Associate Quality Assurance (Incoming QA) Job at Amgen (Breda)

Supervisor, QA Raw Materials

The Supervisor, QA Raw Materials is responsible for leading a team of QA Raw Mat...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in relevant scientific discipline with a minimum of 5+ years’ experience in related GMP industry working in Quality Assurance or Quality Control groups which support receipt, inspection, or release of materials
Equivalent combination of education and experience considered
Knowledge of USP and EP pharmacopoeias, and pharmaceutical raw material compendial testing
Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) and some experience working with international regulations such as EU, ICH
Ability to apply basic scientific principles to solve operational and quality tasks
Experience with RCA, technical writing, and working with quality related investigations

Job Responsibility

Perform review of external documentation and internal GMP documentation associated with incoming raw materials, components, chemicals, excipients, and Active Pharmaceutical Ingredients (API)
Provide Quality Assurance oversight to Materials Management and Quality Control, ensuring that site SOP’s and raw material specifications are adhered to
Responsible for the review and analysis of test results
ability to interpret and comprehend scientific information and data related to QC Micro and QC Analytical testing
Initiation, review, and disposition or closure of raw material quality systems
Assist in the identification, isolation, and containment of potentially nonconforming materials
Assist in the identification and management of expired material
perform scrapping of materials with Materials Management
Assist Materials Management and Project Management with finished product shipments
Provide input, review, and approval of new and revised raw material specifications

Fulltime

Senior Manager Quality Assurance: Incoming Quality and Warehouse

At Amgen, if you feel like you’re part of something bigger, it’s because you are...

Location

United States , New Albany

Salary:

144021.45 - 194852.55 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of Quality/Manufacturing/Engineering experience
Master's degree and 6 years of Quality/Manufacturing/Engineering experience
Bachelor's degree and 8 years of Quality/Manufacturing/Engineering experience
Associate's degree and 10 years of Quality/Manufacturing/Engineering experience
High school diploma / GED and 12 years of quality/Manufacturing/Engineering experience
minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources

Job Responsibility

Lead, coach and develop the QA team, responsible for quality oversight of Incoming Quality, Warehouse Operations, Distribution and Facility and Engineering. Team scope includes disposition of product, materials and components, including on-the-floor support, record review, quality oversight of deviation investigations and changes, document approval
Ensure AOH product is manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Amgen standards, and applicable regulations
Drive investigations and resolution of deviations, ensuring timely, thorough, and compliant outcomes
Lead and participate in Quality Risk Assessments
Provide Quality input to support project or operational design decisions
Build organization according to hiring strategy that supports our growth. Partner with HR to recruit, coach, develop, motivate, and retain staff. Ensure ongoing organizational structure capable of adapting to evolving business needs
Provide oversight to ensure that Amgen Quality Management System is implemented and maintained in accordance with corporate standards
Track performance and drive continuous improvement in the performance and delivery of quality outputs in alignment with Quality strategies
Develop strategies in support of regulatory inspections and site audits
Serve as quality representative to regulatory authorities, Amgen Corporate auditors, and 3rd Parties

What we offer

health and welfare plans for staff and eligible dependents
financial plans with opportunities to save towards retirement or other goals
work/life balance
career development opportunities
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
discretionary annual bonus program
stock-based long-term incentives
award-winning time-off plans
flexible work models where possible

Fulltime

QA Assurance III

Navarro Research and Engineering is recruiting a QA Assurance III (3796) in Carl...

Location

United States , Carlsbad

Salary:

Not provided

Navarro Inc

Expiration Date

Until further notice

Requirements

Associate’s degree in a technical or science-related field and seven years of quality assurance experience
OR a Master’s degree in the specific discipline or subject matter area required by the project and 1 year of relevant work experience
US citizenship is required
Provides intermediate-level quality control support, including detailed inspections and assisting in quality audits
Prepares documentation for compliance checks, assists in managing corrective actions, and develops a working knowledge of quality standards, such as ASME NQA-1
A structured internship with DOE or Government entity can be used to substitute 1 year of experience with recommendation by mentor and/or CO approval

