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Ace Analytical Laboratory Jobs (NOW HIRING)

Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting ... r ace, color, national origin, gender, s exual orientation, gender identity, age, disability ...

Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting ... r ace, color, national origin, gender, s exual orientation, gender identity, age, disability ...

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Ace Analytical Laboratory information

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How much do ace analytical laboratory jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for ace analytical laboratory in the United States is $32.71, according to ZipRecruiter salary data. Most workers in this role earn between $25.96 and $38.46 per hour, depending on experience, location, and employer.

What is Ace Analytical Laboratory?

Ace Analytical Laboratory is a specialized testing facility that provides a range of analytical services, such as chemical, environmental, pharmaceutical, and material analysis. These laboratories use advanced scientific equipment and methodologies to analyze samples for quality control, compliance, research, and safety purposes. Clients typically include manufacturers, healthcare organizations, environmental agencies, and research institutions seeking accurate and reliable data to support their operations or regulatory requirements.

What are the key skills and qualifications needed to thrive as an analytical laboratory technician?

To thrive as an Analytical Laboratory Technician, you need a solid background in chemistry or related sciences, often supported by a relevant degree or laboratory certification. Familiarity with laboratory instruments such as HPLC, GC, spectrophotometers, and laboratory information management systems (LIMS) is typically required. Attention to detail, problem-solving abilities, and strong organizational skills help technicians excel in precise testing and data analysis. These competencies are critical to ensure accurate results, maintain compliance with safety standards, and support reliable laboratory operations.

What are some common challenges faced by laboratory analysts at Ace Analytical Laboratory, and how can they be managed?

Laboratory analysts at Ace Analytical Laboratory often work with complex samples and must follow strict quality control procedures. One common challenge is managing multiple projects simultaneously while ensuring accuracy and timely reporting of results. Effective time management, strong organizational skills, and clear communication with team members help address these challenges. Additionally, staying updated with the latest laboratory protocols and participating in regular training can further support success in this role.

What is the difference between Ace Analytical Laboratory vs Chemist?

AspectAce Analytical LaboratoryChemist
Required CredentialsDegree in Chemistry or related field, certifications may varyDegree in Chemistry, often with specialized certifications
Work EnvironmentLaboratory setting, testing and analysisLaboratory, research, or industrial environments
Employer & Industry UsageTesting labs, environmental agencies, manufacturingResearch institutions, pharmaceuticals, manufacturing
Common Search & ComparisonYesYes

Both Ace Analytical Laboratory professionals and Chemists work in laboratory settings, often requiring similar educational backgrounds and certifications. While Chemists may focus more on research and development, Ace Analytical Laboratory staff typically specialize in testing and analysis services. Understanding these differences helps job seekers and employers align expectations and qualifications.

More about Ace Analytical Laboratory jobs

What states have the most Ace Analytical Laboratory jobs?

States with the most job openings for Ace Analytical Laboratory jobs include:

What job categories do people searching Ace Analytical Laboratory jobs look for?

The top searched job categories for Ace Analytical Laboratory jobs are:

Infographic showing various Ace Analytical Laboratory job openings in the United States as of August 2026, with employment types broken down into 77% Full Time, 15% Part Time, and 8% Nights. Highlights an 100% In-person job distribution, with an average salary of $68,027 per year, or $32.7 per hour.

Senior Quality Laboratory Analyst

Mark Cuban Cost Plus Drug Company

Dallas, TX โ€ข On-site

$39 - $40/hr

Full-time

Posted 29 days ago


Job description

JOB SUMMARY

The Senior Quality Laboratory Analyst (Analytical Chemist) is a pivotal role dedicated to ensuring the quality, purity, and regulatory compliance of pharmaceutical products spanning Small Molecules (Solid Dose) to Advanced Therapies. Operating within a rigorous cGMP environment, this role is responsible for executing complex analytical testing on raw materials, in-process samples, finished products, and stability timepoints. The ideal candidate will possess deep expertise in instrumental analysis—specifically HPLC/UHPLC, GC, and Dissolution—and will act as a Subject Matter Expert (SME) in troubleshooting, method transfer, and data integrity compliance during FDA and PIC/S regulatory inspections.

