Samples Dept Manager Job at ROCK OF AGES CANADA INC. (Bloomington)

New

Account Specialist

Killark is seeking an experienced and driven Account Specialist to directly lead...

Location

United States , Fenton

Salary:

Not provided

Hubbell Incorporated

Expiration Date

Until further notice

Requirements

4-year degree in related field or equivalent work experience in customer service or project management
5+ years of experience in a similar role required
Ability to work and communicate effectively with individuals at all levels of the organization and build relationships across multiple functional groups within the business
Ability to adapt communication style to suit various customer groups
Ability to work autonomously, while escalating where necessary, and possess acumen in executing business decisions
Strategic thinker with a demonstrated ability to successfully develop, launch and execute multiple projects to target goals
Strong facilitation and organization skills
Proficiency with Office Suite, specifically Teams, Excel, OneNote, and PowerPoint

Job Responsibility

Able to work on complex tasks, lead teams, and manage multiple projects to completion
Manage the creation of new accounts with corporate finance, legal teams, and various sales groups
Create pricing and product portfolios for significant projects and key accounts
Work directly with external customers and end users to understand their project requirements, terms, and timelines
Create and manage project specific documentation per customer and/or report out requirements
Work with internal production and procurement teams as well as external vendors or partners to ensure the company meets or exceeds project timeline expectations
Develop key project standard operating procedures and best practices to ensure each new project is handled at ta higher efficiency than the last
Manage project forecast to help drive proper inventory investments, procurement/planning execution
Work with logistics partners on incoming and outgoing deliveries
Work with internal customer service to ensure proper date management

Fulltime

New

Sr Quality Engineer, Validation

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 prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification
To coordinate with cross functional teams of all departments for execution of all validation activities & inform to Manager regarding any non-conformity from planning and execution
To prepare monthly and annual calendars for various periodic qualification/validations & get it reviewed by Manager and approved by Manager
To monitor the QMS elements like Change Control Management, Corrective and Preventive Action, OOS, non-conformance related to the validation activity and prepare investigation report and ensure proper closure of the QMS documents in Track wise
To review the scheduled validation activity as per calendar and send it to the cross functional & PPA department in advance for execution planning before the scheduled date
To ensure samples withdrawal during process validation & keep Manager updated about any non-conformity
To ensure compilation of executed protocols is done online (as applicable) and observation sheets for process validation and other qualifications are duly filled & signed. To ensure the CFS closure of respective documents
To co-ordinate with projects and other cross functional dept. for prior information on new equipment installation and to prepare the protocol in advance, followed by new equipment qualification and get it reviewed by the Manager
To attend training of each protocol before execution of any validation and qualification activity
To collect data & compile summary report for submission to International Regulatory Affairs (IRA) for queries and ANDA

Job Responsibility

Prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification
Coordinate with cross functional teams of all departments for execution of all validation activities
Prepare monthly and annual calendars for various periodic qualification/validations
Monitor QMS elements related to validation activity and ensure proper closure of QMS documents
Review scheduled validation activity as per calendar
Ensure samples withdrawal during process validation
Ensure compilation of executed protocols and observation sheets
Coordinate with projects for new equipment installation and prepare protocol
Attend training of each protocol before execution
Collect data & compile summary report for submission to International Regulatory Affairs (IRA)

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 Quality Engineer, Validation

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 prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification
To coordinate with cross functional teams of all departments for execution of all validation activities & inform to Manager regarding any non-conformity from planning and execution
To prepare monthly and annual calendars for various periodic qualification/validations & get it reviewed by Manager and approved by Manager
To monitor the QMS elements like Change Control Management, Corrective and Preventive Action, OOS, non-conformance related to the validation activity and prepare investigation report and ensure proper closure of the QMS documents in Track wise
To review the scheduled validation activity as per calendar and send it to the cross functional & PPA department in advance for execution planning before the scheduled date
To ensure samples withdrawal during process validation & keep Manager updated about any non-conformity
To ensure compilation of executed protocols is done online (as applicable) and observation sheets for process validation and other qualifications are duly filled & signed
To ensure the CFS closure of respective documents
To co-ordinate with projects and other cross functional dept. for prior information on new equipment installation and to prepare the protocol in advance, followed by new equipment qualification and get it reviewed by the Manager
To attend training of each protocol before execution of any validation and qualification activity

