26 to 50 of 758 Permanent Pharmaceutical Jobs

Role Objectives: The WEP Clinical Global Third-Party and Audit Manager is responsible for the qualification, oversight, and auditing of third-party suppliers and vendors supporting GxP activities, including pharmaceutical manufacturing, distribution, and clinical operations. This includes providers across GMP, GDP, GCP, GLP, and GVP domains. The role ensures partners meet regulatory requirements and internal standards to support the safe More ❯

Facilities Management (or equivalent experience) Essential Qualification in Health & Safety compliance (e.g., IOSH Managing Safely, NEBOSH Certificate) Essential SIA accreditation Desirable Specialist Knowledge & Skills Requirement Importance Experience in research, pharmaceutical, or public sector environments Essential Knowledge of smart building technologies and sustainability initiatives Essential Knowledge of FM software (e.g., Concept Evolution, Planon, Maximo) and FM Operating models Essential Knowledge and More ❯

release process SAP ATTP and SAP IC Hub knowledge Knowledge of legal/government reporting regulations Serialization experience Experience with systems/landscapes specific to the Life Sciences or Pharmaceutical industry Knowledge in Plasma specific processes/fractionation Experience in Computer System Validation (legal requirements and practical knowledge) Exposure to S4HANA Public Cloud or SAP Business By Design solutions Treasury More ❯

in day-to-day interactions with team. Required Qualifications: Bachelor degree in data science, computer science, biomedical engineering or biological sciences. 2+ years of progressive business experience in the pharmaceutical, data science, including life sciences companies, and other companies in the data science ecosystem Track record of collaboration, entrepreneurial skill, and ability to influence and engage strategic and technical partners More ❯

BS, BA) or equivalent professional experience is required, preferably in Health Sciences or Data Sciences. Advanced degrees preferred (e.g., Masters, PhD). Minimum 8-12 years of experience in Pharmaceutical, CRO or Biotech industry or related field or industry! Knowledge of trial site operations and study execution Strong knowledge of regulatory guidelines (e.g., ICH-GCP). Demonstrated strong understanding of More ❯

The role is a core member of the senior leadership team for CF and is focused on driving the growth of a business serving life sciences (pharma, biotech, devices, and diagnostics). This involves supporting the development of the Life Sciences strategy and business plan and taking responsibility for aspects of its delivery including developing brand awareness, securing revenues and More ❯

markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins. Job Description Job Summary: Designs, implements and More ❯

MS Project Top-tier communication and stakeholder management skills A customer-first mindset and ability to manage matrix teams Willingness to travel occasionally Nice to Have: Experience in utilities, pharma, or infrastructure projects Agile/Scrum certification Change and risk management knowledge More ❯

MS Project Top-tier communication and stakeholder management skills A customer-first mindset and ability to manage matrix teams Willingness to travel occasionally Nice to Have: Experience in utilities, pharma, or infrastructure projects Agile/Scrum certification Change and risk management knowledge More ❯

of database performance tuning , indexing, data migration, and security best practices. Experience in server deployment , including virtual environments (e.g., VMware). Desirable Experience: Industry experience in nuclear, defence (MOD), pharmaceutical , or similarly regulated sectors. Familiarity with cloud platforms (e.g., Azure, AWS, GCP). Knowledge of OT Cybersecurity and secure design principles. Experience with database clustering , load balancing, and redundancy. Qualifications More ❯

logistic challenges today. Speed, product diversification, same-day delivery, volume, safety... these concerns are impacting a wide range of industries, from apparel, retail, automotive, to even electronics, energy and pharmaceutical industries. Geek+ was founded to be the solution to these problems. We make logistics affordable, efficient, flexible, safe and agile. Our vision is to establish a fully automatedand intelligent supply More ❯

strong technical documentation writing skills Strong interpersonal, written, and verbal communication skills Desirable experience: Experience in the EC&I industry or highly regulated industries such as Nuclear, MOD, or Pharmaceutical Experience with cloud-based platforms like GCP, AWS, or Azure Knowledge of database clustering, load-balancing, and redundancy Familiarity with integrated SCADA control system applications Experience in OT Cyber Security More ❯

