Engineering Manager
- Central
- Contract
- CAPEX Projects
Our client, a global (bio)pharmaceutical manufacturing organisation, is recruiting for a Engineering Manager to join them on their new expansion project. Based in a charming Nordic location, this is on a contractual basis, and will involve significantly growing the sites capacity for the manufacture of Biologics.
Responsibilities:
- Lead, mentor, and develop a team of engineers, providing guidance and support to achieve individual and team goals
- Oversee the planning, execution, and completion of engineering projects, ensuring they are delivered on time, within scope, and within budget
- Identify opportunities for process optimization and implement engineering solutions that enhance operational efficiency and reduce costs
- Provide technical leadership and expertise in the design, development, and implementation of engineering solutions for pharmaceutical manufacturing processes
- Ensure that engineering practices comply with GMP (Good Manufacturing Practices) and other regulatory standards
- Collaborate with internal stakeholders, including production, quality assurance, and senior management, to align engineering activities with overall business goals
- Communicate project status, risks, and opportunities to senior management and other key stakeholders
- Ensure that all engineering activities comply with relevant regulatory requirements, including FDA, EMA, and other global standards
- Support regulatory inspections and audits by providing technical documentation and expertise
- Develop and manage the engineering budget, ensuring that resources are allocated effectively to meet project and departmental goals
- Monitor expenses and implement cost-saving initiatives where applicable.
- Stay current with the latest engineering trends and technologies in the pharmaceutical industry and evaluate their potential application.
Education, Qualifications, Skills and Experience:
- Bachelor’s degree in Engineering (Mechanical, Chemical, or related field); Master’s degree preferred.
- Minimum of 8-10 years of engineering experience in the pharmaceutical or biotech industry, with at least 5 years in a leadership role.
- Proven track record of managing engineering projects and leading teams in a GMP-regulated environment.
- Strong understanding of pharmaceutical manufacturing processes, regulatory requirements, and quality standards.
- Experience with Lean Manufacturing, Six Sigma, or other continuous improvement methodologies.
- Excellent communication, leadership, and problem-solving skills.
- Ability to work effectively in a fast-paced, dynamic environment and manage multiple priorities.
If this role is of interest to you, please apply now!
#LI-NR1
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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