocols
• Ability to work in a fast-paced environment
• Excellent written and oral communication skills - ability to make presentations and/or give presentations
• Must be able to lift 25lbs
• Must possess a valid US Driver's License

Excited about this role but don't meet every requirement listed? Studies show that often applicants will self-select out if they don't check every box. We encourage you to apply anyway. You may be just the right candidate for this role or another one of our openings.

ADM requires the successful completion of a background check.

"AJCIND"
REF: 82839BR

---