Quality Control Chemist III

Industry

Pharmaceuticals

Advert ID

FOX_BBBH33569

Location

Largo

Job Type

Permanent

Hours

Full-Time

Salary Range

USD30000-32000 per year

No. of Openings

1

Branch Information

Florida Engineering - (USA) 20 North Orange Avenue Suite 702 FL Orlando , FL 32801 Phone : 407-660-6050

ContactNumber

407-660-6050

Job Description

POSITION: Quality Control Chemist III

LOCATION: Largo, FL

TYPE: Direct Hire

SHIFT: 2nd Shift 3pm to 11:30pm



OVERVIEW:

*The QC Chemist III is responsible for supporting the company's Quality Control related requirements.

*This includes the performance of area responsibilities necessary to ensure that Laboratory activities are in accordance to cGMP's and FDA requirements.

*This individual performance must be aligned and consistent with company objectives, applicable department programs, including training, documentation, standard operating procedures, policies and procedures.



RESPONSIBILITIES:

*Performs analytical testing of raw materials, in-process samples, finished products and stability samples in accordance with company SOPs and established cGMP and safety guidelines.

*Prepare Test Solutions as per established test methods and/or compendia requirements.

*Conduct advanced, compendial-based wet chemistry testing of raw materials and components (e.g. - <231> Methods I and II, potentiometric titration, dissolution) consistent with established methods/specifications as well as USP/NF.

*Conduct advanced chromatographic analysis (e.g. - HPLC/GC related substances and GC residual solvents) as part of raw material/in­ process/finished product testing.

*Execute compendia method verification protocols and report results to the QC Analytical Support Group.

*Train QC staff, where qualified to serve as a trainer.

*Execute analytical method transfers and/or participate in co-validation efforts with Analytical Research and Development (AR&D) or Quality Control Analytical Services (QCAS).

*Participate in departmental projects as assigned by laboratory management, including Lean and Process Excellence Initiatives.

*Assist with the implementation of new technology.

*Initiate change controls and document change requests as directed by laboratory management and ensure their timely approval/closure.

*Documents the procedures and results obtained in laboratory notebooks/logbooks according to established procedures consistent guidelines.



QUALIFICATIONS:

*BS Degree or higher in Chemistry or related science field (or equivalent) a minimum of five (S) years of related work experience in a pharmaceutical, chemical or related industrial working environment.

*An equivalent combination of education, training, and experience may substitute.

*Must have strong background in HPLC and GC instrumentation.