Quality Assurance Release Supervisor Job at Baxter (Lessines)

Quality Assurance (FSQA) Tech

Monitor, maintain and improve quality control systems to ensure compliance with ...

Location

United States , Demopolis

Salary:

Not provided

Foster Farms

Expiration Date

Until further notice

Requirements

Must have a high school diploma or equivalent (GED)
1-3 years of experience in food processing
knowledge of USDA regulations, HACCP, GMPs and SSOPs preferred
Must be able to communicate clearly in English (written and verbal)
Must be detail oriented and proficient in mathematics
Proficient on a computer, Excel, Word and Outlook
Must have legible handwriting
Must have good interpersonal skills and communication skills
Must have an overall favorable employment record and attendance record
Must be able to work varying shifts, weekends and holidays as needed

Job Responsibility

Monitor, maintain and improve quality control systems to ensure compliance with company quality standards and USDA regulatory requirements
Provide oversight, training and motivation to the Quality Assurance Representatives to achieve departmental goals
Assist in maintaining, monitoring, and enforcing USDA Regulatory, Corporate Guidelines and Quality Assurance Programs, to include conducting internal audits that may require the participation of management
Interface with Production Supervisors and hourly employees on production and quality procedures
Work with USDA personnel to handle regulatory issues
Assist in maintaining the micro-hold product program
This position has the authority to hold product that does not conform to customer agreements, finished product specifications, or legal requirements and is also authorized to make decision regarding product disposition including release
Provide leadership to QA technicians with regards to their concerns with procedures, product quality, regulatory requirements and corporate procedure
Maintain Quality Reporting Systems

Fulltime

New

Quality Assurance Release Supervisor

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

Location

Belgium , Lessines

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Degree in Science or Engineering
an advanced degree is preferred
Proven experience in a similar QA Release or QA leadership role
Demonstrated experience in people management
Experience with GMP requirements (EU GMP, EudraLex Volume 4) and medical device regulations
Strong knowledge of quality systems, compliance expectations and release processes
QP delegate experience/training is an asset
Strong analytical mindset and structured problem‑solving approach
Excellent communication, presentation and stakeholder‑management skills
Ability to work under pressure and adapt to change

Job Responsibility

Lead, supervise, coach and support a QA Release team of ~10 employees
Plan, coordinate and monitor batch file review activities
Ensure engagement, development and well‑being within the team
Manage and control finished product release for sterile drugs and medical devices
Review and approve deviations/events linked to the manufacturing process
Monitor and continuously improve release performance and associated KPIs
Prepare and present KPI results to site leadership, regional and global Quality teams
Serve as the QA Release representative for interactions with Manufacturing, Supply Chain, CMOs/3rd parties, Product Development, Corporate QA
Ensure efficient and compliant communication across departments
Ensure updates of quality documentation, SOPs and quality agreements

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

New

Quality Assurance Release Supervisor

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

Location

Belgium , Lessines

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Degree in Science or Engineering
an advanced degree is preferred
Proven experience in a similar QA Release or QA leadership role
Demonstrated experience in people management
Experience with GMP requirements (EU GMP, EudraLex Volume 4) and medical device regulations
Strong knowledge of quality systems, compliance expectations and release processes
QP delegate experience/training is an asset
Strong analytical mindset and structured problem‑solving approach
Excellent communication, presentation and stakeholder‑management skills
Ability to work under pressure and adapt to change

Job Responsibility

Lead, supervise, coach and support a QA Release team of ~10 employees
Plan, coordinate and monitor batch file review activities
Ensure engagement, development and well‑being within the team
Manage and control finished product release for sterile drugs and medical devices
Review and approve deviations/events linked to the manufacturing process
Monitor and continuously improve release performance and associated KPIs
Prepare and present KPI results to site leadership, regional and global Quality teams
Serve as the QA Release representative for interactions with Manufacturing, Supply Chain, CMOs/3rd parties, Product Development, Corporate QA
Ensure efficient and compliant communication across departments
Ensure updates of quality documentation, SOPs and quality agreements

What we offer

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

Warehouse Associate Operator Level 3

Reporting to the Warehouse Supervisor, the Warehouse Associate is responsible fo...

