QC Scientist III FM BSD
Company: Bachem
Location: Vista
Posted on: January 12, 2021
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Job Description:
Your Responsibilities The Quality Control Scientist III function
is to perform laboratory day-today operations, guide and interact
with QC and department personnel to accomplish goals and objectives
as directed by the Director of Quality Control. Other duties
include performing in-process testing, GC method validation, raw
material testing, and final product testing, QC documentation and
related GMP activities. Your Tasks Maintain and perform daily
operations of the QC department on a daily basis in coordination
with the QC Director to include testing of in-process, raw
material/peptide samples and prioritizing projects Implement and
maintain GMP procedures such as following SOP's, Standard Testing
Procedures (STP's), written procedure and maintaining proper
documentation as necessary for Quality Control Maintain a cGMP
quality level of work for the QC operations to include training,
documentation and procedural work Test and release in-process, and
raw materials used in the manufacturing facility for GMP.
Performing analytical testing and reviewing data for completeness
and accuracy. Support method validation activities for in-process
samples. Receive, test and release final product peptide
manufactured at Bachem Write/revise specifications as necessary,
performing analytical testing and reviewing data for completeness
and accuracy Write standard operating procedures, standard test
procedures and other related GMP documentation Perform QC analysis
to include: GC, HPLC, Water, Mass Spec, UV, melting point, Optical
Rotation, TLC and misc. wet chemistry lab work and other related
analytical equipment used for control quality of the GMP facility.
This work may include calibration and validation of these methods
Control raw material used in the manufacturing facility for GMP to
include receiving, quarantine, testing and QC release Investigate
any deviation or out of specification as necessary related to QC
work performed as instructed by supervisor Execute validations as
necessary to include QC Analytical methods performed, other
validations to support the quality of the manufacturing facility
Follow safety guidelines for handling, disposal and use for a
peptide manufacturing company using toxic and/or large volumes of
chemicals Support validation, and stability testing activities as
needed, documentation and quality GMP procedures Your Profile BS
Degree in Chemistry or related field Minimum of 8 years' experience
in the GMP industry Experience with the use of analytical
techniques/ instruments, such as, Gas Chromatography (GC), High
Performance Liquid Chromatography (HPLC), Karl Fischer (KF), etc.
May work with hazardous materials and chemicals Ability to train
others in analytical methodology Ability to take the technical lead
working with other scientists Excellent written and oral
communication skills Basic computer knowledge, including Microsoft
Word, Excel and PowerPoint 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 May involve second shift testing activities Flexibility
of working hours based on business needs, may include some nights
and occasional weekends Preferred: Experience with Peptides
Master's degree in Chemistry or related field Experience with use
of Master Control We Offer You will be part of a motivated team
overseeing the entire development cycle of respective APIs. If you
are l 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 Scientist III FM BSD, Other , Vista, California
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