Production Operative

Manpower UK Ltd; Stone Cross; On-site; GBP 24,000 - 29,000; Full time

Job summary

A leading recruitment agency is seeking a Production Operative in Stone Cross to coordinate manufacturing activities in-line with GMP standards. The successful candidate will ensure compliance, record detailed information, and contribute to maintaining productivity within the production laboratory. Prior experience in a pharmaceutical setting and the ability to lift heavy loads are preferred. This full-time, permanent role offers a competitive salary of up to £28,446.60 per year.

Benefits

Referral programme

Life insurance

Company pension

On-site gym

Private medical insurance

Canteen

On-site parking

Qualifications

• Preferred 1 year of experience in the pharmaceutical industry.
• GMP experience recommended for at least 1 year.
• Ability to work a shift rota 5 days out of 7.

Responsibilities

• Daily coordination of manufacturing activities in the Production Lab.
• Maintain GMP standards and ensure compliance with procedures.
• Perform manufacturing processes as per instructions to produce finished goods.
• Record precise and accurate information during production.

Skills

Experience in a manufacturing setting

Knowledge of GMP

Ability to lift heavy loads

Team collaboration

Tools

HPLC

Job description

Benefits

Referral programme

Life insurance

Company pension

On‑site gym

Private medical insurance

Canteen

On-site parking Full job description

My client is seeking a individual to join our growing team in the position of Production Operative. The role is full‑time and permanent. If successful, you will be joining a team of proactive, motivated and self‑driven individuals with a passion for ensuring the success of this exciting company.

Section 2. Role Summary

Daily coordination of manufacturing activities within the Production Laboratory. Responsible for the operational setup, operation, control, monitoring and cleaning of various manufacturing process equipment to produce finished goods. We are looking for individuals with experience of cGMP, but it is not essential.

Key Accountabilities

• Maintain GMP standards within Production laboratory.
• Adhere to 'right first time' documentation standards.
• Highlight and report all processing deviations.
• Ensure compliance by following all policies and procedures.
• Ensure cost effectiveness in your role as much as practicable.
• Complete planned and necessary maintenance, troubleshooting and production engineering duties.
• Record precise and accurate information.
• Liaise with the QA department to meet the highest standards possible.
• Ensure thorough cleaning of working environment.
• Deliver improving productivity and quality with skilled team members.
• Ensure all equipment is fit for purpose upon using that equipment.
• Responsible for taking in deliveries.
• Maintain stock levels.
• Carry out the manufacturing process as per manufacturing instructions to produce finished goods.
• Update production documentation as and when required.

Job Types : Full-time, Permanent

Pay : Up to £28,446.60 per year

Application question(s) : Are you able to work a shift rota 5 days out of 7 from Sunday to Saturday This role will involve some heavy lifting. Please confirm you can lift heavy loads.

Experience :

pharmaceutical : 1 year (preferred)

GMP : 1 year (preferred)

HPLC experience

Work authorisation : United Kingdom (required) Work Location : In person