Location

Canada , Milton, ON

Salary:

41800.00 - 64350.00 CAD / Year

Cencora

Expiration Date

Until further notice

Requirements

High school diploma or equivalency
2 Years minimum experience in a related industry
Must be proficient in English language (reading, written, oral and mathematics)
Ability to lift and move up to 50 lbs daily
Ability to perform repeated reaching, bending and lifting daily
Able to work in a cold environment daily
Ability to maintain confidentiality and use appropriate judgment
Ability to work accurately with a strong attention to detail
Works well under pressure in time sensitive situations
Good organizational and multi-tasking abilities

Job Responsibility

Ensuring the daily shipping, receiving, and inventory control aspects of the warehouse are maintained
Receiving: logging and verifying all in bound shipments for material identity, quantity and any shipping damage
Quarantining of product: relating to all inbound receipts and returns as outlined by Innomar’s SOP’s
Picking of product: the picking of all orders provided by the CSR or Management
Packing of product: all orders that have been picked require a blind check to ensure product and quantity are correct
Stock Replenishment: Responsible for replenishing the stock picking locations utilizing material operating equipment as required
Returns Processing: Responsible for ensuring returns are processed as per established timelines
Ensuring that all documentation is completed accurately, including preparing shipping documentation
Managing inventory movement in a FIFO or FEFO manner
Maintains data integrity of the inventory management systems

What we offer

Medical
dental
and vision care
comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness
support for working families
which may include backup dependent care
adoption assistance
infertility coverage
family building support
behavioral health solutions

Fulltime

Supervisor, QA Raw Materials

The Supervisor, QA Raw Materials is responsible for leading a team of QA Raw Mat...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in relevant scientific discipline with a minimum of 5+ years’ experience in related GMP industry working in Quality Assurance or Quality Control groups which support receipt, inspection, or release of materials
Equivalent combination of education and experience considered
Knowledge of USP and EP pharmacopoeias, and pharmaceutical raw material compendial testing
Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) and some experience working with international regulations such as EU, ICH
Ability to apply basic scientific principles to solve operational and quality tasks
Experience with RCA, technical writing, and working with quality related investigations

Job Responsibility

Perform review of external documentation and internal GMP documentation associated with incoming raw materials, components, chemicals, excipients, and Active Pharmaceutical Ingredients (API)
Provide Quality Assurance oversight to Materials Management and Quality Control, ensuring that site SOP’s and raw material specifications are adhered to
Responsible for the review and analysis of test results
ability to interpret and comprehend scientific information and data related to QC Micro and QC Analytical testing
Initiation, review, and disposition or closure of raw material quality systems
Assist in the identification, isolation, and containment of potentially nonconforming materials
Assist in the identification and management of expired material
perform scrapping of materials with Materials Management
Assist Materials Management and Project Management with finished product shipments
Provide input, review, and approval of new and revised raw material specifications

Fulltime

Supervisor, Quality Assurance Internal Operations

Responsible for leading QA Associates, who provide QA support in the manufacturi...

Location

United States , Madison

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

BS degree in a scientific discipline
Minimum 5+ year’s relevant GMP experience
Knowledge of FDA/ISO regulatory requirements as well as industry trends
Computer knowledge, including Microsoft Office, Windows
Excellent interpersonal skills, must be able to lead and make decisions
College Level Mathematical Skills

