Science,Science|Quality Assurance Scientist,Science|Quality Control Scientist Jobs

Pay Rate: $22 per hour - $27 per hour Summary:

• Duration: 2-3 month assignment
• 40 hours per week

Responsibilities:

• Prepare for new software implementation.
• Upload all control plans and PFEMAs using quality principles.
• Ensure conformance to customer, plant, and regulatory standards.
• Analyze quality data.

Job Responsibilities: (Primary Duties, Roles, and/or Authorities):

• Complete Inspections of Materials and file quality records including receiving files and non-conforming material reports.
• Maintain the receiving area in a neat and orderly manner.
• Ability to check and unload incoming shipments.
• Inspect the received goods to ensure their quality.
• Ability to work with other departments if a problem or discrepancy is found and keeping careful records.
• Count, weigh or measure items of incoming shipments to verify information against invoices, orders, bills of lading or other records.
• Read and understand drawings and specifications is not required, but a plus.
• Route items to various departments
• Examine and unpack incoming shipments; record shortages and reject damaged items
• Examine incoming shipments to ensure they meet specifications and Identify Non-Conforming materials/Bad Materials
• Check in inbound inventory and administer the processing
• General knowledge of measuring tools
• Good mechanical aptitude and close attention to detail
• Ensure that all documents and material received in the receiving are of satisfactory quality
• Must possess the ability to perform various testing procedures and simple statistical analysis as related to sampling.
• Provides supplemental quality support to on-going projects

Educational Qualifications & Previous Experience:

• High School Diploma or GED required. Technical degree or professional certification preferred
• At least one year experience performing mechanical inspections in an FDA or ISO regulated environment preferred, but negotiable.
• Previous quality experience preferred.
• Professional Skills & Key Competencies
• Duties require basic knowledge of inspection/sampling techniques and familiarity with ANSI/ASQ Z1.4
• Basic familiarity with FDA QSR and/or ISO 9000/ISO 13485 Quality System Requirements
• Knowledge of mechanical and physical inspection techniques (callipers, micrometres, depth gauges, etc.)
• Demonstrated strong attention to detail and "do it right the first time attitude
• Ability to work in a fast-paced warehouse environment.
• Ability to read and interpret distribution documents and operational procedures / specifications.
• Desired / Additional Skills & Knowledge
• Basic familiarity with MS Office Products (Word, Excel, Outlook)
• Ability to utilize a computer to enter data and prepare reports
• Ability to lift a 30 lb load from the floor
• Majority of time is spent standing and/or walking for more than four (4) hours per day
• Ability to be able to work with limited supervision.

At-a-Glance:
Are you ready to build your career by joining a certified technology solutions and compliance consulting services company? If so, our client is hiring a QA Deviation Specialist.

Position Type:

• Contract
• On-Site

Required:

• Bachelor's degree from an accredited college or university.
• 10+ years of experience working in Aseptic Processing facilities, with demonstrated expertise in manufacturing deviation investigations and technical report writing.
• Expert-level understanding of deviation management, manufacturing process investigations, Root Cause Analysis, and CAPA development and execution.
• Previous experience supporting or executing remediation plans in response to US FDA observations or regulatory requirements.
• Extensive Quality Assurance experience across multiple areas, including PQR, auditing, change control, complaints management, OOS investigations, batch record review, and documentation management.
• Experience with training programs, supplier quality management, and broader pharmaceutical quality systems within regulated manufacturing environments.
• Excellent written and verbal communication skills in English and other relevant languages, with strong collaboration, conflict resolution, and problem-solving abilities, and a demonstrated focus on KPIs and project goals. 

