Validation Expert

  • Beschäftigungsart Permanent und Temporär - bis auf weiteres
  • Ort
    BASEL
  • Referenz 127516-251-1
  • Eintrittsdatum ab sofort
  • Sektor Chemie & Life Sciences
  • Publikationsdatum 10.10.2019
  • Bewerben

For our client - a pharmaceutical company situated in the region of Basel - we are looking for a:

Validation Expert

Ihr Einsatz

Major Accountabilities
-Support writing and maintaining Validation Master Plan for process, cleaning and packaging validation.
-Support the strategy for continued process verification (CPV) and annual monitoring batches that ensures all critical process parameters and quality attributes are defined after validation activities. Contributes to risk assessments for CPV.
-Set local procedures & templates for respective validation processes, documentation and validation master plan, create assessments on component criticality.
-Maintain all responsible activities and projects in an inspection ready status ahead of any internal or external audits to ensure successful inspections e.g. no critical observations related to validation activities.


Validation activities
-Leads, facilitates, elaborates and authors risk assessments for validation together with the site validation team (PU, QC, QA ) and external functions (TRD, DRA).
-Ensures that all respective validation activities are in line with the current requirements and cGMP, handling any deviations associated to these activities including oversight of pre-validation and validation resulting from launch projects as well as major or complex changes.
-Authors and reviews process, packaging or cleaning validation protocols (e.g. launches, transfers, weak point remediation) and related reports, proposes and reviews MBRs and associated change controls. Supports the execution at the shop floor.
-Responsible to translate the critical process parameters and the process control strategy into a focused validation plan for process validation.
-Participates in transfers and launches, contributes to provide experimental data obtained during the validation activities which will be used to prepare the related registration documentation (e.g. P35 module). Supports successful Handover, Submission and Launch with no delay of approval due to PAI or technical issues related to NTO.
-Contributes or writes, reviews and revises any SOPs related to validation activities, provide guidance to facility impact and component criticality assessments. Provides input to Quality Manuals (QM)/Quallity Directives (QD)/global Standard Operating Procedures (SOPs) and Guidance Documents to ensure the document is in line with global/local requirements and industry standards.
-Provides technical expertise and participates in the improvement and remediation of products in the product improvement portfolio.
-Owns the Training Curriculum for its Job Description and provides the necessary training and support to new associates joining this position.

Ihr Profil

-BSc. in Chemistry, Pharmacy, Chemical Engineering or Pharmaceutical Technology.
-Several years experience in manufacturing/ manufacturing science and technology/technical
development/Quality.
-Thorough understanding of manufacturing processes and related process equipment.
-Strong working knowledge of quality systems and regulatory requirements across multiple health authorities.
-Experience in executing process validation.
-Expert in reviewing and writing technical reports.
-Proven project management experience in a cross-functional environment (e.g. multi-site, technical development, other functions).
-Fundamental understanding of standard pharmaceutical analytical testing.
-Fluent in English and in local language.

Interessiert?

This multifaceted temporary employment provides the opportunity to apply and increase your expert knowledge in one of the largest pharmaceutical companies worldwide. To submit your complete CV including diplomas and references just use the button ‘Apply'. We are looking forward receiving your application today!

Über Manpower
Manpower Schweiz weist über 55 Jahre Erfahrung in der Rekrutierung, Evaluierung und Vermittlung von temporären und festen Mitarbeitenden sowie der Erbringung von HR-Lösungen auf. Mit 50 Agenturen in allen Sprachregionen, 20 000 temporären Mitarbeitenden, 1500 Feststellenvermittlungen und über 5000 Kundenunternehmen aller Grössenordnungen und aus allen Wirtschaftszweigen gehört Manpower zu den Branchenführern in der Schweiz.
 
Unsere 3 Versprechen
„Wir lieben, was wir tun. Dank unserer Leidenschaft haben Sie die besten Einsatzchancen.“
„Wir mögen Menschen. Wie Sie. Darum setzen wir auf eine vertrauensvolle Zusammenarbeit.“
„Wir übernehmen Verantwortung. Das verschafft Ihnen Sicherheit und interessante Perspektiven.“
 
 

Ich will den Job!

Ihr/e Manpower-Berater/in
Dr. Anja Glinschert

Life Sciences Competence Center
Picassoplatz 4
4052 Basel

T: +41 58 307 2441



Spontanbewerbung

Nicht gefunden, wonach Sie suchen? Schicken Sie uns eine Spontanbewerbung für weitere Möglichkeiten.

Spontan bewerben
Display shares