Ms&t Process Expert

vor 3 Wochen

Bad Vilbel, Deutschland STADA Arzneimittel AG Vollzeit

**Process Expert**

**Linthwaite Facility**

**OUR MISSION, YOUR HEALTH**

**ONE STADA** - communication and teamwork, it’s our path into the future together.**AGILITY** - do you have the flexibility and decisiveness to drive change?**ENTREPRENEURSHIP** - will you thrive in one of the fastest growing pharmaceutical businesses in Europe?**INTEGRITY** - we are driven by trust, respect, and honesty, are you?**About the Company**:

- Like all success stories, our company history started with a great idea. In 1895, a group of pharmacists had a common objective:

- _The standardized production of medicinal products to ensure an effective and reasonable provision of healthcare for the many._ This was the beginning of STADA’s impressive development.- We are now a leading manufacturer of high-quality pharmaceuticals. With a long-standing heritage rooted in pharmacies, we continue to be a reliable and trustworthy partner. We help people regain and protect a dignified and able life.- As STADA, we fundamentally care for people’s health as a trusted partner.- If you are ready for new challenges where you can make a difference to people’s health, you have come to the right place. We are looking for people with a great attitude and passion, who care about making a difference in the world.**About the Role**:

- In this role within MS&T, you'll be responsible for providing front line expert support for all process-specific issues to production, continuously improving in quality and efficiency, performed in compliance to GMPs, SOPs and applicable guidelines. In this highly varied and fast paced role you will help
- _ _to support the delivery of our strategic vision of
- **Caring for People as a Trusted Partner**.- Key Responsibilities- Support the execution of process validations, re-validations, Annual Batch Monitoring and short-term improvement projects, liaising with all the relevant parties to ensure accurate execution.
- Execute process improvements, raw material assessments and scale-up.
- Support Project Engineering in process related projects.
- Support the selection and installation of new equipment and validation activities
- Lead product and process related investigations and deviations
- Be a resource to other departments as Subject Matter Expert for the product and process knowledge.

**About You**:

- At STADA we talk about diversity as Uniqueness. Everyone is unique and we recognise our differences as a strength. Our values
- **Entrepreneurship, Integrity, Agility** and
- **One STADA** ensure our uniqueness thrives, enabling us to care for people’s health as a trusted partner. Empower your Uniqueness, bring your whole self to STADA.- If you’re keen to add value and see results, thrive under pressure and have the can-do spirit that’s spearheading our success, bring those unique qualities, with the following skills and qualifications:
- A minimum of 5 years of combined experience in Pharmaceutical (i.e., Validation / QA) or allied industries with exposure to cGMP and GDP.
- In-depth knowledge of GMPs and current validation sciences.
- Proven process understanding (Pharma, GMP, Regulatory aspects)
- Analytical thinking / problem solving skills

**What’s in it for you?**
- Rewarding our employees is important to us, which is why we offer a range of fantastic benefits, such as:
- Competitive base salary
- Annual company performance-based bonus.
- 25 days annual leave (plus bank holidays) with the opportunity to buy an additional 5 days leave.
- Generous Company Pension Scheme
- Life Assurance
- Employee Assistance Programme

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