Qc associate Jobs

New

Sr Associate QC - Microbiology

This role will support manufacturing operations on a 24/7 shift pattern and may ...

Location

Ireland , Dun Laoghaire

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor's degree in a science discipline
Biopharmaceutical QC experience in a microbiology lab
Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products

Job Responsibility

Environmental Monitoring of Grade 8/9 Cleanrooms
Environmental Monitoring of Grade 5/7 Cleanrooms & Isolators
Reading of Environmental Monitoring Plates
Bioburden testing of water & disinfectants
Writing technical reports
Water sampling
Testing of In Process samples such as Density & pH
Initiate and/or implement changes in controlled documents
Participate in audits, initiatives, and projects that may be departmental or organizational in scope
Write protocols and perform validation and equipment qualification/verification

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

New

Associate Quality Control

The Associate Quality Control will provide analytical testing support for the Qu...

Location

United States , Thousand Oaks

Salary:

66222.00 - 82012.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school/GED + 2 years Quality Control experience
Associate’s + 6 months Quality Control work experience
Bachelor’s

Job Responsibility

Execution of QC Microbiology assays following assigned procedures
Analysis of analytical test results and reporting of raw data into various laboratory information management systems
Lab support activities such as management of lab consumables and equipment maintenance/work order completion
Operating specialized laboratory equipment
Daily communication and collaboration with cross-functional teams
Implementation of lab improvements to ensure an efficient and productive lab environment
Flexibility in work hours to support demand of work
occasional evening and/or weekend hours may be required

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
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

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

Associate Director, Software Engineering

We are currently seeking an experienced professional to join our team in the rol...

Location

China , Xi'an

Salary:

Not provided

HSBC

Expiration Date

December 31, 2025

Requirements

Excellent skills in Java Experience
Hands-on development experience in building global software product from zero to one
Strong experience working on the frontend and backend of a technology product
Strong knowledge of Agile development and Devops tool (e.g. Confluence, JIRA, Selenium, Jmeter, HP virtual user, Cucumber, Jenkins, QC, etc)
Extensive relevant working experience, involvement in wealth management or investment IT functions preferred
Experience in the areas of retail investment, wealth management, asset management would be an added advantage
You’re comfortable working in a team that deals with ambiguity and aggressive timelines
Strong team player who also has the ability to work under pressure, independently and proactively
A track record of forging strong relationships and building trusted partnerships through open dialogue and continuous delivery

Job Responsibility

Design and develop cloud native software systems that are resilient, secure, fast, easy to manage, and scalable in modern, dynamic environments such as public cloud
Adopt appropriate software architecture design
Contribute with analysis and solutions to fulfill business requirements
Optimize performance of complex systems
Create structured, testable, lightweight code in Java or any programing language that is suitable

What we offer

Flexible working
Continuous professional development
Opportunities to grow within an inclusive and diverse environment

Fulltime

Quality Project Manager

Nemera is a leading global manufacturer of complex drug delivery systems for the...

Location

United States , Buffalo Grove, Illinois

Salary:

120000.00 - 135000.00 USD / Year

Nemera

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering or related field
4+ years of relevant working experience in Quality in a manufacturing environment
1+ year experience in a supervisory role
Excellent communication skill with the ability to understand, read, write, and speak English
Ability to apply advanced mathematical concepts and intermediate statistical (SPC) knowledge
Strong understanding of injection molding, Automation and FMEA
Knowledgeable to equipment/process/product validation practices and principles
Excellent interpersonal, organizational and communication skills
Demonstrated leadership and the ability to motivate and influence others
Able to lift up to 30 lbs

Job Responsibility

Assists Associate Director of Quality in coordinating and executing goals and objectives throughout the company to improve product quality and operating system efficiency
Direct and coordinate the activities of Quality Department employees
Establish and maintain sound relationships with production, technology, supply chain, quality teams and cross functional personnel to identify system and compliance gaps with proposed resolutions
Act as liaison with metrology, QC and compliance team
Ensure adherence to project and company standards, while maintaining quality systems that meet customer, internal, and regulatory requirements (ISO, cGMP, FDA, Health & Safety)
Manage claims non-conformities, investigations, problem solving, root cause analysis, champion creation of effective and sustainable corrective actions
Manage process and equipment Validations for new product and existing business
Change control process owner
Define and implement quality initiatives to meet KPI’s and objectives
Identify opportunities for improvement through data trending and analysis, as well as develop and implement quality and inspection processes

Fulltime

OneLIMS Lead

We are looking for a highly skilled OneLIMS Lead for a hybrid role based in Toro...

Location

Canada , Toronto

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Degree in Life Sciences, Pharmacy, Chemistry, Engineering, Information Systems, or related field
8+ years of experience in pharmaceutical or biotech environments, including 4+ years in LIMS implementation or major LIMS upgrades
Experience working in Quality Control lab operations—ideally Raw Materials testing and release
Strong knowledge of Computer System Validation in GMP/GLP context: GAMP5, Annex 11, 21 CFR Part 11
Proven experience as a functional lead, business analyst, or project manager on laboratory informatics projects, preferably multisite
Demonstrated ability to coordinate cross-functional teams and external vendors, influence decisions, and manage stakeholders
Excellent communication skills with the ability to translate between business and technical teams
Strong documentation skills and high attention to detail
Proven experience with QC or laboratory master data: materials, specs, analytical methods, limits, and static data structures
Hands-on involvement in at least one data migration or large-scale master data harmonization project including mapping, cleansing, and reconciliation

Job Responsibility

Act as the primary interface between QC laboratories, Manufacturing & Supply, Quality, IT, and external suppliers for the OneLIMS Raw Materials scope
Lead planning and execution of the Raw Materials deployment, including scope definition, timeline, risks, interdependencies, and status reporting
Translate Raw Materials and Quality Control processes into OneLIMS configuration and workflows, ensuring harmonization across sites
Oversee master data requirements gathering, pilots, and configuration for ~600 Raw Materials records and associated analytical methods
Supervise the build and verification of LIMS calculations, limits, and business rules, ensuring regulatory compliance and data integrity
Coordinate data migration, cutover, and hypercare activities for the Raw Materials scope
Define and manage User Acceptance Testing and validation strategy in alignment with GMP, GLP, GAMP5, Annex 11, and 21 CFR Part 11
Review and approve UAT scripts, validation plans and protocols, ensuring full traceability
Ensure high-quality configuration documentation and detailed specifications
Support SOP red-lining and updates to align laboratory processes with the new system

What we offer

An international community bringing together more than 110 different nationalities
An environment where trust is central: 70% of our leaders started their careers at the entry level
A strong training system with our internal Academy and more than 250 modules available
A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.)

Fulltime

Qc associate

Randstad

Location:
India, Hyderabad

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 19, 2025

Expiration:
January 16, 2026

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

Similar Jobs for Qc associate

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Qc associate

Randstad

Location:India, Hyderabad

Category:Research and Development

Contract Type:Not provided

Salary:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:December 19, 2025

Expiration:January 16, 2026

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

Similar Jobs for Qc associate

Sr Associate QC - Microbiology

Quality Control Radiochemist

Associate Quality Control

Manager Quality Control - Microbiology Labs

Manager Quality Control - Biochemistry Labs

Associate Director, Software Engineering

Quality Project Manager

OneLIMS Lead

Location:
India, Hyderabad

Category:
Research and Development

Contract Type:
Not provided

Job Posted:
December 19, 2025

Expiration:
January 16, 2026