KEY RESPONSIBILITIES

1. Routine & Advanced Analytical Testing:

  • Execute analytical testing on raw materials, in-process blends, finished dosage forms (solid dose, aqueous solutions), and stability samples in compliance with compendial methods (USP/EP/JP) and in-house specifications.

  • Operate, calibrate, and maintain core analytical instrumentation, including:

  • High-Performance/Ultra-High-Performance Liquid Chromatography (HPLC/UHPLC) with UV, RI, and ELSD detectors.

  • Gas Chromatography (GC) for residual solvent analysis.

  • Automated Dissolution Testers (Apparatus 1 & 2).

  • Spectroscopic equipment (FT-IR, UV-Vis).

  • Wet chemistry techniques (Karl Fischer titration, potentiometric titrations, pH).

  • Prepare complex mobile phases, standards, and sample solutions requiring precise quantitative techniques.


2. Data Review & Regulatory Compliance:

  • Ensure absolute adherence to ALCOA+ data integrity principles; document all work contemporaneously in Electronic Lab Notebooks (ELNs) and Laboratory Information Management Systems (LIMS).

  • Perform peer review and second-person verification of analytical data, instrument printouts, and Empower/Chromatography Data System (CDS) audit trails to ensure 21 CFR Part 11 compliance.

  • Lead Phase I Laboratory Investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), and aberrant results, utilizing root cause analysis (RCA) tools to identify systemic issues.

  • Draft, revise, and approve Standard Operating Procedures (SOPs), test methods, and technical reports.


3. Equipment Qualification & Method Lifecycle:

  • Support the Commissioning, Qualification, and Validation (IQ/OQ/PQ) of new laboratory instrumentation and software systems.

  • Execute analytical method transfer and co-validation protocols (e.g., Linearity, Accuracy, Precision, Robustness) in accordance with ICH Q2(R2) guidelines.

  • Diagnose and troubleshoot instrument performance issues; coordinate with vendors for preventative maintenance (PM) and out-of-tolerance (OOT) calibrations.


4. Laboratory Operations & Mentorship:

  • Manage the qualification, bridging, and inventory of critical Tier 1 and Tier 2 consumable reagents, HPLC columns, and USP reference standards.

  • Ensure safe handling and segregation of chemical waste (flammable solvents, acids/bases, HPAPIs) in compliance with Environmental Health & Safety (EHS) guidelines.


EDUCATION / TRAINING

  • Bachelor’s degree (B.S. or B.A.) in Chemistry, Analytical Chemistry, Biochemistry, or a closely related scientific discipline.

  • Minimum of 8+ years of hands-on analytical laboratory experience within a cGMP pharmaceutical, biotech, or contract testing organization (CRO/CDMO).

TECHNICAL SKILLS & KNOWLEDGE

  • Demonstrated mastery of HPLC/UHPLC troubleshooting, method execution, and quantitative analysis.

  • Extensive experience with Chromatography Data Systems (e.g., Waters Empower 3 or Thermo Chromeleon).

  • Strong understanding of FDA, PIC/S, and ICH regulatory guidelines pertaining to quality control and data integrity.

  • Experience performing analytical investigations (OOS/OOT).

  • Familiarity with cloud-based QMS (e.g., ACE, MasterControl, Veeva) and LIMS platforms is highly preferred.


Work Environment & Physical Demands
  • Ability to work in a laboratory environment, requiring the use of standard Personal Protective Equipment (PPE) such as lab coats, safety glasses, and gloves.

  • Ability to safely handle hazardous chemicals, active pharmaceutical ingredients (APIs), and organic solvents.

  • Ability to lift up to 25 lbs. and perform tasks requiring manual dexterity and prolonged periods of standing or sitting at a bench.

CORE COMPETENCIES

  • Strong leadership, coaching, and communication skills. 
  • High decision‑making aptitude and risk‑based thinking. 
  • Proficient in data trending, problem‑solving, and scientific writing. 
  • Exceptional organization, prioritization, and follow‑through. 
  • Ability to operate independently with minimal supervision. 
  • Strong competency with Microsoft Office and electronic quality systems.