Plant Chemist

Randstad Enterprise; Kingston upon Hull; On-site; GBP 60,000 - 80,000; Full time

Job summary

A global CDMO organization is seeking a skilled Plant Chemist for chemical batch manufacturing in Hull. You will oversee production of high-quality drug substances under GMP conditions, lead teams, and collaborate with various departments to enhance production efficiency. This role requires a PhD or Master’s in Chemistry or related fields and experience in pharmaceutical manufacturing. Excellent communication skills and a proactive approach are essential.

Qualifications

• Advanced degree in Chemistry, Chemical Engineering, or Process Engineering required.
• Experience in chemical/pharmaceutical batch manufacturing under GMP conditions required.
• Strong knowledge of GMP regulations preferred.

Responsibilities

• Lead the timely and cost-efficient production of drug substances under GMP regulations.
• Conduct risk analyses to ensure product quality and safety.
• Document processes and ensure compliance with GMP requirements.

Skills

GMP knowledge

Teamwork

Communication

Initiative

Flexibility

Education

PhD or Master’s in Chemistry, Chemical Engineering, or Process Engineering

Job description

Job Title: Plant ,Chemist Chemical Batch Manufacturing

Location: Yorkshire/Humber

Contract: Permanent, Full Time

Work Hours: 37.5

Randstad Sourceright, a leading provider of RPO & MSP Recruitment Services are currently recruiting for an Plant Chemist, Chemical Batch Manufacturing on behalf of a global CDMO organization.

Role Purpose:

We are seeking a highly skilled and motivated Plant Chemist to join our team in chemical batch manufacturing, producing high-quality drug substances (Active Pharmaceutical Ingredients - APIs) under Good Manufacturing Practice (GMP) conditions for pharmaceutical companies.

In this role, you will oversee the operation of production facilities, ensuring save, timely, cost-efficient, and compliant production while fostering strong collaboration with cross-functional teams involved in manufacturing processes.

This role will have up to 5 reports and 40 indirect reports.

Key Accountabilities

• Lead the save, timely, high-quality, and cost-efficient production of assigned drug substances (APIs) in compliance with GMP regulations and guidelines related to safety, quality, and environmental standards
• Conduct risk analyses to ensure product quality and safety throughout the manufacturing process.
• Identify and implement opportunities for continuous improvement in production performance and processes.
• Collaborate closely with cross-functional teams, including Quality Assurance, Engineering, Supply Chain, and Regulatory Affairs, to achieve organizational goals such as cost-effectiveness, delivery reliability, and compliance.
• Promote an efficient and collaborative work environment, maintaining effective communication with team members across departments and external stakeholders, including clients.
• Adapt to shifting priorities and manage multiple projects simultaneously while maintaining high standards of performance.
• Document processes and ensure accurate record-keeping in accordance with GMP requirements.

Key Requirements

• Advanced degree (PhD or Master’s) in Chemistry, Chemical Engineering, or Process Engineering.
• Several years of professional experience in chemical and/or pharmaceutical batch manufacturing, preferably under GMP conditions.
• Strong knowledge of GMP regulations and business management skills are highly desirable.
• Exceptional teamwork and communication skills, with a proven ability to collaborate effectively across functions.
• Proactive and flexible work approach, with the ability to thrive in a fast-paced environment and work under pressure.
• Strong sense of responsibility and commitment to continuous professional development.