Operator Bulk

NextPharma Technologies Holding Ltd; Livingston; On-site; GBP 20,000 - 30,000; Full time

Job summary

A leading European contract manufacturer based in Scotland is seeking enthusiastic individuals for full-time positions in pharmaceutical manufacturing. Responsibilities include ensuring compliance with GMP regulations, recording data, and supporting all aspects of the manufacturing process. Experience in a cleanroom is a plus, but not essential. This role is shift-based, involving a proactive attitude and attention to detail. Candidates will work flexibly within a team to meet production demands.

Qualifications

• Experience in a cleanroom environment is advantageous but not essential.
• Must comply with GMP regulations.
• Ability to conduct quality checks accurately.

Responsibilities

• Manufacture pharmaceuticals for commercial and clinical applications.
• Record data appropriately in batch records.
• Maintain hygiene standards in production areas.
• Support all stages of the manufacturing process.

Skills

Attention to detail

Flexibility in production

Good practical skills

Demonstrates good literacy skills

Demonstrates good numeracy skills

Job description

We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,500 employees in Germany, France, Finland, UK and Norway. For us, the next step is always the one that matters most. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.

We are offering new and exciting roles to support the continued expansion of our manufacturing facilities which are required to meet growing market demand.

We are looking for enthusiastic, hard-working people who are willing to learn new skills and have a positive, pro-active approach. Previous experience of pharmaceutical manufacture is not essential, but you must be prepared to work in a cleanroom environment and ensure compliance with GMP regulations at all times.

Key Responsibilities:

• Manufacture of pharmaceuticals products for commercial and clinical trial applications
• Ensuring all activities are undertaken in accordance with cGMP, Health and Safety standards, and current SOPs
• Recording data appropriately in batch records and supporting documentation
• Maintaining hygiene standards in all production areas
• Supporting production activities through each stage of the manufacturing process (cleaning, mix preparation, capsule filling and sorting, blister and bottle packing)
• Set-up, operation and strip down of modern high speed production equipment
• Working flexibly within a team to ensure adherence to the production schedule
• Maintaining personal training records

Person Specification:

• Previous experience of pharmaceutical manufacture or working in a cleanroom environment would be an advantage (but not essential)
• Be conscientious and have a good eye for detail - to conduct quality checks and ensure data is accurately recorded
• Be flexibile - to ensure production output and client demands
• Have a high degree of integrity - to maintain compliance with GMP regulations
• Be reliable, and able to make a positive contribution to the production team
• Previous GMP (Good Manufacturing Practice) experience
• Good practical skills
• Demonstrates good literacy and numeracy skills

Job Type:

• Full Time, Permanent, Shift Work (Day/Back or Nights)

It's time for your next chapter:

We look forward to receiving your application.