Manufacturing Technician

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 contribute to the development of pharmaceutical products in a sterile environment. This role involves executing aseptic manufacturing processes, maintaining compliance with regulatory standards, and ensuring operational efficiency. The ideal candidate will possess effective communication skills and demonstrate flexibility in a dynamic setting. Join a team that values collaboration and quality in producing essential pharmaceutical products, and be a part of a mission-driven organization that prioritizes safety and excellence in every aspect of its operations.

Qualifications

• Experience in following manufacturing documentation in a GMP controlled cleanroom.
• Knowledge of pharmaceutical manufacturing and lean manufacturing is desirable.

Responsibilities

• Execute manufacturing processes for aseptic products following cGMP and SOPs.
• Maintain a clean and safe workplace compliant with GMP and Health & Safety standards.

Skills

Effective communication skills

Flexibility and adaptability

Education

5 National 5's or Higher in Mathematics and English

Job description

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Job Title: Manufacturing Technician - Pharmaceutical Aseptic Processing

Location: Stirling

Working Hours: Shifts (7am to 2pm / 3pm to 10pm)

Core Purpose:

The Manufacturing Technician contributes to the development of pharmaceutical products in a sterile (aseptic) environment, ensuring all processes adhere to regulatory standards and contribute to operational efficiency.

Key Responsibilities:

Operational Effectiveness

• Execute manufacturing processes for aseptic products from raw material ordering to finished product dispatch, following cGMP and SOPs.
• Maintain validated aseptic clean room operator status; prepare materials, reconcile supplies, label, and package products.
• Conduct routine cleanroom monitoring and equipment setup for manufacturing.
• Perform filtration of bulk drug solutions and integrity tests, and handle liquid and lyophilized drug products.
• Reconcile materials and conduct sampling of finished products.

Compliance & Quality Management

• Maintain a clean and safe workplace compliant with GMP and Health & Safety standards.
• Assist in Corrective Action/Preventative Action (CAPA), deviation investigations, and out-of-specification reviews.
• Support validation and qualification of equipment and processes as required.

Management & Development of Team

• Assist in the induction of manufacturing staff, ensuring clarity in their roles and contributions to organizational goals.
• Provide support, feedback, and collaboration with team members to enhance performance and operational effectiveness.

Managing Relationships

• Participate in staff and management meetings to contribute insights and updates on manufacturing activities.
• Foster relationships across teams and management to ensure cohesive operations and meet service expectations.
• Act as a company ambassador, promoting a positive image of the organization.

Person Specification:

Qualifications

• Essential: Educated to a minimum of 5 National 5's or Higher in Mathematics and English.

Experience

• Essential: Experience in accurately following manufacturing documentation in a GMP controlled cleanroom environment.
• Desirable: Knowledge of pharmaceutical manufacturing, lean manufacturing experience.

Skills

• Effective communication skills to collaborate within a team environment.
• Flexibility and adaptability to perform multiple tasks efficiently in a dynamic setting.