1,000+ matching jobs for “Shift Manager Operations”

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Senior Manager, New Product Introduction Operations

Tlaquepaque, Jalisco, Mexico

Full time
Reg Employee

The Senior Manager, NPI Operations ensures HP’s creative and marketing engine runs smoothly at scale. You’ll lead and grow the …

Added Oct 12, 2026

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Defective Operations and Cost Optimization Manager

Singapore, Singapore

Full time
Reg Employee

This role manages end‑to‑end local defective return operations, ensuring adherence to defined processes, performance metrics, and cost and recovery targets. Acting as the …

Added Oct 12, 2026

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Ferguson Enterprises

Distribution Center Shipping Manager - 2nd Shift

Chandler, Arizona, United States

Full time
Regular

Pay posted by employer$4,331.70–$9,529.30

… and ensure all safety and regulatory compliance in a proactive and positive manner Lead all aspects of shift operations to include selection, shipping, receiving, cross docking and trailer loading operations …

Added Oct 27, 2026

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IQVIA Holdings

Clinical Trial Material Manager (2nd Shift)

Marietta, Georgia, United States

Pay posted by employer$77,700–$161,800

The Clinical Trial Material Manager leads daily second-shift (2:00 PM to 11:00 PM) manufacturing operations in a regulated, high-volume …

Added Oct 15, 2026

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Walmart

2nd Shift Manager, Production Systems, NSO

(USA) AR ROGERS 05169 WM ON CAMPUS/RX FACILITIES

Pay posted by employer$76,000–$114,000 per year

... As a 2nd Shift Production Systems Manager, you’ll plan and schedule daily production to ensure safe, productive, and …

Added Oct 27, 2026

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Abbott Laboratories

Senior Manager, TPM Manufacturing and Operations

New Brighton, Minnesota, United States

Pay posted by employer$129,300–$258,700

… to work for diversity, working mothers, female executives, and scientists. MAIN PURPOSE OF ROLE The Senior Manager, Third-Party Manufacturing – Process Development and Operations is responsible for leading a team of …

Added Oct 15, 2026

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Xcel Energy

Operations Instructor/Sr. Operations Instructor

Monticello, MN, 55362

Full time
Regular

Pay posted by employer$84,900–$138,600 per year

below and responsibilities reflect the Operations Instructor level role. The successfully chosen candidate will be placed at a level that is commensurate …

Added Oct 27, 2026

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Abbott Laboratories

Manager Clinical Site Operations, Site ICRA

Maple Grove, Minnesota, United States +1 location

Pay posted by employer$99,300–$198,700

… CA locations. This position is responsible for the supervision of a team of personnel within Clinical Site Operations (CSO) which supports US, Canada, and LATAM. Assists management in hiring, training, developing, and …

Added Oct 23, 2026

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State Street

Claude Support Operations Lead - Senior Manager

Bengaluru, India +1 location

Full time

… SOPs, runbooks, escalation matrices, and support readiness controls. Lead workforce planning, shift coverage strategy, and resource forecasting. Support business continuity, resiliency, and disaster recovery …

Added Oct 27, 2026

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Block

Senior Manager, GTM Strategy & Operations, Square

Bay Area, CA, United States of America

Remote
Regular
Senior

As the Senior Manager, GTM Strategy & Operations, you'll be a strategic partner to Square's Revenue leaders and own the most …

Added Oct 4, 2026

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Merck (MSD)

Operations Intern

Singapore, Singapore

… operational decisions that optimize supply chain and financial targets. -Supports and provide guidance to shift personnel to deliver excellent operational results in a highly regulated, fast-paced API production …

Added Oct 16, 2026

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Workday

Senior Technical Account Manager (APJ Shift)

IND.Pune

Flex
Full time

Workday Support is looking for a dedicated, ambitious and self-driven Technical Account Manager with a passion for customer relations. This role requires a self-motivated professional with technical …

Added Oct 27, 2026

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Bank of America

Senior Operations Manager | BPRO Financial Transaction Review

Pennington

Pay posted by employer$72,100–$109,200

… This job is responsible for managing a unit for a site, region, or product line within the bank's internal operations. Key responsibilities include identifying, analyzing, and resolving highly complex problems, ensuring …

