
Principal Specialist, Quality Systems, Product Summary Reports
Athens, GAContract / Full-time / TemporarySeen todaySeen in employer's feed today
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At a glance
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Requirements
Credentials this posting asks for.
Job overview
The Principal Specialist is responsible for annual product reviews, data trend analysis, product quality complaint and logistic deviation systems, and site corrective and preventive action plans. The role also supports audits, leads projects, completes investigations, and develops KPIs and monthly reports. It is a 12-month BI contract role, scheduled full-time and on-site.
Skills & qualifications
Skills
Qualifications
Full job description
Description
The position is responsible for preparation and managing the the annual product reviews quality system. This individual will prepare and/or evaluate data for trends associated to the annual product reviews. This position is also responsible for managing the product quality complaint quality system and investigating product quality complaints and logistic deviations. The position is also responsible for approving all site Corrective Action ' Preventative Action plans, and compiling KPIs for site management. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
This is a BI Contract role effective for 12 months - December 2026 - December 2027
Duties & Responsibilities
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Independently prepares the annual product reviews and data trend analysis. Ensures all other areas that contribute to the annual product review process provides the required data prior to the due date.
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Assist with internal, regulatory or Corporate audits to ensure compliance with domestic and international regulations, quality requirements and guidance documents.
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Lead projects and ensure department and individual priorities are aligned with corporate, operational and functional priorities.
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Track and complete product quality complaints and logistic deviations in the electronic system. Complete assigned complaint investigations and logistic investigations by due date.
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Responsible for managing the quality system for annual product reviews, product quality complaints, and logistic deviations.
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Development and maintenance of KPIs and applicable monthly reports; manage continuous process improvement initiatives.
Requirements
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Minimum of a Bachelor's degree from an accredited institution in a relevant scientific field with eight-plus (8+) years of GxP experience
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Work experience in a regulated GxP industry required.
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In depth understanding of regulatory and corporate requirements, cGMPs, technical writing and root cause analysis.
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Influencing the understanding of cGMP's, compliance requirements, and regulatory requirements to assess product, procedures, recommended improvements to make quality decisions.
Eligibility Requirements
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Must be legally authorized to work in the United States without restriction.
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Must be willing to take a drug test and post-offer physical (if required).
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Must be 18 years of age or older.
JOB ID
38485
Job function
Quality
Career level
Experienced professionals
Organization
Boehringer Ingelheim Animal Health USA
Working time
Full-Time
Job flexibility
On-Site
Boehringer Ingelheim is an equal opportunity global employer who takes pride in maintaining a diverse and inclusive culture. We embrace diversity of perspectives and strive for an inclusive environment, which benefits our employees, patients, and communities. All qualified applicants will receive consideration for employment without regard to a person’s actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law
How this job compares
Set against the 5,050 open Quality Assurance jobs on Olive Jobs, counted November 3, 2026.
- Pay
- This postingNot listed
- Georgia median$77–140K/yr56 salary ranges
- US median$26–31/hr825 hourly ranges
- Openings
- Olive Jobs lists 121 open Quality Assurance jobs in Georgia and 5,050 across the US. 3% of them nationwide are listed as remote or flexible.
- Hiring the most in Georgia
- CDM Smith5 open
- PwC5 open
- Lockheed Martin4 open
- Experience
- This posting asks for at least 8 years of experience — more than three in four Quality Assurance postings that state a minimum ask for (median 5 years, across 3,868 postings).
- Education
- This posting asks for a bachelor's degree; 1,735 of the 5,050 open Quality Assurance jobs (34%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 3, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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