Boehringer Ingelheim Scientist I, Bio QC in SAINT JOSEPH, Missouri
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.
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 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:
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
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
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
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
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
Uses Word and Excel, QM software for data management (LIMS) and use of MRP inventory software, deviation software (Trackwise), monitoring software (PDCS), and IDEA for Con (Document system) to complete duties
Bachelor’s degree in a relevant scientific discipline required plus two (2) years relevant experience preferred or Master’s degree in a relevant scientific discipline. Associate’s degree plus six (6) years of relevant BIVI experience, or
Ten (10) years of relevant BIVI experience may be substituted for the Bachelor degree requirement
Demonstrated understanding of scientific concepts and principles and complex lab techniques.
Demonstrates ability to manage portions of projects with supervision or minor projects independently.
Performs and documents work following established methods, SOP’s and/or GXP with limited supervision.
Good understanding of applicable regulations.
Comprehensive understanding of processes in immediate area and familiarity of processes in other areas which affect immediate area.
Makes routine decisions with limited guidance from supervisor.
Recognizes and reacts to the significance of data/results.
Able to effectively communicate procedures, thoughts and ideas in a clear concise and appropriate manner.
Communicates with cross-functional groups.
Documents and reviews lab results/data as required by applicable SOP’s and methods.
Organizes data generated for inclusion in reports.
Write and revise SOP’s, methods, and protocols.
Works and interacts mainly within own group to complete tasks assigned.
Able to train others on methods and routine lab work.
Cooperates and shares information with other groups to accomplish goals.
May contribute original suggestions and may act independently to find answers and solutions.
Must be legallyauthorized to work in the United States without restriction.
Must be willing totake a drug test and post-offer physical (if required)
Must be 18 years ofage or older
Boehringer Ingelheim is one of the world’s top 20 pharmaceutical companies and operates globally with approximately 50,000 employees. Since our founding in 1885, the company has remained family-owned and today we are committed to creating value through innovation in three business areas including human pharmaceuticals, animal health and biopharmaceutical contract manufacturing. Since we are privately held, we have the ability to take an innovative, long-term view. Our focus is on scientific discoveries and the introduction of truly novel medicines that improve lives and provide valuable services and support to patients and their families. Employees are challenged to take initiative and achieve outstanding results. Ultimately, our culture and drive allows us to maintain one of the highest levels of excellence in our industry. We are also deeply committed to our communities and our employees create and engage in programs that strengthen the neighborhoods where we live and work. Boehringer Ingelheim, including Boehringer Ingelheim Pharmaceuticals, Inc., Boehringer Ingelheim USA, Boehringer Ingelheim Animal Health USA, Inc., Merial Barceloneta, LLC and Boehringer Ingelheim Fremont, Inc. is an equal opportunity and affirmative action employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender identity or expression; affectional or sexual orientation; disability; veteran or military status, including protected veteran status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
Boehringer Ingelheim is firmly committed to ensuring a safe, healthy, productive and efficient work environment for our employees, partners and customers. As part of that commitment, Boehringer Ingelheim conducts pre-employment verifications and drug screenings.
Title: Scientist I, Bio QC
Location: Americas-United States-MO-Saint Joseph
Requisition ID: 185845