Manufacturing Technician (28k to32k) Plus shift allowance 5k with no weekends)

JR United Kingdom; Grangemouth; On-site; GBP 26,000 - 32,000; Full time

Job summary

An established industry player in pharmaceutical manufacturing is seeking Manufacturing Technicians to join their new facility in Grangemouth. This role involves adhering to stringent cGMP procedures while manufacturing high potency ADC/APIs for clinical trials and launched products. You will be part of a dynamic team, ensuring compliance with ESH standards and maintaining audit readiness. The company offers a competitive salary package with no weekend work, providing a great work-life balance. If you are detail-oriented and passionate about contributing to innovative drug development, this opportunity is perfect for you.

Qualifications

• Adhere to cGMP procedures for manufacturing high potency ADC/APIs.
• Maintain high ESH standards and complete GMP documentation accurately.

Responsibilities

• Execute procedures to manufacture ADC/API products to GMP standards.
• Accurately record batch information and update plant documentation.

Skills

GMP Knowledge

Communication Skills

Teamwork

Risk Management

Flexibility

Education

Relevant Technical Qualification

Tools

SAP Inventory

Job description

Social network you want to login/join with:

Manufacturing Technician (28k to 32k) Plus shift allowance 5k with no weekends, Grangemouth

Client:

Piramal Pharma Solutions

Location:

Grangemouth, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

8

Posted:

18.04.2025

Expiry Date:

02.06.2025

Job Description:

Piramal Pharma Solutions is a leading global CDMO of advanced drug development and manufacturing solutions to the pharmaceutical industry.

We are expanding with our new 45 million pound facility in Grangemouth and have a need for 6 x Manufacturing Technicians to support our projects. You will be adhering to defined cGMP procedures to manufacture high potency ADC/APIs in support of launched products and clinical trial programmes. Proactive approach to suite readiness, structured monitoring, line clearance, BOM/stock levels, sample control and SAP inventory. Complete GMP documentation accurately.

Maintain high ESH standards, carrying out all work in accordance with appropriate ESH systems. Adhere to 5s and housekeeping standards so that suites are audit ready at all times.

Key Roles/Responsibilities

1. Execute defined procedures to manufacture high potency ADC/API products in support of launched products and clinical trial programmes to GMP standards.
2. Work effectively in an organized manner to adhere to the planned schedule.
3. Contribute effectively to a team working environment but also have the ability and confidence to work on an individual basis within the production team.
4. Accurately record information required for batch records.
5. Update and review plant documentation, from PI Sheets to SOPs.
6. Maintain high ESH standards, carrying out all work in accordance with appropriate EHS systems.
7. Have a working knowledge of risk management systems and procedures enabling escalation of deviation as appropriate.
8. Demonstrate flexibility, self-control, and interpersonal awareness within the team environment.
9. Process manufacturing.
10. Good working knowledge of GMP.
11. Understand chemical unit operations and process chemical reaction hazards.
12. Possess good verbal and written communication skills.
13. Experience of working in clean rooms (desirable).

Salary: 26k to 32k with 5k Shift allowance - No weekends.