Production Operator - GFAM Nights

Salesforce Sites; Romford; Hybrid; GBP 21,000 - 30,000; Full time

Benefits offered by this job

Shift allowance 31%

Performance-based pay

25 days annual leave + bank holidays

Pension plan

Medicash health plan

Job summary

Ethypharm is seeking a Production Operator for the GFAM Night Shift at our Romford site. You will work in a cGMP environment producing pharmacological products, recording batch data, and ensuring quality throughout the manufacturing process.

The role requires attention to detail, good communication, and the ability to work a Sunday-Thursday night schedule with a 37.5-hour week. Training will be provided in GMP and operating procedures.

Qualifications

• GCSE (or equivalent) including Maths and English.
• Good written and spoken English.
• Experience operating machinery in a regulated environment.
• Experience working in a structured, process-driven environment.
• Knowledge of cGMP in manufacturing.

Responsibilities

• Complete batch records accurately with integrity.
• Follow GMP working instructions to produce quality products.
• Collaborate with Engineering to resolve machine issues.
• Maintain batch-to-batch quality and minimize downtime.
• Perform quality checks to ensure product and patient safety.

Skills

GMP knowledge

Machinery operation

Numerical skills

Documentation

English proficiency

SAP experience

Education

GCSE Maths & English

Tools

SAP

Job description

Full details of the job.

Vacancy Name

Vacancy Name Production Operator - GFAM Nights

Contract

Contract Permanent

Location

Location Romford, Bampton Road

Salary Up to xxx

Daily Work Times

Daily Work Times Sunday to Thursday. In line with operational requirements, your shift start time will fall between 10:00pm and 10:30pm, and your finish time between 6:00am and 6:30am. You will be scheduled to work 7.5 hours per day.

Basic Hours Per Week

Basic Hours Per Week 37.50

What you will do

As a Production Operator, you will work as part of a team producing high-quality pharmaceutical products focused on the treatment of pain, addiction, and critical care. You will ensure all production activities are carried out in line with current Good Manufacturing Practice (cGMP) standards.

Key responsibilities:

• Accurate documentation: Complete batch manufacturing records accurately, neatly, and with integrity to ensure compliance at all times.
• GMP compliance: Follow detailed GMP working instructions and guidelines to produce high-quality products.
• Collaboration with Engineering: Work closely with the Engineering team to support the resolution of machine breakdowns.
• Teamwork: Work effectively with colleagues to complete batch-to-batch tasks efficiently and minimise downtime.
• Quality control: Carry out quality checks at various stages of the process to maintain product and patient safety.

This role is critical to ensuring products meet required quality standards and are delivered safely to end users.

Working environment

• You will be required to wear cleanroom garments, including a one-piece suit and PPE (including powered respirators).
• Candidates must be able to stand for extended periods and undertake manual handling.
• You must demonstrate good hygiene practices and apply training to minimise contamination risk.

About you

You will ideally have knowledge of cGMP and experience in pharmaceuticals or a similar regulated environment (full training will be provided). You will be process-driven, detail-focused, and an effective communicator.

Basic qualifications and skills

• GCSE (or equivalent) including Maths and English
• Basic PC literacy (Word, Excel, Outlook)
• Strong numerical skills and ability to read/understand numerical data
• Experience working in a structured, process-driven environment
• Experience operating machinery
• Good written and spoken English
• Able to follow written and verbal instructions
• Self-motivated, adaptable, and able to work under pressure
• Clear communicator and motivator
• Able to perform manual handling in line with HSE guidelines
• Experience in a pharmaceutical manufacturing environment
• Experience using SAP
• Good understanding of cGMP in a manufacturing environment

Production Operator – GFAM Night Shift

Location: Bampton Road, Romford (Onsite)

Contract type: Full time, Permanent

Right to work: Sponsorship not currently available

Please note that, if your application is successful following the initial review, you will be invited to attend an assessment centre on Sunday 4th October, from 10pm - 4am. The assessment centre will include maths and literacy assessments, a team activity and a comptency-based interview.

