Scientist Consultant (QC/AS) III
Location: Rockville, MD
Job Responsibilities:
Review analytical data for pharmaceutical products to ensure accuracy and compliance with our client's standards and GxP requirements.
Initiate and monitor stability studies for products tested by contract labs.
Manage and maintain stability data for various pharmaceutical products.
Create and manage studies in LIMS for multiple projects.
Enter and review sample test results in LIMS.
Assist in technical investigations and manage documentation in compliance with GDP and data integrity standards.
Skills Required:
Bachelor's degree in chemistry or related field with 5 years of experience in a GxP environment.
Experience in a GMP environment with analytical lab testing, including HPLC and Dissolution.
Strong communication and interpersonal skills for effective collaboration.
Proficiency in MS Office, especially Excel.
Experience in data review and excellent communication skills.
Nice to Have:
Familiarity with electronic document management systems like Veeva or CREDO.
Experience with investigation software, such as Trackwise.
Strong planning, coordination, and project management skills.
About SSI People:
With over 26 years of industry experience, SSi People has built its reputation and expertise on putting people first. Everything we do works toward delivering an exceptional experience for our consultants, our clients, and our internal team. Through a genuine commitment to people in everything we do. We have developed refined processes and a stellar internal team to deliver talent quickly. More importantly, we focus on building long-term relationships, not transactions. Putting people first is just what we do well.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from SSi People and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our
Location: Rockville, MD
Job Responsibilities:
Review analytical data for pharmaceutical products to ensure accuracy and compliance with our client's standards and GxP requirements.
Initiate and monitor stability studies for products tested by contract labs.
Manage and maintain stability data for various pharmaceutical products.
Create and manage studies in LIMS for multiple projects.
Enter and review sample test results in LIMS.
Assist in technical investigations and manage documentation in compliance with GDP and data integrity standards.
Skills Required:
Bachelor's degree in chemistry or related field with 5 years of experience in a GxP environment.
Experience in a GMP environment with analytical lab testing, including HPLC and Dissolution.
Strong communication and interpersonal skills for effective collaboration.
Proficiency in MS Office, especially Excel.
Experience in data review and excellent communication skills.
Nice to Have:
Familiarity with electronic document management systems like Veeva or CREDO.
Experience with investigation software, such as Trackwise.
Strong planning, coordination, and project management skills.
About SSI People:
With over 26 years of industry experience, SSi People has built its reputation and expertise on putting people first. Everything we do works toward delivering an exceptional experience for our consultants, our clients, and our internal team. Through a genuine commitment to people in everything we do. We have developed refined processes and a stellar internal team to deliver talent quickly. More importantly, we focus on building long-term relationships, not transactions. Putting people first is just what we do well.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from SSi People and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our
Job ID: 486673866
Originally Posted on: 7/24/2025
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