Reponsibitlies:

• Lead Minor, Major, and Critical Deviation investigations within assigned areas, ensuring thorough documentation and compliance with established quality procedures.
• Collect, review, and analyze relevant raw data, records, and supporting information to facilitate comprehensive investigations.
• Lead Root Cause Analysis (RCA) activities to identify probable root causes, assess potential product impact, and establish appropriate CAPAs with assigned owners and due dates.
• Perform deviation trending and data analysis to identify adverse trends, recurring issues, and opportunities for corrective action.
• Prepare, review, and finalize comprehensive investigation reports, ensuring accuracy, quality, and completion within established timelines.
• Develop and implement effective Corrective and Preventive Actions (CAPAs), including follow-up mechanisms to verify implementation and long-term effectiveness.
• Manage client communications, provide regular project progress updates, and report performance metrics to Project Leadership while ensuring timely approval and closure of investigation reports.

Get in Touch:
We want to hear from you! If you think you'd be a good match, submit your resume and reach out to XXXXXXX at XXX-XXX-XXXX to learn more.

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Job Title: QC Tech I 2nd shift

Location: 948 Meridian Lake Dr, Aurora, IL 60504

Duration: Temp-to-hire

Pay Rate: $21/h + $2/h shift diff on W2 (Including all benefits)

Shift: 2:00pm 10:30pm M-F

First day hours: 8AM-5PM

Summary:

The Quality Technician is responsible for managing and enforcing Quality Program procedures and company established policies regarding the powder process and storage, of all goods manufactured at the 948 GPN Aurora facility.

Description

" Perform in-process and packaging checks to ensure products meet specifications per the batch production records (BPR)

" Perform sensory evaluations on in-process and finished product.

" Perform Final Inspection for FG Distribution

" Data entry in Logs pertaining to Quality Metrics

" Perform SAP transactions for releases, holds, reworks and High Jump where applicable

" Perform cleaning verifications using ATP swabs and visual inspections to approve manufacturing rooms prior to production.

" Verify production and quality records are accurately completed in real-time during production.

" Report any process or SOP/GMP deviations to Quality Supervision or Management.

" Support Simple Root Cause Investigations, Validations, CAPA, Environmental Control Program ECA, Customer Complaints Investigations and Document Control

" Fully understand the receiving process flow for raw and packaging materials.

" Fully understand the Distribution Centers and Warehouses process in regards to Finished Goods inspections, SAP transactions and releases.

" Enter results into a computerized system, track and report results (GP/SAP/MS Office programs).

" Understand microbiological concepts, procedures, and knowledge of aseptic technique for Environmental Program ECA's coordination.

" Perform and Sign-off on raw material and packaging samples and inspections.

" Perform and Sign-off on Finished Good Inspections and Releases and report to Quality Management for dispositions.

" Prepare and/or collect samples for laboratory testing for Raw Material receipts and FG investigations.

" Flexibility to perform other duties as assigned by Quality Management.

Education: High School or GED

Food or Pharmaceutical Quality Experience Preferred

Other Experience

• Understand GMP/Food Safety Requirements
• Computer Skills / MS Office / SAP

Physical Demands

The work is classified as Light - Medium Physical Demand Level (PDL) by the US Dept. of Labor's Dictionary of Occupational Titles. Frequencies: Occasional (1-33%); Frequent (34-66%); Constant (67-100%)

Postural Demands

Demand Frequency

Sitting Occasional

Standing Frequent

Walking Frequent

Bending/Stooping Frequent

Lifting Demands

Demand Frequency Designation

Lift up to waist

Lift on up to shoulder

Lift on up to overhead

Carry on up to 25 feet

Carry up stairs

Lifting Demands (Manufacturing)

948 Quality Control: 1) Lift 25 lbs. from 6 inches to waist level x 5 reps.

This job description is not intended, nor should it be construed to be an exhaustive list of all responsibilities, duties, skills, or working conditions associated with the particular job. It is intended only to be a general description of the essential functions common to positions of this type.

Job Title: QC Tech I 3rd shift

Location: 948 Meridian Lake Drive. Aurora, IL

Duration: Temp-to-hire

Pay Rate: $21/h + $3/h shift diff on W2 (Including all benefits)

Shift: 3 rd Shift - 10pm 6:30am M-F

Summary:

The Quality Technician is responsible for managing and enforcing Quality Program procedures and company established policies regarding the powder process and storage, of all goods manufactured at the 948 GPN Aurora facility.

