Compounder Level 1 (2nd Shift: 2-10:30p M-F)

PAI Holdings LLC•Greenville, SC

2h•Onsite

About The Position

Preparing materials and equipment for formulation of liquid pharmaceutical products in accordance with FDA cGMP requirements. To mix ingredients as directed in batch record instructions to make liquid pharmaceutical products. To maintain cleanliness of facilities and equipment.

Requirements

Ability to read and understand simple instructions, short correspondence, notes, letters and memos
Ability to write simple correspondence.
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals
Ability to compute rate, ratio, and percent and to prepare and interpret bar graphs.
Ability to use common sense understanding in order to carry out detailed written or oral instructions
Ability to deal with problems involving a few known variables in situations of a routine nature.
Mental alertness and adaptability to office and field area work routines
Equivalent to four years of high school, with particular emphasis during high school in office skills, shop skills, or others, plus to 6 months related experience or training
Or equivalent combination of education and experience.

Responsibilities

Follows all policies, procedures, SOPs, cGMPS, Work Instructions, and supervisor instructions.
Read batch record for batch to be produced and ask questions as needed to ensure understanding.
Prepare tank and equipment for batch production. Take pre-weighed materials to the batch production area.
Perform mixing operation according to instructions.
Record all process information on batch records and in logbooks.
Clean equipment and store properly.
Perform periodic department housekeeping activities per SOP.
Perform all functions in compliance with written company Standard Operating Procedures.
Notify management immediately upon discovery of any discrepancy or manufacturing problem.
Perform all duties following company safety procedures.
Accountable for accurate preparation of pharmaceutical products free from contamination in accordance with FDA cGMP requirements.
Perform any other related duties as required or assigned.