Top 21 Software quality assurance specialist Jobs in Dayton, Oh

Quality Assurance Specialist
Adare Pharma Solutions —Vandalia, OH
- Full-time
- Microsoft Excel
- Mid-level
- Ability to climb stairs
- Paid holidays
- Disability insurance
12d
Quality Assurance Specialist - 1st Shift
Dayton-Phoenix Group, Inc. —Dayton, OH
- Full-time
- Microsoft Word
- Mid-level
- High school diploma or GED
Quick Apply
10d
Quality Documentation Specialist
Coldwell Banker Heritage —Dayton, OH
- $41,000 - $48,000 a year
- Full-time
- Writing skills
- Mid-level
Quick Apply
ISD Support* (26.24)
SIERTEK LTD —Wright-Patterson AFB, OH
- Full-time
- Microsoft Excel
- Microsoft Outlook
- 5 years
Quick Apply
Data Analytics
NPower Michigan —Dayton, OH
- $55,000 - $75,000 a year
- Temporary
- Hybrid work
- Computer literacy
- High school diploma or GED
- US work authorization
Quick Apply
Data Visualization Specialist
BRS —Wright-Patterson AFB, OH
- Full-time
- Computer science
- Computer Science
- HIPAA
- Profit sharing
- Paid holidays
9d
Technical Writer
Entegrity Consulting Group —Dayton, OH
- Remote
- Microsoft Excel
- Computer Science
- Mid-level
Quick Apply
5d
Coding Compliance Specialist
Prestige Billing Services, Ltd. —Miamisburg, OH
- Full-time
- HIPAA
- Analysis skills
- Continuous improvement
Quick Apply
Data Visualization Specialist* (26.25)
SIERTEK LTD —Wright-Patterson AFB, OH
- Full-time
- Computer Science
- HIPAA
- Mid-level
Quick Apply
DATA VISULATIONZATION SPECIALIST
LTSi - Laredo Technical Services, Inc. —Dayton, OH
- $85,000 - $101,000 a year
- Online Application
- Computer science
- Computer Science
- HIPAA
- Paid holidays
- Health insurance
Quick Apply
Data Visualization Specialist
BESTICA INC —Dayton, OH
- Full-time
- Computer science
- Computer Science
- HIPAA
- Paid time off
Quick Apply
Customer Service Administrator
Orkin —Dayton, OH
- $20 an hour
- Full-time
- Sales
- Computer literacy
- Office
- Employee stock purchase plan
- Paid holidays
2d
Information Technology Specialist AFLCMC/IN-10.21
Credence —Wright-Patterson AFB, OH
- $90,000 - $110,000 a year
- Urgently hiring
- Doctoral degree
- Master's degree
- Ability to lift 50 pounds
- AD&D insurance
- Disability insurance
Quick Apply
Information Technology (IT) Specialist
Applied Research Solutions —Dayton, OH
- Urgently hiring
- Doctoral degree
- Master's degree
- Ability to lift 50 pounds
Quick Apply
Integrated Master Scheduler
BTAS —Wpafb, OH
- Full-time
- Bachelor of Science
- 11+ years
- Research
- Paid holidays
- Health insurance
Quick Apply

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Quality Assurance Specialist

Adare Pharma Solutions -
Vandalia, OH

Apply Now

Job Details

Full-time
12 days ago

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Tuition reimbursement
Paid time off
Vision insurance
Life insurance
Retirement plan
Pet insurance

Qualifications

GMP
Manufacturing facility experience
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Microscopy
Respirator
Pharmaceutical manufacturing facility experience

Full Job Description

Our Business
Adare Pharma Solutions is a global Contract Development and Manufacturing Organization (CDMO) with locations across North America and Italy. We offer a wide range of manufacturing, packaging, and research and development services. Our clients range from growing biotech firms advancing groundbreaking clinical trials to established pharmaceutical companies producing high volumes of approved, widely used medicines.
By combining top talent from the life sciences industry with modern research and manufacturing technologies, Adare enables clients to deliver potentially lifesaving medicines in more easily consumable formats - particularly for patients such as infants or the elderly. This is the meaning behind “Transforming Drug Delivery – Transforming Lives.”
Our Culture
When it comes to being an employee of Adare, although we are located across multiple countries and come from diverse backgrounds, we work together toward a common purpose. Supported by leadership that is experienced and highly regarded in the industry, we are paving the way for a brighter and better future by attracting top talent from both within and beyond the CDMO space.
In addition to delivering high-quality results for our external clients, we foster a collaborative, client-centric culture internally - one where employees support one another, share knowledge, and encourage each other to bring their best selves to work each day.
Why Come to Adare?
Adare is Private Equity owned and poised for growth. Employees are provided with internal development opportunities to progress within the organization, enhancing their professional skills and industry knowledge through Adare’s investment in their growth.
We offer a variety of fields to embark in, including manufacturing, engineering, quality, chemistry, formulations, analytical research and development, finance, supply chain, sales, marketing, project management, human resources, and environmental health and safety. Our benefits package is highly competitive, offering medical, dental, and vision coverage; a retirement plan with company match, paid time off and company holidays, tuition reimbursement with no waiting period, life insurance, pet insurance, Flexible Spending Accounts (medical and dependent care), and disability coverage.

