Our client is a leading Biologics manufacturing operation globally. They are seeking a technically astute drug substance manufacturing professional to develop into a Manufacturing Lead role for their start-up manufacturing facility.

The Role

• You will be responsible for the Bio press associates assigned to the shift on an ongoing basis.
• Providing training and communication in order to achieve business targets and objectives providing guidance and performance management.
• Assisting in the designing and implementation of processes and procedures for the manufacturing shift performing safety audits and walks downs when required.
• Participating in HAZOPs and documentation reviews when needed.
• Acting as the authoriser in permit to work in manufacturing during normal day shifts.
• Ensuring the plant and equipment is operating in a compliant manner and that all activities are meeting GMP regulations.
• Making technical decisions when needed supporting all technical transfer activities to the site.
• The Shift Lead will write, review and approve SOPs, batch records, logbooks and training competencies.

The Person

• Degree qualified in Science or technical discipline.
• 4+ years' experience in a supervisory role within Biologics/Pharma/Vaccine Conjugation manufacturing or similar position.
• You will have an in-depth knowledge of cGMP, safety and environmental regulations.
• Excellent technical communicator with strong problem solving and decision-making capabilities.
• Experience either managing a team or stepping up to supervisory responsibilities for a team from time to time.

The Benefits

• Competitive salary
• Bonus
• Pension
• Health Insurance
• Shift Bonus

To learn more apply online or email your CV to Paul McDonogh to arrange a confidential discussion.