Vacant job

Are you available immediately and looking for a workplace where you can perform chemical laboratory work, collaborate with friendly colleagues, and be part of an improvement initiative? Our client, a leading player in the pharmaceutical industry, offers an exciting position with great development opportunities!

About the position

This is a full-time consulting assignment lasting for 4 months. You will be employed by Bravura and work as a consultant for the company. There are good opportunities for extension of the assignment.

About the company

Our client is a leading company in the pharmaceutical industry that offers development and manufacturing of pharmaceuticals and drug administration for both large and small companies. With a global presence and modern production facilities, they work to develop and produce medicines that contribute to better health.

Job responsibilities

As a laboratory engineer, you will belong to the Quality Control department. QC is part of the production flow and is responsible for the chemical analysis of raw materials, process samples, intermediates, and finished products, packaging control, as well as the disposition of raw materials and packaging materials. The department also handles stability and sustainability samples.

Your role also includes fulfilling assigned responsibilities for methods, equipment, and facilities, as well as using scientifically sound methodology and working in accordance with regulatory quality and GMP expectations, as well as the company's quality standards. You may also participate in qualification work and method transfers. The work is performed in accordance with and governed by GMP, which means clear frameworks for how the work is to be carried out. Education, experience, and personal qualities

Requirements:

• Completed academic education in chemistry, biology, natural sciences, or pharmaceutical studies

• At least 2 years of work experience from a similar role in a GMP-controlled QC laboratory

• Experience in performing wet chemical analyses and interpreting pharmacopoeias and/or in titration, release, and UV.

• You are fluent in Swedish and English, both spoken and written

Preferred:

• Experience in reporting in LIMS

• Experience in HPLC

To fit this role, we believe that you possess analytical skills and have the ability to independently drive your work forward within set deadlines. Since the role involves significant responsibility in working with substances that are crucial for life and health, it is very important that you are meticulous, structured, and flexible. Finally, you have good collaboration skills but can manage your tasks both independently and in a team. Being part of Recipharm is synonymous with being part of an environment with good prospects. Recipharm's global reach means that there is a wide variety of paths to choose from as part of your future development. Other information

Start: Immediately Location: UppsalaSalary: According to agreement We use a competency-based methodology in all recruitment processes to ensure unbiased selection. We also work with ongoing selection, which means that we will take down the advertisement when enough candidates have applied. If you are shortlisted for the position, we will contact you for an initial phone interview. Regardless of whether you proceed in the process or not, you will receive feedback on your application.

If you have questions about the position or your application, please feel free to contact our support by emailing info@bravura.se or calling 010-171 47 10, and we will assist you. Please specify which position you are referring to. We recommend that you submit your application promptly as we conduct ongoing selection.

Welcome with your application!

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