Partner with Connexaire to Deliver Innovation

At Connexaire, we enable brilliant minds and pioneering organisations to deliver impactful results across the Life Sciences industry and emerging fields such as Quantum Computing.

We’re actively building partnerships with independent consultants, start-ups, global companies, and technology innovators to support project delivery through flexible, B2B consultancy models. Our goal is to create a collaborative ecosystem that drives excellence and accelerates progress.

If you’re an expert or an organisation in any of the following disciplines, we’d love to connect:

🔹 Project Management & Construction

Project Managers, MEP Managers, Schedulers, Cost Controllers, HSE Leads, and more.

🔹 Engineering & CQV

Process Engineers, EC&I Engineers, CQV Specialists, Validation Leads, and Technical Directors.

🔹 Regulatory & Compliance

Regulatory Affairs professionals, QA/QC experts, Qualified Persons (QPs), and Compliance Directors.

🔹 MSAT & Manufacturing

Scientists, Biotechnologists, Technology Transfer Leads, and MSAT Managers.

🔹 Automation, Digital & Quantum

Automation Engineers, AI/ML Specialists, Robotics Experts, Software Developers, Data Scientists, and Quantum Computing innovators (algorithm design, quantum hardware integration, advanced simulation).

Whether you’re an individual consultant, a start-up with cutting-edge solutions, or a global enterprise seeking collaboration, Connexaire offers a clear, honest, and personalised engagement experience—from first contact to project completion.

Let’s collaborate to deliver excellence.

📩 Submit your profile or partnership details via our contact form and become part of a network that empowers innovation and drives results.

Location: Denmark

Engagement Type: Full-time, onsite consultancy

Duration: Until 2028 (12-month renewable contracts)

Start Date: May 2026

Assignment Overview

Connexaire is seeking an experienced Project Controls Lead (cost focussed) to deliver expert consultancy services for a major construction project in Denmark. This landmark initiative, valued at a few billion DKK, requires a seasoned professional to lead project controls and ensure successful execution.

Key Responsibilities

As a Connexaire consultant, you will:

• Lead and manage all aspects of Cost controls and take on a Project Controls overview for the following, including:

  • Cost management

  • Scheduling

  • Risk management

  • Change management

  • Performance tracking

• Ensure compliance with corporate standards and budgetary constraints.

• Collaborate with contractors, internal stakeholders, and cross-functional teams.

• Support contract management activities (excluding procurement).

Requirements

• Proven experience in project controls leadership within large-scale projects.

• Broad expertise across cost, and understanding of risk, scheduling, and change management.

• Background in major construction projects, ideally within the pharmaceutical sector.

• Strong interpersonal and leadership skills.

• SAP experience preferred.

• Fluency in English; Danish language skills are an advantage.

• Must be eligible to work in Denmark. International consultants will be engaged via a payroll partner and may benefit from Denmark’s Expat Tax Scheme.

 Work Environment

• Full-time, onsite presence required (Monday–Friday).

Collaborative office culture with close interaction across engineering and facilities teams.

Why Partner with Connexaire?

At Connexaire, we connect exceptional consultants with high-impact projects. By joining our network, you gain:

• Access to prestigious assignments in the pharmaceutical and life sciences sector.

• Streamlined engagement through our payroll partner for international consultants when working in Denmark.

• Support from a consultancy that values expertise, integrity, and client success.

Location: Germany
Engagement Type: Contract or permanent
Start Date: June 2026
Sector: Biotech / Biopharma / Life Sciences

Connexaire is seeking an experienced Automation Manager to support a next-generation biotech manufacturing environment focused on advanced biologics production.

This role will support a highly automated GMP facility covering Drug Substance, Drug Product, fill & finish, packaging, Quality Control, warehouse, and supply chain operations. The successful candidate will lead automation activities across manufacturing and supporting systems, ensuring strong project delivery, compliance, and operational performance.

Key Responsibilities

As a Connexaire consultant or placed professional, you will:

• Lead automation activities across GMP manufacturing and supporting systems.

• Manage automation projects from design through to commissioning, qualification, and handover.

• Provide technical leadership across DeltaV DCS, Siemens PLCs, OT networking, and process control systems.

• Support automation strategy across USP, DSP, fill & finish, QC, packaging, warehouse, and supply chain operations.

• Ensure automation systems meet GMP, validation, data integrity, and regulatory expectations.

