Quality Control Scientist Compunnel Inc. - 3.6 Round Rock, TX Job Details Temp-to-hire $35 - $38 an hour 14 hours ago Qualifications Bachelor of Science High-performance liquid chromatographs

GMP ISO 9001

Bachelor's degree Gas chromatographs Chemistry Quality systems

Full Job Description Job Title:

Quality Control Scientist Location:

Round Rock, TX, 78665

Duration:

12 months, temp to perm potential

Pay Rate :

$35-38/hr on W2 (no prior benefits)

Shift:

Monday-Friday:

8am-5pm may go to 2nd shift at a later date. shift not approved yet. 12pm-9pm

Duties :

Must have: chromotography,

HPLC and GC Essential Job Functions:

Undertake assigned projects, stability studies, writing of reports, test specifications and batch records in the

QC Laboratory Product & Application Development:

run analytical methods and stability assessments- primarily by HPLC and GC, evaluate manufacturing formulations, support validations, technical transfer, training, and testing Follow regulatory, customer, and quality system requirements in product development. Process results of project work, document methods on project/product design, test specifications, write batch records, test specifications etc. Collaborate and work other staff (Scientists and Technicians) to complete testing on products. Other projects as assigned to support innovation and process improvements. Take responsibility for assigned tasks in consultation with the project team. Manage tasks and time to meet development schedules. Participate in training colleagues for technical transfer. Work with team and other departments to implement validation and tech transfer requirements. Develop and expand technical and subject matter expertise in assigned technical areas. Perform equipment qualifications and maintenance/troubleshooting of analytical systems. Develop knowledge on critical quality, safety and delivery requirements. Contribute to project planning though communication with manager, project manager and team: Identify and communicate resource requirements for specified projects. Provide timely updates and communicate project status to management and the project team. Communicate, in a timely manner, issues related to schedule, planning and resources that may stall or prevent the execution of the project. Technical Expertise Operation of chromatographic instrumentation including HPLC and GC. Operation of chromatographic detectors including UV-Vis, RI, ELSD, FID and others. Develop and expand technical and subject matter expertise in assigned technical areas by seeking out trainings and knowledge-sharing. Process and project review for certified reference materials by mass balance techniques that may be traceable to primary pharmacopeias. Documentation Write reports on results of project work, document methods on project/product design, test specifications, write batch records, test specifications etc. for transfer to QC. Maintain lab notebooks, logbooks, batch records, and other documentation.

BASIC QUALIFICATIONS

Education:

BS or MS in chemistry or relevant life science related field.

Knowledge and Skills:

Experience:

BS or MS will have 2+ years prior work experience in a related field. Knowledge of the

ISO 9001, ISO

17025 and

ISO 17034

requirements. May have prior work experience in a GLP, GMP and/or ISO environment. May have knowledge of quality system requirements of the medical device, pharmaceutical and/or clinical industries. "TA01"

Pay:

$35.00 - $38.00 per hour Expected hours: 40.0 per week

Work Location:

In person