Quality Associate Jobs

FLEX Associate Quality Engineer

Temporary entry-level quality engineering role focused on supporting development...

Location

United States , Bethesda

Salary:

44.90 - 74.04 USD / Hour

Marriott Bonvoy

Expiration Date

Until further notice

Requirements

Experience in software testing
Undergraduate degree or equivalent experience/certification
Technology certifications
Experience in Agile methodologies

Job Responsibility

Collaborates with product team members on QE tasks and procedures
Functions as a working SDET where needed
Assists in setting best practice quality procedures
Reviews and edits product documentation
Drives the adoption of TDD, BDD and related test-first development methodologies
Performs quantitative and qualitative analyses for delivering automated testing processes and tools
Implements tooling such as Tosca, NeoLoad, Cucumber, etc.
Validates solutions with enterprise architecture team
Facilitates achievement of expected deliverables and obligations of Service Providers
Ensures proper coordination with appropriate IT and vendor teams

What we offer

Medical coverage
Dental coverage
Vision coverage
Health care flexible spending account
Dependent care flexible spending account
Life insurance
Disability insurance
Accident insurance
Adoption expense reimbursements
Paid parental leave

Fulltime

Quality Lab Associate I

Conduct microbiological analysis, perform endotoxin and particulate matter testi...

Location

United States , Marion

Salary:

56000.00 - 77000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. degree in Microbiology, Biology, or related science
2-5 years of experience or Master’s Degree in biological sciences with 0-3 years experience, preferably in the pharmaceutical or medical device industry
computer literate/knowledge of Microsoft office applications (Word, Excel)
proficient in quality based computer systems such as LIMS, POMS, Endoscan-V software, Sampler Sight Pharma, and AS400
attention to detail and ability to prioritize multiple tasks
proficient in the operation of laboratory instrumentation and equipment such as laminar flow hoods, micro-pipettors, pH meters, analytical balances, and instruments used to perform particulate matter and endotoxin testing
good documentation skills and knowledge of GDPs (Good Documentation Practices)
knowledge of aseptic sampling and testing techniques and microbiological testing according to FDA, cGMP, GLPs and USP testing methodology
must be able to communicate effectively with supervisors and peers
must be experienced in executing general microbiology procedures

Job Responsibility

Prepare samples and perform endotoxin testing on raw materials, solution, and water for bioburden
perform particulate matter testing on solution
perform daily pH meter, balance, and pipette verification
perform daily Honeywell automated temperature checks and manual temperature monitoring
perform peptidoglycan and gel clot testing as needed
manage reagent inventory
generate monthly trend reports
calibration of micro-pipettes, analytical balance, water bath, dry heat bath, depyrogenation ovens, light obscuration particle counters and spectrophotometer
responsible for daily lab upkeep including cleaning, glassware washing and depyrogenation, supply replenishment, syringe and endotoxin prep
assist in method validation and protocol testing as needed

What we offer

Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement
short-term and long-term disability insurance
Employee Assistance Program
childcare benefits

Fulltime

Quality Laboratory Associate II

The position encompasses biological, chemical, and physical analyses on pharmace...

Location

United States , Round Lake

Salary:

60000.00 - 90000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor degree in Chemistry or physical science with 2 or more years' experience
good oral and written communication skills
strong analytical skills
being detail-oriented
knowledge of current Good Manufacturing Practices preferred
advanced laboratory skills with basic knowledge of statistical methods
strong technical problem solving skills
ability to handle multiple tasks concurrently and in a timely fashion
knowledge of Empower Chromatography Data System and LIMS preferred but not required
knowledge of GLP, cGMP requirements and familiarity with USP/ICH guidelines preferred but not required

Job Responsibility

Conduct critical chemical and physical analysis on raw materials, initial, in-process and final products, and samples collected from the environmental monitoring programs
work under minimum supervision
serve as mentor to Quality Laboratory Associate I positions
provide training and work direction for Quality Laboratory Associate I positions
perform review of test data including overall documentation practices
perform release functions in LIMS or other computerized systems
use sophisticated laboratory instrumentation (e.g., HPLC, GC) and computer systems
perform advanced chemical assays requiring precise analytical skills and understanding of biology and chemistry principles
complete all testing including special project/protocol testing in a timely and appropriate manner
maintain data integrity

What we offer

Support for parents
continuing education/professional development
employee health and well-being benefits
paid time off
2 days a year to volunteer
medical and dental coverage
insurance coverage for basic life, accident, short-term and long-term disability
business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)

Fulltime

Senior quality assurance associate

Senior Quality Assurance Associate at Global Animal Health Pharmaceutical Compan...

