QC Chemist – HPLC, Dissolution & GMP Specialist

Supernus Pharmaceuticals Inc; Rockville (MD); On-site; USD 50,000 - 60,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Paid time off

401k company match

Company paid life insurance

Health and wellness benefits

Stock equity awards

Employee stock purchase programs

Discretionary annual bonus program

Job summary

Supernus Pharmaceuticals is seeking a QC Associate to perform testing of pharmaceutical solid dosage forms, primarily by dissolution and HPLC, while maintaining strict GMP documentation and data integrity.

The role includes initiating quality records, CAPA actions, SOP revisions, instrument calibration, and data management within a fast-paced team dedicated to high-quality pharmaceutical testing.

Qualifications

• Bachelor's degree in Chemistry or related science.
• 1+ years of practical related experience preferred.
• Experience with HPLC and/or dissolution testing preferred.
• Experience with GMPs, GCPs, and/or GLPs preferred.
• Knowledge of ALCOA+ and Good Documentation Practices.

Responsibilities

• Initiation of quality records (deviation, OOS/OOT).
• Perform CAPA actions as assigned by management.
• Support senior staff in their responsibilities and tasks.
• Revise SOPs or Test Methods as needed.
• Perform testing (dissolution, spectroscopy, HPLC, visual inspection).
• Maintain equipment logbooks per cGMP guidelines.
• Utilize lab data systems for data acquisition/processing (Empower, LIMS).
• Perform data management, data review and report writing.
• Calibration of laboratory instruments.
• Backup for training newer employees.

Skills

HPLC

Dissolution testing

Technical writing

English communication

Education

Bachelor's degree in Chemistry

Tools

Empower

LIMS

Job description

Supernus Pharmaceuticals is seeking a QC Associate to perform testing of pharmaceutical solid dosage forms, primarily by dissolution and HPLC, while maintaining strict GMP documentation and data integrity.

The role includes initiating quality records, CAPA actions, SOP revisions, instrument calibration, and data management within a fast-paced team dedicated to high-quality pharmaceutical testing.