Associate Quality Control Jobs

New

Associate Quality Control (Analytical)

Amgen is one of the world’s leading independent biotechnology companies. For ove...

Location

Singapore , Tuas

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Chemistry, Biochemistry, Life Science or related technological field and 2 years of directly related experience
Associate’s Degree in Chemistry, Biochemistry, Life Science or related technological field and 4 years of directly related experience
High School Diploma in Chemistry, Biochemistry, Life Science or related technological field / GED and 6 years of directly related experience
1-2 years of relevant laboratory experience in the commercial manufacturing environment within the pharmaceutical or biopharmaceutical industry and analytical testing experience preferred
Knowledge and understanding of GMP pharmaceutical production, pharmaceutical plant operation and associated testing methods
Experience with Quality Control testing and laboratory operations for common testing methods and equipment (e.g. including but not limited to UPLC, HPLC, LC-MS, GC-HS, LOD, Auto-titration, KF, Optical Rotation, wet chemistry, FT-IR, pH, conductivity, TOC, Potency, ELISA, Capillary Electrophoresis, DNA Testing)
Good communication skills (technical writing and verbal communication/ presentation)
Interact effectively with variety of communication and working styles and ability to work well in teams
Ability to manage multiple simultaneous activities in a rapidly changing environment
Problem solving skills and troubleshooting skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality

Job Responsibility

Perform analytical testing of in-process control, drug substance intermediate, final release, stability and plant cleaning samples in a GMP pharmaceutical environment
Support laboratory operations including but not limited to equipment qualification, calibration, cleaning and maintenance, reagent/ buffer preparation
Responsible for maintenance of chemicals and consumables inventory
Ensure proper handling, storage, disposal of all chemicals used in the lab
Responsible for laboratory housekeeping and document archival duties
Participate in laboratory investigations and assist in timely closure of investigations, CAPAs and deviations
Participate in method verification and method validation/ transfer for new product introduction (when required)
Perform review of laboratory data/ records
Assist in SOP/ protocol/ report writing
Assist in periodic review of laboratory procedures and risk assessment

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

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

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

New

Manager Quality Control - Microbiology Labs

Lead all microbiology laboratories during the night shift—ensuring compliant, ac...

Location

United States , Juncos

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
OR Master’s degree and 3 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR Bachelor’s degree and 5 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR Associate’s degree and 10 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR High school diploma / GED and 12 years of Manufacturing Support, Quality Control and/or Laboratory experience
Experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources

Job Responsibility

Lead and develop a successful QC team, fostering a culture of safety, compliance, and continuous improvement
Oversee daily QC operations to ensure timely, accurate, and reliable testing aligned with production schedules
Serve as the QC subject matter expert during audits and inspections, ensuring inspection readiness
Provide technical guidance and troubleshooting support for complex assays and testing issues
Drive training initiatives and ensure team members are appropriately cross-trained for operational flexibility
Monitor assay results and documentation to ensure compliance with cGMP, SOPs, and regulatory standards
Communicate clear expectations on safety, quality, and compliance, addressing discrepancies promptly
Organize and prioritize team tasks based on impact and deadlines, adjusting as needed to meet changing requirements
Use data and dashboards to monitor QC performance metrics, identify trends, and implement improvements
Collaborate with cross-functional stakeholders to align QC activities with broader site and organizational goals

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans and an annual site shutdown

Fulltime

New

Manager Quality Control - Biochemistry Labs

Lead all Biochemistry laboratories during the night shift (including Wet Chemist...

Location

United States , Juncos

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
Or Master’s degree and 3 years of Manufacturing Support, Quality Control and/or Laboratory experience
Or Bachelor’s degree and 5 years of Manufacturing Support, Quality Control and/or Laboratory experience
Or Associate’s degree and 10 years of Manufacturing Support, Quality Control and/or Laboratory experience
Or High school diploma / GED and 12 years of Manufacturing Support, Quality Control and/or Laboratory experience
Experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources

Job Responsibility

Lead and develop a successful QC team, fostering a culture of safety, compliance, and continuous improvement
Oversee daily QC operations to ensure timely, accurate, and reliable testing aligned with production schedules
Serve as the QC subject matter expert during audits and inspections, ensuring inspection readiness
Provide technical guidance and troubleshooting support for complex assays and testing issues
Drive training initiatives and ensure team members are appropriately cross-trained for operational flexibility
Monitor assay results and documentation to ensure compliance with cGMP, SOPs, and regulatory standards
Communicate clear expectations on safety, quality, and compliance, addressing discrepancies promptly
Organize and prioritize team tasks based on impact and deadlines, adjusting as needed to meet changing requirements
Use data and dashboards to monitor QC performance metrics, identify trends, and implement improvements
Collaborate with cross-functional stakeholders to align QC activities with broader site and organizational goals

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans and an annual site shutdown

Fulltime

New

Manager Quality Control - HPLC Labs

Lead the HPLC Labs during the 2nd shift —ensuring compliant, accurate testing an...

