Evotec

Engineer

• Lead the generation of key deliverables in a phase appropriate compliance manner as part of global CQV strategy for F&U, Equipment, QC/Analytical, Cleaning and Shipping
• Document a strategy for validations programs including the generation of validation master plans
• Liaise with the equipment, operations, logistics, qc, tech transfer, process development teams and third-party contractors, as applicable, to define and identify and perform cycle development, qualification and validation activities
• Author validation documentation including, but not limited to, risk and gap assessments, cycle development protocols / reports / procedures, qualification/validation protocols and reports, and validation discrepancies.
• Lead validation discrepancy resolution including troubleshooting and root cause analysis
• Support the development of the qualification and validation programs at Just including the transition from paper based to digital validation software to configure globally scalable end to end paperless solutions to manage the validation lifecycle
• Develop and strategize compliant and novel ways to comply with regulatory requirements
• Support inspection readiness activities, Health Authority and Client audits, and support corrective actions based on audit findings
• Lead CQV activities across global expansion sites

Validation Engineer III

• Work with key stakeholders and vendors to evaluate new technologies for implantation into the manufacturing process to increase efficiency and facility throughput.
• Develop design documents (user requirement specifications, software functional specifications) based on platform process requirements and validation commissioning and qualification protocols
• Collaborate with the automation team on design and development of the Distribute Control System (DCS) with the manufacturing suite.
• Support technical evaluations of the facility utility requirements.
• Lead evaluation of single-use technologies and design single-use manifolds and assemblies.
• Work with vendors to develop data and validation packages supporting technologies.
• Facilitate procurement and implementation of approved new technologies.
• Develop business processes, guidelines, SOPs, and training for processing equipment and technologies .
• Lead the development equipment maintenance & life cycle plans.
• Lead non-conformance/deviation investigations and provide process impact evaluations of equipment/technology issues.
• Lead technical exchanges problems and solutions throughout the manufacturing network.
• Participate in internal and external audits/inspections.

Process Engineer III, Global MSAT

Manager

• Schedule and document maintenance related services for manufacturing equipment activities, including facilities and utilities.
• Actively partner and communicate with key internal/external stakeholders to develop a maintenance strategy and definition of facilities maintenance activities within the manufacturing, QC, PD and utilities and facilities areas.
• Serve as a Subject Matter Expert (SME) for facilities and utilities reliability centered maintenance for control systems; including support to predictive maintenance to main electrical distribution systems and life safety systems to ensure full compliance with the good facilities management guidelines and regulations.
• Develop maintenance strategies, plans, SOPs, parts lists, BOMs, and frequency schedules for new and modified equipment.
• Collaborate with safety, quality engineering, and manufacturing teams to perform equipment assessments.
• Review, improve, and update maintenance SOPs, parts lists, BOMs, and ensure CMMS data integrity for existing equipment.
• Analyze CMMS data to identify trends and prioritize areas for improvement.
• Conduct functional equivalency assessments for spare parts.
• Support or lead equipment troubleshooting efforts in collaboration with engineering, manufacturing, and facilities maintenance team.
• Lead and facilitate Root Cause Failure Analysis (RCFA) and Failure Mode and Effects Analysis (FMEA).
• Drive Reliability Centered Maintenance (RCM) improvement initiatives within assigned areas.
• Serve as the Reliability Engineering subject matter expert (SME) during audits.
• Lead the implementation of predictive maintenance technologies to enhance equipment up time.
• Participate in technical reviews for equipment design projects.
• Contribute to Factory Acceptance Testing (FAT) and commissioning of new or modified equipment as needed.
• Identify and lead cost, waste, and energy reduction opportunities.
• Lead carbon footprint reduction initiatives.
• Manage assigned tasks related to change control, Quality CAPAs, and Safety CAPAs.
• Track, maintain, and publish maintenance performance metrics/statistics.
• Perform other duties as assigned.

Senior Facilities Manager, Reliability

Security Engineer

• Design, implement, and maintain security controls and solutions across various technological domains
• Plan, implement, and maintain cybersecurity tools
• Collaborate with security architects and the SOC
• Conduct security assessments, vulnerability scans, and penetration tests
• Support the SOC and participate in incident detection and response activities
• Work with cross-functional teams and IT stakeholders
• Develop and maintain system documentation, technical guidelines, standards, and procedures
• Stay updated on the latest security trends, technologies, and best practices

Cyber Security Engineer

Vice President

• Define and drive Evotec’s global Quality strategy across Drug Discovery and Drug Development
• Lead large-scale transformation initiatives across systems, structures, processes, and capabilities
• Position Quality as a visible differentiator in client partnerships, business development, and strategic growth
• Build strong executive relationships internally and externally across pharma, biotech, and regulatory bodies
• Ensure world-class GXP compliance while enabling agility, scalability, and operational performance
• Lead and inspire an international Quality organisation across the UK, Germany, France, Italy, and the USA

