Quality Assurance Specialist
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 a Quality Assurance Specialist to join our Quality Assurance Team …
If any of the below describes you, we would love to meet you!
JOB SUMMARY
This position 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 ensuring adherence to cGMP.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
* Audit Analytical testing and executed Batch Production Records.
* Review and approve Deviations and Lab Investigations.
* Coordinate and support Quality Assurance aspects of Product Development and Contract Manufacturing activities.
* Perform cleaning verification visuals and swabs.
* Release in-process materials for further processing and finished products for shipment.
* Interact with Customer’s Quality associates as necessary.
* Maintain and assure correctness of documentation.
* Interface with all departments within the company.
* Ensure facility adherence to cGMP.
* Maintain the confidentiality of pertinent information.
* 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.
* Attends work on a regular and predictable basis.
* Completes assigned tasks in a safe manner and in a constant state of alertness.
* Upholds Company policies, including the Professional Conduct Policy and Prohibition Against Harassment Policy, and the Business Ethics and Conduct Code.
* Works in a cooperative manner with managers, supervisors, coworkers, customers and the public.
* Works effectively under deadlines.
* Perform other tasks as required.
REQUIRED SKILLS AND QUALIFICATIONS
* Bachelor’s Degree preferred, wit...
- Rate: Not Specified
- Location: Vandalia, US-OH
- Type: Permanent
- Industry: Engineering
- Recruiter: Adare Pharmaceuticals
- Contact: Not Specified
- Email: to view click here
- Reference: DF222
- Posted: 2025-07-16 08:33:35 -
- View all Jobs from Adare Pharmaceuticals
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