Scope

To take over, lead and manage already running Process Automation project sub-workstream responsible for DeltaV-based process automation modifications. Ensure alignment with business goals, challenging project schedule, regulatory requirements and technical standards. The role involves a thorough planning and tracking of activities, cross-functional coordination of vendors/internal team/internal clients, vendor management, stakeholder management and adherence to project governance frameworks. The project is already in execution stage, software design & coding is in progress. This project workstream only covers Delta-V software.

Key Responsibilities:

Project Execution & Leadership

•      Lead DeltaV modifications required in the project and their implementation through design, coding, commissioning and qualification.

•      Drive project planning, scheduling and tracking with internal clients and with contractors.

•      Ensure project delivery in compliance with GMP, GAMP5, and 21 CFR Part 11 standards.

•      Manage project scope, risks, and changes through structured change control processes.

•      Coordinate all project activities with other project workstreams, internal clients and external vendors.

•      Track and report project performance metrics to leadership.

Stakeholder & Vendor Management

•      Act as the primary point of contact for internal stakeholders and external vendors.

•      Facilitate interface agreements and align deliverables across contractors and departments

Quality Oversight

•      Ensure quality deliverables through adherence to Quality Plans and validation protocols

•      Team Leadership & Coaching

•      Provide direction and motivation to cross-functional project team consisting of internal employees and contractors.

Documentation & Compliance

•      Oversee the preparation and approval of project documentation including PQMP, FAT/SAT protocols, and validation reports.

•      Ensure timely delivery of documentation and compliance with internal document trackers.

Qualification requirements

•      Bachelor’s or Master’s degree in Engineering, Automation, or related field.

•      5+ years of experience in project management within PROCESS AUTOMATION, preferably with DeltaV systems.

•      Strong knowledge of GMP, GAMP5, and automation lifecycle documentation.

•      Proficiency in project management tools and methodologies

•      Very good communication, negotiation, and leadership skills. Very good vendor management skills.

•      Fluent English is a must, Czech language is a benefit, not a condition

Location: Near Prague, Czech Republic
Start: Rolling onboarding from September / October 2025
Contract Duration: Until June 2026 (potential extension)
Engagement: Independent Consultants (EU passport holders)
Hourly Rate: Based on experience level
Expense package: (flights, accommodation, transport - tbc)

About the Project:

Connexaire is assembling a high-performance CQV team for a critical, fast-track retrofitting project at a GMP biologics facility near Prague.

We are seeking experienced, hands-on CQV Leads across key workstreams.

This is a site-based engagement ideal for seasoned professionals seeking to lead commissioning and qualification on a strategically important European facility retrofit.

Current CQV Lead Openings:

• CQV Lead – Upstream incl. Recovery (Stainless Steel, CIP, SIP)

• CQV Lead – Downstream Process

• CQV Lead – Clean/Black Utilities

• CQV Lead – Facilities

• CQV Lead – IT/Automation (DeltaV DCS / CSV experience beneficial)

Role Overview:

As a CQV Lead, you will take ownership of your assigned workstream—leading all CQV activities from protocol development through to system handover. You will work cross-functionally with engineering, QA, automation, and vendor teams to ensure compliance, operational readiness, and seamless delivery.

Key Responsibilities:

• Lead CQV efforts for assigned systems or workstreams (e.g., process equipment, utilities, facilities, automation).

• Generate, review, and execute protocols (FAT, SAT, IQ, OQ) in line with GMP and project requirements.

• Conduct and lead field activities, including system walkdowns, punch lists, and hands-on testing.

• Manage deviations, change controls, and validation documentation to closure.

• Represent your workstream in project meetings, audits, and technical discussions.

• Mentor Technicians and Operators to execute protocols and support resource coordination to keep workstream on track.

Consultant Profile:

• 10+ years' CQV experience in GMP-regulated biotech/pharma environments.

• Proven ability to lead and deliver in fast-paced, site-based projects.

• Deep technical expertise in one or more areas:

  • Bioprocess (Upstream/Downstream)

  • Clean/Black Utilities

  • GMP Facilities & Cleanrooms

  • Automation (DeltaV - Process Automation), CSV

• Strong documentation, communication, and coordination skills.

• Comfortable interfacing cross-functionally and resolving field issues in real-time.

 Must hold a valid EU passport or work authorisation to work on-site in the Czech Republic.

Compensation & Covered Expenses

• Hourly Rate: € — Based on experience and scope.