strong technical documentation writing skills Strong interpersonal, written, and verbal communication skills Desirable experience: Experience in the EC&I industry or highly regulated industries such as Nuclear, MOD, or Pharmaceutical Experience with cloud-based platforms like GCP, AWS, or Azure Knowledge of database clustering, load-balancing, and redundancy Familiarity with integrated SCADA control system applications Experience in OT Cyber Security More ❯

strong technical documentation writing skills Strong interpersonal, written, and verbal communication skills Desirable experience: Experience in the EC&I industry or highly regulated industries such as Nuclear, MOD, or Pharmaceutical Experience with cloud-based platforms like GCP, AWS, or Azure Knowledge of database clustering, load-balancing, and redundancy Familiarity with integrated SCADA control system applications Experience in OT Cyber Security More ❯

process owner (LPO) to uplift his/her knowledge to reflect industry best practices Your profile Deep understanding and experience of computer system validation and data integrity in a pharma manufacturing environment Experience in API environment preferred with knowledge of systems like DeltaV, PI, PCS7 along with practices as effective alarm management. Deep understanding of both FDA and EMA requirements More ❯

volumes of documentation, electronic and paper Good attention to detail for data entry tasks and understanding of Good Documentation Practices A basic understanding of computer system validation in the pharmaceutical sector Experience and knowledge of working in a regulated environment, specifically with regards to record retention Knowledge of GCP and GMP with regards to QMS activities Responsible for ensuring that More ❯

is looking for a Migration Architect who will become a leading member of our EU Professional Services group, providing migration solutions on project teams implementing Veeva Vault R&D (pharmaceutical development) applications and Vault Platform cloud solutions to companies in the Life Sciences industry. You will lead customer migration implementations by providing expertise with data and document content migration, Vault More ❯

with great attention to detail. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic More ❯

be a decisive and solutions-orientated individual with a track record of successful achievements and accomplishments in a quality-related role in a regulated environment (such as medical devices, pharmaceutical or healthcare manufacturing), and bring experience of working with New Product Introduction projects. You will be degree qualified in a scientific, engineering or associated field. As you'd expect from More ❯

release process SAP ATTP and SAP IC Hub knowledge Knowledge of legal/government reporting regulations Serialization experience Experience with systems/landscapes specific to the Life Sciences or Pharmaceutical industry Knowledge in Plasma specific processes/fractionation Experience in Computer System Validation (legal requirements and practical knowledge) GENERAL •Career opportunities exist along multiple route maps from people and leadership More ❯

with great attention to detail. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic More ❯

/CEO Internal: Manufacturing, R&D, Engineering, Technology ESSENTIAL DUTIES AND RESPONSIBILITIES: System Design, Development, Integration and Testing: Lead the design and development of diode laser spectrometer systems for pharmaceutical test and measurement applications. Specify, select, and evaluate electro-optical devices, including tunable lasers, detectors, and beam optics. Oversee the integration of optical hardware with electronic and software systems. Design More ❯

s degree in engineering, Business, Marketing, or a related field; MBA is a plus. Have proven experience in sales management within the European market, specifically in industrial automation, manufacturing, pharmaceutical, and energy sectors. Have proven experience with working strategically through partners and distribution. Have experience creating and implementing sales strategies. Have a strong track record of achieving sales targets and More ❯

Engagement: Work closely with enterprise clients to understand business challenges and identify opportunities where AI/ML can drive value (e.g. predictive maintenance in manufacturing, drug discovery insights in pharma, or risk modeling in insurance). Translate these needs into solution roadmaps and technical plans. Technical Leadership: Provide hands-on technical leadership to delivery teams. Guide Azure AI Engineers and More ❯

Engagement: Work closely with enterprise clients to understand business challenges and identify opportunities where AI/ML can drive value (e.g. predictive maintenance in manufacturing, drug discovery insights in pharma, or risk modeling in insurance). Translate these needs into solution roadmaps and technical plans. Technical Leadership: Provide hands-on technical leadership to delivery teams. Guide Azure AI Engineers and More ❯