Expert Quality Engineering (m/f/d)* Mainz
Specialty board certificationIdeally, candidate will have a minimum 2 years clinical trials experience as an investigator or medical /clinical expert in the Pharma, CRO, or Biotech industry.Ability to establish and maintain effective working relationships with co-workers, managers and clients.
Medical Director- Psychiatry (m/w/d) Frankfurt, Hesse, Germany
Specialty board certificationIdeally, candidate will have a minimum 2 years clinical trials experience as an investigator or medical /clinical expert in the Pharma, CRO, or Biotech industry.Ability to establish and maintain effective working relationships with co-workers, managers and clients.
Facilities & Utilities Engineer (m/f/d) Neuchatel
Serve as the primary technical contact (SME) for assigned installationsProvide expertise in Building & HVAC, Black Utilities, Clean Utilities, and Chemical storage and distributionLead or support design, installation, commissioning and qualification of system improvements or upgradesAssess technical condition of equipment and propose corrective actions or optimizationsCoordinate corrective maintenance, improvements, and modificationsEnsure alignment with cGMP, GEP, SUVA/ASIT and other relevant industry standardsEnsure safety measures are in place to prevent all risks of injuryDevelop and apply engineering procedures and company standardsSupport the implementation of site-wide and corporate processesParticipate in internal and external audits as system expertEngineering degree (BS/MS or equivalent) in Biotechnology, Chemistry, Food Processing, Mechanical Engineering, or similarSolid experience in the Pharma/Biotech industry (Process or Plant/Engineering)Strong experience in installation, commissioning & validation of pharmaceutical facilities, especially in Facilities & UtilitiesMaintenance & Utilities expertise is an assetStrong knowledge of GEP, cGxPs, FDA guidelines, ISPE guidelines, ASTM2500, ASME/BPEFluent in French & English; German is advantageousProficient with MS Office and MS Project A very renowned companyFlat hierarchiesFlexible working times
Metrology Supervisor (m/f/d) Lengnau, Berne
Lead and oversee daily metrology and calibration activities across GMP areas (manufacturing, QC, labs, utilities) Ensure all measuring and test equipment is calibrated and maintained in compliance with GMP, FDA, EMA, and ISO standards Manage the full calibration lifecycle: planning, execution, review, approval, and documentation Review and approve calibration certificates, OOT results, deviations, and technical assessments Drive and manage deviation, CAPA, and change control processes related to metrology Ensure data integrity according to ALCOA+ principles in all records and electronic systems Support internal/external audits and regulatory inspections, ensuring inspection readiness Collaborate with QA, Engineering, Validation, and Manufacturing on equipment qualification (IQ/OQ/PQ) Monitor and report KPIs (compliance, turnaround time, right-first-time performance) Train, mentor, and develop metrology technicians in GMP and technical competencies Bachelor’s degree in Engineering, Life Sciences, or a related technical field Experience in metrology/calibration within a GMP-regulated pharma/biotech environment Proven leadership or supervisory experience Strong knowledge of GMP regulations (21 CFR 210/211, Annex 11) and regulatory expectations Solid understanding of measurement uncertainty, risk-based calibration, and critical instrumentation Experience with computerized system validation (CSV) and ALCOA+ data integrity requirements Familiarity with QMS processes, including deviations, CAPA, and change control Strong analytical and problem-solving skills with a structured, quality-driven mindset Excellent communication and cross-functional collaboration skills Continuous improvement mindset with experience in process optimization Renowned pharmaceutical company Attractive salary package HAYS Benefits
Principal - EMEA Integrated Research London, United Kingdom
What You’ll Be DoingOwning client engagements and being responsible for ensuring actionable, on-target and timely proposals for client satisfactionMeeting or exceeding revenue targets by developing and delivering insightful, value-added solutions that address complex issuesSeeking out and identifying new revenue opportunities and ensuring a continuous flow of business from clientsApplying consultative problem-solving skills to become a solutions-based expertIdentifying issues to develop tangible and commercial offeringsContributing to the awareness of IQVIA Consulting Group in the marketplace through speaking engagements, client meetings, and publicationsStrengthening your expertise through on-the-job experience and participating in conferences and eventsMentoring, coaching, and sharing expertise
Who You AreA degree holder with 10+ years’ experience in life sciences or healthcare consultingProven seller of complex engagements to the top Pharma/Life Sciences companiesAn established leader with a record of management and people developmentAn expert in the identified teams’ solutions, that can produce new and creative ideasA successful mentor, talent retainer and confident leader that can enable creativity in others
BenefitsVisit our benefits page for information on everything from perks to well-being initiatives and career enhancement.
Sound, hands-on expertise in client delivery, project management and business development, incl. selling complex strategy and operations engagements to top Pharma/Life Sciences companies.Several years of project experience with pharma and other healthcare industries - sound knowledge of the pharma industry and its core processes is a must.
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