Job Responsibility

To prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification
To coordinate with cross functional teams of all departments for execution of all validation activities & inform to Manager regarding any non-conformity from planning and execution
To prepare monthly and annual calendars for various periodic qualification/validations & get it reviewed by Manager and approved by Manager
To monitor the QMS elements like Change Control Management, Corrective and Preventive Action, OOS, non-conformance related to the validation activity and prepare investigation report and ensure proper closure of the QMS documents in Track wise
To review the scheduled validation activity as per calendar and send it to the cross functional & PPA department in advance for execution planning before the scheduled date
To ensure samples withdrawal during process validation & keep Manager updated about any non-conformity
To ensure compilation of executed protocols is done online (as applicable) and observation sheets for process validation and other qualifications are duly filled & signed
To ensure the CFS closure of respective documents
To co-ordinate with projects and other cross functional dept. for prior information on new equipment installation and to prepare the protocol in advance, followed by new equipment qualification and get it reviewed by the Manager
To attend training of each protocol before execution of any validation and qualification activity

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

Qa technician - no shift

SUMMARY Reporting to the Quality Assurance Supervisor. This position is primari...

Location

United States , Richmond

Salary:

22.65 USD / Hour

THE VAIL CORPORATION

Expiration Date

Until further notice

Requirements

HS Diploma or Equivalent is required
1-3 years previous manufacturing, quality or food safety experience is desired
Strong interpersonal skills are required
Must have knowledge and proficiency in Microsoft Office Suite (Excel, Word, Powerpoint)

Job Responsibility

Daily QA factory audit and process verification
First point of contact to respond to all Food Safety and Quality incidents on NO shift
Track and process finished product holds and dispositions using SAP warehouse inventory management system
Completion of various Quality clerical duties, including: Document verification and archiving, Document distribution, Quality document updates, creation and control, Data entry
COA verification, filing and working with vendors for required documentation
Analytical Instruments and Equipment verification, maintenance & calibration
Environmental Monitoring and laboratory testing
Daily Taste Panel setup and ship product samples to Corporate for sensory review
Support all QA Dept. roles in managing Food Safety and Quality systems

What we offer

competitive health benefits
dental benefits
401k benefits
wellness benefits

Fulltime

Administrative Coordinator and Receptionist

Are you looking to join a dynamic team for an industry that specializes in the d...

Location

Canada , Pointe-Claire

Salary:

40000.00 - 48000.00 CAD / Year

Randstad

Expiration Date

June 22, 2026

Requirements

Cegep or equivalent work experience
Office skills and capacity to respond and take reception calls
Computer knowledge (Word, Excel & Outlook) and comfortable working in computer databases
3-5 years of experience in an office setting
Good interpersonal skills, organized, Team player
Filing (minimal lifting of boxes)
Fluent in French and English - written, spoken and comprehension

Job Responsibility

Order Processing: Responsible for Order entry in our database
Create new customer profiles in our database
Invoicing for certain distributors in our database
Back-up in programming Specials in our ERP system
Upselling to our clients ordering by phone/promoting our monthly specials
Daily filing as well as year-end filing
Client Inquiries: Credit request follow ups
Track shipments/retrieve proof of deliveries
data entry of all logistics coming and going through locations
Sales Support: Follow-up on Territory Managers requests for Car Stock

What we offer

Permanent full time position
Monday-Friday 8:30 am to 5PM, 2 paid 15 min breaks and 1 hour lunch not paid
Salary 40,000-48,000$
1K yearly Bonus depending on performance
Medical and Dental after 3 months probation
2 weeks vacation after one complete year of employment
Birthday (paid day off)

Fulltime

!