Description

" Perform in-process and packaging checks to ensure products meet specifications per the batch production records (BPR)

" Perform sensory evaluations on in-process and finished product.

" Perform Final Inspection for FG Distribution

" Data entry in Logs pertaining to Quality Metrics

" Perform SAP transactions for releases, holds, reworks and High Jump where applicable

" Perform cleaning verifications using ATP swabs and visual inspections to approve manufacturing rooms prior to production.

" Verify production and quality records are accurately completed in real-time during production.

" Report any process or SOP/GMP deviations to Quality Supervision or Management.

" Support Simple Root Cause Investigations, Validations, CAPA, Environmental Control Program ECA, Customer Complaints Investigations and Document Control

" Fully understand the receiving process flow for raw and packaging materials.

" Fully understand the Distribution Centers and Warehouses process in regards to Finished Goods inspections, SAP transactions and releases.

" Enter results into a computerized system, track and report results (GP/SAP/MS Office programs).

" Understand microbiological concepts, procedures, and knowledge of aseptic technique for Environmental Program ECA's coordination.

" Perform and Sign-off on raw material and packaging samples and inspections.

" Perform and Sign-off on Finished Good Inspections and Releases and report to Quality Management for dispositions.

" Prepare and/or collect samples for laboratory testing for Raw Material receipts and FG investigations.

" Flexibility to perform other duties as assigned by Quality Management.

Minimum High School or GED

Food or Pharmaceutical Quality Experience Preferred

Other Experience

• Understand GMP/Food Safety Requirements
• Computer Skills / MS Office / SAP

The Quality Inspection associate will be responsible for monitoring the molding process to ensure conformance to all requirements. The position will require lifting of containers weighing up to 40 pounds. The associate must be able to read, understand and follow written work instructions. This associate must have some experience in inspection. Must be able to do sorting/visual inspection of parts. Must have advance knowledge of Quality requirements

• Verify parts are in the proper/correct totes/containers.
• Sort rework parts as needed.
• Release approved parts and move to the rack area dedicated to each part number.
• Sort rework parts as needed.
• Complete the Temporary work instruction for reworked parts and ensure the documentation is processed according to instructions.
• Complete 5-S activities to maintain the molding area.
• Transfer/move molded parts form the molding area to the work-in-process storage area as needed.
• Follow all general and job specific safety and operating requirements established at YAMI.
• Provide suggestions for improvements in the warehouse and other work areas.
• Other duties either temporary or permanent as required or assigned to support Quality Assurance activities at Yahagi America Molding, Inc.
• Scan nonconforming parts to nonconforming in the c-core system when placing into nonconforming cage and log parts on cage log.

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

• Review of event documentation such as Batch records, Exceptions, and Regulatory filings
• Production record review and Product disposition for drug substance, drug product, device assembly and finished goods
• Support design development plan including design verification and DHF deliverables
• Build and maintain Product Specification Files (PSF) for Alnylam program

• Knowledge of relevant government regulations and agency rules for labeling (CFR & EudraLex Volume 4, Annex 13)
• Understanding of ICH, GLP, CGMP requirements, GXP regulations and current industry practices.
• Demonstrated teamwork, initiative, and problem-solving skills
• Ability to prioritize and work independently with minimal supervision
• Ability to accurately determine deadlines and ask for help if needed
• Detail oriented with solid problem-solving acumen.
• Ability to work effectively in a team environment with great organization skills.
• Ability to independently analyze and reconcile moderate to complex issues.
• Must have demonstrated initiative and accountability in a fast-paced environment.
• Excellent verbal and written communication and interpersonal skills.
• Proficient with computers and word processing software (i.e., Microsoft Office products)

• Minimum, a BS degree in life sciences, engineering or related field
• Minimum of 5 years pharmaceutical quality assurance experience in a GMP manufacturing and supply chain environment
• Good understanding of FDA and EMA regulations and guidelines
• Excellent organizational, communication, and interpersonal skills.

