Plant Production Manager

Randstad Enterprise; Kingston upon Hull; On-site; GBP 45,000 - 70,000; Full time

Job summary

A global CDMO organization is seeking a highly skilled Plant Production Manager for its chemical batch manufacturing facilities. The role involves leading a team to ensure the production of high-quality drug substances in compliance with GMP regulations. Candidates should possess an advanced degree in Chemistry or related fields, along with significant experience in batch manufacturing. Strong communication and teamwork skills are essential, as the role requires collaboration across various departments to improve production performance and processes.

Qualifications

• 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.

Responsibilities

• Lead the safe, timely, high-quality, and cost-efficient production of assigned drug substances (APIs) under GMP.
• Conduct risk analyses to ensure product quality and safety throughout the manufacturing process.
• Collaborate closely with teams in Quality Assurance, Engineering, Supply Chain, and Regulatory Affairs.

Skills

Teamwork

Communication

Problem-solving

Education

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

Job description

Job Title: Plant Production Manager, 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.