Associate Director- Process & Procedures Operations Lead, GCO
- Employer
- Regeneron Pharmaceuticals, Inc.
- Location
- Tarrytown, NY, United States
- Start date
- Sep 17, 2019
View more
- Discipline
- Engineering, Manufacturing & Production, Process
- Required Education
- Bachelors Degree
- Position Type
- Full time
- Hotbed
- Pharm Country, Best Places to Work
Job Details
Summary:
The Global Development Process & Procedures (P&P) Operations Lead is directly responsible for driving the operations of the development and management of streamlined, procedural documents (Standard Operating Procedures (SOP), Work Instruction (WI), Guideline Document (GD), Job Aids, Forms and Templates) portfolio.
Responsibilities:
• Accountable for the delivery of quality procedural documents to functional areas/stakeholders
• Oversee and manage the day-to-day operations of P&P Operation Managers to ensure adherence to standards and compliance for creating, updating and retiring procedural documents
• Contribute to continuous improvements in standards (content and style) and procedural document templates in partnership with P&P Quality Lead
• Analyze impact assessments for new and revised procedural document requests
• Liaise with P&P Quality to ensure procedural document quality checks are performed in the agreed timeframe
• Collaborate with P&P Quality Lead to identify trends in metric reports and provide recommendations for continuous improvements to further strengthen procedural document development methods
• Maintain the master Global Development procedural document portfolio
• Collaborate with P&P Business Partners for prioritization and forecasting workload
• Manage and maintain electronic document management system (EDMS) including workflows, folder structure, etc. and interact with system owners as needed
• Liaise with P&P Quality and oversee the preparation of documents for inspection requests (SOP lists, etc.)
• Liaise with P&P Quality Lead to support internal Quality Auditing & Assurance Corrective Actions/Preventive Actions (CAPAs) that result in procedural document changes
• Liaise with GCP Quality Improvement Representatives to identify trends for open process deviations
Supervisory Responsibilities:
• Manages several direct reports
Requirements:
BS/BA Degree with 10+ years relevant experience. MS degree and 8+ years relevant experience.
• A minimum of 10 years' experience in a global regulated organization
• A minimum of 8 years' experience in a quality role with experience in controlled procedural document principles, process design and styles, and leading process improvements
• A minimum of 5 years' experience in Line Management including experience in mentoring and coaching direct reports
• In-depth knowledge of GCP and regulatory requirements
• Strong leadership with demonstrated ability to interact with all levels of the organization
• Demonstrated success in managing teams and projects by maintaining a high level of productivity and quality work products
• Demonstrated success in project management, stakeholder management, collaboration and negotiation of complex situations
• Self-motivated with the ability to work effectively in a dynamic environment
• Excellent problem solving, written and verbal communication skills
• Negotiates complex situations without direct authority
• Advanced technical skills: Word, Excel, Visio, electronic document management system
• Ability to effectively manage multiple priorities with a sense of urgency
• Provides close attention to detail and accuracy of work
Core Behavioral Competencies:
• Leadership
• Executive Presence
• Stakeholder Management
• Project Management
• Process Management
• Line Management
• Strategic Thinking
• Critical Thinking & Problem Solving
• Integrity and Trust
• Negotiating
• Organizational & Political Savvy
• Dealing with ambiguity & paradox
This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.
To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.
Company
Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to seven FDA-approved treatments and numerous product candidates in development, all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye disease, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, infectious diseases, pain and rare diseases.
Regeneron is accelerating and improving the traditional drug development process through our proprietary VelociSuite® technologies, such as VelocImmune® which produces optimized fully-human antibodies, and ambitious research initiatives such as the Regeneron Genetics Center, which is conducting one of the largest genetics sequencing efforts in the world.
Stock Symbol: REGN
Stock Exchange: NASDAQ
- Website
- https://www.regeneron.com/
- Phone
- 914-847-7000
- Location
-
Corporate Headquarters
777 Old Saw Mill River Road
Tarrytown
New York
10591
United States
Get job alerts
Create a job alert and receive personalized job recommendations straight to your inbox.
Create alert