Procedural Document Assoc Manager

Profile

Job Information

Bristol Myers Squibb

Procedural Document Assoc Manager

in

New Brunswick

New Jersey

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Support the Operational Controls document management business unit for the Quality Management System (QMS) process framework (GMP/GDP). This includes, but are not limited to: manage procedural document change requests, collect and share best practices through direct communications and communities of practice, send document change notifications, SME in electronic document management systems.

This position is responsible for supporting the document management process within operational controls including: Qualification & Validation, Facilities Design & Maintenance, Vendor & Materials Management, Production & Disposition, and Product Distribution.

Responsible to create a process to track new or existing procedural document change requests.

Ensure document timelines adhere to established schedule and communicate status.

Schedule and facilitiate the community of practice forums, prepare material and share best practices and project updates.

Create and maintain department Sharepoint site.

Collect metrics to identify trends and take appropriate action.

Support document managers with authoring, coordination of review and comments resolution, approval, issuance, implementation, periodic review, and retirement, as needed.

Responsible for assisting with compliance assessment of procedural documents against evolving global health authority regulations and health authority inspection observations.

Maintain a contemporary knowledge of current industry trends, standards and methodologies as it relates to quality systems and management.

Support Global Product Development & Supply organization as the SME for BMS electronic document management system.

Support strategic initiatives and continuous improvement projects related to QMS

Synthesize feedback from SMEs/procedural document teams to identify and resolve issues in order to accurately document current and future processes

Proactively use judgment to manage risk and uncertainty, and to anticipate the need for and implement contingency plans

Effectively manage projects, escalate issues as necessary and identify/meet key milestones

Work with limited guidance and seek input as needed

Team leadership skills that contribute to meeting team goals and resolving complex issues

Exercise sound judgment, using a risk-based approach, to ensure compliance with procedural document regulations, practices, and policies

Education:

Minimum of a Bachelor’s degree

3 years experience in the Biopharm/Pharmaceutical industry with cross-functional experience in one or more areas (i.e. research, analytical, quality, engineering, manufacturing, regulatory CMC, or IT)

Experience with demonstrated leadership in quality and/or compliance discipline with in-depth knowledge of cGMP requirements and global health authorities’ regulations

Experience/Knowledge:

In depth knowledge of cGMP requirements and global health authority regulations with ability to interpret, apply and implement.

Demonstrated ability to successfully manage competing deadlines and balance priorities while meeting or exceeding expectations

Strong negotiating and influencing skills in a matrixed organization.

Ability to drive consensus, performance and to lead strategically

High level of competency in procedural document writing including the appropriate use of grammar, syntax and organization of ideas

Ability to build teams, foster partnerships across multidisciplinary teams and to resolve complex issues and differences in a creative, constructive and diplomatic manner

Demonstrated ability to work independently and mentor team members

Ability to identify, manage, and/or escalate issues and risks to timelines

Skills/Competencies:

Proficient in MS Office and Collaboration applications.

Experience with electronic documentation management systems.

Project management concepts, strategies and skills

Strong verbal and written communication skills

Critical thinking skills in analyzing and exercising judgment on complex issues, guided by a thorough understanding of quality philosophy.

Excellent technical writing skills.

Proven ability to understand complex processes/problems and propose alternate solutions to implement global procedures requires critical thinking and analysis skills

Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Company info

Bristol-Myers Squibb Company
Website : http://www.bms.com