Top 31 chemistry Jobs in camarillo, ca

Quality Control Analyst III
Curia —Camarillo, CA
- $85,000 - $106,500 a year
- Overtime
- Background check
- Pass drug screening
- Master's degree
- Paid training
- Paid holidays
Scientist – Protein Engineering – Organic Chemist: ADC Research & Development
Amgen —Thousand Oaks, CA
- $111,695.10 - $151,116.90 a year
- Doctoral degree
- Mid-level
- Master's degree
- Disability insurance
- Health insurance
Scientist - Protein Biochemist
Amgen —Thousand Oaks, CA
- $116,032.65 - $156,985.35 a year
- Doctoral degree
- Master's degree
- Bachelor's degree
- Disability insurance
- Health insurance
R&D Laboratory Supervisor
Meissner —Camarillo, CA
- $73,050 - $93,600 a year
- Full-time
- 6 years
- Bachelor of Science
- Senior level
- Profit sharing
- Health savings account
ADC Development: Organic and Conjugation Chemist
Amgen —Thousand Oaks, CA
- $123,777 - $167,463 a year
- Doctoral degree
- Mid-level
- 3 years
Quality Control Validation Scientist
Katalyst Healthcares & Life Sciences —Thousand Oaks, CA
- Contract
- Mid-level
- Bachelor's degree
- Organizational skills
Quick Apply
Process Development Principal Scientist
Amgen —Thousand Oaks, CA
- $148,363 - $171,657 a year
- Online Application
- Hybrid work
- 3 years
- Doctor of Philosophy
- Mentoring
- Disability insurance
- Health insurance
9d
Clinical Lab Scientist PRN
Los Robles Regional Medical Center —Thousand Oaks, CA
- $58.42 - $77.01 an hour
- PRN
- 1 year
- Entry level
- Employee stock purchase plan
- Disability insurance
Quick Apply
Process Development Sr Scientist
Amgen —Thousand Oaks, CA
- $126,066.05 - $170,559.95 a year
- Management
- Doctoral degree
- Office
- Disability insurance
- Health insurance
Sr Scientist
Amgen —Thousand Oaks, CA
- $126,066.05 - $170,559.95 a year
- 3 years
- Analysis skills
- Bachelor's degree
- Disability insurance
- Health insurance
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
1d
Material Scientist
PTI Technologies —Oxnard, CA
- $111,795 - $186,325 a year
- Full-time
- 5 years
- Engineering
- Data analysis skills
- Health savings account
- Employee stock purchase plan
Quick Apply
Field Specialist II -Intervention Services & Drilling Tools
Weatherford —Santa Paula, CA
- Full-time
- Customer service
- Computer literacy
- Writing skills
2d
Clinical Laboratory Scientist, Evening Shift, Full Time
Adventist Health —Simi Valley, CA
- $51.09 - $70.07 an hour
- Full-time
- Hospital
- HIPAA
- Mid-level
- Health insurance
5d
Senior Principal Scientist – Chemical Biology & Proximity-Based Therapeutics
Amgen —Thousand Oaks, CA
- $162,509.80 - $219,866.20 a year
- Doctoral degree
- Master's degree
- Bachelor's degree
- Disability insurance
- Health insurance
Postdoctoral Fellow - Cardiometabolic Disorders (Discovery)
Amgen —Thousand Oaks, CA
- $81,178.40 - $109,829.60 a year
- Doctor of Philosophy
- In-person
- Senior level
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
6d
Assistant Director of Hospital Laboratory Services
Ventura County —Ventura, CA
- $56.30 - $78.83 an hour
- Online Application
- Bilingual
- Hospital
- Supervising experience
Principal Scientist – Lead Discovery and Targeted Protein Degradation Biochemistry
Amgen —Thousand Oaks, CA
- $140,123.35 - $189,578.65 a year
- Management
- Master's degree
- Bachelor's degree
- Disability insurance
- Health insurance
3d
Principal Investigator, Polymer Chemistry
HRL Laboratories —Malibu, CA
- $154,500 - $197,900 a year
- Full-time
- 5 years
- Doctor of Philosophy
- Travel
- Health insurance
- Dental insurance
Quick Apply

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Quality Control Analyst III

Curia -
Camarillo, CA

Apply Now

Job Details

Full-time
$85,000 - $106,500 a year

Benefits

Paid training
Paid holidays
Tuition reimbursement
401(k) matching
Opportunities for advancement

Qualifications

Pharmaceutical company experience
Data-driven problem-solving
Pharmaceutical manufacturing facility experience

Full Job Description

Quality Control Analyst III in Camarillo, CA

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

The Quality Control Analyst III is responsible for supporting the manufacturing department and external customers. Routine functions include testing of raw materials, in-process, end product, and stability samples.

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.

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!

Responsibilities

Perform complex testing and data evaluation, such as HPLC, ELISA, etc.
Troubleshoot equipment issues promptly and communicate resolutions to management
Participate in or assist with test method validations
Evaluate data for trends
Support and/or investigate OOS events by performing thorough root cause analyses, assessing potential product impact, and implementing appropriate CAPAs
Interact with outside departments including attending meetings, providing updates, etc.
Coordinate testing performed at outside testing labs, raw materials, etc.
Maintain a detailed and accurate recording of activities and results
Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries
Perform risk assessment as needed
Write/revise test methods, standard operating procedures, etc.
Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures
Support equipment upkeep
Prepare and order supplies, as necessary
Enter data into relevant data management systems and perform tracking and trending of data. Compile data and provide/present data summaries to management
Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry
Collaborate with cross-functional departments to coordinate testing, scheduling needs, and prioritization
Lead departmental projects and participate in cross-functional teams, including continuous improvement initiatives and new customer project teams
Lead the stability program, including management of test points, reporting of data, and investigations of out of specification or aberrant stability results

Required

Bachelor's Degree in Chemistry or related field and 5+ years related work experience;

Master’s Degree in Chemistry or related field and 3+ years related work experience;

PhD in Chemistry or related field and 1+ years related work experience
Experience working in cGMP or GLP pharmaceutical industry environment
Willing to work flexible hours (nights and weekends), as-needed (overtime eligible)

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 procedures
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 handle 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

Other Qualifications

Must pass a background check
Must pass a drug screen
May be required to pass Occupational Health Screening
May be required to obtain and maintain gowning certification
May be required to obtain and maintain media qualification

Pay Range: $85,000-$106,500/year

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

We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.

All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia 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, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

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Refine Your Search

chemistry jobs in camarillo, ca

Quality Control Analyst III

Scientist – Protein Engineering – Organic Chemist: ADC Research & Development

Scientist - Protein Biochemist

R&D Laboratory Supervisor

ADC Development: Organic and Conjugation Chemist

Quality Control Validation Scientist

Process Development Principal Scientist

Clinical Lab Scientist PRN

Process Development Sr Scientist

Sr Scientist

Organic and Conjugation Chemist

Material Scientist

Field Specialist II -Intervention Services & Drilling Tools

Clinical Laboratory Scientist, Evening Shift, Full Time

Senior Principal Scientist – Chemical Biology & Proximity-Based Therapeutics

Postdoctoral Fellow - Cardiometabolic Disorders (Discovery)

Process Development Senior Scientist - Synthetic Peptides, Oligonucleotides, ADCs

Assistant Director of Hospital Laboratory Services

Principal Scientist – Lead Discovery and Targeted Protein Degradation Biochemistry

Principal Investigator, Polymer Chemistry

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