Quality Control Inspector

45444 Dayton, Ohio Creative Composites Group

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Job Description

Quality Control Inspector

Creative Composites Group - Composite Advantage - Dayton, Ohio

The Quality Control Inspector position is critical in ensuring that all products meet customer expectations by assuring the quality of finished parts and conformance to product requirements. This is done by inspecting parts and documenting inspections and non-conformances. The Quality Control Inspector will interact daily with Operators, Supervisors and Management Staff.

Essential Functions

•Perform first piece, in-process, and final inspections.

•Receiving raw material inspections and testing.

•Blueprint interpretation

•Document Control

•Photographic documentation of materials

•Audit ERP lot number and work order completions for ISO compliance.

•Provide QC data for customer submissions.

•Identify non-conformances and generate QC reports.

•Lead further activities when non-conformance product/material is identified.

•Communicate with Quality Manager and Production Supervisor when non-conforming processes and/or product are identified.

•Responsible for observing all applicable safety requirements. Promotes and maintains a safe work environment; reinforces safety standards and sets the example for PPE, safety training and safe work practices.

Other Duties:

Please note this job description is not intended to be a complete or exclusive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

Supervisory Responsibility

This position has no supervisory responsibility.

Work Environment

While performing the duties of this job, the employee is frequently exposed to fumes or fiberglass and airborne particles, forklift movements and overhead crane usage. The noise level in the work environment and job sites can be loud. The employee will use the following tools and equipment to perform his/her job: tape measures, calipers, steel detector, Barcol reader, angle finder, angle grinder, cordless drills, appropriate PPE, flashlight, and stencils.

Physical Demands

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stoop; bend; climb on top and under parts; twist on a regular basis; stand for prolonged periods of time; walk; use hands to finger, handle or feel; and reach with hands and arms. Specific vision abilities required by this job include close vision and ability to adjust focus, as well as the ability to see and respond to potential worksite hazards. This position requires the ability to lift up to 50 pounds.

Travel

Occasional travel is expected for this position. The employee must have a valid driver's license.

Education and Experience

•2+ years of ISO 9001 experience preferred

•2+ years of experience using measuring devices (tape measure, calipers, gauges, etc.)

•Basic computer skills (Email, Microsoft Office, ERP experience is a plus)

Additional Eligibility Qualifications

•Ability to read measurements in English and Metric.

•Ability to count and perform simple math operations.

•Read/interpret blueprints, CAD drawings and work orders.

•Exceptional oral and written communication skills

•Strong interpersonal and organizational skills.

•Attention to detail.

•Positive attitude. Pleasant demeanor when interacting with co-workers.

EEO Statement

Composite Advantage is an equal opportunity employer, and does not discriminate on the basis of race, color, religion, sex, sexual orientation, age, disability, veteran or marital status, or based on any individual's status in any group or class protected by applicable federal, state or local law. The company also provides reasonable accommodations to qualified individuals with disabilities in accordance with the Americans with Disabilities Act and applicable state and local laws

Keywords

Quality, Quality Control, Inspector, Quality Inspector, Document Control, Production Quality, Manufacturing, Production
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Quality Control Inspector

45444 Dayton, Ohio Stolle Machinery

Posted 5 days ago

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Job Description

(the purpose and general nature of the job): This position is responsible for dimensionally inspecting in-process and final machined parts primarily using CMM (Coordinate Measuring Machine) and other typical inspection equipment. This position will a Quality Control, Inspector, Control, Inspection

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Quality Control Chemist

45377 Vandalia, Ohio Adare Pharmaceuticals

Posted 11 days ago

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Job Description

Permanent

Are you ready to join a growing, global drug development and manufacturing organization that puts people first?  Come to Adare!  We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world.  Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact and is critical to our success.  With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!

Join our mission at Adare !

What can Adare offer you?

  • Medical/dental/vision/life – low employee premiums
  • 401k with a highly competitive match
  • Generous PTO, including floating holidays
  • Career growth and internal opportunities
  • Tuition reimbursement
  • Relocation assistance
  • Performance-based bonus
  • Employee Recognition Programs

We are seeking to hire a Quality Control Chemist to join our Laboratory Operations team

If any of the below describes you, we would love to meet you! 

JOB SUMMARY

The QC Chemist performs moderately complex physical and chemical testing of intermediate and finished products according to written procedures and trains less experienced Chemists as required. Also responsible for testing of cleaning samples for more complex systems and more advanced instrument maintenance. Responsible for timely analytical data reporting based on project timelines.