Location

Japan , Tokyo

Salary:

6000000.00 - 8000000.00 JPY / Year

Randstad

Expiration Date

January 27, 2026

Requirements

Pharmacist Degree (Mandatory)
Fluent English communication skills (TOEIC over 750 preferred)
Proficient in Microsoft Office Suite (Word, Excel, Outlook)
At least 2-5 years of Quality Assurance experience in a GMP/GQP environment is preferred
Strong analytical and problem-solving skills
Excellent communication and interpersonal skills
Strong organizational and time management skills
Experience with SAP inventory systems and/or within the pharmaceutical or animal health industry is highly desirable

Job Responsibility

Oversee warehouse operations, ensuring compliance with GMP and GQP standards
Manage product quality, investigating and resolving issues effectively
Implement and monitor quality systems, ensuring regulatory compliance
Execute assessment plans for GMP service providers
Manage and improve quality processes using a data-driven approach
Lead internal training programs focused on quality control
Handle product complaints and adverse events
Collaborate with regulatory agencies

What we offer

健康保険
厚生年金保険
雇用保険
土曜日
日曜日
祝日

Fulltime

Quality Control Associate

The primary responsibility of the Quality Control Associate is to provide servic...

Location

United States , Remote

Salary:

25.00 - 37.50 USD / Hour

LHH

Expiration Date

Until further notice

Requirements

2 years of experience in a fast-paced virtual customer service role
2 years Career Transition Consulting or Recruiting experience is a significant bonus
Proficiency with Excel and MicroStrategy or another reporting system or database
Strong communication and relationship skills
Experienced customer service professional with a professional image and attitude
Customer service oriented, sensitive to and enjoys helping people
Detail oriented, understands the value of documentation and process
Resourceful, methodical and ability to troubleshoot challenges quickly and independently
Curious mindset, driven to understand data results
Handles deadlines, commitments, and high pressure with grace, and remains motivated in fast-paced environments

Job Responsibility

Manage all Career Transition service evaluations assigned to them
Assess evaluation detail, analyze referral activities
Outreach to candidate and expertly deescalate issues they communicate
Document outreach in internal systems, following proper procedures
Manage the intervention with the assigned Delivery Consultant and their Lead Consultant as appropriate, ensuring a delicate and supportive experience of the Candidate
Manage the reopening of the Career Transition program as-needed, and assignment to new Consultants as appropriate
Ensure all outstanding negative feedback is addressed and resolved with candidate and within internal systems
Strive for and maintain a remediation rate of 20%
Manage a light caseload of candidates to remain current on the LHH career transition experience and enhance the quality control experience
Review consultant activity and candidate utilization to ensure candidates are receiving Career Transition services according to LHH delivery standards

What we offer

Growth opportunities within a human resources global leader
We prioritize learning to stay agile in an increasingly competitive business environment
We foster an open-minded environment where people spark new ideas and explore alternatives
Comprehensive benefits package including health, vision and dental
Unique opportunity to work from the comfort of your own home while providing post-service support to Career Transition service participants from a variety of backgrounds and industries
Paid Training @ $25 per hour
$35 per hour for Quality Control support
$37.50 per hour for Consulting

Parttime

Quality Assurance Associate Manager

Lead and grow a team, ensuring product quality and safety for a prestigious glob...

Location

Japan , Tokyo

Salary:

7000000.00 - 9000000.00 JPY / Year

Randstad

Expiration Date

March 26, 2026

Requirements

Bachelor's degree in Food Science, Food Technology, or a related field
5+ years of experience in QA within the food and beverage industry
Experience in conducting quality and food safety audits
Strong understanding of food laws, regulations, and labeling requirements
Knowledge of QA systems and certification standards (e.g., ISO, BRC, HACCP, FSSC)
1-3 years of supervisory experience
Excellent communication skills in both Japanese and English
Strong leadership, project management, and problem-solving skills
Strategic thinking and decision-making abilities
Proficiency in relevant computer software.

Job Responsibility

Lead the development and implementation of QA processes and guidelines across the product lifecycle
Conduct quality and safety audits for suppliers and retail locations
Investigate consumer complaints and implement corrective and preventive actions
Manage crisis situations and critical quality incidents
Provide food safety and quality training to relevant teams
Collaborate with product development and regulatory teams to ensure compliance
Develop and maintain strong relationships with internal and external stakeholders.

What we offer

健康保険
厚生年金保険
雇用保険
土曜日、日曜日、祝日休暇

Fulltime

New

Associate Director, Analytical Development and Quality Control

The Associate Director, Analytical Development and Quality Control will support ...

