Vision
Improving Patient Outcomes
Mission
To provide Reliable and Accurate Results, using Innovative Solutions, that result in Affordable Analytical Testing and Consultative Services to our Customers
Guiding Principles
Patient Safety, Affordable Healthcare, Business Success
Core Values
Innovation, Collaboration, People and Performance Driven
Business Approach
Continuous Quality Improvement (CQI)
PLEASE NOTE:
We have moved and changed our local phone and fax numbers.
DYNALABS
2327 Chouteau Avenue
Saint Louis, MO 63103
tf: 888.DYNALAB
pn:
314.241.3962
fx: 314.241.5227
The services provided by DYNALABS are protected by U.S. Patent No. 7,197,405.
Careers
At DynaLabs we strive to provide the best solutions for our customers, with our goal of optimizing their pharmacy compounding business. We offer a fast-paced work environment that includes teamwork and accountability of results.
DynaLabs has some of the best testing capabilities within our industry, a talented trained staff, and is also a fun place to work. Our company is growing and expanding each year, which will provide new and challenging opportunities for every employee. We are eager to bring more talented employees on board with strong core characteristics to help strengthen our organization and meet our customer's goals.
To inquire about a position, please send us an email at careers@dynalabs.us and attach your resume.
Current Open Positions:
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Reports To: Laboratory Manager
Department Name: Laboratory Operation
Classification: Non-Exempt
Job Summary: Performs required analytical testing of customer's (pharmacies') samples (compounded medications) in accordance with established procedures.
Essential Job Functions include the following:
(Note: other duties may be assigned.)
- Perform routine preparation of samples and reagents used for testing analysis.
- Perform standard testing of samples using various methods and instruments including HPLC, UV-VIS, NIR, Dissolution devices, Titrations, pH Meter, Light Scattering Particulate Matter Analysis and/or Colorimetric Endotoxin Analysis.
- Analyze results of testing to identify concerns or issues and discuss with supervisor as needed.
- Report and document results following established procedures.
Job Requirements
- Bachelor's degree in chemical or biological sciences or related field from an accredited college or university.
- Able to perform calculations necessary for sample preparation.
- Demonstrates strong communication skills (both verbal and written.)
- Competent, with high quality standards, versatile and adaptable to work environment requirements.
- Highly efficient, accustomed to problem solving and multitasking in a deadline-driven environment.
- Capable to complete projects independently, but work in a team environment.
- Assumes responsibility for the accuracy and timeliness of the completed work.
- Quick learner who is willing to learn and improve on the job.
- Must have a positive attitude, be self-motivating and dependable.
Work Experience
- 1 - 3 years within lab environment performing similar tasks listed in "Job Function" section - (preferred)
Equipment Used to Perform the Job
- Laboratory equipment including HPLC, UV-VIS, NIR, pH meter
- Standard office equipment including telephones, copiers, fax machines
Working Conditions
- Frequently requires the use of potentially hazardous chemicals and agents.
Physical Abilities
- Requires close visual acuity to perform activities such as: preparing and analyzing data and figures; transcribing; viewing a computer monitor/terminal; visual inspection involving small details; using measurement devices.
- Requires frequent talking, hearing, using fingers to manipulate an object.
Reports To: Laboratory Manager
Department Name: Laboratory Operation
Classification: Non-Exempt
Job Role: Essential Job Functions include the following. Other duties may be assigned.
- Define, scope and implement internal projects and/or other customer defined projects.
- Develop UV/HPLC/GC/MS methods used to test Potency/Purity of a variety of APIs in various drug forms.
- Where appropriate, prove that methods used for testing Potency/Purity of various API’s are stability indicating.
- Develop extraction methods for various APIs contained within various drug forms including but not limited to Creams, Troches, Suppositories, Gels Ointments, Capsules, Tablets etc.
- Develop methods for testing the dissolution claims of various drug forms such as capsules, tablets and pellets.
- Validate dissolution and extraction methods using appropriate standards such as USP Chapter <1225>
- Establish expiration periods for standards
- Report on status of projects to management, while maintaining a visible project list
- Assist in troubleshooting production (issue) samples
- Author technical reports
- Working knowledge of regulatory and compendial guidelines concerning the establishment, validation, and documentation of test procedures.
Job Requirements
- Bachelors degree (or advanced degree) in chemistry from an accredited college or university
- Minimum of 3 years work experience within a analytical lab setting, preferably in a GMP environment
- Actual Method Development experience and expertise is a must
- Able to perform complex calculations necessary for data analysis and solution preparation
- Demonstrated strong communication skills, both verbal and written
- Highly efficient, ability to multi-task in an environment of competing priorities
- Assist with establishing & maintaining safe work standards in Lab
- Capable to complete projects independently, but work in a team environment
- Independently responsible for the driving project execution while assuring the accuracy and timeliness of the completed work
- Assume role of timely progress reports to senior management
- Must have a positive attitude, be self-motivating and dependable
- Takes responsibility for decisions, actions and results; demonstrates credibility and trustworthiness while producing quality results
- Able to balance, reprioritize and assign tasks and/or negotiate resources when needed to optimize schedules and outcomes on multiple projects managed simultaneously with minimal guidance.
- Author technical reports.
Metrics
- Method Development output
- Adherence to defined timeline
- Quality of Methods
Reporting
- Supervisor: Lab Manager