Sr Quality Engineer, Validation

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 prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification.
To coordinate with cross functional teams of all departments for execution of all validation activities & inform to Manager regarding any non-conformity from planning and execution.
To prepare monthly and annual calendars for various periodic qualification/validations & get it reviewed by Manager and approved by Manager.
To monitor the QMS elements like Change Control Management, Corrective and Preventive Action, OOS, non-conformance related to the validation activity and prepare investigation report and ensure proper closure of the QMS documents in Track wise.
To review the scheduled validation activity as per calendar and send it to the cross functional & PPA department in advance for execution planning before the scheduled date.
To ensure samples withdrawal during process validation & keep Manager updated about any non-conformity.
To ensure compilation of executed protocols is done online (as applicable) and observation sheets for process validation and other qualifications are duly filled & signed. To ensure the CFS closure of respective documents.
To co-ordinate with projects and other cross functional dept. for prior information on new equipment installation and to prepare the protocol in advance, followed by new equipment qualification and get it reviewed by the Manager.
To attend training of each protocol before execution of any validation and qualification activity.
To collect data & compile summary report for submission to International Regulatory Affairs (IRA) for queries and ANDA.

Job Responsibility

To prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification.
To coordinate with cross functional teams of all departments for execution of all validation activities & inform to Manager regarding any non-conformity from planning and execution.
To prepare monthly and annual calendars for various periodic qualification/validations & get it reviewed by Manager and approved by Manager.
To monitor the QMS elements like Change Control Management, Corrective and Preventive Action, OOS, non-conformance related to the validation activity and prepare investigation report and ensure proper closure of the QMS documents in Track wise.
To review the scheduled validation activity as per calendar and send it to the cross functional & PPA department in advance for execution planning before the scheduled date.
To ensure samples withdrawal during process validation & keep Manager updated about any non-conformity.
To ensure compilation of executed protocols is done online (as applicable) and observation sheets for process validation and other qualifications are duly filled & signed. To ensure the CFS closure of respective documents.
To co-ordinate with projects and other cross functional dept. for prior information on new equipment installation and to prepare the protocol in advance, followed by new equipment qualification and get it reviewed by the Manager.
To attend training of each protocol before execution of any validation and qualification activity.
To collect data & compile summary report for submission to International Regulatory Affairs (IRA) for queries and ANDA.

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

Production Operator - Level 3

Life changing therapies. Global impact. Bridge to thousands of biopharma compani...

Location

Ireland , Dundalk

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Ensure that all product produced conforms to the approved specification
All materials required for the batch are booked in and documented accurately and conform to the packaging instruction & batch packaging record
Sampling tests are carried out at the required frequency
Visual inspections are carried out at required frequencies
Liaise with the QA dept. for support in area / line clearances along with any other specific quality issues which may arise during production
Approval of area / line clearances and pre-production samples as required as per defined procedures
QC samples are collected as per the batch packaging record
Ensure consistent adherence to operating, quality and machine cleaning and safety procedures in production
Deviations are reported to the immediate supervisor
Yields are being monitored versus goals & timely corrective actions are being taken

Job Responsibility

Responsible, in conjunction with the immediate supervisor for shift output, quality and yield in compliance with the requirements of current Good Manufacturing Practice

Fulltime

Production Operator - Night Shift

Responsible, in conjunction with the immediate supervisor for shift output, qual...

Location

Ireland , Dundalk

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Capability to meet clear goals, communicate clearly and ensure progress to completion meeting predefined targets
Fluent English

Job Responsibility

Ensure that all product produced conforms to the approved specification
All materials required for the batch are booked in and documented accurately and conform to the packaging instruction & batch packaging record
Sampling tests are carried out at the required frequency
Visual inspections are carried out at required frequencies
Liaise with the QA dept. for support in area / line clearances along with any other specific quality issues which may arise during production
Approval of area / line clearances and pre-production samples as required as per defined procedures
QC samples are collected as per the batch packaging record
Ensure consistent adherence to operating, quality and machine cleaning and safety procedures in production
Deviations are reported to the immediate supervisor
Yields are being monitored versus goals & timely corrective actions are being taken

Fulltime

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Samples Dept Manager

Job Responsibility

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