Associate Scientist, QC Chemistry

Alcami Corporation•Wilmington, NC

1d•Onsite

About The Position

The Associate Scientist, QC Chemistry is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist, QC Chemistry may also assist with method development/method validation projects. For this position, UV-Vis, Dissolution, HPLC, GC, Titration, and/or KF based methodologies are commonly employed in the described testing.

Requirements

Bachelor’s degree in chemistry or a related field.
0 - 4+ years of related work experience.
Excellent verbal and written communication and documentation skills required.
Excellent detail orientation and organizational skills required.
Excellent problem-solving and basic trouble-shooting ability required.
Basic knowledge of Laboratory equipment and safety required.
Basic knowledge of Laboratory Documentation is required.
Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.
Applies job skills, company policies and SOPs to complete a variety of tasks.
Receives general instructions on routine work, detailed instructions on new projects or assignments.

Nice To Haves

Prior laboratory experience or work experience in Pharmaceutical, CDMO, or cGMP preferred.
Working knowledge of cGMP in a pharmaceutical or regulated environment preferred.

Responsibilities

Performs one or more of the following techniques: residual solvents, assays (potencies, related substances), dissolution, moisture content, identification, and other various analytical techniques.
Maintains working knowledge of routine instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
Performs assigned tasks carefully and on schedule according to standard operating procedure and supervisor instructions.
Analyzes information for technical correctness and accuracy.
Complies with applicable GMPs, peer checks information and signs for GMP review. Brings aberrant information to the attention of supervisor.
Maintains a safe, clean, and organized work environment free of safety hazards.
Suggests improvements for safety, work quality, and productivity.
Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
Seeks to cultivate mentorship, build leadership skills, and foster a culture of ‘team first’.
Other duties as assigned.