Label Operator Job at Greencore Group (Selby)

Infrastructure Engineer / IT Manager

Robert Half (Technology Solutions) is searching for an Infrastructure Engineer /...

Location

United States , Huntington Beach

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

background in Azure AD/Entra
AD
Leadership
Vendor Relations
VMware
FortiGate
GPO
Windows Infrastructure
user administration
Distribution / Security Groups and object attributes

Job Responsibility

Active Directory
Microsoft 365 admin center user license assignment and Microsoft MFA user configuration and troubleshooting
Conversion / creation of Shared Mailboxes and permissions / forwarding
Azure AD Connect installation and troubleshooting
Group Policy troubleshooting
Creation of new GPOs and modification of existing ones
VMware ESXi / vCenter
VM creation / cloning
VM resource allocation modification
VM snapshots and rollbacks

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

Fulltime

New

Delford operative

Label Checker (Delford Operative). You would be responsible for ensuring all lab...

Location

United Kingdom , Hull

Salary:

Not provided

Crown Chicken LTD, Division of Cranswick PLC

Expiration Date

Until further notice

Requirements

Previous experience in a similar role - label checking / quality assurance / experienced production operative
Previous experience in fast moving consumer goods manufacturing
Able to work in fast-paced environment to daily targets
Strong levels of attention to detail
Knowledge of food safety and hygiene

Job Responsibility

Work closely with line leader to ensure the production plan is completed, maintaining a high level of quality of work
Efficiently fill out relevant paperwork and documentation in accordance with our legislations
Perform Gas checks and label scan checks
Be familiar with quality and customer specifications using the on the line QAS
Ensure that lost production time is kept to a minimum by maintaining the speed of the line, and to minimise the waste of raw materials, packaging and consumables
Ensure labels are correct and signed off when collecting from stores

What we offer

Job stability at a growing and expanding company
Commitment to progression and personal development - this will include machine specific training and upskilling
Time and a quarter pay for overtime
20 days annual leave with option to purchase additional 5 days
Purchase company shares via discounted share scheme
Company pension scheme - up to 10% employer contribution
Access to retail discount app, bike to work scheme, health and wellbeing platform

Fulltime

Production Operator II

At CVS Health, we’re building a world of health around every consumer and surrou...

Location

United States , Glasgow

Salary:

17.00 - 25.65 USD / Hour

CVS Health

Expiration Date

Until further notice

Requirements

At least 6 months of experience in customer service
Ability to be fully on-site in the Glasgow, KY office
Demonstrated ability to see and read fine prints
Demonstrated finger dexterity for repetitive operative use of facility equipment
Ability to push, pull, and/or climb as required for position
Repetitive motions using hands/wrists required

Job Responsibility

Verification of materials and products as directed by procedures and/or batch record requirements
Labeling, inspecting, and production of final container products with manual and/or automated systems
Set-up, changeover, and operation of labeling and production equipment
Data entry and computer-generated labels
Maintains records and production area to comply with regulatory requirements, good manufacturing practices, and standard operating procedures
Performs reconciliation activities and determines compliance to specification, floats on all lines
Performs final production check of completed documents for completeness and accuracy
Review of completed batch records for compliance with cGMPs, validation, and standard operating procedure requirements
Reconciles labeling and product components to determine compliance with specifications
Assists in investigation of non-confirming results related to either reconciliation or production activities

What we offer

Affordable medical plan options
401(k) plan (including matching company contributions)
Employee stock purchase plan
No-cost programs for all colleagues including wellness screenings, tobacco cessation and weight management programs, confidential counseling and financial coaching
Paid time off
Flexible work schedules
Family leave
Dependent care resources
Colleague assistance programs
Tuition assistance

Fulltime

End Point Engineer I

The Endpoint Systems Engineering team crafts, builds, deploys and maintains a wi...

Location

United Kingdom , London

Salary:

Not provided

Take-Two Interactive Software, Inc.

