Quality Control Chemist I

Kindeva Drug Delivery Company; Bridgeton (MO); On-site; USD 50,000 - 70,000; Full time

Job summary

Kindeva Drug Delivery Company in Bridgeton, Missouri is seeking a Chemist I to perform quality control testing and support laboratory operations. This role will contribute directly to patient health outcomes by ensuring the quality and efficacy of life-saving drug products.

The ideal candidate will have a Bachelor's degree in Chemistry or related field, with relevant laboratory experience preferred. Strong analytical skills and ability to adhere to cGMP principles are essential. Join us and make a difference in healthcare!

Qualifications

• 0–3 years of laboratory experience or equivalent combination of education and experience.
• Experience in a GMP-regulated pharmaceutical or regulated laboratory environment preferred.
• Ability to read and interpret compendial methods, SOPs, and scientific literature.
• Must be able to work effectively under strict production and quality deadlines.
• Experience with SDS-PAGE, Western Blot, or similar technologies preferred.

Responsibilities

• Perform routine and non-routine quality control testing.
• Analyze samples within established procedures.
• Document and record analytical testing activities accurately.
• Collaborate with various teams to address operational challenges.
• Participate in improvement activities for laboratory processes.

Skills

Knowledge of compendial requirements

Analytical instrumentation experience

Ability to author scientific reports

Mathematical calculation abilities

Ability to multitask

Knowledge of laboratory safety procedures

Education

Bachelor’s Degree in Chemistry, Biochemistry, Pharmaceutical Sciences

Tools

HPLC

UPLC

GC

UV/Vis

Empower

Job description

At Kindeva we make products that save lives, ensuring better health and well‑being for patients around the world.

Why Kindeva?

• Collaborative team culture
• Direct impact on patient care

The Impact You Will Make

Transform Lives Through Innovation. Join a rapidly expanding pharmaceutical CDMO where your work directly impacts patient health outcomes worldwide. Kindeva offers a rewarding and fast‑paced cGMP pharmaceutical environment where your work contributes to the safety, quality, and efficacy of life‑saving drug products.

As a Chemist I, you will perform routine and non‑routine quality control testing of raw materials, in‑process materials, finished products, and stability samples, contribute to investigations and continuous improvement initiatives, and develop your analytical skills alongside a dedicated and collaborative team.

Our St. Louis facility continues to grow, creating exciting opportunities for professional development and career advancement. Join us during this dynamic phase of growth and expand your expertise in analytical chemistry, GMP laboratory operations, investigation support, and pharmaceutical quality systems while contributing to life‑saving healthcare solutions.

Responsibilities

Laboratory Operations & Testing

• Perform and coordinate routine setup, calibration, operation, and maintenance of laboratory instruments and equipment.
• Analyze samples using a variety of analytical techniques and instrumentation in accordance with established procedures and specifications.
• Lead or coordinate testing schedules to support business priorities and timely completion of laboratory activities.
• Prepare solutions and standardize test solutions as defined by analytical methods or compendial requirements.
• Perform assigned work in a timely and safe manner while complying with regulatory, company, and compendial requirements.
• Practice cGMP principles, including proper laboratory documentation, maintenance of records, archival of raw data, attention to specification limits, and immediate notification of any out‑of‑specification (OOS) results.
• Document and record analytical testing activities and data, ensuring reports are accurate, complete, and traceable to procedures, equipment, instruments, and reagents utilized.
• Demonstrate practical laboratory skills and a strong understanding of chemistry theories, analytical techniques, and quality procedures.
• Review and revise SOPs, analytical methods, and related laboratory documentation as required.

Instrumentation, Technology & Continuous Improvement

• Participate in routine calibration, verification, and maintenance activities for laboratory instrumentation.
• Identify, propose, and implement process and method improvements that enhance efficiency, robustness, compliance, and data quality.
• Support data collection, trend analysis, and peer review activities associated with process improvement opportunities.
• Collaborate closely with Manufacturing, Quality Assurance, Validation, Technical Services, and Process Transfer teams to address technical and operational challenges.
• Ensure compliance with Good Documentation Practices (GDP), data integrity requirements, and cGMP expectations.

Qualifications

• Knowledge of compendial requirements including USP, EP, and other applicable references; cGMP guidelines; FDA regulations; laboratory safety procedures; SDS requirements; laboratory instrumentation; and inorganic and organic chemistry principles.
• Bachelor’s Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline with 0–3 years of laboratory experience or an equivalent combination of education and experience/training. Experience in a GMP‑regulated pharmaceutical, biotechnology, medical device, or other regulated laboratory environment is preferred.
• Ability to read and interpret compendial methods, SOPs, technical procedures, scientific literature, professional journals, and governmental regulations. Ability to author scientific reports, business correspondence, and departmental procedures. Ability to perform mathematical calculations using whole numbers, fractions, decimals, and basic statistical functions, including graphing and interpretation of data.
• Ability to define problems, collect and analyze data, establish facts, and draw valid conclusions.
• Experience with analytical instrumentation and laboratory techniques such as HPLC, UPLC, GC, Dissolution, UV/Vis, FTIR, Karl Fischer, particle size analysis, or similar technologies is preferred.
• Knowledge of Windows‑based software applications such as Word, Excel, and Outlook; experience with chromatography data systems and data processing software, particularly Empower, is preferred.
• Must have the ability to multitask across multiple priorities and responsibilities while maintaining attention to detail and compliance requirements.
• Must be able to work effectively under strict production, quality, and performance deadlines. Willingness and ability to support business needs outside of standard work hours when required, including occasional evenings, weekends, and holidays.
• Experience with SDS‑PAGE, Western Blot, icIEF, Plate Reader, ELISA, and large molecule testing is preferred.
• Recent graduates with relevant internship, co‑op, undergraduate research, or academic laboratory experience are encouraged to apply.

Physical Demands / Qualifications

• Employee is required to regularly use hands to handle materials and supplies.
• Employee is required to use computers for an extended period each day.
• Employee must effectively use electronic communication.
• Employee is required to regularly stand and walk for extended periods of time.
• Employee must occasionally lift and/or move up to 20 pounds.
• Ability to use proper PPE and be conscious of the work area hazards.
• Employee is required to follow all site safety procedures.

Equal Opportunity Employer

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.