• Expenses: (TBC)

  • ✈️ Economy return flights (EU origin)

  • 🏨 Hotel accommodation

  • 🚗 Local transportation (rental car and transfers)

Why Partner with Connexaire:

• Join a dynamic, high-performing CQV team delivering a vital biologics retrofit.

• Engage as an independent consultant with a fully covered expenses package.

• Work near vibrant Prague, offering both career-defining impact and quality of life.

• Be part of a project that matters—supporting critical GMP upgrades with future contract extension potential or access to further Connexaire opportunities.

Location: Kalundborg, Denmark (Onsite)

Employment Type: Contract

Duration: 12 Months +

Start: ASAP or 1 Month

Rates: Daily Rate

Languages: English (Fluent)

Our client, is seeking Process Automation Engineers to join their teams and contribute to cutting-edge projects in the Pharma and Biotech industries. We are seeking a highly skilled DCS Process Automation Engineer to work on large, data-driven greenfield plants with modular and scalable designs. You will be instrumental in the design, development, implementation, and validation of automation solutions using ABB 800xA.

Key Responsibilities:

• Design, develop, program, commission, and qualify DCS applications using ABB 800xA.

• Perform Factory Acceptance Tests (FAT), Site Acceptance Tests (SAT), User Acceptance Tests (UAT), and handover activities.

• Collaborate with process experts and colleagues on the integration of systems like MES, Historian, instruments, and production equipment.

• Develop and optimize automation methods and strategies to meet client needs.

• Support the development of automation strategies and architectures for international projects.

• Work in a GMP/GAMP environment.

Required Experience & Skills:

• 4+ years of experience in process automation within the Pharma or Biotech industries.

• Strong technical background in automation and related engineering principles.

Essential:

• Extensive experience with Pharma Processes including Fermentation, Purification, Upstream/Downstream.

• Proven expertise in 800xA DCS Programming (Application Engineering/Control Builder).

• Demonstrated experience with 800xA Batch Management/Recipe Management.

• Strong understanding and practical application of GMP/GDP principles.

• Hands-on experience with FAT/SAT and Commissioning activities.

Nice to Have Skills:

• Experience with Documentation and Qualification & Validation.

• Knowledge of S.88 standards and Batch Pharma processes.

• Familiarity with 800xA Pcdevice/Equipment Library.

• Excellent communication and collaboration skills.

• Ability to prioritize tasks and work in a team-oriented environment.

• Knowledge of MES, Historian systems, instruments, and production equipment.

Client Expectations:

• Ability to work independently and as part of a team.

• Strong understanding of GMP/GAMP regulations.

• Proactive approach to problem-solving and process optimization.

• Commitment to delivering high-quality automation solutions.

Why Apply?

• Contribute to innovative projects in the Pharma and Biotech industries.

• Work with cutting-edge 800xA DCS technology and data-driven automation solutions.

• Collaborate with a skilled and diverse team of process automation experts.

• Competitive contract terms.

Location: Kalundborg, Denmark (Onsite)

Employment Type: Contract

Duration: 12 months+

Start: ASAP or 1 Month

Rates: Hourly Rate

Languages: English (Fluent)  

We are seeking skilled and hands-on Commissioning & Qualification (C&Q) Engineers with a strong mechanical background to join our team for a Pharmaceutical facility project.

Key Responsibilities:

• Review and interpret P&IDs, isometrics, and other technical documentation.

• Verify equipment installation according to manufacturer specifications and industry standards.

• Perform boundary marking and isolation of systems.

• Coordinate with construction and installation teams to resolve issues.

• Maintain accurate records of inspections and activities.

• Ensure compliance with safety regulations and procedures.

Key Activities:

• Plan and execute flushing and pressure testing of piping systems.

• Connect hoses, start pumps, drain pipes, and manage filters.

• Interpret and work with P&IDs to ensure proper system setup.

• Document and verify flushing and pressure test results.

• Perform hands-on installation, inspection, and troubleshooting of mechanical equipment and systems.

• Conduct system walkdowns and inspections to verify installation accuracy.

• Develop and manage punch lists for identified deficiencies.

• Ensure proper mechanical integrity and resolve installation issues.

Required Experience & Skills:

• Bachelor’s or master’s degree in an engineering or related scientific discipline.

• Proven experience in commissioning and qualification activities within the pharmaceutical or life sciences industries.

• Strong mechanical background with expertise in system testing and verification.

• Ability to interpret and work with P&IDs and technical documentation.

• Experience with hands-on mechanical equipment and systems.