RESPONSIBILITIES AND LEARNING OPPORTUNITIES

  • Demonstrate a more advanced knowledge of various test methods and instrument analysis techniques and be proficient with all sample types and test methods. Perform more advanced troubleshooting/maintenance of the instrumentation.
  • Responsible for more complex physical and chemical testing of raw material, intermediate, and finished products as described in the documented procedures to support product release and process validation protocols.
  • Demonstrate proficient ability to operate the instrument software applications, set up advanced sequences, troubleshoot software and report data while executing the higher complexity test methods that utilize instruments such as UV, FTIR, GC, and HPLC, and IC.
  • As required, perform swabbing and analysis of more complex manufacturing equipment with no supervision in accordance with cGMP guidelines. Provide input on cleaning related issues and investigations.
  • Evaluate and maintain assigned calibrations for equipment in the laboratory as required and review the required documentation for compliance. Review instrument qualification documents to support system change control actions and assist vendors during installation and PM’s.
  • Investigate Out of Specification results, Out of Trend results and deviations in accordance with cGMP guidelines.
  • Assist Management with writing and completion of investigation sections and product impact as required. Train others as required as it pertains to LIR/OOS procedures.
  • Perform method validation and method transfer activities as required.
  • Train other Chemists, Lab Assistants, and temporary personnel.
  • Assist with customer and regulatory audits as required for Data Integrity and/or instrument file review.
  • Author, revise and update laboratory test methods and Standard Operating Procedures.
  • Accurately maintain notebooks and files compliant with current GMPs and internal Standard Operating Procedures. Peer review and/or audit others work as required for verification of GMP compliance.
  • Auditing of laboratory testing data as required.
  • Demonstrate consistent ability to perform testing with limited investigations and repeat analyses. Ability to accurately report test data in various formats along with advising less experienced Chemists.
  • Perform cost savings and process improvement projects as required
  • Observes all safety procedures and regulations

REQUIRED SKILLS AND QUALIFICATIONS

Level is commensurate with candidates’ amount of education, experience, as well as demonstrated level of knowledge and skills.

  • Bachelor’s degree in Chemis try or closely related field
  • 0-2 years’ experience for a Chemist I, 3-5 years’ experience for a Chemist II; experience working in a Chemistry Laboratory, Quality Control or Research and Development Laboratory, in the pharmaceutical industry OR M.S. in Chemistry or closely related field and 2-3+ years of experience working in a Chemistry Laboratory, Quality Control or Research and Development Laboratory in the pharmaceutical industry.
  • Moderate to advanced knowledge of laboratory procedures, equipment, instrumentation, safety procedures and laboratory practices. Good understanding of chromatography methods and problem solving.
  • Has a thorough understanding of cGMP and Data Integrity documentation requirements.

Adare Pharma is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status.

PRINCIPALS ONLY
NO AGENCIES OR THIRD PARTIES

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Quality Control Lab Assistant

45377 Vandalia, Ohio Adare Pharmaceuticals

Posted 11 days ago

Job Viewed

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Job Description

Permanent

Are you ready to join a growing, global drug development and manufacturing organization that puts people first?  Come to Adare!  We work closely with our pharmaceutical industry partners during all phases of drug development with a mission of improving the lives of patients and medicines essential to people all over the world.  Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact, and is critical to our success.  With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!

Join our mission at Adare !

What can Adare offer you?

  • Medical/dental/vision/life – low employee premiums
  • 401k with a highly competitive match
  • Generous PTO, including floating holidays
  • Career growth and internal opportunities
  • Tuition reimbursement
  • Relocation assistance
  • Performance-based bonus
  • Employee Recognition Programs

We are seeking to hire an QC Lab Assistant  to join our Quality Control Team

If any of the below describes you, we would love to meet you! 

JOB SUMMARY

Performs general laboratory cleaning and simple laboratory solutions duties for Chemists and other QC personnel.  Works a standard M-F schedule.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Prepare various mobile phase, buffers, and standard solutions as required.
  • Perform some sample preparation for non-complex methods.
  • Clean various glassware and load/empty dishwasher.
  • Take out lab waste
  • Stock all laboratory supplies
  • Clean dissolution baths
  • Monitor solutions for expiration and dispose
  • Put away incoming inventory supplies
  • Perform some basic tests such as pH on buffers and loss on drying on various samples.
  • Verify daily checks on balances and various instruments as required. Attend work on a regular and predictable basis.  This position may require a standard 40 hour work week, but may also require working either of the day or night shifts, overtime, weekend hours, and/or holidays.
  • Complete assigned tasks in a safe manner and in a constant state of alertness.
  • Uphold all Company policies, including but not limited to, the Adare Pharmaceuticals, Inc. (Adare) Code of Conduct and the Professional Conduct Policy and Prohibition Against Harassment Policy.
  • Work in a cooperative manner with managers, supervisors, coworkers, customers and the public.
  • Support the Adare vision and mission and exemplify Adare values.
  • Perform other tasks as required
  • Works effectively under deadlines.
  • Acts as the company’s representative by showing respect and being ambassador for the established beliefs and behaviors of the Company.
  • Participates in the development and implementation of methods, procedures and regulations necessary for the smooth operation of the business.
  • Respects policies, procedures and regulations in force in the company.
  • Completes assigned tasks in a safe manner and in a constant state of alertness.
  • Upholds Company policies, including the Professional Cond uct Policy and Prohibition Against Harassment Policy, and the Business Ethics and Conduct Code
  • Perform other tasks as required.