Job Responsibility

Provide QA support for cGMP manufacturing operations
Coordinate with cross-functional teams to continually improve procedures with respect to area line clearances, labeling, packaging and material release
Support QA scheduling activities by monitoring the production, and visual inspection schedules and project management deliverables, and reviewing factors that may impact schedules
Oversee Quality System Events (QSEs) by verifying a Quality reviewer has been assigned to the QSE and monitor that the QSEs are being completed on time
Lead Associates in providing QA on the floor oversight of manufacturing
Oversee and assist employees with product / material labeling and disposition functions, routine manufacturing area line clearances, AQL Sampling and Inspection of Final Package Lots
Supervise the employees in the Quality Assurance Department
Ensure all training is performed by employees, including aseptic gowning, facility flow and visual inspection
Maintain Quality Metrics for the company
Review of master and executed raw material records. Release raw materials, as necessary

Fulltime

Quality Assurance Lead Person

Foster Farms is always looking for talented individuals to join the Foster Farms...

Location

United States , Fresno

Salary:

21.30 - 25.10 USD / Hour

Foster Farms

Expiration Date

Until further notice

Requirements

Must have a high school diploma or equivalent (GED)
1-3 years of experience in food processing
knowledge of USDA regulations, HACCP, GMPs and SSOPs preferred
Must be able to communicate clearly in English (written and verbal)
Must be detail oriented and proficient in mathematics
Proficient on a computer, Excel, Word and Outlook
Must have legible handwriting
Must have good interpersonal skills and communication skills
Must have an overall favorable employment record and attendance record
Must be able to work varying shifts, weekends and holidays as needed

Job Responsibility

Assist in maintaining, monitoring, and enforcing USDA Regulatory, Corporate Guidelines and Quality Control Programs, to include conducting internal audits that may require the participation of management
Interface with Production Supervisors and hourly employees on production and quality procedures
Work with USDA personnel to handle regulatory issues Assist in maintaining the micro-hold product program
This position has the authority to hold product that does not conform to customer agreements, finished product specifications, or legal requirements and is authorized to make decision regarding product disposition including release
Provide leadership to QC technicians with regards to their concerns with procedures, product quality, regulatory requirements and corporate procedure
Maintain Quality-Reporting Systems
All persons employed or associated with Foster Farms are responsible for the quality and food safety of company products
Special projects or assignments as specified by supervisor

What we offer

More than half of our job openings are filled by internal promotion
We encourage Team Members to gain a variety of experiences across different functional groups

Fulltime

Quality Assurance Lead Person

Foster Farms has been serving families since 1939. Since the founding days, Fost...

Location

United States , Fresno

Salary:

21.30 - 25.10 USD / Hour

Foster Farms

Expiration Date

Until further notice

Requirements

Must have a high school diploma or equivalent (GED)
1-3 years of experience in food processing
knowledge of USDA regulations, HACCP, GMPs and SSOPs preferred
Must be able to communicate clearly in English (written and verbal)
Must be detail oriented and proficient in mathematics.
Proficient on a computer, Excel, Word and Outlook
Must have legible handwriting
Must have good interpersonal skills and communication skills
Must have an overall favorable employment record and attendance record
Must be able to work varying shifts, weekends and holidays as needed

Job Responsibility

Assist in maintaining, monitoring, and enforcing USDA Regulatory, Corporate Guidelines and Quality Control Programs, to include conducting internal audits that may require the participation of management.
Interface with Production Supervisors and hourly employees on production and quality procedures.
Work with USDA personnel to handle regulatory issues Assist in maintaining the micro-hold product program.
This position has the authority to hold product that does not conform to customer agreements, finished product specifications, or legal requirements and is authorized to make decision regarding product disposition including release.
Provide leadership to QC technicians with regards to their concerns with procedures, product quality, regulatory requirements and corporate procedure
Maintain Quality-Reporting Systems.
All persons employed or associated with Foster Farms are responsible for the quality and food safety of company products.
Special projects or assignments as specified by supervisor

Fulltime

Quality Assurance Release Supervisor

Baxter

Location:
Belgium , Lessines

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 04, 2026

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March 04, 2026