Analyst / Chemist 1

Analyst / Chemist 1 Sanford, FL Job Details Full-time 23 hours ago Benefits Health insurance Dental insurance 401(k) Paid time off 401(k) matching Qualifications Stability testing Computer operation CGMP Document review (document control) Empower (software) Laboratory inventory control Laboratory safety GLP Laboratory instruments Technical documentation Pharmaceutical regulatory compliance Word processing Computer literacy Bachelor of Science Spreadsheets High-performance liquid chromatographs GMP Mid-level Laboratory equipment calibration 3 years Databases ICH guidelines Bachelor's degree Scientific protocols Pharmaceutical analysis Laboratory compliance Laboratory quality control Laboratory techniques Technical writing Chemistry Communication skills Bachelor's degree in chemistry Full Job Description HILL DERMACEUTICALS, Inc. is a privately-owned pharmaceutical company that develops and manufactures innovative dermatology products for children and adults. We provide unique products that enhance the treatment of difficult-to-treat diseases such as scalp psoriasis, atopic dermatitis/eczema, chronically itchy ears, melasma (of the face) and actinic keratosis (pre-cancerous skin conditions). The Quality Control Chemist is well grounded in a scientific discipline performing testing and test related activities for testing incoming raw materials, in-process samples, utility samples and general testing in support of production. The QC Chemist has responsibility to ensure current procedures are followed; test instrument performance is suitable for the intended test requirements; allocate resources for the timely completion of tasks; responsible to review, interpreted, analyze and audit all laboratory data; investigate as necessary to provide input on decisions regarding acceptability of test results, review and approve assigned documents. Has good written and oral communication skills, including the ability to generate written instructions, and its computer literate.

Key Responsibilities:

Follow procedures for sampling, analytical equipment set-up/operation and testing of the following: Raw Materials Packaging components and materials In-process drug products Finished drug products Customer complaint samples Stability samples Environmental control samples Cleaning verification Calibration of Instruments Perform routine laboratory procedures according to SOP's including (but not limited to) testing of special samples as required for validation, qualification, protocol studies and developmental projects. Assist with the administration of laboratory systems, including laboratory safety, documentation, SDS, and laboratory inventory maintenance. Maintaining all program documentation requirements with respect to content, completeness, accuracy and timeliness of completion. Participate in lab investigations as required. Report any unexpected or anomalous findings to supervisor or manager. Assist with laboratory investigations and the execution of protocols as needed. Additional assignments may be given by management.

Requirements:

Bachelor's degree (BS or BA) in chemistry or equivalent. At least 3 years' experience in a cGMP pharmaceutical laboratory setting preferred.

Skills/Experience Requirements:

Appropriate laboratory techniques in relevant scientific discipline. Technical writing ability Good understanding of GMP, GLP, ICH and USP/NF guidelines Good compliance knowledge Familiarity with databases, spreadsheets and word processing programs Knowledge with HPLC and database acquisition program (Knowledge with Empower database acquisition a plus)

Job Type:

Full-time Benefits:

401(k) 401(k) matching Dental insurance Health insurance Paid time off

Work Location:

In person