Product Transfer Coordinator

The Process Life Cycle Team, a division of Product Transfer, acts as the technical partner to several Swedish and International functions within Cepheid. Our team leads/coordinates post-launch changes, improvement projects, transfers of assays between manufacturing sites, and supports expansions into new markets. As part of these activities, we solve problems and develop new processes, methods and procedures, assuring manufacturability and continued production of cost-effective high-quality products.


In your role as Product Transfer Coordinator, you will work with changes that affect Cepheid's products available on the market. You will be responsible for participating in and supporting projects and activities related to the manufacture, quality control and compliance of GX assay products. Daily interaction with Operations, Quality Control, Regulatory, R&D, Global Supply and other national and international functions within Cepheid is expected. Continuous production of cost-effective and high-quality products through effective implementation of changes to both products and processes, participation in improvement initiatives, transfers of assays between manufacturing sites and expansions into new markets are key activities.


Your main responsibilities will be to coordinate and participate in projects, and implement operations-related activities such as:
Changes to manufacturing processes and test procedures
Updates of BOMs, procedures and worksheets
Investigations, troubleshooting and risk assessments
Initial assessment of requests/tasks
Test method validations, and qualifications



Required Education:
MS in Life Sciences with 1+ years of relevant professional experience, or
BS in Life Sciences with 3+ years of relevant professional experience



Required knowledge, skills and abilities:
Proficiency in Molecular Biology Techniques including PCR
Excellent communication skills both in Swedish & English (oral and written)
Excellent organizational and planning skills
Demonstrated track-record of successful coordination of tasks and activities
Ability to successfully interact with cross-functional teams in a global environment
Experience within Operations/Manufacturing and/or from working in a regulated environment (ISO or GMP)



Preferred qualifications:
Experience with Design for Manufacturing
Familiarity with medical device regulations in US and CE markets
Experience from participating in projects
Experience within validation/qualification
In order for you to succeed in this role, you need to be efficient and organized. You are a responsible person who thrives in a continuously changing environment, prioritizing among parallel on-going tasks. You communicate clearly in all parts of the organization and are easy to cooperate with and keen to achieve results in your work.
This position is a temporary position due to a maternity leave between- 2022-02-01 until 2022.01.31.



Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.