EVP, Global Quality

• Lead validation efforts for Manufacturing (MFG), Quality Control (QC), enterprise, and PP&D systems within the Sandoz remediation initiative.
• Ensure adherence to client requirements, regulatory compliance, and project timelines.
• Collaborate with cross-functional teams to execute complex Computer System Validation (CSV) projects, including remediation and new system implementations.
• Develop validation strategies and author validation documents such as validation master plans, data migration plans, protocols, reports, and discrepancy resolutions.
• Manage and optimize validation testing processes, ensuring risk-based validation approaches align with current FDA Computer Software Assurance (CSA) principles and GAMP5 practices.
• Standardize and enhance CSV framework templates and procedures to drive continuous improvement initiatives.
• Support and oversee risk management activities, including risk-based assessments and gap remediation efforts.
• Ensure compliance and maintain the validated state of all GxP systems.
• Manage external CSV consultants and oversee their contributions to CSV projects.
• Serve as a subject matter expert (SME) for Data Integrity, CSV lifecycle management, and compliance with global regulatory expectations.
• Own CSV-related deviations and CAPAs, managing remediation efforts related to CSV and Data Integrity.
• Partner with IT to establish backup/restore protocols, disaster recovery strategies, adherence to data retention schedules, and infrastructure qualification requirements.
• Assist business and technical owners in developing requirements and specifications for computerized systems used in GxP operations.
• Oversee the authoring and execution of IQ, OQ, and PQ test scripts.

IT CSV Engineer

• Lead the design, development and procurement of new equipment and technologies for the Just-Evotec manufacturing network
• Evaluate new technologies for implementation into the manufacturing process to increase efficiency and facility throughput
• Develop design documents based on platform process requirements and validation commissioning and qualification protocols
• Collaborate with the automation team on design and development of the Distributed Control System (DCS)
• Support technical evaluations of the facility utility requirements
• Lead evaluation of single-use technologies and design single-use manifolds and assemblies
• Work with vendors to develop data and validation packages supporting technologies
• Facilitate procurement and implementation of approved new technologies
• Develop business processes, guidelines, SOPs, and training for processing equipment and technologies
• Lead the development equipment maintenance & life cycle plans
• Lead non-conformance/deviation investigations and provide process impact evaluations of equipment/technology issues
• Lead technical exchanges problems and solutions throughout the manufacturing network
• Participate in internal and external audits/inspections

Process Engineer III

• Work with key stakeholders to evaluate new and existing technologies to increase efficiency and facility throughput
• Develop design documents (user requirement specifications, software functional specifications) based on platform process requirements and validation commissioning and qualification protocols
• Assist project leads and automation team with integrating equipment and technologies into the Distribute Control System (DCS) with the manufacturing suite
• Evaluate single-use technologies and design single-use manifolds and assemblies
• Work with vendors to develop data and validation packages supporting technologies
• Facilitate procurement and implementation of approved new technologies
• Develop business processes, guidelines, SOPs, and training for processing equipment and technologies
• Lead the development equipment maintenance & life cycle plans
• Partner with Site MSAT Manufacturing Technology & Science teams on global and site objectives
• Participate in non-conformance/deviation investigation and provide process impact evaluations of equipment issues
• Participate in exchange of technical problems and solutions throughout the manufacturing network
• Participate in internal and external audits/inspections

Process Engineer II

Compliance

• guide the successful logistical support for quality records for clinical and commercial manufacturing operations while ensuring cGMP compliance
• supervise a team of technical subject matter experts in biologics operations
• guide investigations, demonstrate strong technical and problem-solving skills
• support team in tracking to deviation closure deliverables to meet lot disposition timelines
• improve the technical capabilities and quality practices within the department
• coordinate activities and resolve issues across the department, other groups, and/or projects
• ensure response to and/or resolve recurring technical or processing issues
• drive safety, quality and accountability culture
• communicate information effectively through updates, reports, and summaries
• lead improvements in processes and methods that reinforce cGMP within the department and/or across the site
• participate directly in internal, external, and global health authority audits/inspections
• apply systematic thinking processes and technical knowledge to independently address a broad range of non-routine to moderately complex problems
• establish goals of the department
• assist in providing leadership on project teams when appropriate
• provide routine updates on progress, status, and issues associated with campaigns/projects
• provide support and/or direction to junior staff when necessary
• exercise sound judgment when making decisions
• make critical decisions in collaboration with key stakeholders
• demonstrate accountability for personal, departmental, and organizational initiatives