Working hours

Sunday to Thursday. Subject to operational needs the night shift will start between 10:00pm and 10:30pm and finish between 6:00am and 6:30am. This equates to 37.5 hours per week.

What you will do

As a Production Operator, you will work as part of a team producing high-quality pharmaceutical products focused on the treatment of pain, addiction, and critical care. You will ensure all production activities are carried out in line with current Good Manufacturing Practice (cGMP) standards.

Key responsibilities:

• Accurate documentation: Complete batch manufacturing records accurately, neatly, and with integrity to ensure compliance at all times.
• GMP compliance: Follow detailed GMP working instructions and guidelines to produce high-quality products.
• Collaboration with Engineering: Work closely with the Engineering team to support the resolution of machine breakdowns.
• Teamwork: Work effectively with colleagues to complete batch-to-batch tasks efficiently and minimise downtime.
• Quality control: Carry out quality checks at various stages of the process to maintain product and patient safety.

This role is critical to ensuring products meet required quality standards and are delivered safely to end users.

Working environment

• You will be required to wear cleanroom garments, including a one-piece suit and PPE (including powered respirators).
• Candidates must be able to stand for extended periods and undertake manual handling.
• You must demonstrate good hygiene practices and apply training to minimise contamination risk.

About you

You will ideally have knowledge of cGMP and experience in pharmaceuticals or a similar regulated environment (full training will be provided). You will be process-driven, detail-focused, and an effective communicator.

Basic qualifications and skills

• GCSE (or equivalent) including Maths and English
• Basic PC literacy (Word, Excel, Outlook)
• Strong numerical skills and ability to read/understand numerical data
• Experience working in a structured, process-driven environment
• Experience operating machinery
• Good written and spoken English
• Able to follow written and verbal instructions
• Self-motivated, adaptable, and able to work under pressure
• Clear communicator and motivator
• Able to perform manual handling in line with HSE guidelines
• Experience in a pharmaceutical manufacturing environment
• Experience using SAP
• Good understanding of cGMP in a manufacturing environment

Personal qualities

The ideal candidate will be a methodical and self-motivated individual who is approachable and flexible in their work. They should demonstrate diligence, a hardworking and positive attitude, and strong team player qualities. Adaptability and a willingness to learn are essential. A technically minded approach, with the capability to see beyond processes, is highly valued.

What we offer you

• £25,000 per annum
• 31% shift allowance
• Opportunity to increase salary through a tiered performance-based system
• 25 days annual leave, plus bank holidays with an opportunity to buy or sell up to an additional 5 days
• Holidays rising to 30 days with length of service
• Eligible to participate in the Company’s Business bonus scheme with a potential earning of 3% of salary
• Wellbeing and benefits platform
• Medicash - health cash plan
• Salary Sacrifice scheme - electric vehicles with Tusker (dependent on meeting policy eligibility)
• Pension Plan - employer contribution of 5%

Why Ethypharm?

Ethypharm is a leading mid-sized international pharmaceutical company, with strong European roots, that manufactures and provides essential medicines, with a focus on hospital care, central nervous system (severe pain and addiction) and internal medicine.

Ethypharm has 1,700 employees dedicated to its various pharmaceutical activities. Our six production sites located in France, UK, Spain, and China have expertise in injectables and complex oral solid forms.

At Ethypharm, you will be part of a team dedicated and committed to improving patients lives.

Our Romford facility is located 20 miles from the centre of London and consists of over 6700 square metres of a high-quality, modern pharmaceutical facility where we mix, fill, sterilise, inspect, pack, and label a wide range of medicines.

We provide a workplace which is one of collaboration, teamwork and innovation. We are all different and we embrace this uniqueness in each and every one of our employees. Our commitment to you is that we want to help you unleash your full potential by supporting your training and development.We want you to be the best that you can be.

At Ethypharm we recognise the value of diversity in the workplace and provide equal opportunities for all. We are always open to discussing flexible working arrangements where this meets with the needs of our business.