Associate, Weigh & Dispense, Supply Services

Description

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 Ingelheims high regard for our employees.

The Associate, Weigh & Dispense, Supply Services performs fundamental unit operations in weigh and related to the manufacturing of bulk drug substance in a multi-product facility. This position performs duties with oversight and according to standard operating procedures.

Duties & Responsibilities

Documents work according to cGMP and cGDP.

Adheres to established regulations and follows cGMP established by site.

Reports abnormalities and deviations in a timely and accurate manner.

Adheres to safety standards and identifies unsafe situations / habits and escalates appropriately.

Maintains production areas according to predefined standards (5s).

Keeps own training on track and trains other technicians and associates on operations.

Contributes to Quality activities as investigations and area walk-throughs.

Executes with oversight of qualified staff: with adequate training non-complex fundamental operations such as weigh and dispense, equipment prep, kits assembly, and staging. Performs internal support duties, including:

Stocking consumables/materials.

Updating controlled SOP binders.

Appropriately discarding expired chemicals.

Recognizing and reporting process and equipment anomalies.

Executes with oversight of qualified staff fundamental tasks such as:

Weigh and Dispense operations.

Schedule adherence.

Associated warehouse operations.

Daily analytics and maintenance of analytical equipment.

Cleaning and setup of equipment.

Requirements

High school degree required, entry level position; Associates/bachelor’s degree or biotechnology vocational training preferred.

One (1) or more years of experience in cGMP regulated industry preferred.

Ability to concentrate on detail-oriented work in a complex technical setup with a Quality and Right the first-time mindset.

Strong written and verbal communication skills.

Ability to work with computer-based systems.

Ability to read and understand SOPs and work instructions and document work in a written format applying cGMP standards.

Ability to work as part of a high performing team and collaborate effectively with staff.

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.

Desired Skills, Experience and Abilities

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.