Top 34 Chemists Jobs in Camarillo, Ca

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
6d
Laboratory Analyst I/II (Extra-help) - Ventura Water
City of Ventura —Ventura, CA
- $35.64 - $47.62 an hour
- Part-time
- Clean driving record
- Mid-level
- Associate's degree
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
6d
Chemist II
Parker Hannifin Corporation —Oxnard, CA
- $88,790 - $148,155 a year
- Full-time
- Mid-level
- Master's degree
- Analysis skills
- Paid parental leave
- Paid holidays
Quality Control Validation Scientist
Katalyst Healthcares & Life Sciences —Thousand Oaks, CA
- Contract
- Hybrid work
- Mid-level
- Bachelor's degree
- Organizational skills
Quick Apply
Junior Analytical Chemist / Application Scientist: Gas Chromatography-Mass Spectrometry (GC-MS)
Entech Instruments Inc —Simi Valley, CA
- Full-time
- English
- Mid-level
- Travel
- Health insurance
- Dental insurance
Quick Apply
Senior VOC & GC/MS Chemist
AmSpec Group —Camarillo, CA
- Full-time
- 7 years
- Ability to walk for extended periods
- Bachelor of Science
Organic and Conjugation Chemist
Amgen —Thousand Oaks, CA
- $84,454.30 - $114,261.70 a year
- Mid-level
- Master's degree
- High school diploma or GED
- Disability insurance
- Health insurance
Senior Scientist
Amgen —Thousand Oaks, CA
- $127,121.75 - $171,988.25 a year
- Pass drug screening
- 3 years
- Bachelor's degree
- Disability insurance
- Health insurance
7d
Sr. Analytical Chemist – Organics in Water by GC/MS
Entech Instruments Inc —Simi Valley, CA
- Full-time
- English
- Analysis skills
- Doctor of Philosophy
- Health insurance
- Dental insurance
Quick Apply
Scientist - LC-MS / MS Bioanalytical
Amgen —Thousand Oaks, CA
- $109,020.15 - $147,497.85 a year
- 3 years
- Analysis skills
- Supervising experience
- Disability insurance
- Health insurance
Process Development Senior Associate
Amgen —Thousand Oaks, CA
- $80,044.50 - $108,295.50 a year
- Mid-level
- Master's degree
- High school diploma or GED
- Disability insurance
- Health insurance
Process Development Senior Scientist
Amgen —Thousand Oaks, CA
- $126,066.05 - $170,559.95 a year
- 3 years
- Bachelor's degree
- Doctor of Philosophy
- Disability insurance
- Health insurance
Senior RNA Chemist – RNA Therapeutics
Amgen —Thousand Oaks, CA
- $123,777 - $167,463 a year
- Presentation skills
- Bachelor's degree
- Doctor of Philosophy
- Disability insurance
- Health insurance
Analytical Sr Scientist
Amgen —Thousand Oaks, CA
- $126,066.05 - $170,559.95 a year
- Management
- 3 years
- Analysis skills
- Disability insurance
- Health insurance
Process Development Sr Scientist
Amgen —Thousand Oaks, CA
- $126,066.05 - $170,559.95 a year
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
- Disability insurance
- Health insurance
13d
Process Development Sr. Scientist
Amgen —Thousand Oaks, CA
- $126,066.05 - $170,559.95 a year
- Bachelor's degree
- Doctor of Philosophy
- Senior level
- Disability insurance
- Health insurance
Process Development Principal Scientist
Amgen —Thousand Oaks, CA
- $141,836.95 - $191,897.05 a year
- Bachelor's degree
- Doctor of Philosophy
- In-person
- Disability insurance
- Health insurance
Senior VOC & GC/MS Chemist
Amspec LLC. —Camarillo, CA
- Full-time
- 7 years
- Ability to walk for extended periods
- Bachelor of Science
Quick Apply
Process Development Senior Scientist - Synthetic Peptides, Oligonucleotides, ADCs
Amgen —Thousand Oaks, CA
- $126,066.05 - $170,559.95 a year
- 3 years
- Bachelor's degree
- Doctor of Philosophy
- Disability insurance
- Health insurance

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Quality Control Analyst II

USDM Life Sciences -
Thousand Oaks, CA

Apply Now

Job Details

Full-time
$40 - $60 an hour
6 days ago

Benefits

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

Qualifications

High school diploma or GED

Full Job Description

Job Title:

Quality Control Analyst II

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 Analyst will support various activities within the QC department. Key responsibilities are to execute analytical method transfers, including raw materials, for use in a cGMP environment in Quality control. You will be responsible for conducting biological or chemical and physical analyses on raw materials, in-process samples, drug substance and final product samples and other samples collected from manufacturing areas.

Primary Responsibilities

Conduct biological, chemical, and physical analyses on samples including raw materials, initial, in-process and final products, and samples collected from environmental monitoring according to SOP and pre-approved protocols.
Drive implementation of new methodologies, or new sample types into existing methods in a QC laboratory
Support Investigation of nonconformances and troubleshoot unexpected results.
Handle multiple tasks concurrently including testing and inventory management in a timely and appropriate manner.
Perform review of test data, which includes overall documentation practices (CGDP). May perform release functions in LIMS or other computerized systems.
Support generation and documentation of validation protocol deliverables.
Draft and update, as required, QC SOPs.
Perform test equipment, equipment maintenance and calibrations as required.

Additional Responsibilities

Performs other related duties and assignments as required

Qualifications

General understanding & knowledge of the following areas:
Laboratory functions, test methods, equipment (including but not limited to analytical equipment (e.g. HPLCs, plate readers, processes and applicable procedures.
Laboratory safety including standard precautions and hazardous and biohazardous chemical handling.
Wet and instrumental methods of analyses.
Operating and troubleshooting procedures for lab equipment
General knowledge of FDA regulations, application of Good Laboratory Practices, application of Good Manufacturing Practices and application of Good Documentation Practices is preferred.
Knowledge of quality and regulatory requirements pertinent to pharmaceutical manufacturing labs is a plus.
Ability to write detailed investigation reports, knowledge of how to implement investigation strategies and apply root cause failure analysis is a plus.

Education & Certifications

High School degree or equivalent required; Bachelor’s Degree in Chemistry, Microbiology or Biological Sciences strongly preferred
Minimum 2 years of related work experience
Experience in quality operations, biotechnology, pharmaceutical or similar GMP manufacturing environment is strongly preferred.

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 40.00 - 60.00

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

chemists jobs in camarillo, ca

Quality Control Analyst II

Laboratory Analyst I/II (Extra-help) - Ventura Water

Quality Control Validation Scientist

Chemist II

Quality Control Validation Scientist

Junior Analytical Chemist / Application Scientist: Gas Chromatography-Mass Spectrometry (GC-MS)

Senior VOC & GC/MS Chemist

Organic and Conjugation Chemist

Senior Scientist

Sr. Analytical Chemist – Organics in Water by GC/MS

Scientist - LC-MS / MS Bioanalytical

Process Development Senior Associate

Process Development Senior Scientist

Senior RNA Chemist – RNA Therapeutics

Analytical Sr Scientist

Process Development Sr Scientist

Process Development Sr. Scientist

Process Development Principal Scientist

Senior VOC & GC/MS Chemist

Process Development Senior Scientist - Synthetic Peptides, Oligonucleotides, ADCs

I want to receive the latest job alert for chemists in camarillo, ca

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