Record label and Marketing Assistant Job at BCE Apprenticeships (London)

Record Label Marketing Apprentice

We are looking for an Apprentice to join our team and work across all areas of t...

Location

United Kingdom , Cookham Maidenhead

Salary:

15700.00 GBP / Year

BCE Apprenticeships

Expiration Date

Until further notice

Requirements

16+ years old
English & maths GCSE or equivalent grade above C/4

Job Responsibility

Assist with scouting new artists online
Research ideas to support artist marketing and new business opportunities
Liaise with labels and partners on release plans
Manage artist diaries and book sessions with producers and songwriters
Help coordinate artist travel plans
Occasionally travel with artists for filming, promo, or live shows
Attend meetings with artists and partners, take notes, and follow up on action points
Support artists with their social media and encourage them to stay on track with plans
Contribute ideas to help market artists and grow their profiles
Manage and screen communication (email, phone, WhatsApp)

Driver Local

Responsible for safely transporting hazardous and non-hazardous materials from t...

Location

United States , Groves

Salary:

Not provided

Veolia

Expiration Date

Until further notice

Requirements

High School diploma or General Educational Development (GED) required
Prior commercial driving experience required
Familiarity with U.S. Department of Transportation (DOT) regulations pertaining to the transportation of hazardous and non-hazardous materials
Strong team player
Excellent interpersonal and communication skills
Time management: the ability to organize and manage multiple tasks
Strong customer service orientation
Valid Class A Commercial Driving License (CDL) as required
Hazmat (H) endorsement required
40-Hour HAZWOPER training preferred

Job Responsibility

Perform daily inspections of vehicle and/or trailer prior to driving to ensure the safety and integrity of equipment going to designated sites
Prior to transporting materials reviews shipment records, manifests, container labeling, vehicle placards, and integrity of loaded drums, roll-off boxes or bulk tankers
Driving within the local market, ensures that DOT requirements such as load weight limits, driver log books, Vehicle Inspection Records, transportation permits, insurance cards, fuel trip reports, IFTA fuel stickers, or other paperwork is up to date and valid
Consults with customers pertaining to load conditions, drum counts or paperwork inconsistencies to ensure that materials can be properly transported to designated site(s)
Notify immediate supervisor of any moving violations and/or accidents in-route to and/or from sites
Assist in the loading/unloading of materials at designated sites utilizing appropriate equipment
Responsible for assisting with housekeeping as required
Other duties as assigned

What we offer

paid time off policies
health insurance
dental insurance
vision insurance
life insurance
savings accounts
tuition reimbursement
paid volunteering
employer sponsored 401(k) plan

Fulltime

Senior Associate, Labeling Compliance

The Senior Associate, Labeling Compliance will support the planning, coordinatio...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelorâ€™s degree or Masterâ€™s degree with 5 to 9 years of directly related experience in Regulatory Affairs, labelling compliance, artwork management, quality, or a related pharmaceutical or biotechnology function
Equivalent combinations of education and relevant experience may also be considered

Job Responsibility

Coordinate day-to-day labelling activities to support timely and compliant implementation of approved labelling changes across EU and global markets
Manage labelling change requests, track deliverables, monitor timelines, and maintain accurate records in applicable labelling, artwork, or document management systems
Serve as an operational point of contact for labelling activities, providing guidance to internal stakeholders on labelling processes, document requirements, formats, and timelines
Ensure labelling updates are aligned with approved Product Information, internal procedures, quality standards, and market-specific implementation requirements
Identify potential compliance risks, delays, inconsistencies, or documentation gaps and escalate issues to the appropriate stakeholders for timely resolution
Support EU labelling activities across applicable procedures, including centralised, decentralised, mutual recognition, and national procedures, as relevant
Coordinate updates to EU Product Information components, including the Summary of Product Characteristics, Package Leaflet, outer labelling, inner labelling, mock-ups, and related packaging text
Support alignment of labelling content with approved Marketing Authorisations, regulatory commitments, internal procedures, and country-specific requirements
Coordinate with regional and local Regulatory Affairs contacts to gather requirements, clarify expectations, resolve queries, and support implementation of approved labelling changes
Track EU labelling milestones, review comments, approvals, and implementation status to ensure visibility across stakeholders and support delivery against agreed timelines

Fulltime

New

Cdl Local Driver

Position Purpose: Responsible for safely transporting hazardous and non-hazardou...

