Sr Production Supervisor Job at Baxter (Cartago)

Production Coordinator

For twenty years OnQ has been at the forefront of retail innovation. We’re trust...

Location

United States , Akron, Ohio

Salary:

Not provided

OnQ

Expiration Date

Until further notice

Requirements

Familiarity with Production techniques
Willing to help within all areas on the production floor and other depts
Knowledge of retail industry – preferred
Some people management background is a plus
Strong mathematical abilities
Moderate computer skills and familiarity with Microsoft Office products, especially Excel
Comfortable with Excel, Google, and SmartSheet forms
Well-organized
Great eye for detail
Ability to analyze and assess production lines

Job Responsibility

Work well within a team
Assist the Sr. Production Manager with Production planning and evaluation tasks
Perform preliminary assignment of tasks to Production Lines based on anticipated Capacity
Able to understand complex BOMs and interpret them well enough to recognize and communicate potential issues that may arise during production
Run Time Studies to estimate time required for current and future Production activities
Assist the Sr. Production Manager in identifying and evaluating personnel who may be a good fit for the Jr. Line Supervisor position when one is available
Assist the Sr. Production Manager in evaluating the progress of Jr. Line Supervisors to help determine if/when they are ready to be hired on as mid-level Line Supervisors
Lead lines if a Line Supervisor is out sick, on vacation, etc.
Enforce rules and best practices on the Production floor
Lead Production activities and determine next kits/tasks for lines when Sr. Production Manager is unavailable

Fulltime

Sr Exec I, Quality Assurance

This is where you make a difference in our patients’ safety. As a member of the ...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

To take instructions from Supervisor and shift lead to perform the shift activity
To verify the correct raw material, primary packaging material, and Quantities are issued and dispensed as per the approved Batch records
To perform the line clearance activity at various stages of manufacturing and packaging activity as defined in the BMR
To perform routine In process checks, sampling, periodic verification, online documentation as defined in batch records and escalate any nonconformances to shift lead and supervisor and ensure appropriate actions (CAPA) in place
To collect In-process samples, finished product samples, and other samples timely submission into QC/micro
To review and verification of electronic records/Audit trails and printout of the equipment’s like autoclave, sterilizer, filter integrity machine and any other equipment’s etc.
To ensure the respective documents to be destructed as per approved procedure
To ensure the compliance and GDP of logbooks, online documents, records, and other supporting documents related to products manufactured in the plant and data integrity is ensured
To ensure & provide support to Shift Lead or Supervisor in investigation, in case of any product complaints or non-conformities or Out of Specification
To execute the approved Corrective and Preventive Action (CAPA) with in define timeline

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Sr Executive I, Quality Assurance

This is where you make a difference in our patients’ safety. As a member of the ...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

To take instructions from Supervisor and shift lead to perform the shift activity
To verify the correct raw material, primary packaging material, and Quantities are issued and dispensed as per the approved Batch records
To perform the line clearance activity at various stages of manufacturing and packaging activity as defined in the BMR
To perform routine In process checks, sampling, periodic verification, online documentation as defined in batch records and escalate any nonconformances to shift lead and supervisor and ensure appropriate actions (CAPA) in place
To collect In-process samples, finished product samples, and other samples timely submission into QC/micro
To review and verification of electronic records/Audit trails and printout of the equipment’s like autoclave, sterilizer, filter integrity machine and any other equipment’s etc
To ensure the respective documents to be destructed as per approved procedure
To ensure the compliance and GDP of logbooks, online documents, records, and other supporting documents related to products manufactured in the plant and data integrity is ensured
To ensure & provide support to Shift Lead or Supervisor in investigation, in case of any product complaints or non-conformities or Out of Specification
To execute the approved Corrective and Preventive Action (CAPA) with in define timeline

Job Responsibility

Any other responsibility assigned by shift lead and reporting manager

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Sr Executive I, Quality Assurance

This is where you make a difference in our patients’ safety. As a member of the ...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

To take instructions from Supervisor and shift lead to perform the shift activity
To verify the correct raw material, primary packaging material, and Quantities are issued and dispensed as per the approved Batch records
To perform the line clearance activity at various stages of manufacturing and packaging activity as defined in the BMR
To perform routine In process checks, sampling, periodic verification, online documentation as defined in batch records and escalate any nonconformances
To collect In-process samples, finished product samples, and other samples timely submission into QC/micro
To review and verification of electronic records/Audit trails and printout of the equipment’s like autoclave, sterilizer, filter integrity machine and any other equipment’s etc.
To ensure the respective documents to be destructed as per approved procedure
To ensure the compliance and GDP of logbooks, online documents, records, and other supporting documents related to products manufactured in the plant and data integrity is ensured
To ensure & provide support to Shift Lead or Supervisor in investigation, in case of any product complaints or non-conformities or Out of Specification
To execute the approved Corrective and Preventive Action (CAPA) with in define timeline

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Sr Executive I, Quality Assurance

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

To take instructions from Supervisor and shift lead to perform the shift activity
To verify the correct raw material, primary packaging material, and Quantities are issued and dispensed as per the approved Batch records
To perform the line clearance activity at various stages of manufacturing and packaging activity as defined in the BMR
To perform routine In process checks, sampling, periodic verification, online documentation as defined in batch records and escalate any nonconformances
To collect In-process samples, finished product samples, and other samples timely submission into QC/micro
To review and verification of electronic records/Audit trails and printout of the equipment’s like autoclave, sterilizer, filter integrity machine and any other equipment’s etc.
To ensure the respective documents to be destructed as per approved procedure
To ensure the compliance and GDP of logbooks, online documents, records, and other supporting documents related to products manufactured in the plant and data integrity is ensured
To ensure & provide support to Shift Lead or Supervisor in investigation, in case of any product complaints or non-conformities or Out of Specification
To execute the approved Corrective and Preventive Action (CAPA) with in define timeline

Job Responsibility

This is where you make a difference in our patients’ safety
As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives
Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Lead, Production Technician

Responsible for manufacturing and assembly of clinical and commercial products. ...

