Packaging Engineer Contractor

K-Recruiting GmbH; Schweiz; Vor Ort; CHF 110.000 - 150.000; Vollzeit

Zusammenfassung

K-Recruiting GmbH is seeking a Packaging Engineer contractor (M/F/D) for a 14-month assignment located in Zurich, Switzerland. The role focuses on cGMP packaging documentation, Trackwise management, and regulatory labeling requirements across EU/ROW markets.

The candidate should hold a Bachelor's degree in packaging or related engineering field, have about 5 years of pharmaceutical experience, and be able to work with minimal supervision while coordinating with global teams.

Qualifikationen

• Maternity Leave Cover for Packaging Engineer contractor role.
• Bachelor's degree in an engineering field; Packaging Engineers preferred.
• 5 years pharmaceutical experience or equivalent.
• Strong knowledge of cGMP documentation requirements.
• Experience with electronic documentation systems (Trackwise)

Aufgaben

• Manage CMO activities and documentation for Packaging operations.
• Develop, review, and approve technical profile drawings and specs.
• Lead change control, non-conformances, and CAPA with QA and Global Labeling.
• Support qualification of packaging components on equipment.
• Oversee regulatory template inclusion and global labeling requirements.
• Coordinate platform harmonization and BOM management.

Kenntnisse

cGMP documentation

Cross-functional collaboration

Project management

Leadership

Ausbildung

Bachelor's degree in engineering (Packaging preferred)

Tools

Trackwise

Veeva

Jobbeschreibung

PackagingEngineerContractor(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