Top 11 Quality control validation Jobs in Oxnard, Ca

Quality Control Validation Scientist
USDM Life Sciences —Thousand Oaks, CA
- $65 - $75 an hour
- Full-time
- Mid-level
- Bachelor's degree
- Critical & Intensive Care
- Disability insurance
- Dental insurance
2d
Quality Control Validation Scientist
Katalyst Healthcares & Life Sciences —Thousand Oaks, CA
- Contract
- Hybrid work
- Mid-level
- Bachelor's degree
- Organizational skills
Quick Apply
Quality Control Inspection Engineer
ECA Medical Instruments —Newbury Park, CA
- $75,000 - $113,000 a year
- Full-time
- Microsoft Outlook
- Customer service
- 5 years
- Health savings account
- Health insurance
Quick Apply
Quality Control Specialist, Microbiology
Amgen —Thousand Oaks, CA
- $100,450.45 - $135,903.55 a year
- Doctoral degree
- Master's degree
- High school diploma or GED
- Disability insurance
- Health insurance
Quality Control Analyst II
USDM Life Sciences —Thousand Oaks, CA
- $40 - $60 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Bachelor's degree
- Disability insurance
- Dental insurance
2d
Sr. Quality Control Technician
Avantor —Carpinteria, CA
- $50,000 - $80,500 a year
- Full-time
- Microsoft Outlook
- Computer literacy
- Basic math
Product Quality Engineer
Rently —Camarillo, CA
- $75,000 - $85,000 a year
- Full-time
- Google Workspace
- Engineering
- Mid-level
- Disability insurance
- Health insurance
7d
QC Analytical Chemist
Avantor —Carpinteria, CA
- Full-time
- Oracle
- Microsoft Outlook
- Bachelor of Science
Quality Technician II
AeroVironment —Simi Valley, CA
- $20 - $30 an hour
- Overtime
- Clean driving record
- Mid-level
- High school diploma or GED
- Paid holidays
- Health insurance

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Quality Control Validation Scientist
USDM Life Sciences —Thousand Oaks, CA
Strong technical writing skills and able to write generate technical documents and reports that meet company and regulatory requirements.
$65 - $75 an hour
2d
Quality Control Validation Scientist
Katalyst Healthcares & Life Sciences —Thousand Oaks, CA
Strong technical writing skills and able to write generate technical documents and reports that meet company and regulatory requirements.
Quick Apply

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Process Quality Engineer
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Interpret customer, internal, product, testing, and manufacturing process requirements and develop appropriate quality controls, testing methods, inspection…
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Quality Engineer
Engineered Profiles LLC —Columbus, OH
Working knowledge of Statistical Process Control, capability studies, MSA/Gage R&R, and basic statistical analysis tools such as Minitab.
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Quality Control Validation Scientist

USDM Life Sciences -
Thousand Oaks, CA

Apply Now

Job Details

Full-time
$65 - $75 an hour
2 days ago

Benefits

Disability insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Life insurance

Qualifications

Content creation for technical audiences
Analytical chemistry
Technical writing experience within manufacturing
Statistical analysis
Test validation method

Full Job Description

Job Title:

Quality Control Validation Scientist

Job Function:

Quality Consultant

Location:

Thousand Oaks, CA

About USDM

USDM Life Sciences is a premier consulting company with 20+ years of experience assisting heavily regulated biotech, medical device, and pharmaceutical companies with their GxP technologies to accelerate growth. Our deep domain knowledge and technology expertise in life sciences business processes are what set us apart. From strategy to implementation and adoption, we have delivered thousands of GxP projects globally.

As part of the USDM team, you have the opportunity to work with cutting-edge technologies through our many partnerships with companies like Microsoft, Google, Oracle, DocuSign, Box, and many more. From molecule to market, you will help connect technology, people, and data in new ways to generate real-time insights to improve business outcomes for USDM’s clients. Are you ready to make an impact and drive real digital transformation in life sciences?

Founded in Santa Barbara in 1999, USDM has grown to a progressive, global company with 300+ remote employees and offices throughout the US, Canada, and Germany.