REQUIRED SKILLS AND QUALIFICATIONS

  • High school diploma or equivalent.
  • Some interest and knowledge of science is a plus.
  • Ability to understand and follow procedures; including safety procedures.
  • Good interpersonal skills are required.

PHYSICAL REQUIREMENTS

  • Stand, walk, push, pull, twist, reach overhead, and bend to the floor.
  • Occasionally move items or equipment weighing up to 100 pounds – potential to handle heavier materials with mechanical assistance.
  • Occasionally required to climb ladders and/or steps to reach equipment.
  • Reading precision measuring equipment, machine dials, gages, and thermometers; must be able to observe fine details utilizing a microscope.

Adare Pharma is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status.

PRINCIPALS ONLY
NO AGENCIES OR THIRD PARTIES

Apply Now

Quality Control Chemist, Raw Materials

45377 Vandalia, Ohio Adare Pharmaceuticals

Posted 11 days ago

Job Viewed

Tap Again To Close

Job Description

Permanent

Are you ready to join a growing, global drug development and manufacturing organization that puts people first?  Come to Adare!  We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world.  Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact, and is critical to our success.  With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!

Join our mission at Adare !

What can Adare offer you?

  • Medical/dental/vision/life – low employee premiums
  • 401k with a highly competitive match
  • Generous PTO, including floating holidays
  • Career growth and internal opportunities
  • Tuition reimbursement
  • Relocation assistance
  • Performance-based bonus
  • Employee Recognition Programs

We are seeking to hire a Raw Materials Chemist I or II  to join our Quality Control team…

If any of the below describes you, we would love to meet you! 

JOB SUMMARY

The Raw Materials Chemist will perform chemical and physical testing on pharmaceutical raw materials (APIs, Excipients and Packaging components).  

RESPONSIBILITIES AND LEARNING OPPORTUNITIES

  • Perform sampling, physical testing, and chemical testing of raw materials as described in the documented procedure or compendia with minimal supervision in accordance with cGMP guidelines.
  • Compile samples for send out testing and maintain associated documentation. 
  • Maintain laboratory equipment and work areas in good working condition.
  • Ensure Raw Material documentation is accurate and up to date and revise as needed (i.e. certificates of analysis, test methods, Standard Operating Procedures)
  • Monitor compendia for changes that effect current raw materials testing and procedures.
  • Perform assigned calibrations and preventative maintenance for equipment in the laboratory. 
  • Recognize and troubleshoot equipment issues.
  • Recognize and investigate Out of Specification results, Out of Trend results and deviations in accordance with cGMP guidelines and report results to supervisor.
  • Audit laboratory documentation.
  • Assist with training of Raw Material Analysts and temporary personnel.
  • Responsible for laboratory systems as assigned (i.e. logbooks, calibrations, standards)
  • Perform new material verifications with minimal supervision. 
  • Assist with method validations.
  • Assist with installation of new laboratory equipment.
  • Accurately maintain notebooks and files compliant with current GMPs and internal Standard Operating procedures.
  • Observes all safety procedures and regulations.
  • Other job-related tasks as required

REQUIRED SKILLS AND QUALIFICATIONS

Level is commensurate with candidates’ amount of education, experience, as well as demonstrated level of knowledge and skills.

  • Bachelor or Master’s degree in Chemistry or related field
  • 0-2 years’ experience for a Chemist I, 3-5 years’ experience for a Chemist II; working in a Quality Control, Raw Materials or Research and Development Laboratory, preferably in the pharmaceutical industry; years’ + type of experience and Education level will determine level
  • Working knowledge of laboratory procedures, equipment, instrumentation, safety procedures and laboratory practice
  • Working knowledge of current Good Manufacturing Practices (GMPs)
  • Proficient in Microsoft Excel, Word.  Microsoft Access experience a plus
  • Basic knowledge of technical writing coupled with good oral communication skills.

PHYSICAL REQUIREMENTS

  • Stand, walk, push, pull, twist, reach overhead, and bend to the floor.
  • Occasionally move items or equipment weighing up to 50 pounds – potential to handle heavier materials with mechanical assistance.
  • Occasionally required to climb ladders and/or steps to reach equipment.
  • Reading precision measuring equipment, machine dials, gages, and thermometers; must be able to observe fine details utilizing a microscope.

Adare Pharma is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status.

PRINCIPALS ONLY
NO AGENCIES OR THIRD PARTIES

Apply Now
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