• Collaborate with Engineering, Manufacturing, Quality, Validation, IT/OT, QC, Supply Chain, vendors, and system integrators.

• Drive reliability, process control, alarm management, data traceability, and continuous improvement.

Requirements

• Proven automation leadership experience in Pharma, Biotech, Biologics, CDMO, Biosimilar, or another GMP-regulated environment.

• Demonstrable experience leading automation projects in Pharma or other regulated industries.

• Strong hands-on experience with DeltaV DCS and Siemens PLCs.

• Practical experience with OT networking, automation infrastructure, and system integration.

• Strong understanding of GMP documentation, validation, change control, data integrity, and automation lifecycle management.

• Strong leadership, communication, and stakeholder management skills.

• Fluency in English, German is advantageous.

• Must be eligible to work in the EU.

Advantageous Experience

• CDMO or biosimilar manufacturing.

• Fed-batch processes.

• SUB and SUM technologies.

• AVEVA OSIsoft PI Historian.

• EMS systems.

• LabWare LIMS.

Work Environment

• Advanced biotech / biopharma manufacturing environment.

• GMP-regulated facility with high automation and data traceability.

• Cross-functional collaboration with technical, quality, manufacturing, and external partner teams.

• Contract or permanent engagement considered.

Why Partner with Connexaire?

Connexaire connects specialist consultants and technical professionals with high-impact opportunities across pharmaceutical, biotech, and life sciences projects.

You will gain access to confidential opportunities, professional engagement support, and assignments where technical expertise, integrity, and delivery quality matter.

Location: Germany
Engagement Type: Contract or permanent
Start Date: June 2026
Sector: Biotech / Biopharma / Life Sciences

Assignment Overview

Connexaire is seeking an experienced Senior Automation Engineer to support a next-generation biotech manufacturing environment focused on advanced biologics production.

This role will provide hands-on automation engineering support across a highly automated GMP facility covering Drug Substance, Drug Product, fill & finish, packaging, Quality Control, warehouse, and supply chain operations.

The successful candidate will support process control systems, OT infrastructure, GMP automation systems, commissioning, qualification, troubleshooting, and lifecycle activities.

Key Responsibilities

As a Connexaire consultant or placed professional, you will:

• Support automation engineering activities across GMP manufacturing and supporting systems.

• Configure, troubleshoot, optimise, and maintain DeltaV DCS, Siemens PLCs, and OT infrastructure.

• Support design, testing, commissioning, qualification, and operational readiness activities.

• Participate in FAT, SAT, IQ, OQ, PQ, and validation-related documentation.

• Support integration with historian systems, EMS, LIMS, and manufacturing-related systems where applicable.

• Investigate and resolve automation issues in live GMP manufacturing environments.

• Prepare and maintain specifications, test protocols, change controls, technical reports, and lifecycle documentation.

• Work closely with Engineering, Manufacturing, Quality, Validation, IT/OT, QC, Supply Chain, vendors, and system integrators.

Requirements

• Proven hands-on automation engineering experience in Pharma, Biotech, Biologics, CDMO, Biosimilar, or another GMP-regulated environment.

• Strong practical experience with DeltaV DCS and Siemens PLCs.

• Experience with OT networking, industrial communication, automation infrastructure, and system integration.

• Experience supporting commissioning, qualification, troubleshooting, and lifecycle management of GMP automation systems.

• Good understanding of GMP documentation, validation, change control, deviation/CAPA support, and data integrity.

• Strong communication and problem-solving skills.

• Fluency in English, German advantageous.

• Must be eligible to work in the EU.

Advantageous Experience

• CDMO or biosimilar manufacturing.

• Fed-batch processes.

• SUB and SUM technologies.

• AVEVA OSIsoft PI Historian.

• EMS systems.

• LabWare LIMS.

Work Environment

• Advanced biotech / biopharma manufacturing environment.

• GMP-regulated facility with high automation and data traceability.

• Hands-on technical role working with manufacturing, engineering, validation, and IT/OT teams.

• Contract or permanent engagement considered.

Why Partner with Connexaire?

Connexaire connects specialist consultants and technical professionals with high-impact opportunities across pharmaceutical, biotech, and life sciences projects.

You will gain access to confidential opportunities, professional engagement support, and assignments where technical expertise, integrity, and delivery quality matter.