Scientist III - Bioassay
Alcami Corporation · Wilmington, NC · 2 mo ago
AnalystFull-time
Responsibilities
- Performs laboratory analysis of pharmaceutical and biopharmaceutical products utilizing analytical instrumentation.
- Analyzes and documents data in accordance with Alcami SOPs.
- Documents results in electronic laboratory notebook.
- Performs one or more of the following techniques: cell-based potency assays, ELISA, real-time PCR, enzymatic activity assays, binding kinetic assays and other biochemical testing methods.
- Supports troubleshooting and problem solving activities for cell-based and biochemical tests.
- Evaluates and interprets generated data.
- Contributes to operational initiatives to support continued growth of the organization.
- Develops and validates biological tests to determine purity, identity and potency of pharmaceutical and biopharmaceutical products.
- Writes standard operating procedures (SOPs), test procedures, specifications and summary reports.
- Maintains working knowledge of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
- Affords assistance in removal of hazardous waste, routine equipment cleaning, and restocking of consumable products and reagents.
- Interacts with team members, management and clients to discuss data and project progress.
- Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
- Effectively uses various laboratory software packages (SoftMax, ProCal, Master Control, ELN, etc.).
- Maintains a safe, clean, and organized work environment free of safety hazards.
- Safely handles potent compounds.
- Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
- Other duties as assigned.
Qualifications
- Associate’s degree and 16+ years of related experience.
- OR Bachelor’s degree and 6+ years of related experience.
- OR Master’s degree with 2+ years of related experience.
- OR PhD with 0+ years of experience required.
- 2+ years of experience in Pharmaceutical, CDMO, or cGMP preferred.
- Knowledge, Skills, And Abilities:
- Working knowledge of peptides, monoclonal antibodies, recombinant proteins is required, and knowledge of cell therapy and gene therapy is preferred.
- Knowledge of Cell-based Bioassays required.
- Working knowledge of Real-time PCR preferred.
- Strong knowledge of ELISA/immunoassays required.
- Working knowledge of Enzymatic Activity Assays preferred.
- Working knowledge of Laboratory Documentation is required.
- Working knowledge of cGMP in a pharmaceutical or regulated environment is preferred.
- Strong verbal communications and presentation skills required.
- Strong time management and organization skills required.
- Strong knowledge of Laboratory equipment and safety required.
- Good problem solving and trouble shooting ability required.
- Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.
- Working knowledge of SoftMax and Empower preferred.