Manufacturing Technician- Pharmaceutical Processing

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

Job summary

An established industry player is seeking a Manufacturing Technician to enhance their dynamic team in Stirling. This role is pivotal in ensuring compliance with stringent regulations while performing operational tasks in a fast-paced environment. The ideal candidate will thrive in a regulated setting, showcasing their expertise in manufacturing processes and GMP standards. With opportunities for growth and a supportive work culture, this position offers a chance to contribute to the production of high-quality pharmaceutical products. If you are dedicated, detail-oriented, and ready to meet challenges head-on, this could be the perfect opportunity for you.

Benefits

Opportunities for growth

Benefits package

Compensation for shifts

Qualifications

• Experience in manufacturing or production environments is essential.
• Knowledge of GMP practices is crucial for compliance.

Responsibilities

• Perform operational activities including start-up and processing.
• Maintain an audit-ready state through housekeeping and maintenance.

Skills

Manufacturing experience

GMP knowledge

Science degree

Cleanroom experience

Attention to detail

Strong communication skills

Teamwork

Deadline management

Education

Relevant science degree

Job description

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Manufacturing Technician- Pharmaceutical Processing, Stirling

Client:

SRG

Location:

Stirling, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

5

Posted:

24.04.2025

Expiry Date:

08.06.2025

Job Description:

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

The ideal candidate will have production experience within a regulated environment or relevant GMP industry experience.

This role involves early and back shift work from Monday to Friday, with compensation. The company offers benefits and opportunities for growth.

Main Responsibilities:

• Perform operational activities including start-up, processing, cleaning, and handling highly potent substances.
• Complete batch manufacturing records and documentation in accordance with cGMP and SOPs accurately and promptly.
• Maintain the facility in an audit-ready state through housekeeping and maintenance.
• Set up clean rooms, prepare, and 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.
• Adhere to Health and Safety regulations.
• Record information accurately to meet deadlines.
• Participate in 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 in a busy team and achieve goals.
• Dedication and ability to meet deadlines.