Location

United States , Phoenix

Salary:

Not provided

Veolia

Expiration Date

Until further notice

Requirements

High School Diploma/GED is required
Prior commercial driving experience required
Familiarity with U.S. Department of Transportation (DOT) regulations pertaining to the transportation of hazardous and non-hazardous materials
Strong team player
Excellent interpersonal and communication skills
Time management: the ability to organize and manage multiple tasks
Strong customer service orientation
Valid Class A, B, or C Commercial Driving License (CDL) as required
Hazmat (H) endorsement required
40-Hour HAZWOPER training preferred

Job Responsibility

Perform daily inspections of vehicle and/or trailer prior to driving to ensure the safety and integrity of equipment going to designated sites
Prior to transporting materials reviews shipment records, manifests, container labeling, vehicle placards, and integrity of loaded drums, roll-off boxes or bulk tankers
Driving within the local market, ensures that DOT requirements such as load weight limits, driver log books, Vehicle Inspection Records, transportation permits, insurance cards, fuel trip reports, IFTA fuel stickers, or other paperwork is up to date and valid
Consults with customers pertaining to load conditions, drum counts or paperwork inconsistencies to ensure that materials can be properly transported to designated site(s)
Notify immediate supervisor of any moving violations and/or accidents in-route to and/or from sites
Assist in the loading/unloading of materials at designated sites utilizing appropriate equipment
Responsible for assisting with housekeeping as required
Other duties as assigned

What we offer

Paid time off policies
health insurance
dental insurance
vision insurance
life insurance
savings accounts
tuition reimbursement
paid volunteering
employer sponsored 401(k) plan

Sales Support

Sales Support position at LWC Drinks in Andover, UK. The role involves driving n...

Location

United Kingdom , Andover

Salary:

Not provided

Webrecruit

Expiration Date

Until further notice

Requirements

Excellent Customer service skills
Use of Microsoft Excel for spreadsheets and records
Ability to use the trinity system and LWC drinks quote system
Good team work skills
Good communication and relationship building skills
Good specialist knowledge of the drinks industry, products and the on trade market.

Job Responsibility

To drive new business in the depot via Lead Generation
To increase customer retention by closely managing retention reports and keeping attrition to a minimum
Providing key support for account managers
informing them of results from the 5 weekly report, ensuring that they stay aware of business retention and setting up appointments for new business
Reviewing Down Traders and reporting to Sales Manager
Follow up actions for the above report for either Telesales and or Account Managers
To ensure a high standard of customer service with creating an initial business relationship with all new customers
Set up initial orders and delivery requirements
Take ownership of solving customer issues through pro-active customer service
Ensure that own label POS is permanently available at depot level whilst managing the cost budget

What we offer

A discretionary £2000 bonus may be granted annually, subject to performance against defined KPIs

Fulltime

Label Review Support Specialist

We are looking for a detail-oriented Label Review Support Specialist to join a m...

Location

United States , Pasadena

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Demonstrated attention to detail with the ability to identify inconsistencies in text, formatting, and artwork
Strong written and verbal communication skills for working effectively with cross-functional teams
Experience using Microsoft Office applications, including Word and Excel, in a work setting
Working knowledge of Adobe Acrobat for reviewing, annotating, and managing document files
Ability to maintain accurate data entry, documentation, and audit-ready tracking records
Familiarity with label review, document control, auditing, or compliance-related processes
Ability to manage multiple priorities while meeting deadlines in a structured work environment

Job Responsibility

Review printed product labels, including text and graphic elements, to confirm consistency with approved regulatory content before release
Partner with marketing and other internal teams to coordinate updates, clarify discrepancies, and obtain corrected label revisions when needed
Maintain organized records and tracking logs for label review status, approvals, and related documentation
Conduct careful checks of label materials to identify errors, omissions, or compliance concerns prior to printing
Support efficient day-to-day document control activities by keeping review workflows accurate, timely, and well documented
Communicate review findings clearly and professionally to stakeholders across different levels of the organization
Assist with additional label compliance and administrative duties as business needs require

What we offer

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

Fulltime

Regulatory Specialist

Charlie Gilmur with Robert Half is looking for a Regulatory Specialist to help s...

