Associate Scientist - QC Chemistry

22h22 hours ago

Alcami Corporation

Wilmington, US · Full-time · $60,000 – $85,000

About this role

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization through trusted partnerships and proven expertise. The Associate Scientist - QC Chemistry drives results in a fast-paced environment by performing routine and non-routine analytical testing for pharmaceutical product development or manufacturing. Common methodologies include UV-Vis, FTIR, HPLC, GC, Titration, and AA.

Day-to-day responsibilities involve executing techniques such as residual solvents analysis, assays for potencies and related substances, dissolution, elemental impurities, moisture content, and identification tests. Tasks are performed carefully per standard operating procedures and supervisor instructions. Data is analyzed for technical correctness and accuracy.

This is a 100% on-site position with 1st shift hours Monday through Friday from 8:30am to 5:30pm. The role requires maintaining a safe, clean, and organized work environment free of hazards while complying with applicable GMPs. Peer checks and supervisor notifications ensure quality and compliance.

Suggest improvements for safety, work quality, and productivity while ensuring timely completion of cGMP training. Cultivate mentorship, build leadership skills, and foster a 'team first' culture. Other duties as assigned support ongoing pharmaceutical operations.

Requirements

Bachelor’s degree in chemistry or a related field
0 - 4+ years of related work experience
Prior laboratory experience or work experience in Pharmaceutical, CDMO, or cGMP preferred
Excellent verbal and written communication and documentation skills
Excellent detail orientation and organizational skills
Excellent problem-solving and basic trouble-shooting ability
Basic knowledge of Laboratory equipment and safety
Proficiency with Microsoft Office (Word, Excel, PowerPoint)

Responsibilities

Perform analytical techniques including residual solvents, assays (potencies, related substances), dissolution, elemental impurities, moisture content, and identification
Maintain working knowledge of routine instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks
Perform assigned tasks carefully and on schedule according to standard operating procedure and supervisor instructions
Analyze information for technical correctness and accuracy
Comply with applicable GMPs, peer check information, and bring aberrant data to supervisor attention
Maintain a safe, clean, and organized work environment free of safety hazards
Suggest improvements for safety, work quality, and productivity
Ensure timely completion and compliance with cGMP and relevant company training requirements