Talent.com
ASSOCIATE DIRECTOR, GMS STABILITY
ASSOCIATE DIRECTOR, GMS STABILITYBristol Myers Squibb • New Brunswick, NJ, US
ASSOCIATE DIRECTOR, GMS STABILITY

ASSOCIATE DIRECTOR, GMS STABILITY

Bristol Myers Squibb • New Brunswick, NJ, US
11 hours ago
Job type
  • Full-time
Job description

Associate Director Stability

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

The Associate Director Stability is responsible for stability product strategy and oversight of product stability programs for commercial large molecules Drug Substances and Drug Products. Activities include those associated with product stability strategy, stability program requirements, stability sample management, preparation, review and approval of stability reports and regulatory filings.

The Associate Director is responsible for leading high-performance technical team, developing team and fostering company culture.

Responsibilities

  • The Associate Director Stability is accountable for the stability commercial program for large molecules Drug Substances and Drug Products.
  • Accountable for new products commercialization and providing support to the sites or external manufacturing for new products commercialization.
  • Serves as stability representative on project teams covering post-approval changes, designs and executes required premarket stability program in support of the change.
  • Accountable for the handling of annual commercial stability program for assigned products in coordination with sample management group.
  • Provides technical expertise to the stability team.
  • Provides support for authoring stability sections of filling dossiers for post-approval filings, and stability related responses to health authority inquiries.
  • Approves the stability sections of filling dossiers, annual reports, product renewals, Annual Product Stability Reviews.
  • Provide support for OOT / OOS investigations, Market Action Fact Finding, and other investigations related to potential quality issues or capacity issues.
  • Accountable for stability procedures and ensures consistency with site department and BMS groups procedures.
  • Leads OpEx initiatives to streamline and standardize management of stability programs.
  • Supports health authorities' inspection internal and external.

Leadership skills :

  • Leads the team and focus on the pipeline complexities to achieve milestones and objectives, while providing technical oversight, mentorship, and coaching.
  • Leads with a global mind-set to direct and influence multiple remote teams
  • Drives sense of team responsibility for group's success, promoting a high commitment to business goals and objectives
  • Accountable for stability resources definition and budget.
  • Fosters a culture focused on demonstrating high capacity for executing with company values and behaviors.
  • Provides continuing development opportunities, including ongoing performance assessments
  • Qualification :

  • 10 years of relevant work experience required, preferably in a pharmaceutical environment.
  • 2 years' experience as team manager.
  • Expert knowledge and understanding of stability ICH Guidelines (Q1A, Q5C) and associated policies, directives and guidance documents. A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs in a pharmaceutical manufacturing facility.
  • Expert Knowledge of US / EU / ROW Requirements, Corporate Directives and industry best practices.
  • Expert Knowledge of Drug Substance and Drug Product manufacturing and good understanding of analytical and / or Microbiology methods.
  • Significant Experience with authorship and able to critically review investigations, interpret results, and generate technical conclusions consistent with Quality management principles.
  • Excellent skills to drive development of technical or scientific initiatives for solving complex problems / issues, recommending and drive science-based decisions / implementation of solutions.
  • Significant experience on health authorities' inspections in front room.
  • Excellent written and verbal communication skills.
  • Leadership experience : Team, conflict management, coaching others, talent selection, developing others, decision-making, building relationships, innovation management, and resource allocation.
  • Advanced knowledge of Microsoft office applications, LIMS, Quality Management system (e.g. TrackWise or Veeva), Statistics software (e.g. SlimSTAT, JMP).
  • #LI-ONSITE
  • Compensation Overview : Devens - MA - US : $168,930 - $204,702 New Brunswick - NJ - US : $157,880 - $191,312 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following : Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility / infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.

    Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

    On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role : Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

    Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations / adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation / adjustment prior to accepting a job offer. If you require reasonable accommodations / adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com / eeo-accessibility to access our complete Equal Employment Opportunity statement.

    Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

    If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information : https : / / careers.bms.com / california-residents / .

    Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https : / / careers.bms.com / fraud-protection

    Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

    Create a job alert for this search

    Associate Director • New Brunswick, NJ, US

    Related jobs
    Athletic Director

    Athletic Director

    InsideHigherEd • Branchburg, New Jersey, United States
    Full-time
    Administrative and Professional.About Raritan Valley Community College : .New Jersey, Raritan Valley Community College has been serving as an academic and cultural center for Somerset and Hunterdon C...Show more
    Last updated: 25 days ago • Promoted
    Associate Director, Rare Hematology, US Patient Advocacy

    Associate Director, Rare Hematology, US Patient Advocacy

    Novartis Group Companies • East Hanover, NJ, United States
    Full-time
    The Associate Director, Rare Hematology, US Patient Advocacy collaborates with relevant malignant and non-malignant Hematology and focused rare patient communities to understand unmet needs that in...Show more
    Last updated: 30+ days ago • Promoted
    Associate-Director, Human Factors and Usability Engineering

    Associate-Director, Human Factors and Usability Engineering

    Sanofi • Morristown, NJ, United States
    Full-time
    Associate-Director, Human Factors and Usability Engineering.With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their famili...Show more
    Last updated: 30+ days ago • Promoted
    Associate Director, Marketing - Care Pathway Education T1D

