Job Description
Job Description
Job Description
Job Title: Chemist / QC Analytical Chemist
Summary:
The Chemist will perform chemical, quantitative, and qualitative analysis on intravenous solutions, raw materials, and plant water using wet chemistry techniques and analytical instrumentation. The role involves supporting investigations, ensuring compliance with cGMP and SOPs, documenting results accurately, and maintaining a safe and clean work environment.
Key Responsibilities:
- Conduct chemical analyses (quantitative/qualitative) on IV solutions, raw materials, and devices.
- Utilize wet chemistry and analytical instrumentation for testing.
- Collect and record data using computer systems and MS Office.
- Perform investigations, troubleshooting, and write deviation/exception reports.
- Support protocol development and execution.
- Maintain compliance with cGMP, SOPs, and regulatory standards.
- Complete and peer-review documentation accurately.
- Maintain lab cleanliness following 6S principles.
- Follow environmental, health, and safety regulations.
- Work occasional off-shift hours and weekends as needed.
Knowledge, Skills & Abilities:
- Proficiency in MS Office and lab software systems.
- Strong analytical and problem-solving skills.
- Knowledge of chemistry principles and lab instrumentation.
- Excellent organizational and time-management skills.
- Strong written and verbal communication skills.
- Ability to work independently in a fast-paced environment.
Education & Experience:
- Bachelor’s degree in Chemistry, Chemical Engineering, Physical Chemistry, or Biology (with Chemistry coursework).
- 2–4 years of laboratory experience in analytical chemistry.
- Experience with instrumental analysis (e.g., HPLC, GC, spectroscopy) required.
- Experience in GMP-regulated environments preferred.
Physical Requirements:
- Must pass Ishihara’s Color Vision Test (not color blind).
- Must meet near vision visual acuity requirements annually.
Top Skills & Must-Haves:
- Wet chemistry and instrumental analysis (HPLC, GC, UV-Vis)
- cGMP / GLP compliance
- Data documentation and peer review
- Deviation and investigation reporting
- Lab safety and 6S compliance
- Strong analytical and problem-solving ability
Thanks
Suchi
Company DescriptionVastek Inc is managed by a group of dedicated professionals having rich experience of over years in Healthcare, IT consulting and staffing. We are a certified minority owned, Small business company head quartered out of San Diego, with coverage all across United States, Canada, Mexico, Italy and India. We specialize in Engineering, Validation, Regulatory, IT and NON-IT related areas primarily focused on Pharmaceutical / Life Sciences and Medical device companies.
Company Description
Vastek Inc is managed by a group of dedicated professionals having rich experience of over years in Healthcare, IT consulting and staffing. We are a certified minority owned, Small business company head quartered out of San Diego, with coverage all across United States, Canada, Mexico, Italy and India. We specialize in Engineering, Validation, Regulatory, IT and NON-IT related areas primarily focused on Pharmaceutical / Life Sciences and Medical device companies.