Nature and Scope of Job

The QC Analytical Scientist will support various Quality Control activities within the AQC department. Key responsibilities are to transfer and execute analytical methods, including raw materials, for use in a cGMP environment in Quality control, both analytical quality control methods (AQC) and Quality Control Microbiology methods (QCM).

Primary Responsibilities

Drive analytical method validation/ transfer of laboratory methodologies
Support the execution and issue resolution (e.g., discrepancies) and completion approval of test plans/protocols
Support troubleshooting of analytical methods
Ensure laboratory equipment is maintained in a validated state and that all analytical methods transferred follow company and regulatory requirements.
Responsible for protocol and report generation and other technical documents as required. This may include supporting raw material qualification for new products
Use sound scientific principles and statistical techniques to solve problems and make recommendations.
May Support the installation, operational qualification (IOQ), maintenance and troubleshooting of instrumentation in the AQC group.
Responsible for deliverables to ensure timelines and milestones are met.
Other duties as assigned.

Qualifications

Strong technical writing skills and able to write generate technical documents and reports that meet company and regulatory requirements
Knowledge of analytical methods and operations with strong emphasis in problem-solving.
Knowledge about analytical method validation.
Intermediate statistical knowledge and experience with data analysis
Knowledge concerning cGMP, especially lab related topics such as method validation and unexpected results investigation.
Basic knowledge about regulatory requirements concerning analytical instrumentation, and test methods
Substantial knowledge and understanding in terms of regulatory standards requirements e.g., CGMP, QSR, USP, 21CFR, ICH etc.
Ability to complete tasks with minimal direction, demonstration of basic project management skills.
Ability to multi‐task in a highly dynamic and diverse environment.
Attention to detail, good organization, and time management skills to meet deadlines.
Proficient in Microsoft Office.
Strategically and business-oriented thinking

Additional Qualifications

Nice to have the KNEAT Program, not required
Experienced in reviewing and approving Life Cycle Validation Documents including:
Familiar with paperless validation software for life sciences
Commissioning, Installation, Operational and Performance Qualification protocols and reports for Equipment, Facilities & Utilities at Biopharmaceutical Manufacture plant.
Computer System Validation protocols and reports, including SCADA, MES.
QC/Micro Laboratory Instrument Qualification and method validation.

Education & Certifications

Bachelor’s Degree in biotechnology, Microbiology, Pharmacy, Chemistry or equivalent.
Minimum of 1 year of analytical development or validation experience in Pharmaceutical, Biopharmaceutical or related manufacturing environment, or an advanced degree.

Working Conditions

The working conditions described here are representative of those that must be met by an employee to successfully perform the essential responsibilities and functions of the job and are not meant to be all-inclusive. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential responsibilities and functions of the job.

Unless reasonable accommodations can be made, while performing this job the staff member shall:

Prolonged periods of sitting or standing at a desk and working on a computer in an environmentally controlled home office environment.
Operate other office productivity machinery, such as a calculator, scanner, or printer.
Frequently communicate with stakeholders via telephone, email, or instant message. Must be able to exchange accurate information in these situations.

Equal Opportunity Statement

USDM Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Disclaimer

This job description is intended to describe the general nature and the level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. USDM Life Sciences reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.

Compensation

Salary/Hourly Rate Range (W2): USD 65.00 - 75.00

The base salary/hourly rate range represents the anticipated low and high end of the USDM’s compensation range for this position. Actual salaries/hourly rates will vary and will be based on various factors, such as the candidate’s qualifications, skills, competencies, and proficiency for the role. The compensation described above is subject to change and could be higher or lower than the range described based on market survey data or budget.

Full-time employees are eligible for health, vision, and dental insurance, life insurance, short and long-term disability, hospital indemnity, accident, and critical care coverage.

Both full and part-time employees, who are at least 21 years of age, are eligible to participate in USDM's 401k plan. Full and part-time employees may be eligible for paid time off.

All employees are eligible for USDM's rewards and recognition program.

Apply Now

Refine Your Search

quality control validation jobs in oxnard, ca

Quality Control Validation Scientist

Quality Control Validation Scientist

Quality Control Inspection Engineer

Quality Control Specialist, Microbiology

Quality Control Analyst II

Sr. Quality Control Technician

Product Quality Engineer

QC Analytical Chemist

Quality Technician II

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