Quality Administrator

Job Title: Quality Administrator

Type: Contract on w2

Location: Coppell, TX, 75019

Duration: 8 months (with a possibility of extension)

Description:

As a member of the Quality Control (QC) team contribute through the completion of all assigned and routine laboratory related tasks in compliance with Client, GMP & SHE standards

Key Accountabilities:

• Ethical conduct and compliance

• Adherence to GLP and GDP

• Provides support services for analysts and chemists in the quality control laboratory including cleaning and maintaining the general laboratory facilities and glassware through 5S

• Responsible for ordering laboratory chemicals and supplies, and inventory management

• Responsible for preparing and shipping testing samples to contract lab

• Responsible for cleaning, organizing, and maintaining lab glassware

• Performs sampling of purified water, compressed air, and environmental monitoring for testing

• Accurately completes all data entry requirements for methods or tasks performed

• Performs actives supporting sample receipt, retain storage, and dispositioning of samples

• Executes analytical methods and/or SOPs, with appropriate documentation

• Reviews data for completeness and accuracy using the applicable method/SOP's

• Execute test plan to support laboratory investigation if needed

• Work with document control department for issuing/archiving logbooks and sample folders if needed

• Work with warehouse team for events occuring during sample receipt

• Perform daily check of lab equipment to assist chemists for testing

• Participate in problem solving activities, including ownership of action items identified through the problem-solving activities

• May fulfill other jobs/responsibilities as directed by management consistent with skill level and training

Qualifications and Experience

• Bachelor or Associates Degree, preferably in the chemical or biological sciences with previous experience in a pharmaceutical laboratory

• Must be able to perform activities to support QC sampling activities including climbing ladders and working in areas with limited access and on catwalks around production equipment.

• Must be day/time, weekend and holiday flexible to support QC sampling activities/testing (routine, validation studies, PW sanitization, etc.).

• Must be able to retrieve, dispense, and dispose of chemicals and reagents according to according to approved procedures.

• Must be adequately trained in Good Laboratory Practice (GLP and GMP) standards and be able to complete all forms legibly and accurately and/or notebooks.

• Must be able to attain proficiency in using Client analytical applications required for the completion of assigned tasks.

• Must be able to work at a lab bench or hood and perform the necessary procedures required for sample preparations and clean-up using the current prescribed or validated methodologies

• Excellent verbal communication skills

• Teamwork

• Professionalism

• English Language Skills

SHIFT

Monday through Friday (7am - 4pm)

Potential weekend work required according to business needs

DRESS CODE

Business casual, Required PPE will be provided