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Biotech Quality Control Jobs in Dallas, TX (NOW HIRING)

Danone

Quality Systems Coordinator

Dallas, TX · On-site

SPOC for contracted Pest Control Program on site. * All other duties as assigned Physical Demands ... S. in Food Science or Food Technology, Microbiology, Pharmacy, Biotechnology or related science ...

Danone

Quality Systems Coordinator

Dallas, TX · On-site

SPOC for contracted Pest Control Program on site. * All other duties as assigned Physical Demands ... S. in Food Science or Food Technology, Microbiology, Pharmacy, Biotechnology or related science ...

Danone

Quality Systems Coordinator

Dallas, TX · On-site

SPOC for contracted Pest Control Program on site. * All other duties as assigned Physical Demands ... S. in Food Science or Food Technology, Microbiology, Pharmacy, Biotechnology or related science ...

synergy

Analytical Chemist

Dallas, TX

Synergy Bioscience is a pharmaceutical and biotech CRDMO providing research, development ... Experience interacting and collaborating with QA/QC teams. * Experience supporting regulatory and ...

synergy

Analytical Chemist

Dallas, TX · On-site

Synergy Bioscience is a pharmaceutical and biotech CRDMO providing research, development ... Experience interacting and collaborating with QA/QC teams. * Experience supporting regulatory and ...

synergy

Analytical Chemist

Dallas, TX · On-site

Synergy Bioscience is a pharmaceutical and biotech CRDMO providing research, development ... Experience interacting and collaborating with QA/QC teams. * Experience supporting regulatory and ...

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Biotech Quality Control information

See Dallas, TX salary details

$27.9K

$74.4K

$118.5K

How much do biotech quality control jobs pay per year?

As of Aug 29, 2026, the average yearly pay for biotech quality control in Dallas, TX is $74,401.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,300.00 and $91,500.00 per year, depending on experience, location, and employer.

What is a biotech quality control?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What does a biotech quality control do?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

What are the key skills and qualifications needed to thrive in biotech quality control?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What are the most commonly searched types of Biotech Quality Control jobs in Dallas, TX?

The most popular types of Biotech Quality Control jobs in Dallas, TX are:

What are popular job titles related to Biotech Quality Control jobs in Dallas, TX?

For Biotech Quality Control jobs in Dallas, TX, the most frequently searched job titles are:

What job categories do people searching Biotech Quality Control jobs in Dallas, TX look for?

The top searched job categories for Biotech Quality Control jobs in Dallas, TX are:

What cities near Dallas, TX are hiring for Biotech Quality Control jobs?

Cities near Dallas, TX with the most Biotech Quality Control job openings:

Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Dallas, TX as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $74,401 per year, or $35.8 per hour.

Senior Quality Laboratory Analyst

Mark Cuban Cost Plus Drug Company

Dallas, TX • On-site

$39 - $40/hr

Full-time

Posted 25 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.

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