Added Oct 27, 2026

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Cencora

Operations Supervisor

Munich, Bavaria, Germany

Full time

… World Courier business. In our brand-new Kirchheim branch, we are looking for a Supervisor on our dedicated Operations team. You will supervise operational activities in accordance with corporate policies and procedures and …

Added Oct 27, 2026

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Bank of America

Global Credit Operations- Change & Transformation Program Manager

Charlotte, North Carolina, United States +2 locations

… programs impacting people, process, and technology changes. Key responsibilities include working with Operations and Technology leaders to develop a plan to implement sustainable change and monitor the execution to …

Added Oct 31, 2026

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Merck (MSD)

Tech, Operations

Singapore, Singapore

JOB PURPOSE Perform manufacturing operations per production schedule in compliance with cGMP and achieve the operational objectives. Meet Site's safety, …

Added Oct 16, 2026

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Supply Chain Business Operations Manager (Chonburi Based)

T.Nongchak A.Ban Bueng, Chon Buri, Thailand

Full time
Reg Employee

… of complex supply chain processes, such as inventory analysis and planning, demand planning, import/export operations, and sales and operations planning (SOP). Identifies opportunities for process improvement and …

Added Oct 26, 2026

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Bank of America

Senior Technology Manager Global Data-Network Operations

Chandler, Arizona, United States +1 location

… fostering leadership skills, and managing stakeholders. Position Summary: The global head of data network operations is a senior technology management role responsible for the strategy, governance and day-to-day reliability …

Added Oct 27, 2026

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Sonoco Products

Shift Supervisor

Holyoke, Massachusetts, United States

In person
Full time
Regular

Pay posted by employer$105,520–$118,710 per year

… brilliant solutions every year. Today we are a world leader in global packaging solutions with diversified operations in over 34 countries. We're extremely proud of our portfolio of brands, our achievements in sustainability …

Added Oct 27, 2026

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Live Nation Entertainment

LN Venues, Operations Manager - Punch Line Irving

Irving, Texas, United States

Full time
Regular

… (department director sign off) · Maintain positive staff relations (in all areas outlined in Manager evaluation form) Manages, coordinates and aids in execution/facilitation of all on-site training programs, …

Added Oct 18, 2026

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Abbott Laboratories

Manager Clinical Site Operations, Site ICRA

Maple Grove, Minnesota, United States +1 more

Pay posted by employer$99,300–$198,700

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Required Qualifications · employer excerpt

Two-year degree or equivalent experience, with at least 5 years people management. Experience with clinical research and/or specific functions that the manager is overseeing.
Preferred 4-year college degree and 5 or more years of clinical research experience, 2 or more years of people management, and/or the specific function that the manager is overseeing.
Must have strong written and verbal communication, interpersonal, presentation, analytical, organizational skills, and the ability to interpret basic clinical data, to meet deadlines as well as the ability to communicate effectively with…
Must be proficient in Microsoft Office Suite and relevant clinical applications.
Ability to work independently when necessary.

2 more in the full description below.

About this opportunity

Original employer description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

Career development with an international company where you can grow the career you dream of.
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
An excellent retirement savings plan with a high employer contribution
Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position is an on-site full-time role and can be located at our Maple Grove, MN or Plano, TX or Sylmar, CA locations.

This position is responsible for the supervision of a team of personnel within Clinical Site Operations (CSO) which supports US, Canada, and LATAM. Assists management in hiring, training, developing, and retaining qualified staff for CSO. In addition, this position supports work during the lifetime of Abbott clinical trials including start-up, conduct and closure working independently with minimal guidance, direction and ensuring compliance to study protocol, domestic and international Good Clinical Practices, applicable regulatory standards, and Abbott Standard Operating Procedures.

Able to solve complex problems; consider alternative or new perspectives using existing tools and standard processes. The Assistant Manager, Clinical Site Operations is accountable for functional oversight within CSO. For this role, they will be responsible for a team of In-house Clinical Research Associates.

What You’ll Work On

Responsible and accountable for ensuring the team reaches defined goals for core deliverables of assigned clinical studies (in partnership with Site and Project Management) such as but not limited to:

- Site Invitation.

- Site Activation (incl. checklist and appropriate tracker- and CTMS updates).