• Ability to perform system walkdowns and inspections.

• Experience in developing and managing punch lists or similar issue-tracking systems.

• Knowledge of risk assessments and quality assurance.

• Excellent problem-solving and troubleshooting skills.

• Strong attention to detail and ability to maintain accurate records.

• Fluency in English.

Client Expectations:

• Ability to work independently and as part of a team.

• Strong commitment to safety and quality.

• Flexibility to adapt to various C&Q tasks.

• Hands-on approach and willingness to perform physical work.

Why Apply?

• Contribute to a critical Pharmaceutical facility project.

• Work in a dynamic and challenging environment.

• Competitive contract terms.

Location: Kalundborg, Denmark (Onsite)

Employment Type: Contract

Duration: 12 Months

Start: ASAP or 1 Month

Rates: Hourly Rate

Languages: English (Fluent)

About the Role:

Our client, a leading pharmaceutical company, seeks an experienced Automation Team Lead to oversee the integration of vendor-based automation solutions within their API production facility. This role involves leading a team of up to 5 engineers, ensuring seamless integration of PLC/SCADA systems, and acting as a Subject Matter Expert (SME).

Key Responsibilities:

• Lead a team of up to 5 automation engineers, providing direction and mentorship.

• Oversee the integration of vendor-based systems into the client's IT/OT infrastructure.

• Ensure quality and compliance with GMP/GAMP standards.

• Manage network setup and security.

• Review design, test protocols, and conduct FAT.

• Act as the primary point of contact for clients and vendors.

Required Experience & Skills:

• 7-10 years of experience in pharmaceutical (API) automation.

• Proven team leadership and management skills.

• Expertise in PLC/SCADA integration.

• Strong knowledge of GMP/GAMP.

• Experience with vendor system integration.

• Proficiency in network and security protocols.

• Excellent communication and stakeholder management.

• Experience with SCADA: iFix/WinCC/Aveva/Ignition, PLC’s: Siemens, Allen Bradley.

Why Apply?

• Lead a high-performing automation team in a critical pharmaceutical project.

• Work with cutting-edge technology and international stakeholders.

• Competitive contract terms.

Location: Kalundborg, Denmark (Onsite)

Employment Type: Contract

Duration: Initial 12 Months

Start: July / August 2025

Rates: Daily Rate

Languages: English (Fluent)

Our client, a leading pharmaceutical company, is seeking a proactive LOTO Mechanical Specialist to manage LOTO procedures on site. You will be responsible for both preparing and executing mechanical LOTO activities, reviewing P&IDs, managing work permits, and ensuring site safety.

Key Responsibilities:

• Prepare LOTO documentation, including boundary markings, P&ID reviews, locker and tag management, and valve closure lists.

• Develop and maintain isolation procedures and safety checklists.

• Execute mechanical LOTO procedures, ensuring safe isolation of equipment.

• Deliver LOTO equipment to workers.

• Clearly communicate isolation requirements and responsibilities.

• Manage the work permit system, ensuring compliance and coordination.

• Enforce safety protocols, including the use of personal protective equipment (PPE).

• Conduct risk assessments and identify potential hazards.

• Stop unsafe work and address safety concerns.

• Communicate with the permit office and stakeholders.

• Prepare Lockout/Tagout out for commissioning activities or activities interfacing with live systems.

Required Experience & Skills:

• Minimum 2 years of experience in LOTO procedures and systems, preferably in commissioning and qualification within the pharmaceutical or life sciences industries.

• Practical experience in plant isolation for mechanical systems.

• Profound understanding of Safety Rules/Lock Out Tag Out (LOTO) procedures.

• Ability to review and interpret P&IDs.

• Experience with work permit systems.

• Strong understanding of safety procedures and risk assessment.

• Proficiency in relevant IT software (e.g., Dalux, Microsoft, SharePoint, Permit Vision).

• Excellent communication and organizational skills.

• Certifications and training in safety procedures are an advantage.

• Fluency in English.

Why Apply?

• Be part of a growing LOTO team in a leading pharmaceutical project.

• Opportunity to establish and manage critical safety procedures.

• Work in a dynamic and challenging environment.

• Competitive contract terms.

Location: Spain, Barcelona, Catalonia Region

Employment Type: B2B (Autonomo)

Duration: 12 Months - 24 Months

Start: As soon as possible

Rates: Daily Rate

Languages: Spanish Fluent (Mandatory) and English

About the role:

Our client, an international company specialising in advanced industrial materials in Europe is seeking an experienced Civil Engineer to support a large-scale CAPEX investment. This role requires a versatile professional with a strong foundation in civil engineering, capable of overseeing design, quality management, and process implementation across diverse aspects of industrial construction.