    Associate Director, Marketing - Care Pathway Education T1D

    Sanofi • Morristown, NJ, United States
    Full-time
    Associate Director, Marketing - Care Pathway Education T1D.Associate Director, Marketing - Care Pathway Education T1D.Type 1 Diabetes (T1D) early detection and intervention.TZIELD marketing team, t...Show more
    Last updated: 30+ days ago • Promoted
    Special Education Coordinator

    Special Education Coordinator

    Uncommon Schools • Florence, NJ, US
    Full-time
    Uncommon Schools is a nonprofit network of high-performing public charter schools dedicated to providing an exceptional K-12 education in economically disadvantaged communities.Operating in Boston,...Show more
    Last updated: 6 days ago • Promoted
    Associate Director, Programmatic (NY, 20974)

    Associate Director, Programmatic (NY, 20974)

    IPG Mediabrands • New York, NY, United States
    Full-time
    KINESSO is the technology-driven performance marketing agency that sits at the very heart of IPG Mediabrands, providing actionable growth for both our agency partners and clients.We turn 'action' i...Show more
    Last updated: 30+ days ago • Promoted
    Director / Associate Director Finance (GTN)

    Director / Associate Director Finance (GTN)

    AdvaGen Pharma • East Windsor, NJ, United States
    Full-time
    Director / Associate Director Gross to Net, Finance.Ensure proper recording and reporting of all components of Net Sales for Generic and Branded business units. This includes Chargebacks, Rebates, Cu...Show more
    Last updated: 4 days ago • Promoted
    ASSOCIATE MEDICAL DIRECTOR

    ASSOCIATE MEDICAL DIRECTOR

    The Institute for Family Health • New York, NY, United States
    Full-time
    Walton Family Health Center and Center for Counseling - Bronx, NY.Responsible for the overall clinical management of the practice and program assigned to the practice as above, including direct sup...Show more
    Last updated: 30+ days ago • Promoted
    Director, Acct Mgmt & Pricing Strategy -Remote

    Director, Acct Mgmt & Pricing Strategy -Remote

    Novartis Group Companies • East Hanover, NJ, United States
    Remote
    Full-time
    This position can be based remotely anywhere in the U.Please note that this role would not provide relocation as a result. The expectation of working hours and travel (domestic and / or international)...Show more
    Last updated: 5 days ago • Promoted
    Director, Division of Infectious Diseases

    Director, Division of Infectious Diseases

    Hackensack Meridian Health • Neptune Township, US
    Full-time +1
    Director, Division of Infectious Diseases.Jersey Shore University Medical Center.Hackensack Meridian Health – Neptune, New Jersey. Hackensack Meridian Health is seeking a Director, Division of...Show more
    Last updated: 30+ days ago • Promoted
    Cardiology Business Manager

    Cardiology Business Manager

    Deborah Heart and Lung Center • Browns Mills, NJ, US
    Full-time
    Job Details Description Position Summary : The Cardiology Business Manager is responsible for the daily business, data, and financial operations of the cardiology product line.This manager-level lea...Show more
    Last updated: 23 hours ago • Promoted
    Director, Global Trial Lead

    Director, Global Trial Lead

    Bristol Myers Squibb • Princeton, NJ, US
    Full-time
    Director, Global Trial Lead (Gtl).Those aren't words that are usually associated with a job.But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every d...Show more
    Last updated: 11 hours ago • Promoted • New!
    Associate Director, Launch Project Management

    Associate Director, Launch Project Management

    Sandoz Inc. • Princeton, NJ, United States
    Full-time
    The Associate Director, Launch Project Management leads and executes launch activities to bring Generics and Biosimilars products to market on time, with defined launch quantities and a coordinated...Show more
    Last updated: 1 day ago • Promoted
    Associate Vice President of Technology Services

    Associate Vice President of Technology Services

    InsideHigherEd • Branchburg, New Jersey, United States
    Full-time
    About Raritan Valley Community College : .New Jersey, Raritan Valley Community College has been serving as an academic and cultural center for Somerset and Hunterdon County residents for over 50 year...Show more
    Last updated: 30+ days ago • Promoted
    Associate Director, Growth Analytics

    Associate Director, Growth Analytics

    IPG Mediabrands • New York, NY, United States
    Full-time
    IPG Mediabrands is the media and marketing solutions division of Interpublic Group (NYSE : IPG).Mediabrands Content Studio, Orion Holdings, Rapport, and the IPG Media Lab. IPG Mediabrands clients inc...Show more
    Last updated: 30+ days ago • Promoted
    Associate Director, Specialty Contracting

    Associate Director, Specialty Contracting

    Sandoz Inc. • Princeton, NJ, United States
    Full-time
    Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambi...Show more
    Last updated: 30+ days ago • Promoted
    Asset Management Associate

    Asset Management Associate

    B&D Holdings • Warren, NJ, United States
    Full-time
    Asset Management Associate – Industrial, B&D Holdings.Mountain Boulevard, Suite 201, Warren, NJ (On-Site).B&D Holdings, a fast-growing national real estate investment and development firm, is expan...Show more
    Last updated: 30+ days ago • Promoted
    Associate Director of Quality Control

    Associate Director of Quality Control

    Evergreen Theragnostics • Springfield, NJ, United States
    Full-time
    Evergreen Theragnostics is a Lantheus owned company, headquartered in Bedford, Massachusetts with offices in Springfield, New Jersey. Evergreen Theragnostics is an entrepreneurial, agile, growing or...Show more
    Last updated: 30+ days ago • Promoted