Location

United States , Cypress, California

Salary:

49300.00 - 66700.00 USD / Year

Diasorin

Expiration Date

Until further notice

Requirements

Requires High School Degree or higher
Experience working on complex machinery as a Sr. Production Technician or equivalent is preferred
Good interpersonal and verbal communication skills
Ability to read, analyze, and interpret general, technical procedures, or governmental regulations
Ability to write reports
Ability to effectively present information and respond to questions from groups of supervisors, engineers, or managers
Ability to add, subtract, multiply, and divide
Ability to round numbers to the nearest whole number, tenths, hundredths, or thousandths
Knowledge of metric system with ability to convert units – weight (milligram, gram, kilogram, etc.), volume (milliliter, liter, etc.), and distance (centimeter, millimeter, meter, etc.)
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists

Job Responsibility

Manufacture of subassemblies, components, and/or kits per documented methods
In-process testing of product with ability to interpret results and perform any required adjustments to product
Execute validation protocols and/or experiments
Ability to perform investigation to identify potential root cause of an issue. Ability to identify and implement CAPA (Corrective Action and Preventative Action)
Understand, comply, support, and enforce FDA and ISO regulatory requirements
Understand, comply, support, and enforce all policies and procedures
Lab maintenance per documented cleaning requirements
Inventory maintenance, replenish raw materials and supplies as required
Proper storage of raw materials, subassemblies, components, and kits
Equipment operation and maintenance per documented procedures, calibrate as required

What we offer

comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks
may also be eligible to participate in an annual incentive program

Fulltime

Client Onboard Sr Supervisor

The Client Onboard Sr Supervisor provides leadership and supervisory responsibil...

Location

Colombia , Bogotá

Salary:

Not provided

Citi

Expiration Date

Until further notice

Requirements

2-5 years of experience preferred with corresponding supervisory experience
Finance or economics education background
Good interpersonal communication skills
Consistently demonstrates clear and concise written and verbal communication skills
Demonstrated Project management skill including financial cost management skills
Advanced execution skills in a multi-tasking mode
Exposure to Customer Service and handling of system, testing and rollouts
Ability to achieve business objectives without compromising on controls and risk parameters established
Ability to interact confidently with senior management and / or regulators
Ability to coach and develop people, identifying and retaining talent

Job Responsibility

Responsible for customer interaction, documentation issuance, review and system setups
Demonstrates high level of diligence, motivation and organizational skills
Focuses on timely and accurate delivery of all account opening functions, as well as delivering superior customer service and resolution of customer issues
Performs day to day management of the account opening and maintenance processing
Responsible for various types of project management in the account services space, and managing cross-functional relationships with all teams
Determines new work procedures, analyzes complex and variable issues with significant departmental impact
Supports the motivation of staff through constant interaction with the team
Ensures team delivers as per service level agreements
Understands client requirements and implements them correctly
Monitors customer satisfaction and service level and drives process changes

Fulltime

Sr. Engineer - Facilities

This position is responsible for ensuring full compliance with all regulatory re...

Location

United States of America , Aibonito

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

B.S degree in electrical or mechanical engineering
One to three years of experience in facilities/utilities maintenance
Ability to speak and present information effectively before plant groups meetings
Knowledge in how to read and interpret mechanical drawings and P&IDs
Experience with thermal systems and high‑voltage electrical infrastructure is highly desirable and will be considered a strong advantage for candidates
Fluently in English and Spanish languages

Job Responsibility

Ensure full compliance with all regulatory requirements associated with Building Maintenance, the electrical system, HVAC systems, and clean room operations
Supervise and manage the facility’s Cogeneration System
Lead the site’s Lean Energy Program
Reviews and approves all documentation generated and verifies the accomplishment of them to the company policies
Executes projects, protocols, presentations and other assigned duties related to the area
Reviews changes in specifications (Certification Document Reviews-CDRs) and compliance with local SOP’s
Conducts investigations looking for root causes of non-conformances
Generate change controls and CAPA events
Fill out department reports such as calibration, study documents, particles, etc
Assists the supervisor in ln looking for improvements to optimize workload, efficiency, coordination and compliance to specifications and gap assessments

What we offer

Medical, Dental, Disability and Life Insurance coverage
Vision Plan
Paid Vacation Days and Paid Holidays
Paid Parental Leave
Retirement Plan 165e
Employee Stock Purchase Program
Educational Assistance Plan
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits

Sr Production Supervisor

Baxter

Location:
Costa Rica , Cartago

Category:
Manufacturing

Contract Type:
Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 21, 2025

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