BD (Becton, Dickinson and Company) R&D Manager in New Hope, Minnesota
Category: R&D Manager
Job ID: 2018-11355
Career Level: experienced
Relocation: No relotation provided
Location: New Hope,Minnesota,United States
Summary of Position with General Responsibilities:
The individual in this position is responsible for the coordination of department and division activities during the product development process and management of assigned departmental personnel.
Essential job Functions:
Coordinates and/or directs all aspects of product development activity related to a product line.
Coordinates product development activities of R&D/Product Development teams, including integration of RA, QA/QE, Operations, Clinical, Marketing, Sales and Packaging Engineering for a product line.
Participates as team leader or as an active member of the team to meet company objectives and ensure department responsibilities are completed.
Assesses priorities and makes assignments to direct reports to ensure project and company priorities are met.
Performs supervisory responsibilities for direct reports, including but not limited to, performance reviews, recommending salaries and promotions, training, interviewing and hiring decisions and disciplinary actions.
Identifies development needs and potentials of employees, and provides or recommends project assignments and training to increase expertise to meet current or future division needs.
Provides technical support and feedback for direct reports.
Coordinates with team members, internal and external suppliers and outside professionals to ensure project output meet users’ needs as well as applicable regulatory requirements.
Actively participates in training and providing input to training of employees on division procedures and policies.
Creates, tracks and meets project schedules, plans and budgets.
Reviews and analyzes costs in order to identify and implement cost improvements.
Provides input, feedback and maintenance for department and division procedures and policies.
Complies with company procedures and policies, government regulations.
Experience with balloon catheters, stents and stent delivery systems preferred
Experience in process validation (IQ, OQ and PQ), including writing protocols and reports to support verification and validation activities for product commercialization
Experience in drug coating, active pharmaceutical ingredient handling, and working in controlled environment
Knowledge of cGMP and GLP is a plus.
US FDA QSR and ISO 13485 requirements for design controls
Strong skills in communicating with all levels of technical and operating management.
Demonstrated positive communication and human relation skills.
Strong ability to analyze and use technical data and resources.#LI-NL1
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status