Manufacturing Technician- Pharmaceutical Processing

SRG; Stirling; On-site; GBP 25,000 - 35,000; Full time

Job summary

An established industry player is seeking a dedicated Manufacturing Technician to join their vibrant team in the pharmaceutical sector. This role offers the opportunity to work in a regulated environment, ensuring compliance with GMP standards while performing essential operational tasks. You will be involved in the complete manufacturing process, from start-up to cleaning, while contributing to audits and maintaining a cleanroom environment. If you thrive in a dynamic setting and are passionate about achieving team goals, this position could be the perfect fit for you. Join a growing company that values your contributions and offers additional benefits for your hard work.

Qualifications

• Experience in a manufacturing or production environment to GMP standards.
• Strong attention to detail and communication skills are essential.

Responsibilities

• Perform operational activities including start-up, processing, and cleaning.
• Complete batch manufacturing records accurately to cGMP and SOPs.
• Maintain the facility in an 'audit-ready' state.

Skills

GMP Experience

Attention to Detail

Strong Communication Skills

Team Player

Cleanroom Experience

Education

Relevant Science Degree

Job description

Manufacturing Technician- Pharmaceutical Processing

SRG are working with a busy manufacturing company who are looking for a Manufacturing Technician to join a busy team.

If you have production experience within a similarly regulated environment or relevant GMP industry experience then this could be the role for you.

This role does require early and back shift work Mon-Fri, which you will receive compensation for so you must be able to get to site for these times. There are also additional benefits and the chance to join an expanding company and team.

MAIN RESPONSIBILITIES:

• Performing all operational activities including start-up, processing and cleaning and dealing with highly potent substances
• Complete all batch manufacturing records and all associated documentation to cGMP and SOPs in an accurate and timely manner.
• Undertake general house-keeping and maintenance of the facility in an 'audit-ready' state at all times
• Set up the clean room and prepare and filter bulk drug solutions
• Cleaning and maintaining work areas
• Visual inspection activities
• Working to strict regulations and standards
• You will follow and review SOPs and work instructions
• Confirming your work is aligned with the relevant Health and Safety regulations and requirements
• Ensuring all information that you record is accurate to ensure set deadlines are met
• Contributing to internal and external audits

SKILLS/EXPERIENCE REQUIRED:

• Prior experience working in a manufacturing or production environment to GMP or relevant science degree
• Cleanroom experience would be beneficial
• Attention to detail and strong communication skills
• You will be passionate about working within a busy team and achieving goals
• You will be dedicated and able to work to set timelines
• Flexible and team player

Seniority level

Associate

Employment type

Full-time

Job function

Science

Industries

Pharmaceutical Manufacturing