Manufacturing Technician- Pharmaceutical Aseptic Processing

TN United Kingdom; Stirling; On-site; GBP 25,000 - 35,000; Full time

Job summary

An established industry player is seeking a Manufacturing Technician specializing in pharmaceutical aseptic processing. This role offers a chance to work in a dynamic manufacturing environment, contributing to the production of high-quality pharmaceutical products. The ideal candidate will have experience in regulated environments, particularly with GMP standards, and will play a crucial role in maintaining operational excellence. Join a growing team that values dedication and attention to detail, ensuring compliance with health and safety regulations while supporting internal and external audits. This is an exciting opportunity to advance your career in a vital industry.

Qualifications

• Experience in manufacturing or production environments.
• Knowledge of GMP and cleanroom procedures.

Responsibilities

• Perform operational activities including start-up and processing.
• Complete batch manufacturing records in accordance with cGMP.
• Maintain the facility in an audit-ready state.

Skills

GMP knowledge

Manufacturing experience

Attention to detail

Communication skills

Cleanroom experience

Education

Relevant science degree

Job description

Social network you want to login/join with:

Manufacturing Technician- Pharmaceutical Aseptic Processing, Stirling

Client:

SRG

Location:

Stirling, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

87ea8d21fdfc

Job Views:

6

Posted:

05.05.2025

Expiry Date:

19.06.2025

Job Description:

SRG is collaborating with a busy manufacturing company seeking a Manufacturing Technician to join their team.

If you have production experience within a regulated environment or relevant GMP industry experience, this role might be suitable for you.

The position involves early and back shift work from Monday to Friday, for which you will be compensated. Additional benefits include the opportunity to join an expanding company and team.

Main Responsibilities:

• Perform operational activities including start-up, processing, cleaning, and handling highly potent substances.
• Complete batch manufacturing records and related documentation in accordance with cGMP and SOPs accurately and promptly.
• Maintain the facility in an audit-ready state through general housekeeping and maintenance.
• Set up clean rooms and prepare/filter bulk drug solutions.
• Clean and maintain work areas.
• Conduct visual inspections.
• Work in compliance with strict regulations and standards.
• Follow and review SOPs and work instructions.
• Ensure work aligns with Health and Safety regulations.
• Record information accurately to meet deadlines.
• Contribute to internal and external audits.

Skills and Experience Required:

• Experience in manufacturing or production environments, GMP knowledge, or a relevant science degree.
• Cleanroom experience is advantageous.
• Attention to detail and strong communication skills.
• Ability to work effectively within a busy team and meet goals.
• Dedication and ability to adhere to set timelines.