Position
Quality Assurance Specialist
Location
Vandalia, OH
Summary
The Quality Assurance Specialist is key player on the Quality Assurance team, and is responsible for the audit of batch production documentation (manufacturing records, analytical records, deviation investigations), Development support, Contract Manufacturing oversight, disposition of product, approving quality documents (e.g. SOP, protocols, methods), and overall adherence to cGMP.

Responsibilities

Disposition Product
Review executed Production Records, Packaging Records and Analytical results for compliance to established internal procedures, methods, specifications and industry standards
Resolves minor issues found during documentation review (documentation errors, missing information) as directed by SOP and resolves major issues that are not defined by SOP.
Conduct product release activities for intermediates, drug product and finished goods including review and approval of master batch records and executed batch records.
Investigations
Ensure deviations are properly documented and investigated.
Approve Corrective and Preventive Actions.
Interact with Customers
Ensure compliance with Quality Agreements.
Support customer service-related business activity, as appropriate.
Maintain the confidentiality of pertinent information.
Third Parties
Review and approve master and executed manufacturing / packaging records.
Work with CMOs to raise, investigate and resolve deviations and investigations prior to lot disposition.
Projects:
Actively participates on project teams as assigned by management.
Training:
Completes all assigned training by target due dates.
Audits/Inspections:
Participates in internal audits as assigned by management.
Interface with all departments within the company
Be an ambassador for Quality within the company
Maintain professional interactions with all departments and other sites
Ensure facility adherence to cGMP
Work as part of the Quality Assurance team to meet company, departmental, and individual goals as outlined by management
Follow other job-related instructions and perform other tasks as required

Experience, Education, and Skills Required

Bachelor’s Degree preferred, with at least 2+ years of Quality experience in a pharmaceutical or other GMP regulated industry.
Experience using a Quality Management System; experience with Veeva preferred.
Experience with using the Microsoft Office Suite of software (Word, Excel, PowerPoint) is preferred.
Knowledge in cGMP as related to records and documentation in a bulk pharmaceutical and solid oral dosage manufacturing environment is preferred.
Knowledge and/or working experience of large processing systems, fluid air systems, and/or coacervation systems is highly preferred.
Accuracy and neatness of compiling documents.
Attention to detail.

Physical Demands

The physical demands here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently required to sit, use hand and fingers, to manipulate objects, tools, or controls; and reach with hands and arms. The employee is occasionally required to stand, walk, stoop, kneel, crouch, or crawl, and talk or hear.
Specific vision abilities required by this job include close vision, color, peripheral, depth perception and the ability to adjust focus.
Stand, walk, push, pull, twist, reach overhead, and bend to the floor.
Must have ability to wear a respirator in order to work with chemicals of a specified potency level
Occasionally move items or equipment weighing up to 25 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

Attention Job Seekers and Applicants: Please be aware of attempted recruiting scams. While Adare does conduct virtual interviews for some positions, we do NOT use Skype or Google Meet. If you are contacted by someone regarding a job opportunity, please be vigilant in reviewing the details of any and all correspondence. Here are some things to look out for: bad grammar; font inconsistencies or formatting irregularity: logos not properly sized, stretched out, blurred; numerous different font styles and sizes within the content of an email or letter; company impersonators (postings that mirror a reputable company, but there’s no link to the business) mismatched email or website domains, or there is difficulty with locating an address, business phone number, and/or email address, financial requests: Do not provide payment or account credentials as part of the application process. Legitimate companies should not require transfers, checks, gift cards or the wiring of funds as a condition of the application process. Additionally, equipment purchases: be cautious if a company asks you to purchase your own equipment (computers, iPads, mobile phones) and requests you to mail it to their IT department. Applicant Follow-up Questions: Proceed with caution if you receive an application follow-up request that requires you to click on a link to answer additional questions; especially if the questions request personal information such as a social security number. General anonymity: proceed with caution if you can’t quickly verify the identity of the poster.

Apply Now

Refine Your Search

software quality assurance specialist jobs in dayton, oh

Quality Assurance Specialist

Quality Assurance Specialist - 1st Shift

Quality Documentation Specialist

ISD Support* (26.24)

Data Analytics

Data Visualization Specialist

Technical Writer

Coding Compliance Specialist

Data Visualization Specialist* (26.25)

DATA VISULATIONZATION SPECIALIST

Data Visualization Specialist

Customer Service Administrator

Information Technology Specialist AFLCMC/IN-10.21

Information Technology (IT) Specialist

Integrated Master Scheduler

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