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Scientist I, Bio Quality Control
Company | Boehringer Ingelheim |
Address | , Gainesville, 30501, Ga |
Employment type | FULL_TIME |
Salary | |
Expires | 2023-07-11 |
Posted at | 1 year ago |
The Scientist I, Bio Quality Control professional performs bio-analytical methods (immunological, in vivo, microbiological, molecular biological, or virological) for various Bio QC tests on raw materials, in-process, release or stability samples in compliance with 9CFR, EU and VICH regulatory guidelines, Outlines of Production and Special Outlines. Initiates, executes, completes, and communicates results and related issues as per validated procedures and within Quality and Compliance guidelines.
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 several 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:
- Skills
- Information/data summarized in concise format
- Demonstrates creativity and contributes original suggestions
- Troubleshoot/Problem solving beyond method defined action
- Locate answers from other areas/consult with other areas
- Seeks development opportunities
- Locate answers from other areas/consult with other areas
- Projects
- In house reagent replacement / validation
- Coordinate projects with supervision
- Coordination of projects within group
- Writes reports and summaries
- Is called upon by other groups in QC for collaboration or SME
- Is called upon by other departments for collaboration or SME
- Coordinate projects with supervision
- Is called upon by other departments for collaboration or SME
- Communicates schedule, test status and concerns
- Prepare reagents and materials
- Plans activities and structures work for others
- Coordinates and participates in assay validation
- Support
- Plans activities and structures work for others
- Prepares work schedule for self
- Uses data analysis to make decisions and recommendations
- Coordinates and participates in assay validation
- Seeks development opportunities
- Troubleshoot/Problem solving beyond method defined action
- Revise a Pre-existing Standard Methods and SOPs
- Demonstrates creativity and contributes original suggestions
- Trains others on methods & procedures
- Create New Standard Methods, SOPs, Protocols
- Is called upon by other groups in QC for collaboration or SME
- Maintains laboratory reagents, supplies and calibrated equipment
- Coordination of projects within group
- Writes reports and summaries
- Prepares work schedule for self
- Write Laboratory Investigations, as needed.
- Calculates results
- Review and approve results and test sheets
- Uses data analysis to make decisions and recommendations
- Perform testing using a significant portion of the existing laboratory assays
- Perform testing using a portion of the existing laboratory assays
- In house reagent replacement / validation
- Information/data summarized in concise format
- Testing
- Perform testing using a portion of the existing laboratory assays
- Perform testing using a significant portion of the existing laboratory assays
- Maintains laboratory reagents, supplies and calibrated equipment
- Prepare reagents and materials
- Calculates results
- Communicates schedule, test status and concerns
- Write Laboratory Investigations, as needed.
- Review and approve results and test sheets
- Revise a Pre-existing Standard Methods and SOPs
- Create New Standard Methods, SOPs, Protocols
- Trains others on methods & procedures
Requirements:
- In lieu of degree, a High School Diploma or GED + 6 years of scientific concepts, principals and/or lap technique experience in cGMP or similar environment, required.
- Bachelor's degree in Biology or relevant scientific discipline, required + 2 years of scientific concepts, principals and/or lab technique experience in a cGMP or similar environment, required OR
- Associate's degree + 4 years of scientific concepts, principals and/or lab technique experience in a cGMP or similar environment, required OR
Eligibility Requirements:
- Must be willing to take a drug test and post-offer physical (if required).
- Must be 18 years of age or older.
- Must be legally authorized to work in the United States without restriction.
Who We Are:
At Boehringer Ingelheim we create value through innovation with one clear goal: to improve the lives of patients. We develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family-owned company, we focus on long term performance. We are powered by 50.000 employees globally who nurture a diverse, collaborative, and inclusive culture. Learning and development for all employees is key because your growth is our growth.
Want to learn more? Visit boehringer-ingelheim.com and join us in our effort to make more health.
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.
Job - Quality/Compliance
Primary Location - Americas-US-GA-Gainesville
Organization - US-Boehringer Ingelheim Animal Health
Schedule - Full-time
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