Quality Control Analyst II - Camarillo CA

ATTENTION MILITARY AFFILIATED JOB SEEKERS- Our organization works with partner companies to source qualified talent for their open roles. The following position is available toVeterans Transitioning Military National Guard and Reserve Members Military Spouses Wounded Warriors and their Caregivers. If you have the required skill set education requirements and experience please click the submit button and follow the next steps.
Unless specifically stated otherwise this role isOn-Site at the location detailed in the job post.


Job Description
QUALITY CONTROL ANALYST II in Camarillo CA

Build your future at Curia where our work has the power to save lives

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia we are on a mission to advance our customers therapies from curiosity to cure and ultimately to improve patients lives.

The Quality Control Analyst II is responsible for performing routine and non-routine analytical chemistry assays of raw materials in-process samples finished APIs and stability samples. This role also participates in special projects method development/transfers and cleaning study qualifications.

Join our talented workforce where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients lives with the pharmaceuticals we develop and manufacture

We proudly offer

Generous benefit options (eligible first day of employment)
Paid training vacation and holidays (vacation accrual begins on first day of employment)
Career advancement opportunities
Education reimbursement
401K program with matching contributions
Learning platform
And more!
Essential job duties

Perform analytical testing for incoming in-process and final products and stability samples using equipment such as balances pipettes pH meter UV/Visible spectrophotometer Total Organic Carbon analyzer etc.
Perform chromatography (HPLC/UPLC GC) with minimal qualification and training wet chemistry assays analytical chemistry assays Capillary Electrophoresis ELISA HPLC/UPLC GC IR UV etc. and raw material testing and/or sampling
Back up for QC analytical instrument maintenance and calibration
Perform QC general laboratory equipment maintenance laboratory housekeeping hazardous waste handling and preparation of the laboratory for audits
Perform or assist with QC method qualifications transfers and validations
Perform QC method development
Perform cleaning validation studies
Assist with the evaluation of new equipment and processes
Assist in the review of QC data and provide summaries to management as needed
Assist QC Management as needed in the completion of OOS deviations and CAPAs investigations for QC
Backup for QC analytical sample receipt for internal testing outside laboratory testing login processing shipment tracking distribution of test results and closure

Additional Qualifications/Responsibilities
Education experience certification and licensures Required

Bachelors degree in Chemistry or related field
Minimum 3-5 years experience in pharmaceutical industry environment or equivalent combination of education and experience
Preferred

Experience working in cGMP or GLP pharmaceutical industry environment
Knowledge skills and abilities

Excellent verbal and written communication skills including the ability to effectively present information and respond to questions from groups of managers clients customers and the general public
Ability to meet deadlines and work under pressure with limited supervision
Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently
Ability to read analyze and interpret general business periodicals professional journals technical procedures or governmental regulations
Ability to write reports business correspondence and procedure manuals
Ability to apply advanced mathematical concepts such as exponents logarithms quadratic equations and permutations
Ability to apply mathematical operations to such tasks as frequency distribution determination of test reliability and validity analysis of variance correlation techniques sampling theory and factor analysis
Ability to define problems collect data establish facts and draw valid conclusions
Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables
Proficient use of computer software including Microsoft Office Suite and instrument manufacture-based systems
Knowledgeable in FDA GMPs (21 CFR 211 820 and/or 600); ISO 9001 and 13485 a plus


Salary: $70000 - $86900/year.

Education experience location and tenure may be considered along with internal equity when job offers are extended.