Location

United States , Newberg

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent relevant experience in the medical device manufacturing industry
extensive industry experience may be considered in place of a degree
Working knowledge of medical device regulatory frameworks across multiple regions, including U.S., Canadian, European, and other international markets
Experience preparing and maintaining regulatory documentation, technical files, registrations, and product compliance records
Familiarity with quality management system standards and risk management principles, including ISO 13485 and ISO 14971
Ability to assess engineering changes, product development updates, and labeling revisions for regulatory significance
Experience participating in internal audits, external audits, or regulatory inspections within a regulated manufacturing environment
Strong document control, organization, and cross-functional communication skills
Proficiency supporting quality assurance and regulatory compliance activities for medical device or closely related regulated products

Job Responsibility

Lead the preparation, organization, and upkeep of regulatory submissions and product files for domestic and international markets
Oversee product registration, licensing, and renewal activities, ensuring approval records remain current and traceable
Evaluate design or engineering changes to determine regulatory impact and identify when additional submissions or notifications are required
Partner with internal teams to review product labeling, instructions for use, and related documentation for compliance with applicable market requirements
Maintain quality system documents such as procedures, templates, and manuals so they remain aligned with current standards and business practices
Plan and perform internal audits, document observations, and follow corrective actions through to completion
Support external inspections and third-party audits by assembling required evidence and assisting with responses to findings
Monitor changes in global regulations and standards, assess operational impact, and communicate necessary updates to stakeholders
Contribute to post-market quality and regulatory activities, including complaint analysis, adverse event reporting support, and recall documentation when needed
Provide training and practical guidance to cross-functional teams on regulatory expectations, risk management, and quality system requirements

What we offer

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

Regulatory Affairs Specialist

Regulatory Affairs - office based - Bogota. ICON plc is a world-leading healthca...

Location

Colombia , Bogota

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor's degree in Pharmaceutical Chemist or next to graduate required
Minimum 1 year of experience in regulatory area within the pharmaceutical or biotechnology industry
Knowledge or awareness of current regional guidelines and regulations is preferred
Technical knowledge in the preparation of a dossier is desirable
Prior experience using computerized information systems required: PC Windows, word processing and electronic spreadsheets
Advanced English level

Job Responsibility

Manage activities associated with obtaining initial, amendment and other central authority approvals i.e. Regulatory Agency (RA), and any other central authorities for the assigned country/ countries
Perform submission and maintenance of new health records, renovations and modifications to keep the products on the market according to the strategic plan established by the company, current Colombian laws and current local health legislation in accordance with the corporate guidelines and policies, procedures and premises
Review of promotional materials for products for human use of their therapeutic line(s) in Veeva Vault or current tool
Perform submission and monitoring of products for human use of their therapeutic line(s) in procedures such as: PSUR, DSUR, RMPs, and safety information according to current Colombian regulations
Back-up to the Head of Regulatory Affairs and analysts of records in the procedures of INVIMA in order to guarantee the operation of the area
Ensure that IP labels are in adherence to country requirements and submitted where applicable
Support the senior level regulatory staff/country consultant in the maintenance of accurate, up-to date Country Knowledge repositor
Contribute to the maintenance and collection of regulatory intelligence by ensuring that tools such as the Country Knowledge Repository and the Country Fact Sheets are up-to-date and communicate new information or changes to the Regulatory Intelligence Consultant team
Preparation of electronic regulatory submission of post-registration requests, HMPs, Labeling notifications, additions, publication corrections and database corrections, among other petitions to be field at MoH
Follow-up on the status of the regulatory submissions (paper dossiers) from dispatch to the receipt of proof of protocol

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fulltime

Select Country

Record label and Marketing Assistant

Job Description

Job Responsibility

Requirements

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