Location

United States , Juncos

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
OR Master’s degree and 3 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR Bachelor’s degree and 5 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR Associate’s degree and 10 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR High school diploma / GED and 12 years of Manufacturing Support, Quality Control and/or Laboratory experience
Experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources
Educational background in Life Sciences, Chemistry, Biochemistry, or related fields
Experience in Quality and/or Biochemistry Laboratory operations within a GMP environment, preferably in HPLC testing
Strong knowledge of analytical techniques such as HPLC
Familiarity with laboratory systems such as LIMS, LMES, CIMS, and Empower for HPLC data management

Job Responsibility

Lead and develop a successful QC team, fostering a culture of safety, compliance, and continuous improvement
Oversee daily QC operations to ensure timely, accurate, and reliable testing aligned with production schedules
Serve as the QC subject matter expert during audits and inspections, ensuring inspection readiness
Provide technical guidance and troubleshooting support for complex assays and testing issues
Drive training initiatives and ensure team members are appropriately cross-trained for operational flexibility
Monitor assay results and documentation to ensure compliance with cGMP, SOPs, and regulatory standards
Communicate clear expectations on safety, quality, and compliance, addressing discrepancies promptly
Organize and prioritize team tasks based on impact and deadlines, adjusting as needed to meet changing requirements
Use data and dashboards to monitor QC performance metrics, identify trends, and implement improvements
Collaborate with cross-functional stakeholders to align QC activities with broader site and organizational goals

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans and an annual site shutdown
Flexible work models where possible

Fulltime

New

Quality Control Radiochemist

We have a fantastic opportunity for a QC Radiochemist to join our Radiopharmacy ...

Location

United Kingdom , Guildford

Salary:

Not provided

Alliance Medical Ltd

Expiration Date

Until further notice

Requirements

BSc/MSc in a scientific field (or expecting to graduate at the end of the academic year)
Analytical Chemistry background
Willingness to work unsocial hours and shift work

Job Responsibility

Operate and maintain routine protocols for the chemistry laboratory in strict adherence to GMP and relevant EU pharmacopoeia standards
Manage raw material sampling, testing and release system
Ensure efficient performance of, and undertake first-line maintenance of, Quality Control equipment including HPLC, Gas Chromatography, pH measurement, Osmolality and LAL
Maintain records of faults on any dysfunction - operational or equipment
In association with the QC Manager to develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for standard PET tracers
Ordering of chemicals, glassware, cleaning and other consumables for routine QC analysis
Formulation of reagents for radiochemistry, mixing of solvents for HPLC and other analyses, cleaning of glassware and disposal of waste chemicals and materials
Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by QA and adoption by the unit
Provide training and support for others selected as rota / backup in undertaking routine QC operations
Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time

What we offer

Routine progress assessments and staged salary uplifts that are awarded as training milestones are achieved
Local shift pattern to assure a harmonious work-life balance is maintained
Extensive training in Good Manufacturing Practice (GMP), radiation safety and Quality Management Systems

Fulltime

Quality Control Engineer

The Quality Control Engineer addresses and resolves quality issues through timel...

Location

United States , Columbus

Salary:

Not provided

ADB Safegate

Expiration Date

Until further notice

Requirements

BS in Engineering (Mechanical, Electrical, Manufacturing, or related) or equivalent experience
Minimum 3 years of hands on manufacturing Quality experience (in line production support, troubleshooting, or test engineering)
Demonstrated experience performing root cause analysis and driving CAPA to completion
Proficient in data analysis and statistical methods (SPC, capability studies, Gage R&R)
Working knowledge of ISO9001 quality systems
Able to read and interpret engineering drawings, assembly drawings, and process documents
Strong working knowledge of MS Office (Excel, Word, PowerPoint, Outlook)
Comfortable working on the production floor, hands on troubleshooting of electrical/mechanical assemblies, and traveling to customer sites when needed
Excellent written and verbal communication skills

Job Responsibility

Act as the frontline investigator for production and field quality issues: collect data, replicate failures, perform hands on testing and inspection, and lead containment and corrective action
Own root cause analysis activities and drive corrective and preventive actions (CAPA) to closure with verification of effectiveness
Work side by side with production associates to identify nonconformance, implement containment and train operators to prevent recurrence
Establish, perform, and improve incoming inspection procedures
receive and disposition nonconforming incoming materials
Maintain and control calibration records for inspection/test equipment and ensure measurement traceability
Collect and analyze quality data (defect rates, scrap/rework, yield, process capability)
generate actionable reports and present trends to stakeholders
Lead or participate in productivity and quality improvement projects (DOE, Kaizen, Lean, SPC), and support engineering design improvements to enhance manufacturability and robustness
Support internal and external audits as required

What we offer

A dynamic and challenging environment that encourages growth and learning
Opportunities to shape the future of our industry and make a significant impact on our company's business
A collaborative culture that values innovation, integrity, and inclusivity
Competitive compensation packages, including health benefits

Fulltime

Associate Quality Control

Amgen

Location:
United States, Thousand Oaks

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 18, 2025

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Job Posted:December 18, 2025

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