922 matching jobs for “Department Manager I”

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Exact titles rank first, then title variations and keywords in descriptions. These labels aren't qualification scores. Without keywords, recently added jobs appear first.

Bristol-Myers Squibb

Manager I, Global Submission Management - CMC

Warsaw - PL

Full time
Regular

The Manager, Submission Management supports end-to-end regulatory activities for assigned projects, including leading …

Added Oct 15, 2026

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Tyson Foods

Manager Maintenance I- Chicago Bruss, IL

Chicago Plant (Bruss) - Chicago, Illinois

Full time

… administer purchasing and use of all parts and equipment materials and supplies utilized in the maintenance department; ensure refrigeration system and wastewater systems are well maintained and meet all regulatory guidelines; …

Added Oct 27, 2026

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Jabil

Buyer I

Ranjangaon

… over the phone or via e-mail. If you believe you are a victim of identity theft, contact your local police department. Any scam job listings should be reported to whatever website it was posted in. Jabil, including its …

Added Oct 28, 2026

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PulteGroup

Host I

Greenville, South Carolina, United States

Part time
Regular

… career with PulteGroup! JOB SUMMARY: Responsible for providing administrative assistance to Senior Sales Manager and Sales Manager(s). PRIMARY RESPONSIBILITIES - Assist in the daily administration of routine sales …

Added Nov 3, 2026

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Jabil

Planner I

Ranjangaon

… reports to Management . Direct supervisor job title(s) typically include: Planning Supervisor, Planning Manager. · Job is NOT directly responsible for managing other employees (e.g., hiring/termination and/or pay …

Added Oct 28, 2026

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Comfort Systems USA

Field Engineer I

Houston, TX (TAS-Cullen HQ)

Full time
Regular

of the Field Service Technician I is to provide field support to our clients. This includes commissioning, troubleshooting, repair or …

Added Oct 27, 2026

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M&T Bank

Commercial Segment Support Manager I - Treasury Management

Buffalo, New York, United States

Hybrid

Pay posted by employer$89,600–$149,300

Evaluate, inform, continually implement Treasury Management Revenue Strategy, aligning department roles, responsibilities, and driving adoption across organization including Product Penetration, Regional …

Added Nov 3, 2026

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Applied Materials

Manager I, Operations Management - (M1) 2nd Shift

Austin, Texas, United States

Pay posted by employer$60,000–$82,500

… the prevention of employee accidents and injuries. Responsible for ensuring and documenting that all department employees (including temporaries) receive and follow appropriate department training including …

Added Oct 27, 2026

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Thermo Fisher Scientific

QC Scientist I

Loughborough, England, United Kingdom

… is safe or helping find cures for cancer. DESCRIPTION Join us at Thermo Fisher Scientific as a QC Scientist I to contribute to global health through quality control testing that ensures the safety and efficacy of …

Added Oct 16, 2026

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Arrow Electronics

Trade Compliance Coordinator I

Yokohama, Kanagawa, Japan

Full time
Temporary

… within trade compliance software for trade control reasons. When necessary, escalate orders to regional department Manager or Program Manager, or regional department leader for guidance. ● Process global supply chain …

Added Oct 31, 2026

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Capital One Financial

Credit Analyst I

Plano, Texas, United States

… of any credit weaknesses and reporting of any significant deterioration of borrowing relationship to department managers. Performs $1-3MM Loan Interim Reviews and prepares Loan Packages for Annual Reviews. Prepare and …

Added Oct 27, 2026

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Elevance Health

Special Programs Case Manager I (Licensed BH professional)

Norfolk, Virginia, United States +8 locations

Regular

Pay posted by employer$61,028–$96,360

Special Programs Case Manager I Field : This field-based role enables associates to primarily operate in the field, traveling to client …

Added Oct 27, 2026

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Ace Hardware

International Merchant I

Panama City, Panamá, Panama

Regular

… analytical merchant to drive category growth across international markets. The International Merchant I is responsible for developing and executing assortment, pricing, promotional, vendor, and category …

Added Nov 3, 2026

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Centene

Intake Representative I

Remote-NJ

Pay posted by employer$15.87–$27.25 per hour

Position Purpose: The Intake Representative I enters specific data/information from physicians’ requests into a medical management authorization system, …

Added Oct 31, 2026

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Expedia Group

Senior Accountant I

Czech Republic - Prague

Full time

… benefits, and support to do their best work. Join us and build for travelers everywhere. Senior Accountant I Our Corporate Functions are made up of teams that support Expedia Group, including our Global Finance Org., …

Added Oct 27, 2026

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Dover

Controls Engineer I

Rosenberg, Texas, United States

… in the oil & gas industry and work alongside a dedicated team of professionals. The role will report to the Manager, Hardware Engineering and will be based in the Rosenberg, TX office. Responsibilities: • Design custom …

Added Nov 3, 2026

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Jabil

Quality Technician I

Florence, Kentucky, United States

To enhance the capabilities of the QA Department by providing administrative and technical support to the Quality Engineer. ESSENTIAL DUTIES AND …

Added Oct 28, 2026

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PulteGroup

Host I - Wilmington

Wilmington, North Carolina, United States

Full time
Regular

Responsible for providing administrative assistance to Senior Sales Manager and Sales Manager(s). PRIMARY RESPONSIBILITIES - Assist in the daily administration of routine sales …