Expiration Date

Until further notice

Requirements

Proficient with Windows, Linux, including installing, configuring and problem solving issues
Experience leading virtualized environments (e.g. VMware, Nutanix)
Practical networking experience (4 layer model, TCP/IP) including diagnosing, and remediating basic network issues (e.g., firewalls)
Demonstrable ability to write and debug automation tools and scripts (e.g. PowerShell, shell scripts, Python)
Experience with software development principles, including version control systems, Agile development methodologies, and automated CI/CD pipelines (e.g., Perforce, Jenkins, Git)
Strong ability to learn new technologies and dive into challenges
Capable of written and verbal communication among both technical and non-technical audiences
Develop and implement a comprehensive endpoint management strategy
Supervise lifecycle management for all endpoint devices, including procurement, deployment, maintenance, and retirement
Design and implement configurations using tools like Microsoft Endpoint Manager (Intune), SCCM, JAMF or similar

Job Responsibility

Coordinate complex engineering projects, providing technical expertise
Collaborate with collaborators, customers, partners, and team members to define project requirements, scope, and objectives
Understanding of full product suite and tool set leveraged by the business
Identify and assess new technologies and methodologies to enhance processes. Align engineering initiatives with business goals. Develop continuous improvement and innovation within the team
Collaboration and Communication: Collaborate closely with various teams, including product management, operations, and marketing. Effectively communicate technical concepts to non-technical collaborators. Maintain relationships with external partners and vendors regarding engineering matters
Coordinate testing, validation, and quality assurance processes. Ensure projects meet or exceed technical and operational standards

What we offer

Private healthcare
Private dental
A double matching pension policy where the employer will double match up to a 4% contribution from the employee
Employee stock purchase scheme with a 15% discount
Eye tests and vouchers towards glasses
Cycle to work scheme
Flu vouchers
Annual health
4X death in service insurance
Income protection (66% salary)

Fulltime

Senior National Account Manager

Our client is a Global Branded Food Player with a market leading UK Business in ...

Location

United Kingdom

Salary:

Not provided

PT Executive

Expiration Date

Until further notice

Requirements

Strong experience in either Brands or Own Label within the FMCG industry
Operating within National Accounts Commercial Role
Category perspective
Strong Relationship skills

Job Responsibility

Drive growth across the channel
Ability to Network & Influence throughout the Customer Matrix Space
Full P&L visibility
Deal with peers, cross functional colleagues, Executive Board members internally and Senior Management externally
Reason and rationalise complex business scenarios
Manage internal strategies and external requirements
Application of Category Management
Negotiate annual Joint Business Plans (JBPs)
Drive distribution of existing and new products
Manage product mix to maximise margin

Fulltime

New

Associate Director, Global Supply Chain

The Associate Director, Global Supply Chain reports to the Senior Director, Glob...

Location

United States , Waltham, MA or San Diego, CA

Salary:

160000.00 - 200000.00 USD / Year

Kailera Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor’s degree and 10+ years of relevant biopharmaceutical industry experience or advanced degree with 5+ years of experience
6+ years of experience in clinical supply management
Knowledgeable in the implementation and workings of IRT systems
Ability to create a collaborative environment and manage multiple project activities
Strong computer skills including MS Office
Hands-on, roll-up-your-sleeves, collaborative approach with high sense of urgency and drive for results
Ability to think outside of the box and challenge the status quo
Desire to work in a fast-paced, innovative environment
Ability to travel up to 20%

Job Responsibility

Assist with investigational drug product supply and logistics activities, including, but not limited to, demand forecasting and supply planning, IRT start-up and maintenance, label generation and approval, packaging and labeling operations, release and distribution, expiry extension, returns, reconciliation, destruction, cold chain management, and inventory management
Maintaining oversight in monitoring inventory levels throughout the life of a clinical trial
Support with oversight of packaging and labeling/distribution vendors, including relationship management
Coordinate the preparation of clinical trial pharmacy manuals, packaging methods, batch records, drug labels, shipping documents, destruction certification, and coordinating the origination, proofing, and translation of clinical study labels and generation
Proactively identify potential issues, notify supervisor in a timely manner, and develop mitigating actions
Interpret clinical synopses and protocols to create clinical IMP demand forecasts
Attend clinical study and cross functional meetings as needed
Assist the global supply chain lead in overseeing the execution of multiple clinical trials and proactively identify potential supply chain issues and recommending solutions to global supply chain lead
Lead clinical study close-out activities, including returned goods reconciliation and inventory destruction
Assist with drug supply delivery through coordination of CMC efforts (including, but not limited to, CMC, Supply Chain, Legal, Procurement, Commercial, Regulatory, Clinical Development, and Clinical Operations)

What we offer

comprehensive health coverage
flexible time off
paid holidays
year-end shutdown
monthly wellness stipend
generous 401(k) match
tuition reimbursement
commuter benefits
disability and life insurance
annual bonus opportunities

Fulltime

New

Director, Global Supply Chain

The Director, Global Supply Chain reports to the Senior Director, Global Supply ...

