200844 - Quality Control Scientist III
Industry
SCI
Region
CA-Southern California - San Diego
City
San Diego
State
CA
Rate
$36 to $37.00 DOE
Duration
12 Months
Description
Chipton-Ross is seeking a Quality Control Scientist III for a contract opportunity in San Diego, CA.

RESPONSIBILITIES:
The Quality Control Scientist III position is a specialized member of the Quality Control team. In this role you will perform work required to ensure product quality is maintained at standards set forth by Mesa Biotech, part of the Quality System and mandated by regulatory agencies.

Perform incoming inspections of all raw materials
Operate all equipment safely, as trained and directed, in accordance with established practices
Maintain material identification and status control
Execute test and inspection procedures in compliance with written and approved standard operating procedures
Summarize data to monitor/trend product performance
Deliver weekly, monthly, and quarterly metrics
Leads and participates in cross-functional teams
Leads continuous improvement and cost improvement projects
Leads troubleshooting and lab investigations
Ability to adhere to standard timeline and escalate actions appropriately for resolution in a timely manner
Responsible for meeting deadlines under a tight timeline and changing priorities
Create and own medium to high-risk Non-Conformances/ Deviations / CAPAs
Recommend and execute test procedure updates
Performs tasks related to QC functional responsibilities such as, stability, validations, sample retention program, customer complaints, inventory maintenance, and continuous improvement efforts
Provide administrative and technical support services during quality assurance audits.
Provides training to other QC personnel
Review’s manufacturing batch records for accuracy, completeness, and GDP
Always complies with Good Lab Practices (GLP) and Good Documentation Practices (GDP)
Embodies cultural values and aligns daily actions with department goals and company culture
Other activities as deemed necessary by the QC management team
Manager project and influence w/
Work effectively with cross functional teams (Validation, Quality Assurance)

REQUIRED EXPERIENCE:
Experience in an FDA regulated and/or cGMP environment required
Proficient in Microsoft Excel and Word
Effective written and oral communication skills
High attention to detail, highly organized, and strong documentation skills
Ability to be self-motivated, proactive, accountable, and flexible
Ability to work well under pressure, handle multiple tasks/projects and meet deadlines
Sets stretch goals and links them to strategic outcomes and business deliverables
Comfortable with ambiguity

EDUCATION: High school diploma (or equivalent)

WORK HOURS: 8am-4:30pm M-F.

Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.

Contact
Zachary Fasano
zfasano@chiptonross.com
CHIPTON-ROSS, INC.
420 Culver Boulevard
Playa Del Rey, CA 90293

Phone: (310) 414-7800 x252 or (800) 927-9318 x252

Candidates responding to this posting must currently possess the eligibility to work in the United States. No third parties please.

Employment will be contingent on candidate clearing pre-employment drug screen and background check.

Chipton-Ross provides equal employment opportunities to all employees and applicants for employment without regard to race, color, creed, religion, national origin, sex (including pregnancy), age, disability, sexual orientation, gender identity and/or expression, protected veteran status, genetic information, or any other characteristic protected by Federal, State or local law. This policy governs all areas of employment at Chipton-Ross, including recruiting, hiring, training, assignment, promotions, compensation, benefits, discipline, and terminations.