What are the responsibilities and job description for the Analytical Chemist position at Bell Pharmaceuticals Inc.?
Overview:
QC Analytical Chemist
The QC Chemist is responsible for performing testing on raw materials, in-process samples, stability samples, and finished products to ensure they meet established quality standards and regulatory requirements. This role involves conducting analytical testing, documenting results, investigating out-of-specification results, maintaining laboratory compliance, and supporting the overall quality control program.
Key Responsibilities:
Laboratory Testing & Operations:
- Perform analytical testing on raw materials, in-process samples, stability samples, and finished products using techniques such as HPLC, FTIR, UV-Vis, dissolution, wet chemistry, pH, conductivity, particle size analysis, moisture analysis, and other established methods.
- Conduct microbiological testing as required.
- Ensure all testing is performed in accordance with approved procedures, compendial standards (USP), and regulatory guidelines.
- Manage sample receipt, logging, and tracking through the laboratory system.
- Operate, maintain, and calibrate laboratory equipment and instrumentation.
- Monitor and maintain laboratory supplies, reagents, and standards inventory.
Quality & Compliance:
- Accurately document all test results, data, and observations in laboratory notebooks or electronic systems.
- Review and verify analytical data for accuracy and completeness.
- Investigate out-of-specification (OOS) results, deviations, and non-conformances following established procedures.
- Support ongoing laboratory programs including stability testing, environmental monitoring, water testing, and equipment preventive maintenance.
- Maintain data integrity practices and ensure compliance with cGMP, GLP, FDA, and other applicable regulations.
- Assist in the development, revision, and implementation of laboratory procedures and test methods.
Technical & Safety Responsibilities:
- Troubleshoot technical issues with laboratory methods and instrumentation.
- Identify and report trends or potential quality issues observed during testing.
- Follow all laboratory safety protocols, including proper handling of hazardous materials and waste disposal.
- Support regulatory inspections and internal audits as needed.
Collaboration:
- Communicate testing results, deviations, and quality concerns clearly to supervisors and cross-functional teams (Production, Quality Assurance, etc.).
- Work effectively with team members to meet testing timelines and priorities.
Required Skills and Qualifications:
- Bachelor’s degree in Chemistry, Biochemistry, or a related scientific field.
- Knowledge of microbiological methodologies is preferred.
- 1–5 years of experience in a pharmaceutical or regulated QC laboratory environment.
- Hands-on experience with analytical instrumentation and techniques (HPLC, FTIR, UV-Vis, dissolution, wet chemistry, etc.).
- Understanding of pharmaceutical regulatory requirements (cGMP, USP, FDA) and quality standards.
- Strong understanding of laboratory safety protocols.
- Proficient in data analysis and interpretation.
- Excellent technical writing skills (protocols, reports, and procedures).
- Strong attention to detail and organizational skills.
- Ability to manage multiple priorities and meet deadlines.
- Good verbal and written communication skills.
Pay: $60,000.00 - $70,000.00 per year
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Work Location: In person
Salary : $60,000 - $70,000