Qa Supervisor Job at The People Co. (Richmond Hill)

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 or QA Head to manage Document Control activity
To ensure the implementation and maintenance of current Good Manufacturing Practice (cGMP) standards
To review and verify that any GDP issues have been addressed
To issue and close Logbooks to the respective plant, as per request of respective department from Controlled Forms System (CFS)
To archive executed Logbooks, Standard Formats, Batch Manufacturing Record in the record room and submit to central record room
To issue completed records from record room and ensure its storage, achieve & timely disposition
To verify BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for each new product introduced for manufacturing, whether for regulatory filings (exhibit batches) or for commercial distribution (approved products)
To review BMR based on initial product transfer input received from Quality or F&D / TTD as per requirement
To Prepare / review BMRs and BPRs by integrating product specifications from Technical Package (TP) and processing parameters from site
To verify BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) in TcU, based on approved BMRs and BPRs production planning schedule and after generating a batch number assignment

What we offer

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

Senior 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 or QA Head to manage Document Control activity
To ensure the implementation and maintenance of current Good Manufacturing Practice (cGMP) standards
To review and verify that any GDP issues have been addressed
To issue and close Logbooks to the respective plant, as per request of respective department from Controlled Forms System (CFS)
To archive executed Logbooks, Standard Formats, Batch Manufacturing Record in the record room and submit to central record room
To issue completed records from record room and ensure its storage, achieve & timely disposition
To verify BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for each new product introduced for manufacturing, whether for regulatory filings (exhibit batches) or for commercial distribution (approved products)
To review BMR based on initial product transfer input received from Quality or F&D / TTD as per requirement
To Prepare / review BMRs and BPRs by integrating product specifications from Technical Package (TP) and processing parameters from site
To verify BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) in TcU, based on approved BMRs and BPRs production planning schedule and after generating a batch number assignment

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 or QA Head to manage Document Control activity
To ensure the implementation and maintenance of current Good Manufacturing Practice (cGMP) standards
To review and verify that any GDP issues have been addressed
To issue and close Logbooks to the respective plant, as per request of respective department from Controlled Forms System (CFS)
To archive executed Logbooks, Standard Formats, Batch Manufacturing Record in the record room and submit to central record room
To issue completed records from record room and ensure its storage, achieve & timely disposition
To verify BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for each new product introduced for manufacturing, whether for regulatory filings (exhibit batches) or for commercial distribution (approved products)
To review BMR based on initial product transfer input received from Quality or F&D / TTD as per requirement
To Prepare / review BMRs and BPRs by integrating product specifications from Technical Package (TP) and processing parameters from site
To verify BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) in TcU, based on approved BMRs and BPRs production planning schedule and after generating a batch number assignment

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 or QA Head to manage Document Control activity
To ensure the implementation and maintenance of current Good Manufacturing Practice (cGMP) standards
To review and verify that any GDP issues have been addressed
To issue and close Logbooks to the respective plant, as per request of respective department from Controlled Forms System (CFS)
To archive executed Logbooks, Standard Formats, Batch Manufacturing Record in the record room and submit to central record room
To issue completed records from record room and ensure its storage, achieve & timely disposition
To verify BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for each new product introduced for manufacturing, whether for regulatory filings (exhibit batches) or for commercial distribution (approved products)
To review BMR based on initial product transfer input received from Quality or F&D / TTD as per requirement
To Prepare / review BMRs and BPRs by integrating product specifications from Technical Package (TP) and processing parameters from site
To verify BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) in TcU, based on approved BMRs and BPRs production planning schedule and after generating a batch number assignment

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

Assoc 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

B.Pharma
Exp- 3-7Yrs

Job Responsibility

To take instructions from supervisor or QA Head to manage Document Control activity
To ensure the implementation and maintenance of current Good Manufacturing Practice (cGMP) standards
To review and verify that any GDP issues have been addressed
To issue and close Logbooks to the respective plant, as per request of respective department from Controlled Forms System (CFS)
To archive executed Logbooks, Standard Formats, Batch Manufacturing Record in the record room and submit to central record room
To issue completed records from record room and ensure its storage, achieve & timely disposition
To verify BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for each new product introduced for manufacturing, whether for regulatory filings (exhibit batches) or for commercial distribution (approved products)
To review BMR based on initial product transfer input received from Quality or F&D / TTD as per requirement
To Prepare / review BMRs and BPRs by integrating product specifications from Technical Package (TP) and processing parameters from site
To verify BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) in TcU, based on approved BMRs and BPRs production planning schedule and after generating a batch number assignment

What we offer

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

Qa p1

As part of our exciting expansion project we are now recruiting a QA position, W...

