Referso Jobs

QC Lab Services Analyst (Analytical Instrument and Lab Systems)

Net2Source · Posted Nov 9, 2026

Open

Wilson, North Carolina, United States
On-site
Contract · Associate
$63–$63 per hour
2+ years

QC Lab Services Analyst (Analytical Instrument and Lab Systems)

Net2Source · Posted Nov 9, 2026

Open

Wilson, North Carolina, United States
On-site
Contract · Associate
$63–$63 per hour
2+ years

Analyst 3 - Quality Assurance

eTeam Inc. · Posted Nov 9, 2026

Open

Wilson, North Carolina, United States
On-site
Full-time · Associate
2+ years

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QC Lab Services Analyst (Analytical Instrument and Lab Systems) responsible for laboratory equipment lifecycle management and CSV support at a Biotherapeutics Manufacturing facility.

Responsibilities

Participate in the qualification of analytical equipment for related testing functions, for example, IQ/OQ/PQ of HPLC, Spectrophotometry, Endotoxin, Cell Culture and Total Organic Carbon equipment.
Author SOP’s, Work Instructions and protocols.
Responsible for the quality control laboratory equipment lifecycle management and CSV support.
Participate in activities to introduce technologies and computer base applications to a new site, for example eLIMS/iLABS, SDMS, Empower and SoftMax Pro, SAP, to improve laboratory efficiency and promote a culture of Innovation.
Interact with the QC Global organization for the different center of excellence for equipment and information technologies.

Requirements

Bachelor’s Degree in Chemistry, Biochemistry, Micro or science related field

Skills

Equipment Lifecycle Management cGMP experience Document Authorship Working knowledge of regulatory requirements, policies and guidelines

Senior Stability Specialist, Quality Control

AstraZeneca · Posted Nov 11, 2026

Open

Santa Monica, California, United States
On-site
Full-time · Senior
$101K–$151K per year
3–7 years

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The successful candidate will contribute to the advancement of our product pipeline by supporting all stability testing across multiple products and sites. This individual is a subject matter expert responsible for coordinating stability testing, facilitating stability execution, authoring stability report, managing EDAs, and leading all investigations related to stability.

Compensation

The annual base pay (or hourly rate of compensation) for this position ranges from $100,786 to $151,179. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.

Responsibilities

Author, review and execute Protocols and relating to Drug Product and Drug substance stability
Serve as Quality Stability Subject Matter Expert (SME) during health authority inspections, client audits, and internal reviews
Author stability protocols, summary reports, and regulatory submission documents
Assess stability data, perform statistical analyses (e.g., using Prism or JMP), and evaluate trends to determine product shelf-life and retest periods
Lead investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), atypical results, and stability-related deviations or CAPAs

Requirements

PhD degree preferably in a related science field
Master’s degree preferably in a related science field
Bachelor’s preferably in a related science field
Associate’s degree preferably in a related science field

Skills

Senior Stability Specialist, Quality Control

AstraZeneca · Posted Nov 11, 2026

Open

Santa Monica, California, United States
On-site
Full-time · Senior
$101K–$151K per year
3+ years

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Senior Stability Specialist, Quality Control responsible for coordinating stability testing, executing protocols, analyzing data, leading investigations, and managing regulatory submissions within AstraZeneca’s QC team.

Compensation

Responsibilities

Author, review and execute protocols related to drug product and drug substance stability
Serve as quality stability SME during inspections, audits, and internal reviews
Author stability protocols, summary reports, and regulatory submission documents
Assess stability data, perform statistical analyses, and evaluate trends to determine product shelf-life and retest periods
Lead investigations for OOS, OOT, atypical results, and stability-related deviations or CAPAs

Requirements

PhD in a related science field
Master’s degree in a related science field
Bachelor’s degree in a related science field
Associate’s degree in a related science field

Skills

CGMP experience Stability design, execution, and management

Analyst 3 - Quality Assurance

Artech LLC · Posted Nov 9, 2026

Open

Wilson, North Carolina, United States
On-site
Full-time · Associate
$60–$62 per hour
2+ years

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QC Lab Services Analyst responsible for laboratory equipment lifecycle management and CSV support at a biotherapeutics manufacturing facility.

Compensation

Pay Range: $60-62/hr

Responsibilities

Participate in qualification of analytical equipment
Author SOPs, work instructions and protocols
Manage quality control laboratory equipment lifecycle
Introduce technologies and computer-based applications
Interact with QC Global organization

Requirements

Bachelor’s Degree in Chemistry, Biochemistry, Micro or science related field

Skills

Equipment Lifecycle Management cGMP experience Document Authorship IQ/OQ/PQ of HPLC Spectrophotometry Endotoxin Cell Culture

Specialist QA Shop Floor

Bristol Myers Squibb · Posted Nov 5, 2026

Open

Summit, New Jersey, United States
On-site
Full-time · Associate
$35–$42 per hour
2+ years

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The Quality Assurance Shop Floor team provides 24x7 Quality collaboration and oversight of site operations, including Manufacturing, Quality Control, Label Operations and Warehouse Operations ensuring compliance with cGMP.

Compensation

$34.92 - $42.32 hour

Responsibilities

Provide routine Quality-the-floor oversight and triage unexpected events
Identify departures from approved procedures and respond to issues
Document operational verification within Manufacturing Execution System (MES)
Review manufacturing records to ensure compliance with approved procedures
Maintain compliance with assigned learning plan

Requirements

Bachelor's degree in STEM field
High school diploma
Associate’s degree with equivalent combination of education and experience
Nice to have: FDA/EMA regulations
Nice to have: biopharmaceuticals

Skills

cGMP experience batch record review change control product complaints deviations

Sr. Process Engineer

PCI Pharma Services · Posted Nov 6, 2026

Open

San Diego, California, United States
On-site
Full-time · Senior
$107K–$134K per year
8+ years

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Design and optimize pharmaceutical and biopharmaceutical manufacturing processes for improved efficiency and yield. Supports manufacturing operations and mentor junior engineers. Lead technical assessment and improvement/scale up projects for manufacturing processes, including managing projects through to successful completion.

Compensation

The base salary hiring range for this position is $106,800 - $133,500 plus eligibility for an annual performance bonus.

Responsibilities

Design and specify processes and manufacturing equipment systems
Evaluate existing systems for continuous improvement
Provide in-depth technical review of all documents
Research new technologies and implement new/upgraded systems
Document changes to systems per change management procedures

Requirements

Bachelor's degree
Bioengineering
Chemical Engineering
Electrical Engineering
Industrial Engineering

Skills

cGMP experience manufacturing processes process flow troubleshooting GMP regulations

QC Lab Services Analyst (Analytical Instrument and Lab Systems)

QC Lab Services Analyst (Analytical Instrument and Lab Systems)

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Requirements

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Benefits

Analyst 3 - Quality Assurance

Responsibilities

Requirements

Skills

Senior Stability Specialist, Quality Control

Compensation

Responsibilities

Requirements

Skills

Senior Stability Specialist, Quality Control

Compensation

Responsibilities

Requirements

Skills

Analyst 3 - Quality Assurance

Compensation

Responsibilities

Requirements

Skills

Specialist QA Shop Floor

Compensation

Responsibilities

Requirements

Skills

Sr. Process Engineer

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CGMP Experience jobs

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