Referso Jobs

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

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

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

Apply with RefersoAI Apply on careers page

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

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 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

Apply with RefersoAI Apply on careers page

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

Apply with RefersoAI Apply on careers page

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

Apply with RefersoAI Apply on careers page

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

Associate II, Shop Floor Quality Assurance Cell Therapy

Bristol Myers Squibb · Posted Nov 5, 2026

Open

Devens, Massachusetts, United States
On-site
Full-time · Entry
$35–$43 per hour
0–2 years

Apply with RefersoAI Apply on careers page

The Quality Assurance Shop Floor team is responsible for 24x7 Quality collaboration and oversight of site operations, including but not limited to Manufacturing, Quality Control laboratories, and Supply Chain Operations.

Compensation

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities.

Responsibilities

Provide Quality on-the-floor oversight to Manufacturing/ QC/ Supply Chain Operations & responding to minor issues or escalating to senior members.
Perform and document operational verification per approved procedures.
Observe manufacturing operations and identify departures from clean room behaviors and aseptic techniques.
Provide quality oversight to maintenance operations and support pre-approved return to service plans.
Perform area walkthroughs to identify quality issues and support remediation to ensure the floor and operations are in adherence with cGMP and approved procedures.

Requirements

Bachelor's degree in STEM field preferred
High school diploma/ Associates degree with equivalent combination of education and work experience may be considered
Nice to have: biopharmaceuticals manufacturing
Nice to have: cell therapy manufacturing

Skills

cGMP experience

GMP Warehouse Specialist

Evotec · Posted Nov 5, 2026

Open

Abingdon, Oxfordshire, United Kingdom
On-site
Full-time · Mid
£35K per year

Apply with RefersoAI Apply on careers page

Experienced Warehouse Specialist working within a GMP Warehouse to manage materials, receipts, forklift operations, and general warehouse duties.

Compensation

£35,000, plus excellent benefits package

Responsibilities

Ensure all activities are conducted in a safe manner and that all equipment and racking is regularly checked and complies with Safety Legislation
The effective and efficient receipt of goods through a centralised receipting location
Managing GMP materials (raw materials and consumables) through receipt, sampling and location transfer
Loading and unloading vehicles (manually and using FLT)
General warehouse duties

Requirements

Nice to have: SAP

Skills

Warehouse ERP Systems Forklift truck experience cGMP Experience COSHH regulation Microsoft Excel SAP

CGMP experience jobs

Compensation

Responsibilities

Requirements

Skills

Benefits

Compensation

Responsibilities

Requirements

Skills

Compensation

Responsibilities

Requirements

Skills

Compensation

Responsibilities

Requirements

Skills

Compensation

Responsibilities

Requirements

Skills

Compensation

Responsibilities

Requirements

Skills

Compensation

Responsibilities

Requirements

Skills

Benefits

Benefits

Benefits

Benefits

Benefits