Key Responsibilities:

·     Ensure civil works provide the necessary foundation and structural integrity for large-scale industrial equipment, enabling seamless mechanical system integration.

·     Facilitate close collaboration between civil, mechanical, and process engineering teams to guarantee civil designs meet the operational demands of industrial production systems.

·     Supervise the construction of critical civil infrastructure, ensuring compliance with load bearing, vibration control, and alignment specifications essential for process equipment performance.

·     Establish and maintain effective interfaces between civil structures and industrial process utilities, piping, and structural supports.

·     Validate civil structure readiness during commissioning, confirming adherence to operational and safety standards for successful equipment startup.

Required Experience & Skills:

·     Minimum 8 years of experience as a Civil Engineer on high-value industrial CAPEX projects, including heavy process equipment integration.

·     Proven ability to implement efficient civil engineering processes for large-scale mechanical installations.

·     Extensive experience in foundations, structural supports, and mechanical interfaces for industrial facilities.

·     Expertise in earthworks, concrete, steel construction, cladding, and utilities, ensuring integration with process systems.

·     Strong understanding of quality management, risk assessment, and dynamic load considerations for heavy machinery.

·     Ability to manage designs from international and Spanish teams, aligning civil works with mechanical needs.

·     Experience with commissioning, including pre-commissioning checks, structural load testing, and resolving civil-mechanical interface issues.

·     Fluency in Spanish and English (Mandatory).

Why Apply?

·     Be part of a high-impact industrial project with global reach.

·     Work with international stakeholders and supply chain partners.

·     Competitive contract terms aligned with industry standards.

Please note: This is a freelance/autónomo contract role. Candidates must possess the legal right to work as an autónomo (self-employed) in Spain. No visa sponsorship is offered. Non-EU/EEA citizens must have the necessary residency and work permits.

Location: Spain, Barcelona, Catalonia Region

Employment Type: B2B (Autonomo)

Duration: 12 Months - 24 Months

Start: As soon as possible

Rates: Daily Rate

Languages: Spanish Fluent (Mandatory) and English

About the role

Our client, an international company specialising in advanced industrial materials in Europe is seeking an experienced Contract Manager to support a large-scale CAPEX investment. This role involves managing and overseeing supplier contracts across multiple international stakeholders. The project requires a strategic professional with strong contract negotiation, risk management, and supplier engagement expertise.

Key Responsibilities

·       Lead contract negotiation, administration, and execution for a high-value industrial CAPEX projects (€500M+).

·       Manage EPCM, Time & Material, and supplier contracts, ensuring compliance with legal and commercial terms.

·       Act as the primary contract liaison between project teams, suppliers, and legal/finance departments.

·       Develop and implement risk mitigation strategies to optimise cost, timelines, and contractual obligations.

·       Handle claims management, contract variations, and dispute resolution in a timely manner.

·       Engage with international suppliers, including travel to supplier locations.

Required Experience & Skills

·       10+ years of experience as a Contract Manager on large-scale industrial CAPEX projects (€500M+).

·       Legal or commercial background in engineering, construction, or procurement.

·       Background in Raw Material Conversion, Oil & Gas, Automotive, or Pharma industries.

·       Strong expertise in EPCM contracts, Time & Material agreements, and supplier negotiations.

·       Experience managing contracts with General Contractors, Designers, and LLE Suppliers.

·       Proven ability to handle complex negotiations, risk assessment, and claims resolution.

·       Willingness to travel internationally, including supplier visits.

·       Languages: Fluency in Spanish and English (Mandatory)

Why Apply?

·       Be part of a high-impact industrial project with global reach.

·       Work with international stakeholders and supply chain partners.

·       Competitive contract terms aligned with industry standards.

Please note: This is a freelance/autónomo contract role. Candidates must possess the legal right to work as an autónomo (self-employed) in Spain. No visa sponsorship is offered. Non-EU/EEA citizens must have the necessary residency and work permits.

Location: Spain, Barcelona, Catalonia Region

Employment Type: B2B (Autonomo)

Duration: 12 Months - 24 Months

Start: As soon as possible

Rates: Daily Rate

Languages: Spanish Fluent (Mandatory) and English

Our client, an international company specialising in advanced industrial materials in Europe is seeking an experienced Project Cost Controller to support a large-scale CAPEX investment. This role will be crucial in managing and controlling project costs, ensuring accurate reporting, and optimising financial performance. The successful candidate will possess strong analytical skills and experience with SAP.

