QC Analyst III Job

QC ANALYST III needed for a CONTRACT opportunity with Yoh's client located in Oceanside, CA.

What You'll Be Doing:
- Summary Conduct routine and non-routine analysis of manufacturing environment and in process commercial and clinical products according to standard operating procedures.
- Responsible for collecting, processing and reporting data.
- Apply knowledge of good manufacturing practices and good laboratory practices on a daily basis.
- Compile data for documentation of test procedures and prepare reports for internal and regulatory submissions.
- Calibrate and maintain laboratory and instrumentation equipment.
- Develop and/or optimize testing methods and troubleshoot testing methods.
- Revise and update standard operation procedures.
- Review and evaluate data for conformance to specifications and report and investigate anomalous data.
- Ensure quality and safety of manufactured products.
- Use state-of-the-art techniques to evaluate and implement new techniques and technologies.

Job Responsibilities Essential
- Proficient in cGMP practices in all aspects of laboratory assignments
- Perform routine testing and basic troubleshooting
- Represent QC and serve as a point of contact for manufacturing and other departments
- Perform microbiological and chemical assays according to established procedures
- Share responsibilities with a team to accomplish all testing needed for QC samples
- Participate in routine projects
- Assist in data trending, data review, lab maintenance, training of new personnel
- Collect data, enter data and generate reports from electronic systems.
- Initiate, compile, and perform lab investigations that include reviewing documents, conducting internal and external interviews, and tracking information.
- Supplementary Responsibilities
- Attend team, department and corporate meetings as required
- Attend seminars and/or classes as necessary to support business demand

Job Requirements Work Environment/Physical Demands/Safety Considerations
- Work in office and laboratory environment
- May work in the clean room environment that requires gowning and no make up or jewelry
- May work in the clean room environment which can be a loud environment from different equipment operating
- Work with some hazardous materials and chemicals
- Available to work over-time, weekends, and holidays as needed

What You Need to Bring to the Table:
- Knowledge, Skills, and Abilities
- Demonstrate excellent organizational skills
- Ability to read and follow Standard Operating Procedures
- Excellent interpersonal, written and verbal communication skills
- Ability to read and interpret technical data cGMP experience
- Proficient with QC systems
- Must have working knowledge in manual and automated chemical and microbiological assays
- Must be able work independently as well as within a team in a fast pace environment
- Ability to stand for 8 to 10 hours a day Ability to lift up to 30lbs
- Ability to climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility
- Ability to sit, stand and move within work space for extended periods
- Ability to perform repetitive tasks including frequent hand to finger manipulations, grasping pushing and pulling

Bonus Points! Otherwise Known As Preferred Qualifications:
- Education and Experience Bachelor's Degree in Biology, Microbiology, Biochemistry, Chemistry or other relevant discipline and one (1) year of related experience or AA and 4 years of related experience or HS and six (6) years of related experience

WHAT ARE YOU WAITING FOR? APPLY NOW!

RECRUITER: Salima Hakim

Yoh, a DayTHIS ADDRESS IS EXCLUSIVELY FOR INDIVIDUALS WITH DISABILITIES REQUESTING APPLICATION ASSISTANCE.

J2W: CLINICAL

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