Location

United States , San Diego

Salary:

160000.00 - 200000.00 USD / Year

Kailera Therapeutics

Expiration Date

Until further notice

Requirements

10+ years of experience, or 5+ with advanced degree, in the pharmaceutical/biotech industry with experience in all phases of innovative drug development and commercial launch in accordance with global CMC regulatory filings (IND/NDA/MAA, etc.)
Strong expertise in analytical techniques HPLC/UPLC, LC–MS, SE-HPLC, dissolution, along with extractables and leachable analysis
Knowledge of drug development activities with respect to cGMP, quality systems, ICH guidelines, global regulatory requirements, and USP, EP, JP, and CHP requirements
Hands-on experience supporting early- and late-stage CMC development, stability programs, and specification setting
Proven experience leading OOS/OOT investigations, deviations, CAPAs, and change controls
Strong track record of working with CROs/CMOs and managing external analytical/testing activities
Excellent technical writing skills for analytical reports and regulatory submissions (IND/IMPD, NDA/BLA)
Demonstrated leadership ability with experience mentoring and developing scientific staff
Strong communication, cross-functional collaboration, and project-management skills
Innovative team-player with high energy for our dynamic company environment

Job Responsibility

Support analytical development and QC activities related to characterization of drug substances and drug products from early-stage clinical development through commercialization
Maintain current knowledge in analytical methods and control strategies supporting a variety of molecule platforms and dosage forms
Oversee and provide scientific leadership on QC testing for DS/DP at vendors, ensuring cGMP compliance, data integrity, and timely delivery of analytical results
Direct investigations including OOS/OOT, deviations, and CAPAs, and provide strong analytical rationale
Design and manage stability programs (accelerated, long-term, bracketing/matrixing) supporting early and late clinical phases
Interpret stability trends and establish shelf-life/retest periods consistent with ICH guidelines and peptide behavior
Support comparability assessments for process changes, analytical method updates, or site transfers
Communicate CMC project status to key stakeholders cross-functionally and assist in driving decision-making
Participate in cross-functional CMC teams for the project(s) assigned to ensure adequate development and execution of CMC plan/strategies as needed
Author and review CMC sections of IND/IMPD and NDA submissions and address regulatory questions

What we offer

Comprehensive health benefits and tax-advantaged savings accounts
Flexible time off, 13 paid holidays, and a companywide year-end shutdown
Monthly wellness stipend
Generous 401(k) match
Disability and life insurance

Fulltime

Production Associate - Fill

The Production Associate contributes to saving and sustaining lives by inspectin...

Location

United States , Marion

Salary:

17.88 USD / Hour

Baxter

Expiration Date

Until further notice

Requirements

Must be at least 18 years of age
Must have basic English written and oral communication skills adequate to communicate with other team members
Understand verbal and written safety and quality instructions and read and comprehend written work instructions including words and drawings
Must be able to perform basic mathematics
Possess or be able to obtain Inspector Certification
One year of manufacturing experience, preferred
CRC (Career Readiness Certification) at the Silver level, preferred
Requires continuous grasping, pushing/pulling up to 12 pounds for up to 25 feet and reaching with hands and arms
Lifting on average up to 16 pounds to/from a height of up to 46 inches constantly throughout the shift
Carrying on average up to 10 pounds for 5 feet constantly throughout the shift

Job Responsibility

Over-pouch and seal the over-pouch, enclosing a bag containing solutions or premixed drugs, at a rate consistent with production needs
Inspect and ensure that the over-pouches, bags and their components meet quality standards
Perform scheduled quality checks using an assortment of gauges and a scale
Perform and document scheduled cleaning activities
Notify the supervisor and take appropriate action if any safety, quality, mechanical or discrepancy issues occur
Learn, understand, and apply rigorous quality standards, Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMP)
Sustain a clean and safe work area using 6S principles
Correct any over-pouch seal or packaging issues previously identified

What we offer

Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement

Fulltime

Quality Associate

Randstad

Location:
India, Tiruvallur

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 15, 2025

Expiration:
January 05, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Quality Associate

FLEX Associate Quality Engineer

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Quality Associate

Randstad

Location:India, Tiruvallur

Category:Manufacturing

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:December 15, 2025

Expiration:January 05, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Quality Associate

FLEX Associate Quality Engineer

Quality Lab Associate I

Quality Laboratory Associate II

Senior quality assurance associate

Quality Control Associate

Quality Assurance Associate Manager

Associate Director, Analytical Development and Quality Control

Production Associate - Fill

Location:
India, Tiruvallur

Category:
Manufacturing

Contract Type:
Not provided

Job Posted:
December 15, 2025

Expiration:
January 05, 2026