QC Supervisor
Company: Bachem
Location: Vista
Posted on: January 12, 2021
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Job Description:
Your Responsibilities The supervisor of Quality Control fulfills
a critical role in the active pharmaceutical ingredient (API)
manufacturing operations within the Quality Control (QC)
department. This individual manages and executes coordination
testing for raw materials, IPC, Final product and Microbial
testing. Additionally, this individual supports the Director of QC
in reviewing data and reports. This role also serves to advance
analytical capabilities and contributes to the development of the
QC department. Your Tasks Manage and execute testing for all type
of QC samples for use in manufacturing Supervise QC scientists and
oversee the testing process in the lab Have a good understanding of
optimization of new and existing analytical methods for
qualification and release testing. Write, review, and approve QC
Standard Operating procedures (SOP's) as needed Oversee QC lab
equipment qualification and ensure the lab is maintained in a
compliant manner consistently. Evaluate, recommend, and implement
new analytical technologies and instrumentation for raw material,
environmental, and water testing Provide training, day-to-day
scheduling, mentoring, and coaching for QC personnel who contribute
to testing. Investigate Out-Of-Specification (OOS) test results,
write reports and implement corrective and preventive actions
(CAPA) to prevent reoccurrences Review test data for completeness
and accuracy Provide timely responses to internal and external
inquiries Stay abreast of new developments in analytical
technologies Contribute to improvements in laboratory operations to
increase efficiency and GMP compliance Ability to work and
communicate effectively with others within the company to ensure
timely completion of tasks and projects Your Profile Bachelor's
Degree with a minimum of 3 years extensive industry experience.
Thorough knowledge and understanding of Analytical Chemistry,
including USP materials testing Experience in GMP laboratory
testing such as UPLC/ HPLC, GC, UV-VIS Spectrophotometer, Karl
Fisher Titrator, FTIR, MS, TOC, etc. Comply with good housekeeping
and safety practices Excellent written and oral communication
skills. Experience in writing standard operating procedures (SOP's)
and test methods Excellent computer knowledge, including Microsoft
Word, Excel, Power Point and Access Ability to effectively
organize, multitask, and work in a fast-paced, deadline driven work
environment Ability to communicate in a proactive and
solution-focused manner, including keeping management aware of
potential issues Detail oriented with the ability to troubleshoot
and resolve problems Ability to work independently and manage one's
time Communicate effectively and ability to function well in a team
environment Preferred: Bachelor or Master's Degree in Analytical
Chemistry or related science field and a minimum of 2 years of QC
testing and GMP/GLP experience We Offer You will be part of a
motivated team overseeing the entire development cycle of
respective APIs. If you are looking for a new challenge and want to
join a motivated team in an internationally renowned company, you
should seize this opportunity. Nearest Major Market: San Diego
Keywords: Bachem, Vista , QC Supervisor, Other , Vista, California
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