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Packaging Engineer Contractor (M/F/D)
Tasks:
This role is will manage CMO activities including all the documentation requirements of Packaging operations
Knowledge of cGMP docuemntation requirements a must
Knowledge and experienced use of trackwise a must
Knowledge of developing and experience in qualifying packaging components on packaging equipment a must
Management (development, review and approval of) new and modifications to technical profile drawings and purchasing/release specifications a must
Ability to multi task and achieve tactical deliverables with little to no supervision, while understanding strategic impact training
Support team in substantiating and qualifying alternate component substrates, suppliers, and processes to mitigate risk of supply the development (input), launch, life cycle management and continuous improvement of primary and/or, Lead or own change control, non-conformances and CAPA activities working with Quality and Global Labeling Operations
Manage implementation of platform (harmonization / standardization) components Manage bill of materials, etc.
Candidate will facilitate template inclusion of regulatory (serialization)and global corporate standard labeling requirements (i.e. authentication)
Scope of work includes all commercial products in the Biologics, Synthetic and Oncology portfolio, packaged within the internal packaging Network and approved contract manufacturing organizations (CMO’s) throughout global footprint with focus on EU/ROW.
Candidate will function EU based above site Packaging Engineer SME. Is responsible, as an individual contributor to managing ALL impacted changes for the group, in US, EU and Rest of World markets GSQ Portfoilio
This role is to support external CMO Packaging Engineering but may include projects/product supplied both from internal and external CMO operations.
cGMP SME in packaging
Technical specification, profile drawing development, review and approval
Packaging Process Validation
Specification development, review, approval and implementation
Managing quality documentation systems such as Veeva or Trackwise (change control, deviation/investigation and CAPA initiation, review and approval mechanisms a must)
Qualification:
Maternity Leave Cover
Language: English
Bachelor’s Degree in an engineering related field; Packaging Engineers preferred
5 years pharmaceutical experience (or equivalent)
Strong knowledge of cGMP documentation requirements
Strong technical, interpersonal, communication and leadership skills.
Demonstrated abilities to manage and collaborate across internal stakeholders such as packaging colleagues, quality…
Demonstrated strength in cross boundary communication, influencing others, working in cross-functional teams
Demonstrated organizational skills including project management
Knowledge of electronic documentation systems (MUST: Trackwise)
Requirements:
Start: 02.11.2026
Duration: 14 months
Capacity: 5 days per week (8 days per month on-site)
Location: Zurich, Switzerland
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