Description

Conduct investigations into somewhat complex deviation events for products produced at BIAH. 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, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

Duties & Responsibilities

Performs the investigation of deviations for somewhat complex products manufactured at BIAH to identify the root cause, impact assessment, and CAPA to assess quality requirements to comply with USDA, EU, FDA, or other GMP regulatory requirements and proposes disposition of the product. Participates on investigation related project teams to evaluate events which are investigated. Complete maintenance of systems associated with the investigation function.
Produces the technical investigation report detailing the findings and assessment of the investigation under some direct supervision. Investigation reports and impact assessments are complete and compliant with regulations. Submits data for weekly/monthly KPI reports.
Serve on assigned internal and external project teams (change controls, process improvements, technology transfer, training, business process excellence, electronic system deployment) as a technical/compliance resource to solve quality related issues. Communicates new requirements/performs training with QA Investigation team.
Assist with internal, regulatory or Corporate audits to ensure compliance with domestic and international regulations, quality requirements and guidance documents. Assist with completion of assigned CAPAs by target due dates. Included is the responsibility for making sure QA Investigation areas are 'inspection ready' at all times.
Serves as a technical participant for quality related questions or issues.
Performs all company business in accordance with all regulations (e.g. GMP, USDA, FDA, EU etc.) and Company policy and procedures.
Demonstrated high ethical and professional standards with all business contacts in order to maintain BIAH's excellent reputation in the community. When violations are noted or observed, they are immediately reported to management.

Requirements

A Bachelor's degree, from an accredited institution, in a relevant scientific discipline plus five (5) years relevant experience; Or Master's degree, from an accredited institution, in a relevant scientific discipline plus three (3) years relevant experience; Or PhD, from an accredited institution, in a relevant scientific discipline is required.
Demonstrating technical writing skills to provide complete, timely investigation reports.
Demonstrating logical skills with excellence in written and verbal communication skills.
Demonstrating theoretical and practical knowledge of regulated processes and technical disciplines such as sterilization, aseptic processing, QC testing, quality and compliance, production excellence, and/or maintenance services.
Ability to work out problems utilizing appropriate previously defined techniques.
Demonstrating ability to lead small projects and teams.
Ability to recommend decisions and propose CAPA with some supervision regarding the acceptability of product based on investigation provided.
Excellent attention to detail.
Requires ability to utilize computer programs such as Microsoft suite, SAP, IDEA for CON, Learning One Source,
TrackWise and other relevant electronic applications.
May be required to travel nationally
NOTE: Relevant BIAH experience may be weighted more significantly.
Physical Demands / Surroundings:
Lifting, pushing and pulling and/or carrying <25 pounds occasionally
Constant periods sitting
Frequent standing, walking or climbing stairs.
Crouching/squatting, bending/stooping, twisting, above the shoulder or low level work, fine finger dexterity/ including grasping required occasionally
Writing and typing constantly
Visual / Hearing Demands:
Color vision required.
May require extended hours at a computer screen.
Must be able to read electronic documents of all types.

Eligibility Requirements

Must be legally authorized to work in the United States without restriction.
Must be willing to take a drug test and post-offer physical (if required).
Must be 18 years of age or older.

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