Engineer - External Manufacturing
Bristol-Myers Squibb (Central New Jersey, New Jersey)

This job posting has expired.

You may wish to try a search for ENGINEER - EXTERNAL MANUFACTURING

Or visit the FlipDog home page
 

Job Responsibilities: This position will play a key role in supporting the External Manufacturing Process and maintaining positive and aligned working relationships both internally and with external manufacturers for ConvaTec. Develops formal Project Plans and continuously reviews plan execution against target and manages the ongoing process. Anticipates problems, develops alternatives and keeps all key contributors fully appraised of changes and developments. Must exercise a high degree of adaptability in dealing with an ambiguous and complex work environment, balances multiplicity of demands on role in a responsive, professional manner. Will be require d to facilitate the project development process by providing internal customerswith an understanding of the sites manufacturing capabilities and by formulating plans based on the sites ability or potential to deliver against the required customer demand. Must understand complex technical issues and communicates their impact effectively in understandable terms to the team and management. Proactively identifies key issues and delivers efficient and innovative solutions to overcome project obstacles. Understand the implications of change control in a regulated environment i.e. raw material, packaging, process changes, etc.. Anticipates impact of changes on volume, customer service, price, quality and recommends effective strategies to address the impact of the change. Uses planning toolsas well as professional project management tools and processes to hold a complex project on schedule and coordinate parallel activities. This position will be expected to identify and manage potential roadblocks through ongoing communication with engineers and cross functional team members. On a day to day basis, the Engineer will Provide support to cross functional teams. Review documentation change requirements. Initiate the change evaluation plans. Develop and execute process verification and validation requirements. Job Requirements/Education: Bachelors degree in Engineering field with 3 to 5 years relevant work experience as well as successful track record in working with and supporting cross functional teams. Preferred candidate will have experience in Pharmaceutical, cosmetic, electronic and or medical device processes. Must have demonstrated ability to analyze and interpret complex problems data gathered from a variety of sources and, through effective analysis and communication deliver superior business solutions. Must have prior work experience with demonstrated success working with a range of technically and culturally diverse people, influencing them to get things done, and delivering value added business results that meet high quality requirements within tight deadlines. Must have successful track record of adaptability required to cope within a global change environment as well as firsthand experience of working directly with customers, management, technical experts and professional staff experience in leading a technically complex project. Must be proactive to manage risks and to meet the project schedule. Working knowledge ofMicrosoft Project, Microsoft Office is required. Must be able to demonstrate a thorough understanding of how specific organizational functions contribute to the development, marketing and management of Pharmaceutical, Cosmetic, and MedicalDevice products. These would include Manufacturing, Marketing, Quality Control and Assurance, Validation, Regulatory Affairs, Materials Management, Research and Development and Engineering. Must be conversant in various site technical capabilities and use of basic business support systems, Change Control, QCQA, Regulatory. International travel will be required.
Salary will be commensurate with experience. Bristol-Myers Squibb is an equal opportunity employer. M/F/V/D