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Uplc Jobs (NOW HIRING)

Astrix Inc

Document Control Specialist II

Vista, CA · On-site

$39 - $52/hr

Review and verify QC data output from chromatographic systems (HPLC, UPLC, or GC), confirming the accuracy of scanned batch records, chromatograms, and associated analytical records, and ensuring ...

Beloteca

ANALYTICAL CHEMIST

San Diego, CA · On-site

Independent execution of various standard laboratory techniques, including but not limited to H/UPLC, GC, water content analysis per USP, appearance assessment, water activity per USP * May ...

TekWissen LLC

Analytical Chemist

Chesterfield, MO · On-site

$32/hr

Develops methods for determining chemical composition and concentrations of analytes present in agrochemical formulations/products and related sample matrices using HPLC/UPLC/LCMS/GC to support ...

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Jobs for Humanity

Analytical Scientists

Hauppauge, NY · On-site

$70K - $90K/yr

Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. Responsibilities: Responsibilities include, but are not limited ...

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How much do uplc jobs pay per year?

As of Jul 5, 2026, the average yearly pay for uplc in the United States is $59,606.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,500.00 and $69,000.00 per year, depending on experience, location, and employer.

What are some common challenges encountered by UPLC (Ultra Performance Liquid Chromatography) operators, and how can they be addressed?

UPLC operators often face challenges such as dealing with instrument maintenance, troubleshooting unexpected results, and managing complex sample matrices. Ensuring proper calibration and regular maintenance of the system can prevent many technical issues. Additionally, thorough training on method development and data analysis helps operators quickly identify and resolve anomalies, leading to more reliable results. Collaborating closely with chemists and laboratory technicians can also facilitate problem-solving and knowledge sharing within the team.

What are the key skills and qualifications needed to thrive as a UPLC (Ultra Performance Liquid Chromatography) Specialist, and why are they important?

To thrive as a UPLC Specialist, you need a solid background in analytical chemistry, laboratory techniques, and experience with chromatographic separation, usually supported by a relevant science degree. Proficiency in operating UPLC instruments, chromatographic data software (such as Empower or Chromeleon), and understanding regulatory requirements like GLP or GMP are commonly expected. Attention to detail, problem-solving, and strong organizational skills help professionals excel in troubleshooting and managing complex analytical workflows. These competencies ensure accurate data generation, compliance, and high-quality results in research or quality control environments.

What is UPLC?

UPLC stands for Ultra Performance Liquid Chromatography. It is an advanced form of liquid chromatography that uses columns with smaller particle sizes and higher pressures to achieve faster, more sensitive, and more efficient separation of compounds in a mixture. UPLC is commonly used in pharmaceutical, environmental, and food industries for qualitative and quantitative analysis. Its high resolution and speed make it a preferred technique for analyzing complex samples with precision.

What is the difference between Uplc vs UPLC Developer?

AspectUplcUPLC Developer
CredentialsTypically requires knowledge of Uplc language and blockchain fundamentalsRequires expertise in Uplc, smart contract development, and blockchain protocols
Work EnvironmentBlockchain projects, smart contract coding, testing, and deploymentDeveloping, testing, and maintaining Uplc-based smart contracts and blockchain applications
Industry UsageUsed in blockchain and decentralized application developmentFocuses on creating and optimizing smart contracts on blockchain platforms

Uplc is a language used for blockchain smart contracts, while a UPLC Developer specializes in developing and deploying these contracts. The roles overlap in blockchain environments but differ in focus: Uplc is the language, and UPLC Developer is the professional implementing it.

More about Uplc jobs
What job categories do people searching Uplc jobs look for? The top searched job categories for Uplc jobs are:
Uplc jobs near you
Infographic showing various Uplc job openings in the United States as of June 2026, with employment types broken down into 84% Full Time, 2% Part Time, 2% Temporary, 11% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $59,606 per year, or $28.7 per hour.
Document Control Specialist II

Document Control Specialist II

Astrix Inc

Vista, CA • On-site

$39 - $52/hr

Full-time

Posted yesterday

Job description

Pay Rate Low: 39 | Pay Rate High: 52
Document Control Specialist II
Position Summary
A growing manufacturer of drug substances is seeking a Document Control Specialist II to join its QA team.
In this role you will help ensure that drug substances are produced in compliance with FDA and international regulatory requirements across research, pre-clinical, clinical, and commercial stages. The position centers on the review and processing of GMP documentation, day-to-day quality oversight, guidance to other functions on cGMP matters, and support for customer and regulatory audits. You will also help maintain GMP records and the supporting electronic quality systems.
Location: Onsite in Vista, CA | Hours: M-F 8-5 | Type: 1-year contract | Compensation: $39-$52/hour
What You Will Do
Core Responsibilities
  • Carry out clearance verifications for production rooms, the dispensary, and shipments as needed
  • Revise standard operating procedures (SOPs) and other GMP documents such as stability protocols, raw material specifications, and environmental monitoring trend reports
  • Administer GMP documentation and the associated workflows for the department
  • Review and verify QC data output from chromatographic systems (HPLC, UPLC, or GC), confirming the accuracy of scanned batch records, chromatograms, and associated analytical records, and ensuring documents are correctly labeled and packaged for archival
  • Provide support during regulatory, customer, and internal audits
  • Help implement and maintain the Quality Management System
  • Scan, verify, and archive internal and external GMP records
  • Represent QA on cross-functional and cross-site projects, including system and process harmonization and the rollout of new systems

Qualifications
Education & Experience
  • Bachelor's degree in organic chemistry or a related field required; master's degree in organic chemistry or a related field preferred, or
  • Bachelor's degree in a science or related field with a minimum of 3 years in a GMP/manufacturing setting, or
  • Associate's degree in a science or related field with a minimum of 5 years in a GMP/manufacturing setting
  • 3-5 years in Quality Assurance and/or Quality Control
  • 3-5 years in internal auditing and in working with regulatory agencies
  • 3-5 years in an ISO 7 and ISO 8 controlled environment, with experience supporting real-time batch record review
  • Demonstrated experience reviewing QC chromatographic data output from HPLC, UPLC, or GC systems in a GMP environment

Knowledge & Skills
  • Working knowledge of cGMP and FDA regulations and guidance
  • Familiarity with Quality Management Systems and GxP
  • Ability to review scanned batch records and QC chromatographic data output (HPLC, UPLC, or GC) with a high degree of accuracy
  • Detail-oriented, with sound problem-solving and troubleshooting ability
  • Able to work independently, manage your own time, and contribute effectively within a team

Certifications
  • ASQ Certified Quality Process Analyst, or
  • Certified Quality Auditor (CQA), or
  • Certified Quality Engineer (CQE)
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
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