Senior Technician, Quality Systems & Compliance

Job Description

For over 130 years, we have pioneered groundbreaking science.  Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology.  Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way.

Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence.  Because when it comes to animal health, no one sees it like we do.

The candidate will audit/inspect/release all incoming company Animal Health pharmaceuticals, third party pharmaceuticals, medical devices, third party biologic and diluents as required. This will include Batch Record reviews per cGMP as required. Manage short-dated inventory. Final compliant stock will be released for Distribution. Maintain completed inspection files.

Adherence to medical product Cold Chain requirements will be addressed buy this candidate via on-line data downloading.

The candidate will be responsible to perform physical inspections of incoming finished products, and approved artwork per AQL (Acceptable Quality Level) inspections.

Manage site Notification of Events (NOE) and Product Quality Complaints within the company's Reliance system, as required.  Perform NOE follow-up and completion through investigations, Corrective Actions, Preventative Actions, etc., as applicable.  Assist in self-inspection audits for the Omaha Distribution Center. 

The candidate Must have experience with cGMP/GDPs and have understand Data Integrity requirements. 

Other Quality Assurance duties and projects will be assigned as applicable.

Required Education:

• High school diploma required.
• BS or BA degree in Biology or related science highly preferred.

Required Experience and Skills:

• Two (2)+ years of Quality Assurance / Quality Control experience.
• Basic knowledge of USDA, FDA, DEA, and /or EPA requirements.
• Must have good planning and organization skills to handle multiple projects.
• Strong communications skills.
• Technical writing skills.
• Ability to assume technical responsibilities with minimum supervision.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

#MSJR

Required Skills:

Aseptic Manufacturing, Aseptic Manufacturing, Biological Sciences, Biopharmaceuticals, Consulting, Corrective Action Management, Data Integrity, FDA Compliance, FDA Regulations, Inventory Management, Manufacturing Audits, Materials Inspection, Medical Device Management, Medical Devices, Microbiology, Operational Quality, Pilot Plant Operations, Preventive Action, Process Improvements, Project Management, Quality Assurance Processes, Quality Improvement Programs, Quality Management Systems (QMS), Quality Process Development, Quality Standards {+ 1 more}

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.  As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.  For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

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