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Gmp Process Chemist Jobs (NOW HIRING)

Agilent

Process Chemist

Folsom, CA

$132K - $207K/yr

As a Process Chemist you will perform a variety of engineering duties to support manufacturing ... Experience working in GMP or regulated environments, including change control, deviations, CAPA ...

Agilent

Process Chemist

Folsom, CA · On-site

$132K - $207K/yr

As a Process Chemist you will perform a variety of engineering duties to support manufacturing ... Experience working in GMP or regulated environments, including change control, deviations, CAPA ...

Caresoft Inc.

Manufacturing Process Chemist

Carlsbad, CA · On-site

$28 - $32/hr

Manufacturing Process Chemist Location: Carlsbad CA - 1st Shift Duration: 9 Months Summary: The ... GMP environment Knowledge/Skills Basic algebraic, statistical and mathematical skills General ...

Bachem

Chemist

Vista, CA · On-site

$31.07 - $33.01/hr

Follow SOPs and approved directions to clean equipment used in GMP processes, maintain cleaning log ... Bachelor's degree in chemistry or related field (in lieu of degree, will consider 10+ years ...

Bachem

Chemist

Vista, CA · On-site

$31.07 - $33.01/hr

Follow SOPs and approved directions to clean equipment used in GMP processes, maintain cleaning log ... Bachelor's degree in chemistry or related field (in lieu of degree, will consider 10+ years ...

Astrix Inc

Production Chemist

Torrance, CA · On-site

Develop processes for purification of chemicals other than peptides * Follow and maintain GMP ... in Chemistry or related field * 1-5 years' work experience * Experience with HPLC and ...

Eurofins Scientific

GMP Chemist

Saint Louis, MO · On-site

The position will be providing analytical support to biotherapeutic process development teams ... Chemistry, Chemical Engineering or other related fields. * 1-3 years of relevant GMP industrial ...

Eurofins

GMP Chemist

Saint Louis, MO · On-site

The position will be providing analytical support to biotherapeutic process development teams ... Chemistry, Chemical Engineering or other related fields. * 1-3 years of relevant GMP industrial ...

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Gmp Process Chemist information

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$41K

$84.8K

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How much do gmp process chemist jobs pay per year?

As of Sep 13, 2026, the average yearly pay for gmp process chemist in the United States is $84,782.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,000.00 and $105,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Gmp Process Chemist jobs?

For Gmp Process Chemist jobs, the most frequently searched job titles are:

Infographic showing various Gmp Process Chemist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $84,782 per year, or $40.8 per hour.

Process Chemist

Folsom, CA

Agilent
Biotechnology Research and Development • 10K+ employees
Learn more about Agilentexternal

$132K - $207K/yr

Full-time

Re-posted 13 days ago

Agilent Technologies rating

8.5

Company rating: 8.5 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

Job description

Job Description

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic, and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us.

As a Process Chemist you will perform a variety of engineering duties to support manufacturing operations and improving products, processes and applications to meet agreed-upon objectives. As part of our diverse and expert team, you will be responsible for:

  • Executing and overseeing complex laboratory work, with focus on GC, GCMS, LC, LCMS to enable timely, customerfocused decision making in a manufacturing environment.
  • Providing onfloor and realtime troubleshooting as needed, prioritizing work to meet manufacturing schedules and ensuring timely, rightfirsttime resolution of analytical questions.
  • Designing and executing statistically sound experiments, interpret complex datasets, and communicate clear, riskbased recommendations to manufacturing and quality stakeholders.
  • Leading process performance evaluations, robustness studies, and root cause analysis to support deviations, CAPA, complaints, and lifecycle improvements.
  • Partnering crossfunctionally with QC, QA, R&D, MSAT, and Global Operations to align analytical strategy with product requirements, control strategies, and operational priorities.
  • Leading and supporting complex investigations related to manufacturing events and customer complaints, applying structured problemsolving methodologies to determine root cause and implement effective corrective and preventive actions.
  • Driving continuous improvement of chromatography capability, including equipment and instrument performance, preventative maintenance strategies, method robustness, and technical engagement with vendors as required.
  • Authoring, reviewing, and approving highquality technical documentation (e.g., protocols, validation and transfer reports, deviations/investigations, change controls), ensuring traceability, compliance, and data integrity.
  • Providing technical leadership through mentoring and coaching, influencing crossfunctional teams and driving adoption of best practices in chromatography and laboratory execution.
  • Ensuring all work is performed in compliance with safety, quality, and regulatory requirements, with a strong focus on good documentation practices and data integrity.
Qualifications

Minimum Qualifications

  • Bachelor's degree in Chemistry, Biochemistry, Materials Science or a related discipline.
  • 8+ years of handson experience with gas chromatography (GC) and liquid chromatography (HPLC/UHPLC), including troubleshooting, validation, and supporting sample preparation techniques.
  • Broad working knowledge of analytical techniques and detectors (e.g., MS, UV, FID, ECD) with the ability to select fitforpurpose analytical approaches.
  • Proven ability to lead complex investigations and translate analytical data into clear, actionable technical recommendations.
  • Strong technical writing skills, with experience authoring protocols, validation documentation, and investigation reports.
  • Demonstrated commitment to laboratory safety, quality systems, and data integrity.

Preferred Qualifications

  • Experience with LCMS and/or GCMS for trace analysis, impurity profiling, and/or materials characterization. Additional analytical technique expertise (e.g., NMR, SEM, Karl Fischer, spectroscopy, microscopy) is a plus.
  • Knowledge of chromatography consumables (columns, stationary phases, sample preparation) and performance chemistry evaluations.
  • Experience working in GMP or regulated environments, including change control, deviations, CAPA, and inspectionready documentation.
  • Experience with method validation, method transfer, and continued process/method verification; familiarity with DOE and statistical tools.

Additional Details

This job has a full time weekly schedule. Applications for this job will be accepted until at least September 8, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $132,851.00 - $207,580.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: OccasionalShift: DayDuration: No End DateJob Function: Manufacturing

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