QA Supervisor Job at Bakkavor (Spalding)

Qa Supervisor

This is an exciting role with an industry leader which manufactures and supplies...

Location

Canada , Richmond Hill

Salary:

Not provided

The People Co.

Expiration Date

Until further notice

Requirements

Degree (BA) in Food Science or related required.
Minimum 1+ years experience as a QA Supervisor in the food manufacturing sector.
Expertise with GFSI quality programs.

Job Responsibility

Ensuring compliance with product specifications, labeling, and regulatory standards
Overseeing and implementing HACCP, GMP, and other food safety and quality programs for the plant.
Providing oversight for the development of robust manufacturing control processes and related reports use throughout the plant.
Managing customer complaint investigations, resolution and tracking.
Performing gap analysis on all Food Safety and Quality processes and procedures.
Training, mentoring, and supervising QA Co Op.
Managing the hold and release program
Establishing finished goods quality standards, monitor down-graded product and work with manufacturing to reduce them to appropriate levels.

What we offer

An attractive salary, benefits, and potential for career progression!
An amazing opportunity to grow your career with a leading food company.

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 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

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

Member Services Team Lead

The Member Services Team Lead is responsible for supporting and driving the team...

Location

United States , Tempe

Salary:

22.00 - 24.00 USD / Hour

Personify Health

Expiration Date

Until further notice

Requirements

High school diploma or equivalent required
Minimum of one year of customer service experience in a call center environment
previous leadership or team lead experience preferred
TPA (Third Party Administrator) experience and familiarity with medical terminology preferred
Excellent written and verbal communication skills
Strong personal computer usage and Internet proficiency skills
Ability to effectively support, guide, and collaborate within a team environment
Flexible with scheduling based on business needs
Attentive listener with the ability to assess and support member needs
Types 30+ WPM with accuracy

Job Responsibility

Assisting agents with their calls and inquiries, both remotely and onsite
Assisting with IT issues (reporting and troubleshooting)
Supervisor Callbacks
Agent Escalations
Assisting supervisors with the QA process
Providing supervisors with agent feedback
Outlining and documenting certain MS procedures
Adding organizations to ZD
Additional tasks, depending on the kind of project currently being worked on, as well as its workload
All other duties as assigned

What we offer

Competitive base salary and benefits effective day one
Comprehensive medical and dental through our own health solutions
Paid Time Off
Mental health support
retirement planning
financial protection
Professional development with clear career progression and learning budgets
Mission-driven culture where diverse perspectives drive real impact on people's health

Fulltime

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

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QA Supervisor

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QA Supervisor

Qa Supervisor

Sr Executive I, Quality Assurance

Senior Executive I, Quality Assurance

Sr Executive I, Quality Assurance

Assoc I, Quality Assurance

Member Services Team Lead

Qa p1

Data Analyst Quality Assurance Lead

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