Location

United States , Waltham, MA or San Diego, CA

Salary:

175000.00 - 230000.00 USD / Year

Kailera Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor’s degree and 10+ years of relevant biopharmaceutical industry experience or an advanced degree with 8+ years
8+ years of experience in clinical supply management
Experience with global pharmaceutical development and manufacturing operations for development-stage and/or commercial products, including formulation development (pre-filled syringes, solid oral dosage forms, etc.), analytical development, and device development
Deep understanding of IRT systems
Ability to create a collaborative environment and manage multiple project activities with global contract CDMOs
Strong computer skills including MS Office
Hands-on, roll-up-your-sleeves, collaborative approach with high sense of urgency and drive for results
Ability to think outside of the box and challenge the status quo
Desire to work in a fast-paced, innovative environment
Domestic or international travel is required (up to 20%)

Job Responsibility

Managing drug product supply and logistics activities, including, but not limited to, demand forecasting and supply planning, IRT start-up and maintenance, label generation and approval, packaging and labeling operations, release and distribution, expiry extension, cold chain management, and inventory management
Communicating supply strategies and supply needs to CMC stakeholders and providing input for developing manufacturing strategies to support those needs
Providing oversight in monitoring inventory levels throughout the life of a clinical trial or commercial product, including taking preventative actions to avoid potential supply issues
Providing day-to-day oversight of packaging and labeling/distribution vendors, including relationship management
Contributing to the preparation of clinical protocols, clinical trial pharmacy manuals, packaging methods, batch records, drug labels, shipping documents, destruction certification, and coordinating the origination, proofing, and translation of clinical study labels and generation
Proactively identify potential issues, notify management in a timely manner, and develop mitigating actions
Interpret clinical synopses and protocols to create clinical IMP demand forecasts
Oversee the execution of multiple clinical trials and proactively identify potential supply chain issues, including providing analysis and recommending solutions with appropriate support from SMEs
Support clinical study close-out activities, including returned goods reconciliation and inventory destruction
Manage and execute drug supply delivery through coordination of CMC efforts assigned to the entire project team (including, but not limited to, CMC, Supply Chain, Legal, Procurement, Commercial, Regulatory, Clinical Development, and Clinical Operations)

What we offer

comprehensive health coverage
flexible time off
paid holidays
a year-end shutdown
monthly wellness stipend
generous 401(k) match
tuition reimbursement
commuter benefits
disability and life insurance
annual bonus opportunities

Fulltime

AI Research Engineer, Data Infrastructure

As a Research Engineer in Infrastructure, you will design and implement a robust...

Location

United States , Palo Alto

Salary:

180000.00 - 250000.00 USD / Year

1X Technologies

Expiration Date

Until further notice

Requirements

Strong experience in building data pipelines and ETL systems
Ability to design and implement systems for data collection and management from robotic fleets
Familiarity with architectures that span on-robot components, on-premise clusters, and cloud infrastructure
Experience with data labeling tools or building dataset visualization and annotation tooling
Proficiency in creating or applying machine learning models for dataset organization and automated labeling

Job Responsibility

Optimize operational efficiency of data collection across the NEO robot fleet
Design intelligent triggers to determine when and what data should be uploaded from the robots
Automate ETL pipelines to make fleet-wide data easily queryable and training-ready
Collaborate with external dataset providers to prepare diverse multi-modal pre-training datasets
Build frontend tools for visualizing and automating the labeling of large datasets
Develop machine learning models for automatic dataset labeling and organization

What we offer

Equity
Health, dental, and vision insurance
401(k) with company match
Paid time off and holidays

Fulltime

Label Operator

Greencore Group

Location:
United Kingdom , Selby

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 05, 2026

Expiration:
January 19, 2026

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Location:United Kingdom , Selby

Category:Manufacturing

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:January 05, 2026

Expiration:January 19, 2026

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Job Posted:
January 05, 2026

Expiration:
January 19, 2026