QA Analyst for a producer of therapeutic peptides for pharmaceutical
and biotech uses located in Torrance, CA. Here are the details:
Primary Job Responsibilities:
Accountable for the non-GMP storage and electronic data base for
custom peptides; updating customer files.
Accountable for weighing and dispensing of GMP and non-GMP key raw
materials to production.
Responsible for ****pping both GMP and non-GMP products to customers.
Responsible for distribution of do***ents. Makes affective new/revised
S.O.P.=92s, Master Batch Records, change control system, specification
and test method mauals.
Responsible for maintaining BSE/TSE files
Team member for internal audits.
Provides backup sup****t for the QA manager
Performs environmental monitoring trending and water system data
trending
Writing and reviewing Standard Operating Procedures (S.O.P.=92s)
Perform related duties as assigned
Required Competencies:
Minimum BA in Science
BA/BS in science
At least 2 to 3 years experience in FDA regulated environment
Team oriented and, performs duties with minimal supervision.
Good computer skills including Microsoft Windows
Excellent oral and written communication
Sound analytical techniques to perform tests.
Ability to work in fast paced environment, at times under pressure
including tight deadlines
Detail oriented multitasking is a must
If you are interested in applying for this op****tunity, please forward
to khristine_anderson@[EMAIL PROTECTED]
the following:
1. Resume in Word or txt format
2. Confirmation that Torrance is commutable
3. Work authorization information (i.e. H1B, TN, citizen, green card
holder, etc)
4. Compensation requirement or salary in most recent position
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