Product, Technical & Quality Manager in Cheltenham

Product, Technical & Quality Manager in Cheltenham

Cheltenham Full-Time On-site
T

1. NPD project management

  • Run the product pipeline end to end, from concept brief and formulation through samples, stability, artwork, first production and launch.
  • Build and own a stage-gate process. Keep one live critical path for every launch, working back from launch dates.
  • Coordinate the founder, nutritionist, marketing, commercial, finance and manufacturers, and flag slippage early with options.
  • Manage NPD budgets, MOQs, sample costs and cost-of-goods targets with finance and commercial.
  • Run range extensions, reformulations, pack changes and delistings with the same discipline as new launches.

2. Technical development

  • Work with our lead nutritionist on formulation, so every product delivers our max-strength promise.
  • Brief and challenge contract manufacturers on feasibility, overages, stability, shelf life and cost.
  • Own raw material and finished product specifications, stability programmes and shelf-life justification.
  • Hold the technical file for every SKU, Scout new ingredients, formats and suppliers that could give us an edge.

3. Regulatory, claims and labelling

  • Sign off every label and pack against UK and EU food supplement law, including the Food Supplements Regulations 2003, FIC and the GB NHC register.
  • Check marketing, Amazon listings and ad copy for claims compliance with the CAP Code.
  • Hold claims substantiation for every product and campaign.
  • Complete retailer technical questionnaires, declarations and product specification portals.

4. Quality management

  • Build and run a proportionate Quality Management System: SOPs, specifications, document control and records.
  • Review and approve batch records and Certificates of Analysis, and own finished product release.
  • Run an independent testing programme so we verify and audit our own quality.
  • Lead investigations into complaints, non-conformances and out-of-spec results.
  • Own change control and risk assessment for any change to formula, supplier, site or pack.

5. Supplier and manufacturer quality

  • Approve and audit contract manufacturers and key raw material suppliers against GMP, BRCGS or equivalent standards.
  • Put quality and technical agreements in place with every manufacturer.
  • Monitor supplier performance and lead supplier reviews.
T

Contact Details:

Tonic Health Recruitment Team