Location

United Kingdom , Eye, Suffolk

Salary:

16.58 GBP / Hour

Crown Chicken LTD, Division of Cranswick PLC

Expiration Date

June 11, 2026

Requirements

Be self-motivated and able to work on your own initiative
Be able to work additional hours as overtime may be required
Ideally have experience of working within a fast-paced food manufacturing environment
Have a good level of both written and verbal English
Ideally have Level 2 Food Hygiene/Safety certification

Job Responsibility

Troubleshooting – ‘Walking the factory floor’ to identify any issues ahead of them arising and taking appropriate action. Dealing with issues as and when required
Managing Corrective actions – making sure corrective actions are completed within appropriate timescales and that the relevant documents have been completed, e.g. hold log, non-conformance log. Reporting any complex issues to QA Supervisor or QA Manager
Audit paperwork – checking the production paperwork has been completed correctly by production staff (Checking production line paperwork)
Hygiene Audits, micro swabbing and micro sampling product
Checking the ‘online’ verifier and dealing with any issues
Formal GMP, Fabrication and Process Control Audits
Conduct documented checks that a % of the production run is within product specification

What we offer

Opportunity to work an overtime outside of your standard hours and potential career progression across other technical departments
Overtime – time and a third after basic hours
Pension – 3% employer contributions/5% employee contributions
Opportunity to buy extra holiday
Discounted share scheme
Discounted local gym membership

Fulltime

Data Analyst Quality Assurance Lead

The Data Analyst/Quality Assurance Lead performs data collection and analysis fo...

Location

United States , Las Vegas

Salary:

95000.00 - 105000.00 USD / Year

Arcata Associates, Inc

Expiration Date

Until further notice

Requirements

Bachelor's Degree in a Quality Assurance, Technical discipline, Business Administration, Management or related discipline
At least four years of related experience
In lieu of a bachelor's degree, a combination of formal education and technical experience is acceptable
Experience with quality methodology, analytical concepts and applications are preferred
American Society of Quality (ASQ) Auditor Certification preferred
must be obtained within the 6-month probationary period if selected candidate does not possess certification
Excellent interpersonal skills and proven ability to communicate effectively in both oral and written form
Highly skilled in the use of a PC and PC-based business applications software such as Microsoft Office, specifically Word, PowerPoint and Excel
Strong planning, organization, data analysis, data management and problem-solving skills are required
Demonstrated skill, knowledge, and technical competence in the reading and interpretation of schematics, plans, manufacturer's manuals, Government procedural documents, management reports, and other similar documents

Job Responsibility

Creates and distributes Quality Metrics (i.e. report cards) to be used in tracking Annex 2 trends for major departments
Acts as the Critical Spares Program Administrator, coordinating and compiling departmental inputs on behalf of the Critical Spares Program
Provides oversight to the QA staff assigned to the Business Operations department as directed by the DM/QA Supervisor
Provides oversight of the Technical Order Distribution Office (TODO) duties performed by the QA department for Technical Orders (TOs), Time Compliance Technical Orders (TCTOs), and Computer Program Identification Numbers (CPINs)
Provide oversight of the ETool Program in conjunction with the IT department and the QA Lead TODO
Continually review the processes governing all aspects of the J-Tech II Annex 2 Quality Management System providing recommendations to management on opportunities to improve the current business model
Reviews the applicable sections of the J-Tech II contract, contract modifications, and external related documents to ensure new requirements are identified and included in the Quality Management System
Performs inspections of equipment, systems, and services required of the QA Department
Performs audits required of the J-Tech contract and perform JT4 Corporate Management audits as assigned
Maintains audit/inspection documentation and records IAW with JT4/Annex 2 practices

What we offer

Medical, Dental, Vision, and much more

Fulltime

Logistics Specialist

To ensure complete accuracy, fulfil and comply with Logistics Objectives, QMS an...

Location

United Arab Emirates , Dubai

Salary:

Not provided

Airbus

Expiration Date

Until further notice

Requirements

Bachelor's in Management/Logistics/Supply Chain/Aviation + 2-3+ years of relevant experience in end to end Warehouse Logistics and Quality Conformance
Proficiency in IT apps - MS Office (Excel, Word, PowerPoint), Gmail, etc.
Experience with logistics software: ERP (SAP), TMS, WMS
Knowledge of shipping software (eg. UPS/FedEx/DHL)
Organizational Skills: Strong planning, time management, and attention to detail
Communication: Excellent verbal & written skills in English
Problem-Solving: Ability to work under pressure, make decisions, adapt
Customer Focus: Service-oriented attitude
Expert in warehouse logistics operations (inbound, inventory handling and outbound) and Quality Conformance
Strong knowledge in order management, logistics management, inventory management, shipping/receiving, warehouse management and Quality Conformance

Job Responsibility

Oversee daily Logistics shopfloor activities to ensure smooth operations and on time delivery of KPIs (daily/weekly/monthly) in line with the agreements
Process Optimization: drive processes, identify bottlenecks, and propose solutions to improve efficiency and optimize costs
Liaise with LSP, suppliers, carriers, Dubai customs and internal teams (sales, production) for seamless operations
Act as a focal point for global to local to global processes (Logistics) coordination, implementation and reporting
Create transparency in the shopfloor operations through timely reporting and escalations
Close collaboration with the Logistics (LSP) WH supervisor and QA team on daily tasks
Coordinate Customs (internal/external) requirements with local/global entities
Participate/Contribute in logistics and QA meetings (Local/Global)
Align with the preparation of rolling shift roaster plans for the QA team
Close monitoring of KPIs, Scraps, Customer claims, Stock Discrepancies and Customer Returns (Red/Blue Channels)

Fulltime

Qa Supervisor

The People Co.

Location:
Canada , Richmond Hill

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
May 03, 2026

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Qa Supervisor

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Location:Canada , Richmond Hill

Category:Quality Control

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:May 03, 2026

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