Key Responsibilities

·       Implement and maintain robust cost control processes for the project.

·       Manage cost allocation, track project expenditures, and identify cost trends.

·       Develop and generate accurate and timely cost reports for project stakeholders.

·       Utilise SAP to organise and manage the project cost structure, ensuring data integrity.

·       Monitor and analyse project budgets, forecasts, and variances.

·       Provide financial analysis and recommendations to support project decision-making.

·       Ensure compliance with financial policies and procedures.

Required Experience & Skills

·       Minimum of 5 years of experience as a Project Cost Controller.

·       Demonstrated ability to apply project controls principles and practices to effectively manage project costs and forecasts.

·       Proven track record of accurate cost allocation, insightful trend analysis, and the delivery of comprehensive cost reports to stakeholders.

·       Proficient in utilising SAP (specifically modules related to project cost controlling) for budget management, cost tracking, and establishing/maintaining project cost structures.

·       Excellent analytical and problem-solving skills.

·       Ability to work independently and as part of a team.

·       Strong attention to detail and accuracy.

·       Languages: Fluency in Spanish and English (Mandatory)

Why Apply?

·       Be part of a high-impact industrial project with global reach.

·       Work with international stakeholders and supply chain partners.

·       Competitive contract terms aligned with industry standards.

Please note: This is a freelance/autónomo contract role. Candidates must possess the legal right to work as an autónomo (self-employed) in Spain. No visa sponsorship is offered. Non-EU/EEA citizens must have the necessary residency and work permits.

Location: Near Prague, Czech Republic
Start: Rolling onboarding from August 2025
Contract Duration: Until June 2026 (potential extension)
Engagement: Independent Consultants (EU passport holders)
Hourly Rate: Based on experience level
Expense package: To be confirmed

About the Project:

Connexaire is building a high-performance CQV team for a fast-track retrofit at a GMP biologics facility near Prague. With CQV leadership and program management already in place, we are now engaging experienced CQV Engineers across multiple workstreams to support hands-on commissioning and qualification of this strategically important site.

This site-based engagement is ideal for motivated engineers looking to make a strong impact within a high-performing team on a vital GMP retrofit project.

Workstreams: Upstream, Downstream, Utilities, Facilities, Automation/IT

Current CQV Engineer Openings:

• CQV Engineer – Upstream incl. Recovery (Stainless Steel, CIP, SIP)

• CQV Engineer – Downstream Process

• CQV Engineer – Clean/Black Utilities

• CQV Engineer – Facilities

• CQV Engineer – IT/Automation (DeltaV DCS / CSV experience)

Role Overview:

As a CQV Engineer, you will support the execution of commissioning and qualification activities within your assigned workstream. Working alongside CQV Leads and cross-functional teams, you will help deliver field readiness, protocol execution, and system handover in compliance with GMP and project standards.

Key Responsibilities:

• Execute CQV tasks for assigned systems (e.g., bioprocess equipment, utilities, facilities, automation).

• Writing and execution of protocols (FAT, SAT, IQ, OQ).

• Perform hands-on commissioning and qualification in the field.

• Support system walkdowns, punch list resolution, and field coordination.

• Maintain detailed validation documentation and assist with deviation resolution.

• Work closely with CQV Leads, QA, and engineering to meet project milestones.

Consultant Profile:

• CQV experience in GMP-regulated biotech/pharma environments (minimum 3–10+ years depending on seniority).

• Strong technical understanding of one or more areas:

  • Bioprocess systems (Upstream or Downstream)

  • Clean/Black Utilities

  • GMP Facilities

  • Automation/DCS (DeltaV), IT or CSV

• Ability to work hands-on in a fast-paced, site-based environment.

• Detail-oriented with strong documentation, coordination, and communication skills.

  Must hold a valid EU passport or work authorisation to be eligible to work on-site in the Czech Republic.

Compensation & Expenses

Hourly Rates (dependent on experience) = EURO / € + Expense Package (to be confirmed)

Why Partner with Connexaire:

• Be part of a high-performing CQV team on a vital GMP retrofit program.

• Engage as an independent consultant.

• Work near vibrant Prague—a rare blend of career impact and lifestyle.

• Contribute to a critical biologics project with real purpose and global importance.

• Build a lasting partnership with Connexaire, with opportunities for future engagements across our growing project portfolio.