Quality Assurance Specialist

Quality Assurance Specialist - (Process / Parenterals)

Location: Schaffhausen, Switzerland

Hours: 40h, Hybrid way of working, on-site 4 days per week

Languages: English (fluent), German (Conversational)

Cilag AG in Schaffhausen, Switzerland, is part of the Johnson & Johnson Innovative Medicine is currently recruiting for an Specialist QA Process Parenterals.

Imagine your next role as a Quality Specialist, based in Schaffhausen.   We manufacture high quality pharmaceutical products and active pharmaceutical ingredients (APIs). Today Cilag AG is one of the largest pharmaceutical manufacturers in Switzerland supplying all the major global markets. The Schaffhausen facility is a Johnson & Johnson strategic launch and growth site for parenteral products, and we have an impressive pipeline of new and innovative products!

The role 

As a Specialist in the QA Process Parenterals team you will join a dynamic team which is responsible for Quality and Compliance guidance, as well as Quality and Aseptic oversight of equipment and premises used for manufacturing in the Business Units Parenterals (compounding and subsequently filling of syringes and vials), Optical Inspection, Device Assembly and Packaging, and Warehouse departments at the JSC Schaffhausen site.

Due to a high number of ongoing projects combined with daily business activities, we are looking for a colleague who can quickly support the team with a focus on processes, equipment and projects in the Optical inspection department.

Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our pharmaceutical products? Apply today for this exciting opportunity!

Key responsibilities:

• Provide Quality and Compliance guidance to Optical inspection department and corresponding supporting departments

• Perform Quality oversight on the shop floor

• Actively contribute to new concepts and projects as well as suggestions for improvement

• Proactive risk mitigation

• Assess and approve Non-conformances and Corrections/ CPAs related to utilities, facility, environment, equipment and processes

• Review and approve Protocols, Reports, SOPs/WIs, Change requests (COCs) and other applicable documents

• Review and approve GMP critical SAP master data (e.g. manufacturing instructions)

• Support ‚customers‘ (Production, Quality Control, Logistics, MSAT, Engineering, etc.) in terms of GMP Compliance

how to succeed:

• You have a Bachelor’s or Master’s Degree in a technical or science field

• You have proven experience (minimum 3 yrs) in a GMP regulated Pharma production environment, or experience in a relevant Quality role (minimum 2 yrs)

• You have experience in the following area and related processes - Optical inspection, e.g. fully automated, semi-automated and manual inspection

• You are used to work in an GMP-environment, and have a genuine quality mindset which is shown in your daily work

• You have experience as team or project lead

• You are fluent in German and English

If you are a team-oriented, open-minded dynamic and highly motivated person with strong interpersonal skills you might be the one we are looking for. For collaboration with different departments, you will need flexibility, social competence, and a reasonable degree of authority. You will take decisions independently and provide advice as needed

Benefits

This role offers a competitive hourly rate & a supportive working environment. This is a 2 year assignment.

About Johnson & Johnson

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years. As a skilled contractor, you’ll play a key part in the thinking, strategy, dynamism - and impact - of this iconic global healthcare company as they touch the lives of nearly a billion people every day. Contribute to the next healthcare breakthrough with your next project at Johnson & Johnson.

https://www.jnj.ch/

application process

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email. Please apply via the link.

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.