Senior Manager, Manufacturing Compliance

QA Engineer

• Execute day-to-day QA responsibilities for GMP manufacturing
• Build and enhance quality assurance systems
• Review and assess all quality events of eQMS to assure compliance
• Provide inputs and reviews on communication about deliverables
• Develop, review, and deliver training regarding QMS process
• Support QA QMS in internal and external client audits
• Monitor and review effectiveness for QMS through trending and analysis

QA Specialist

• lead a QC raw materials testing program to support commercial manufacturing
• oversee the inspection, sampling, and testing of incoming raw materials prior to use in manufacturing, according to US and EU GMP requirements
• ensure materials are sampled in accordance with SOPs, entered into the data management systems, and are available for use on time
• participate in the qualification of raw materials via external and in-house testing
• serve as subject matter expert in review of raw material specifications
• participate in vendor audits as a technical advisor
• oversee the daily routine activities of the raw materials group, provide data review, and ensure the operation remains compliant at all times
• collaborate with Quality Assurance, Manufacturing, Materials Management, external vendors, and other functions to ensure internal timelines, testing TAT, and team milestones are achieved
• author and maintain required cGMP documentation such as SOPs and guidance documents
• oversee verification of assays at external testing labs
• identify gaps, design collaborative solutions, and implement improvements
• participate in external testing labs QC laboratory investigations, deviations, OOS, and CAPAs
• support onboarding and qualification of analytical equipment.

QC Manager, Raw Materials

Risk

• Facilitate and coordinate formal Risk Assessments with cross functional groups to identify risks
• Work with process owners and subject matter experts to identify required mitigations and drive down risk to acceptable levels
• Manage the site risk register for both the Seattle and Redmond facilities
• Communicate major risks and the associated mitigation plans to senior management
• Continue the development and improvement of Just-Evotec Risk Management program
• Mentor and train functional groups in the area of Risk Management to increase risk intelligence within the broader organization
• Partner with both internal/external collaborators, vendors, and regulatory agencies to anticipate and resolve risk and maintain GxP compliance

Quality Risk Manager

Business Development Rep

• Develop and implement a regional sales strategy aligned with global commercial goals, assess and refine sales territories and account assignments across the team to maximize efficiency and growth potential.
• Build and maintain strong, executive-level relationships with key clients in the region, acting as a trusted advisor and understanding their unique needs to ensure Evotec is seen as partner of choice.
• Accelerate top-line growth by being accountable for the achievement of a regional sales target & supporting the team in the identification and closing of new sales opportunities while ensuring sustainable long-term profitability by safeguarding profit margins.
• Monitor team KPIs and report performance to executive leadership.
• Partner with other sales leaders, marketing, commercial strategy and commercial operations to ensure aligned growth strategies and seamless execution across the organization.
• Represent Evotec at industry events, trade shows, and key client meetings, serving as a visible and knowledgeable company ambassador in the region.
• Hire, mentor, train, and motivate sales teams to achieve sales and customer satisfaction targets, ensuring proper staffing and efficient utilization of resources.

VP Business Development – Development, East Coast/Northeast

Director

• Lead and manage a global, fully remote team, fostering a high-performance and accountable culture
• Effectively allocate and prioritise workload across the team, ensuring efficiency and balance
• Drive systematic process optimisation across the proposal lifecycle, identifying bottlenecks and implementing improvements that increase speed, consistency, and quality
• Introduce scalable workflows, automation, and standardisation to reduce cycle time and increase throughput without compromising accuracy
• Partner closely with Sales and Operations leadership, as well as cross-functional teams (Finance, Legal, Project Management), to drive alignment and improvements
• Collaborate closely with client-facing teams and support Sales in client discussions to ensure proposals align with client expectations, including presenting bids, articulating proposal rationale, and contributing to client meetings as needed
• Define, implement, and monitor KPIs, leveraging CRM tools to track efficiency metrics (turnaround time and win rates indicators) and continuously improve outcomes

Director, Head of Discovery Proposal

Learning and Development

• Support our Learning, Leadership, and Talent processes through platforms, tools, and AI solutions.
• Manage and improve EVOacademy (LMS) for user experience and engagement.
• Support EVOconnect / EVOtalks (Workday) for performance and talent processes.
• Work closely with the HRIS team to implement changes and extract data and insights.
• Upload, curate, and maintain digital learning content.
• Support the design and rollout of learning journeys and initiatives.
• Create learning materials and videos using digital and AI tools.
• Manage operational topics such as purchase orders, licenses, and invoicing.
• Use AI tools to improve content creation and team productivity.
• Support the communication of learning initiatives and campaigns.
• Track and report on learning and participation data.