Job Responsibility

Qualify as a QA Auditor under CBFO QAD’s qualification process within two years of service
Perform as a QA Auditor on generator site-related assessments by completing NMED Permit-driven C6-1 Checklists for general QA elements
Assist Lead Auditors in participating as a QA Auditor for WIPP site and other WIPP Participant-related assessments as assigned
Responsible for performing QA verification checks for NMED-related assessment objective evidence submitted with the final audit report
Compare printed objective evidence presented to the NMED and work with the Permit-related QA administrative support person to ensure the evidence submitted to the NMED is accurate
Also, become the alternate support in processing Final Audit Reports and transmitting the associated objective evidence to the NMED
Develop and maintain QA-related spreadsheets
Track CBFO QAD’s incoming requests for QA reviews for generator sites and other WIPP participant procedures and documents
Coordinate the reviews to ensure timely response
Coordinate the effort for CBFO QAD’s Semi-Annual CAR Trend Reports

What we offer

Health Care Plan (Medical, Dental & Vision)
Retirement Plan (401k)
Life Insurance (Basic, Voluntary & AD&D)
Paid Time Off (Vacation & Public Holidays)
Short Term & Long Term Disability

Fulltime

Senior Quality Assurance Technician

Beacon Hill Life Sciences is looking for an experienced QA professional to perfo...

Location

United States , Maryland Heights

Salary:

28.00 - 30.00 USD / Hour

Beacon Hill

Expiration Date

Until further notice

Requirements

Associate degree in life science or a related field, with completion of 4 college-level life science courses required
Bachelor's degree in life science or a related field preferred
Work experience is considered instead of a degree
3+ years of relevant experience required
Experience with computer data entry required
Must be proficient in Microsoft Office

Job Responsibility

Ensure completion of required training, work (including document review, batch release, QA on-the-floor, AQLs), and timely release of materials and batches
Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e., FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.)
Responsible for the thorough and efficient review and disposition of completed batch record documentation, ensuring adherence to Good Documentation Practices, cGMPs, and applicable local procedures
Responsible for performing and/or overseeing performance of Quality Assurance 'On The Floor' tasks, including but not limited to performing AQL inspections, performing clearances for manufacturing areas, and providing Quality input and guidance to manufacturing personnel
Responsible for dispositioning finished product, raw materials/ components, and intermediates through an all-inclusive documentation review and cross-reference of electronic quality systems
Responsible for the release of incoming raw materials and components per applicable local procedures. This may include support for labeling dispositioned raw materials and components with appropriate status indicator labels
Ensure a safe and quality working environment through training, awareness, and compliance with safety/Quality guidelines and SOPs
Ensure the maintenance of the department, premises, and equipment
Ensure that all assigned training is carried out so that assigned tasks are performed confidently and consistently
Perform all work in compliance with site safety and radiation protection guidelines

Fulltime

Associate QA Manager - Labs

Responsible for managing the plant Quality Assurance Soup Laboratories including...

Location

United States , Maxton

Salary:

90400.00 - 130000.00 USD / Year

THE VAIL CORPORATION

Expiration Date

Until further notice

Requirements

High School Diploma or GED
3+ years of Quality Assurance, Laboratory practices or Food experience within a manufacturing environment

Job Responsibility

Managing the plant Quality Assurance Soup Laboratories including Chemistry Lab and Microbiological Lab
Coordinating releases of products, startups of new and reformulated products, supplier and incoming materials COA's, and Noncompliance's
Managing laboratory data and coordinate resolution of specification issues with materials and products
Coordinating test runs, new product/reformulations start-ups with Product Development, Quality System and plant operations management
Reporting outcome of start-ups and reformulations to management
Organizing and reporting on conformance of new product to specifications
Coordinating corrective action plans
Establishing schedule and ensuring sampling of products per specification and Food Safety/Quality requirements
Ensuring Microbiology and chemistry lab compliance with corporate requirements
Ensuring data base and MES system maintenance

What we offer

Medical
Dental
Short and long-term disability
AD&D
Life insurance
Matching 401(k) plan with immediate vesting
Unlimited sick time
Paid time off
Holiday pay
Employee Resource Groups (ERGs)

Fulltime

Quality Associate

Proclinical is seeking a Quality Associate to support quality assurance activiti...