Title: REL Quality Control Specialist I

Location: Winchester, VA
Employment Type: Contract

Compensation:
Pay Range$13.00-$23.00 Per Hr

Description
Engage with a dynamic team to ensure quality control standards are met.
Work in a hybrid setting with a requirement to be onsite three days a week.
Contract position lasting six months with potential for overtime based on business needs.
Utilize a range of technologies to monitor and evaluate service quality.
Provide feedback and identify areas for improvement to enhance service delivery.

Key Responsibilities
Monitor and evaluate interactions to ensure service quality and compliance.
Document feedback and provide recognition for positive performance.
Identify potential fraud or abuse and report findings.
Analyze process changes for impact on service quality.
Collaborate with stakeholders to improve operational efficiency.

Qualifications
2-4 years of relevant experience in quality control or a related field.
Strong interpersonal, verbal, and written communication skills.
Proficient in word processing, spreadsheet, and presentation software.
Experience in cross-functional team environments.
Ability to provide constructive feedback and solutions.

Core Technologies
Word Processing Software | Spreadsheet Software | Presentation Software

Contact Authorization
By applying for this job, you agree to receive AI-generated calls, text messages, and/or emails from Mitchell Martin Inc and its affiliates and contracted partners at various frequency through traditional and automated methods. Message and data rates may apply for texts. Carriers are not liable for delayed or undelivered messages. You can access our privacy policy here (url removed). 

Onboarding Expectations
Learn more about our Onboarding Process here (url removed) 

EEO Statement
Learn more about our EEO policy here (url removed) 


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Primary Duties and Responsibilities:

• Conduct incoming inspection to validate arriving material meets quality standards with moderate supervision.
• Conduct outgoing inspection to validate material moved through the production process meets quality standards with moderate supervision.
• Accurately input data into appropriate data storage locations for all inspected material.
• Validate incoming and outgoing inspection documentation is available, organized, and complete.
• Provide In-Process Inspections as needed.
• Provide training and support for the Production team for quality-related process steps and other topics as needed.
• Inspections are visual as well as with tools.

Qualifications:

To perform this position successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.

• Associate's degree in Electronics preferred or equivalent experience is required, with demonstrated level of technical capability and responsibility.
• Very good written and verbal communication skills are required. Proficiency in Microsoft Office is required, particularly Word and Excel.
• Demonstrated capability as a self-starter in a hands-on environment is required.

This position does require one to be moving and standing, and there is some lifting involved. We inspect product that is up to 35 lbs regularly and the inspectors are on the move between production areas for most of the day, to the point that they have mobile workstations.

Join our team in Robinson Township, PA, where you can grow your career in a vibrant and supportive community. Enjoy the benefits of working in a location that offers a blend of suburban tranquility and easy access to urban amenities.

 

Benefits
PEAK's benefit offerings available for our associates include medical, dental, vision, Flexible Spending Account (FSA), Dependent Care Savings Account (DCA), and 401K plan. PEAK believes that taking care of our team is essential for success and we are proud to provide benefits that enhance both your well-being and your future. Additionally, our associates may be eligible for Paid Sick Leave as required by Federal, State, or local laws.  

Equal Opportunity Employer (EEO) 
PEAK Technical Staffing is committed to creating a diverse and inclusive environment and is proud to be an Equal Opportunity Employer. PEAK does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status, or any other characteristic protected by applicable law. All employment decisions are made based on qualifications, merit, and business need. We encourage all individuals to apply. 

Americans Disabilities Act (ADA) 
The physical and mental requirements described in this job description are representative of those that must be met by an employee to successfully perform the essential functions of the position. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. Must be able to perform the essential physical functions of the position, including sitting, standing, walking, stooping, kneeling, and lifting up to 25 pounds, with or without reasonable accommodation. 