- Site Maintenance activities such as but not limited to:

Site Amendment/Re-activation (incl. checklist and appropriate tracker- and CTMS updates)
Periodic Progress Report distribution and resolution support

-Ensuring both regulatory and clinical protocol compliance is maintained for all assigned clinical projects as appropriate for functional responsibility.

- Trial Master File completion at site level and ensuring an appropriate level of Site Audit Readiness.

- Site Audit preparation and support.

- Study Site Compliance Escalation activities.

- Site Closure and Final Report distribution.

- Responsible for hiring, training, managing, developing, and retaining qualified staff. This may include engagement with service providers that provide staffing contractor services.

- Supports career and personal development of team members as well as creation and maintenance of talent profile, goals, and objectives planning.

- Partners and collaborates with colleagues within Site Management and Operations and GCO to achieve regional and national goals and objectives. - Provides support and training to internal and external clinical personnel on functional processes, as needed.

- Communicates and collaborates with all levels of employees, customers, contractors, and vendors.

- Applies expertise in clinical research processes and regulatory knowledge to the clinical department goals and objectives and actively improves processes and efficiencies.

- Leads small projects and process improvement efforts that are critical to help support departmental goals and objectives.

- Exercises judgment in planning, organizing, and performing work, monitors performance and reports status as necessary.

- Provides input to departmental Standard Operating Procedures (SOPs) and Departmental Work Instruction (DWIs).

- Serves as a Business Unit Champion to at least one BU to support study execution as the main point of contact for the Site ICRA team, drive activation, review of timelines, risk, and finds solutions to drive success.

Other Duties:

- Has strong knowledge of current clinical regulations and common industry practices.

- Engages in relevant professional associations or societies and seeks continuing education about Abbott devices and therapies.

- May support ad-hoc projects and process improvement efforts that are critical to help support departmental goals and objectives.

- May participate in Core Team activities and make additional contributions as assigned.

- This position might require up to 20% travel.

Equipment: Uses standard office equipment, including (but not limited to) personal computer, telephone, FAX, and copier.

Working Conditions: Normally works in a cubicle situated in open landscape office environment. Air conditioned. Well lighted. Moderate noise level.

Physical Demands: Describe the physical demands representative of those that must be met by an employee to successfully perform the essential functions of this job.

Primarily sitting. Some walking. Light effort related to moving, lifting and using office supplies and standard office items. Performs tasks which regularly require good correctable vision and hand/eye coordination.

Required Qualifications

Two-year degree or equivalent experience, with at least 5 years people management. Experience with clinical research and/or specific functions that the manager is overseeing.
Preferred 4-year college degree and 5 or more years of clinical research experience, 2 or more years of people management, and/or the specific function that the manager is overseeing.
Must have strong written and verbal communication, interpersonal, presentation, analytical, organizational skills, and the ability to interpret basic clinical data, to meet deadlines as well as the ability to communicate effectively with all levels of employees.
Must be proficient in Microsoft Office Suite and relevant clinical applications.
Ability to work independently when necessary.
Capable of exchanging straightforward information, ask questions, and check for understanding.
Capable of learning new systems as required for trial master file management and regulatory submissions.

Preferred Qualifications

An excellent understanding of all aspects of clinical research. A strong familiarity with clinical trials research processes. Previous related experience in research within a clinical or corporate setting or relevant clinical experience in a clinical/hospital environment.
Certification as a Research Professional by Society of Clinical Research Associates (SoCRA), Association of Clinical Research Professionals (ACRP) or similar profession society as appropriate for regional assignment.
Work habits include organization, coordination of many tasks, accuracy, and attention to detail.
Regulatory audit experience (e.g. back-room support).
ADA Factors (Physical and Environment Demands).
For each category, check the box that most closely defines the activity required for this position.

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.

The base pay for this position is

$99,300.00 – $198,700.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Research and Discovery

DIVISION:

MD Medical Devices

LOCATION:

United States > Maple Grove : 6820 Wedgwood Road N.

ADDITIONAL LOCATIONS:

United States > Sylmar : 15900 Valley View Court

WORK SHIFT:

Standard

TRAVEL:

Yes, 20 % of the Time

MEDICAL SURVEILLANCE:

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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