Background:

The department Packaging Engineering Parenterals (MMDEDP) is looking for an organized and motivated individual looking to progress in his/her career. This candidate should be ready to lead projects and take the drive him/her-selves. This position focuses more on technical writing and project management for primary and secondary packaging.

Tasks & Responsibilities:

• Author technical documentation to support packaging development organization (e.g. requirements documents, risk assessments, protocol/reports)
• Act as project lead for packaging development projects protocol/reports)
• Manage timeline, budget and activities for the packaging project
• Communicate key risks/challenges to stakeholders as necessary
• Evaluate and develop new materials and/or alternate packaging materials, packaging solutions or packaging systems based on product, regulatory, business or technical requirements.
• Develop and qualify global primary and secondary packaging solutions
• Qualification of global packaging solutions in line with the current valid requirements (e.g. Development of test protocols and reports, execute IQ, OQ, and PQ etc.)
• Maintenance of global packaging solutions (e.g. maintain global specifications, support change control records, provide impact assessments, execute requalification etc.)

Must haves:

• Bachelor’s degree, preferably with an engineering degree in packaging, materials science, or a related field
• Professional background: pharma or medical device industry for 3+ years
• 3 years of experience in medical device regulation and package engineering within the pharma industry
• Strong experience in budget planning, project timeline planning, problem solving
• Profound knowledge of ISO 9001 and ISO 13485
• Knowledge of ASTM D4169, ASTM D7386 and Container closure integrity testing
• Knowledge on equipment IQ, OQ, and PQ and development of qualification protocols / reports for packaging and shipping qualification activities
• First experience in project management within the pharma industry
• Hands on working experience in GMP environment and authoring technical documents
• IT skills: Microsoft office, Visio, timeline programs
• Fluent in English - written and spoken
• Confident presentation, networking, relationship building skills

Nice to haves:

• German or French
• CAD, Artios, palletization software

Our offer:

• A modern workplace with many social- and green zones
• Flexible workplace model
• The ability to work for a company who works towards creating a positive impact on patients livelihood

If you would like an insight into the detailed job description, we look forward to receiving your complete application documents by e-mail to Ms Marica Hug (marica.hug@elan-personal.ch).

Baselland Vollzeit Fulltime Packaging Design Materials Science VerpackungsingenieurIn VerpackungstechinkerIn