Location

Switzerland , Basel

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Strong communication skills to address GMP and logistics-related queries effectively
Knowledge of scientific, technical, and regulatory aspects relevant to quality assurance
Familiarity with drug development processes and cGMP guidelines
Basic understanding of safety and environmental regulations
Good organizational skills to manage documentation and project timelines
Proficiency in English, both written and oral, with fluency in the site language preferred
Must have the right to work in this location or hold an EU passport

Job Responsibility

Review and manage GMP-relevant documents and batch records to ensure compliance
Provide functional expertise and support to teams within the quality assurance unit
Contribute to the development and implementation of quality tools, processes, and initiatives
Support project-related activities such as product portfolio development, quality risk assessments, training, and facility upgrades
Ensure adherence to internal and external quality and safety guidelines, including cGMP, SOPs, and regulatory requirements
Manage incoming documents, including executed batch records and vendor labels
Facilitate the timely release of GMP batches, labels, and investigational medical products
Organize, scan, file, and archive QA-owned documents, such as certificates of compliance and batch review checklists

Quality Lab Technician

The QA Lab Technician is responsible for performing routine and specialized samp...

Location

United States , Hampshire

Salary:

19.73 - 29.60 USD / Hour

PetAg, Inc

Expiration Date

Until further notice

Requirements

High school diploma or equivalent required
Associate degree in Food Science, Microbiology, or related discipline desirable
1–2 years of experience in a laboratory or food manufacturing environment
Proven laboratory and document control skills, including sampling, testing, and analytical
Familiarity with lab equipment and calibration
Knowledge of food safety protocols (HACCP) and GMP requirements
Able to become familiar with FDA, USDA, NASC, and other regulatory guidelines for food safety and labeling
Proficiency in Microsoft Word, Excel, and Outlook
experience with QA systems a
Excellent attention to detail and documentation

Job Responsibility

Perform incoming sampling of carriers, ingredients, and packaging
Monitor and document in-process conditions, materials, and products during
Collect and document samples for microbiological and nutritional testing of ingredients and finished goods
Prepare and ship samples to external laboratories for specialized
Record and maintain accurate lab results for ingredients and finished products in compliance
Audit production processes and documentation using QA checklists to ensure adherence to SOPs and GMPs
Collect, store, and track retain samples for reference and regulatory
Conduct environmental monitoring and microbiological sampling of manufacturing
Assist with GMP audits and report findings to QA
Assist in complaint investigations and root cause analysis as

What we offer

Medical Insurance
Dental Insurance
Vision Insurance
Life Insurance with Accidental Death & Dismemberment (AD&D)
Short- and Long-term Disability
Employee Assistance Program (EAP)
Flexible Spending Account (FSA)
Pet Insurance
Paid Holidays & Paid Time Off (PTO)
Employee Stock Ownership Plan (ESOP)

Fulltime

Quality Associate

Quality Associate- Nanded. Support the QA Team in the effective functioning of t...

Location

India , Nanded

Salary:

Not provided

Randstad

Expiration Date

June 19, 2026

Requirements

Graduate/Postgraduate in chemistry/Biotechnology/Food technology/Microbiology/DIFAT
Minimum 1-2 years’ experience in FMCG (Brewery/Beverage/ food/distillery)
Hands on experience in titration / analysis / evaluation techniques
Hands on experience in handling lab equipment and its maintenance and calibration
Knowledge of Excel, Word, PowerPoint
Hands on experience and in-depth knowledge of QMS or FSMS/FSSC
Exposure in Spirit processing and bottling

Job Responsibility

Support the QA Team in the effective functioning of the QA department in alignment with defined quality systems
Evaluate incoming raw materials, intermediates, and finished products
Conduct routine testing of processed and incoming goods
Calibrate and maintain inspection, measuring, and testing equipment
Ensure raw and packaging materials meet defined standards
Ensure Safety at laboratory
Conduct line inspections and ensure SOP compliance
Maintain lab records and documentation in accordance with ISO, FSSAI, and Excise standard
Assist with chemical and microbiological sampling and analysis
Support regulatory audits and inspections by maintaining accurate documentation

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Associate Quality Assurance (Incoming QA)

Amgen

Location:
Netherlands , Breda

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
May 04, 2026

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Associate Quality Assurance (Incoming QA)

Amgen

Location:Netherlands , Breda

Category:Quality Control

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:May 04, 2026

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Job Posted:
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