Bristol Myers Squibb Company

Associate CMC Technical Writer

Location
New Brunswick, NJ, United States
Posted
Sep 16, 2020
Ref
R1529613
Required Education
Bachelors Degree
Position Type
Full time

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

About Bristol-Myers Squibb

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.

Position Summary

The Associate Technical Writer, is responsible for preparing CMC elements of regulatory filings under a Technical Writer's guidance and supporting the regulatory activities for pre and post submissions for biologic products.

This role requires effective collaboration across technical functions to deliver on timelines for submissions. The candidate must have a working knowledge of regulatory submissions for pre and post filings. The position routinely interfaces with experts in Process Development, Manufacturing Sciences and Technology, Operations, Analytical Science and Technology, Quality and Regulatory Sciences. The successful candidate will work effectively in cross functional project teams and also independently to accomplish company goals.

Detailed Position Responsibilities

Prepare under supervision CMC elements of regulatory filings.

Supports integrated review process for authored sections. Support the operation of the review process and creates updated draft for next phase review.

Participate in initiatives (creation of templates) involved with regulatory filings.

Support the logistical process for regulatory submissions including pre and post submissions while interfacing across the BMS network as needed.

Assist in the facilitation of authoring, review, verification and submission-ready compliance for the finalization of filings as needed.

Participation on various cross-functional project teams, interactions with Technical Operations and GRS-CMC staff at different BMS sites and other key partners both internal and external to the company are necessary.

Must possess the ability to support multiple projects.

Work in a team environment and foster teambuilding for the improvement of processes and enhancement of productivity to align with key business drivers.

Demonstrate commitment to excellence and bring a high energy level to daily activities as well as involve periods of high intensity work under tight timelines.

Works under supervision and collaborates with other groups.

Desired Experience

BS with 2-5 years of pharmaceutical experience or MS degree. Advanced degree is an asset.

Excellent organizational and communication skills are required along with proficient navigation of electronic systems.

Proven experience with regulatory publishing software is required along with proficiency in compliance ready standards for final publication.

Must have a working knowledge of regulatory submissions for pre and post filings.

Must be capable of working in a fast-paced changing team environment, prioritizing multiple tasks to meet filing deadlines.

Possess strong interpersonal skills and demonstrates ability to effectively interact with business functions.

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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 with the resources to pursue their goals, both at work and in their personal lives.