Manages the receipt, storage, organization, and disposal of laboratory reagents, standards and consumables of the Chemistry Laboratory in a high-growth, fast-paced, dynamic work environment while ensuring compliance with FDA and DEA regulations.
Receiving and logging laboratory reagents, standards, and consumables into LIMS while ensuring compliance of QC practices.
Helps maintain a flexible organization of the laboratory reagents, standards, and consumables to allow fast changing manufacturing priorities to occur with minimum disruption and avoid back logs.
Assists in the creation of the purchase requisition's based on laboratory needs.
Performs other duties as assigned or apparent.
Primary Accountabilities
NOTE: The primary accountabilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or most of the primary accountabilities listed below. Specific tasks or responsibilities will be documented in the incumbents' performance objectives as outlined by the incumbents' immediate supervisor or manager.
Manages the receipt, storage, organization, and disposal of laboratory reagents, standards and consumables of the Chemistry Laboratory
Receiving and logging laboratory reagents, standards, and consumables into LIMS while ensuring compliance of QC practices.
Helps maintain a flexible and clean storage area that provides efficient organization of the laboratory reagents, standards, and consumables to allow fast changing manufacturing priorities to occur with minimum disruption and avoid back logs.
Assists in the creation of the purchase requisition's based on laboratory needs.
Communicates with the management team when any discrepancies or concerns are noted and shows the initiative to correct/address any concerns.
Performs other duties as assigned or apparent.
Knowledge, Skills & Abilities:
Minimum High School Diploma or GED.
Good communication skills.
Strong organization skills with the ability to handle numerous details.
The ability to use a computer and different programs efficiently.
Experience with cGMP documentation systems and with implementation of quality control systems.
Knowledge of FDA manufacturing/regulatory quality systems regulations, qualification, facilities and investigation requirements.
Must be detailed oriented and have excellent organizational skills.
Must possess effective written and oral communication skills and be able to handle multiple tasks within limited time frames.
The ability and willingness to change direction and focus to meet shifting organizational and sample demands.
The ability to create and contribute to an environment that values people, encourages trust, teamwork, and open communication, and provides participation, learning, feedback and recognition.
The ability to effectively manage one self demonstrates integrity, be productive under pressure, and achieve development goals.
Position requires bending, typing, climbing, lifting, reaching, vision, standing, sitting (10%), walking, and hearing.
Salary range: Based on experience
EEO Statement:
Nephron is an equal employment opportunity employer and does not discriminate against employees or job applicants on the basis of race, religion, color, sex, sexual orientation, age, national origin, mental or physical disability of a qualified individual, veteran or military status, pregnancy, marital status, familial status, genetic information, or any other consideration made unlawful by applicable federal, state or local law.