Added Nov 3, 2026

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Jabil

Inventory Analyst I

Ho Chi Minh City, Ho Chi Minh City (HCMC), Vietnam 2 postings

… classifying, and finding the root causes of inventory inaccuracies. Give feedback and possible solutions to manager for eliminating further discrepancies. ESSENTIAL DUTIES AND RESPONSIBILITIES · Responsible for …

Added Oct 28, 2026

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Henry Schein

Machine Operator I

Savannah - Georgia

In person
Full time
Regular

… of work; notifies quality when inspections are required and reports any scrap parts/pieces. (5%) Notifies manager of any identified issues/errors on processes and/or tools and machines that require repair and/or …

Added Nov 3, 2026

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Bristol-Myers Squibb

Manager I, Global Submission Management - CMC

Warsaw - PL

Full time
Regular

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About this opportunity

Original employer description

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Position Summary

The Manager, Submission Management supports end-to-end regulatory activities for assigned projects, including leading the preparation, compilation, and delivery of compliant US IND, CTA, and marketing application submissions for global health authorities. The role partners closely with Regulatory CMC, Technical Operations, Quality, Manufacturing, and Supply Chain functions to ensure timely development and submission of CMC regulatory content throughout the product lifecycle while supporting continuous improvement initiatives.

Key Responsibilities:

· Collaborate with stakeholders to define eCTD submission strategies and document requirements, ensuring alignment with regulatory standards and project timelines.

· Collaborate with teams to drive the execution of the Global Submission Plan.

· Track and ensure timely progress of submission components to Health Authorities. Apply risk and critical path management practices.

· Execute submission management and publishing activities in the eCTD publishing system for efficient eCTD production and delivery to HA portals.

· Lead/represent team in regulatory/submission meetings driving deliverable and publishing timelines.

· Lead/participate in department initiatives within scope. Develop/update procedural documentation as needed.

· Execute required activities in RIM systems (Veeva RIM) and use available tools to generate reports and track submission content.

· Coordinate non-eCTD submissions with international teams.

· Partner with Regulatory CMC, Manufacturing, Quality, Analytical Development, and Technical Operations teams to plan, coordinate, and track CMC documentation required for global regulatory submissions and health authority interactions.

· Manage the submission readiness of CMC content for INDs, IMPDs, BLAs, NDAs, MAAs, lifecycle management submissions, variations, supplements, and responses to health authority questions.

· Ensure CMC submission components are complete, compliant, and aligned with current global regulatory requirements and company standards.

· Support regulatory assessment of manufacturing changes, process improvements, site transfers, specification updates, and other post-approval CMC changes impacting global submissions.

· Coordinate CMC contribution to health authority requests, deficiency responses, inspections, and agency meeting packages.

Continuous Improvement Initiatives

· Drive initiatives that promote innovation and simplify processes to enhance efficiencies for BMS teams.

· Lead the ongoing maintenance of regulatory requirements to ensure accurate and current regulatory information.

· Ensure cross-functional alignment for IND and marketing applications across projects, studies, and countries, aligning with regulatory standards and best practices.

· Effectively communicate regulatory changes to the business to maintain compliance and support continuous improvement.

· Drive harmonization and standardization of CMC submission planning, content management, and regulatory processes across programs and regions.

· Support implementation and optimization of regulatory technologies, data standards, and digital solutions that improve CMC submission management and compliance.

Experience and skills required:

· BA/BS degree, science/technology field preferred.

· 5+ years relevant submissions experience.

· Proficient knowledge of global regulatory practices, submission guidelines, and requirements; able to identify and resolve issues with support from senior team members.

· Strong analytical and critical thinking skills for solution development, decision-making, and implementation; generates alternative solutions by weighing risks and dependencies.

· Effective communication skills in English (written and oral), including presenting complex information and collaborating with non-English speakers.

· Solid project management abilities: defines objectives, sets priorities, tracks progress, manages resources, and communicates status and risks within project teams.

· Builds collaborative relationships by understanding stakeholder needs, priorities, and processes; drives team communication for successful project delivery.

· Advanced proficiency with desktop software and regulatory systems with the ability to instruct others; understands how non-regulatory systems interact with regulatory systems. Embrace the use of artificial intelligence and automation tools.

· Experience supporting Regulatory CMC activities and managing CMC submission components for development and/or commercial products.

· Understanding of pharmaceutical and/or biologics manufacturing processes, quality systems, lifecycle management, and global CMC regulatory requirements.

· Experience with Module 3 content, CMC document management, and lifecycle submissions in major markets (FDA, EMA, PMDA, Health Canada, and other global health authorities) is preferred.

· Knowledge of manufacturing change management and regulatory impact assessments is highly desirable.

#LI-Hybrid

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:

Warsaw - PL: zł174,980 - zł212,026


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 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. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

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 [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

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

For roles based in Los Angeles County only: 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.

If this posting is missing required information required by local law or incorrect, contact BMS at [email protected] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1601849 : Manager I, Global Submission Management - CMC

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Keywords also found in description

Full time
Permanent
Regulatory Affairs

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