Candidate Privacy
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to (url removed) and (url removed)  

AI Recruiting Disclosure 
We use AI-assisted tools to help review applications and compare your experience to job requirements, but all hiring decisions are made by human recruiters. You may request a human-only process or opt out of automated communication at any time. Required notices and our latest bias audit are available on our website: (url removed)/ai-disclosure.

Job ID: GN - 17
Job Title: QC Tech I
Location: 948 Meridian Lake Drive. Aurora, IL 60504
Duration: Temp-to-hire
Pay Rate: $21/h + $1/h shift diff on W2 (Including all benefits)
Shift: 10pm 6:30am M-F 3 rd Shift

First Day Hours: 8:00 AM 5:00 PM

Summary: The Quality Technician is responsible for managing and enforcing Quality Program procedures and company established policies regarding the powder process and storage, of all goods manufactured at the 948 GPN Aurora facility.

Duties and Responsibilities:

" Perform in-process and packaging checks to ensure products meet specifications per the batch production records (BPR)
" Perform sensory evaluations on in-process and finished product.
" Perform Final Inspection for FG Distribution
" Data entry in Logs pertaining to Quality Metrics
" Perform SAP transactions for releases, holds, reworks and High Jump where applicable
" Perform cleaning verifications using ATP swabs and visual inspections to approve manufacturing rooms prior to production.
" Verify production and quality records are accurately completed in real-time during production.
" Report any process or SOP/GMP deviations to Quality Supervision or Management.
" Support Simple Root Cause Investigations, Validations, CAPA, Environmental Control Program ECA, Customer Complaints Investigations and Document Control
" Fully understand the receiving process flow for raw and packaging materials.
" Fully understand the Distribution Centers and Warehouses process in regards to Finished Goods inspections, SAP transactions and releases.
" Enter results into a computerized system, track and report results (GP/SAP/MS Office programs).
" Understand microbiological concepts, procedures, and knowledge of aseptic technique for Environmental Program ECA's coordination.
" Perform and Sign-off on raw material and packaging samples and inspections.
" Perform and Sign-off on Finished Good Inspections and Releases and report to Quality Management for dispositions.
" Prepare and/or collect samples for laboratory testing for Raw Material receipts and FG investigations.
" Flexibility to perform other duties as assigned by Quality Management.

• Minimum of High School or GED is required
• Food or Pharmaceutical Quality Experience Preferred

Other Experience

• Understand GMP/Food Safety Requirements
• Computer Skills / MS Office / SAP

Job Description

 

LBF is seeking a qualified candidate to conduct ongoing Quality Control responsibilities on a reverse mortgage (HECM and Proprietary) and HELOC pipeline to ensure adherence with HUD and investor guidelines, and federal, state and regulatory requirements. The Coordinator will be responsible for managing the QC process for pre and post-closing.  

Primary Responsibilities 

• Manage the post-closing QC process for loan selection, delivery of files for review, tracking service level agreements, informing appropriate parties of any findings, and mitigation of findings with QC provider.
• Identifying loans that require FHA Self-report. 
• Identify compliance risks or concerns and report up to Management.
• Analyze results to determine trends and work with Operations Management on solutions for process enhancements where systematic errors are discovered. 
• Summarize and log audit findings for pre- and post-closing and create monthly reports. 
• Communicate audit findings and remediation to management. 
• All other compliance-related assignments as required for agency/regulatory compliance.
• Manage the administration of external programs and vendors used to complete quality control tasks.
• Communicate all alerts (credit policy, state regulatory, compliance, and Operations process) and underwriting guidelines updates to QC vendor.

Additional Responsibilities 

• Select loans for pre-funding QC audits of loans which have final underwriting approval, but not yet closed. Manage the process including:  delivery of files for review; tracking of service level agreements; informing appropriate parties of any findings; mitigation of findings with QC provider; issuing to Operations a clearance to close.
• Provide support to operations to address any pattern of deficiencies discovered during QC. 
• Various other related duties assigned.