Quality Control Chemist - ALL 3 SHIFTS

Quality Control Chemist - ALL 3 SHIFTS Formulated Solutions - 2.3 Largo, FL Job Details Full-time 1 day ago Benefits Health savings account Health insurance Dental insurance 401(k) Tuition reimbursement Paid time off Vision insurance 401(k) matching Life insurance Referral program Qualifications Gas chromatography Computer operation Laboratory safety High-performance liquid chromatographs Laboratory information management systems Bachelor's degree Continuous improvement Data entry Chemical analysis Training & development Full Job Description

PRIMARY PURPOSE

The Chemist II will ensure the timely and accurate testing of raw materials, in-process, and finished products by applying validated analytical methods and sound scientific principles, while maintaining compliance with regulatory and quality standards. Contribute to laboratory efficiency, data integrity, and continuous improvement initiatives, and support the development of team capabilities through training and technical guidance.

MAJOR DUTIES AND RESPONSIBILITIES

: Testing of incoming materials, in process/bulk/intermediate, finished product, and stability samples using wet bench and physical techniques, plus instrumentation such as FTIR, UV-VIS, etc., and basic chromatography while growing and training in complex chromatographic analyses Accurately records raw data and analyzes, calculates, and interprets the results Enters results in appropriate lab systems, such as ERP and LIMS Performs daily verification activities, basic calibration and preventative maintenance tasks, and assists with calibration of

HPLC, GC, AA, TOC

as part of ongoing training Is qualified to review and disposition samples/lots in their respective area Ability to train and qualify junior co-workers Assists in out of specification (OOS) test results and investigation Ensure testing is performed accurately and in compliance with GLP, GMP, USP, SOP and other approved test methods Participates in method verification/validation/transfer tasks as directed by supervisor and may provide review of raw data and/or reports Maintain reagents in laboratory including but not limited to inventory, current

MSDS, PPE

required for handling, waste generation and disposal May flex to other Quality teams/departments to assist when needed Promote GMP and safety throughout the facility Promote continuous improvement and customer satisfaction Assists to follow-up on OOS's and CAPAs to verify compliance Potential exists for exposure to potentially harmful chemicals Participate in other activities as assigned by the Quality Supervisor

QUALIFICATIONS

Required Ability to use a personal computer and peripheral equipment to accurately enter and analyze data and produce reports. Knowledge of chemical safety and protective equipment. Knowledge of various analytical equipment and techniques utilized in an analytical laboratory. Ability to follow established priorities, work independently and productively. Communicate with others clearly and concisely. Ability to work in a dynamic fast paced environment-sometimes rapidly shifting priorities. Ability to concentrate in such an environment and perform quality work. Must be able to lift up to 15 pounds.

EDUCATION AND TRAINING

Bachelor's degree in chemistry or appropriate discipline.

Job Type:

Full-time Benefits:

401(k) 401(k) matching Dental insurance Health insurance Health savings account Life insurance Paid time off Referral program Tuition reimbursement Vision insurance

Experience:

HPLC & GC

3 years (Required)

CDMO:

3 years (Preferred)

Work Location:

In person