Regulatory CMC Associate till AstraZeneca

Arbetsbeskrivning

Regulatory CMC Associate
On behalf of AstraZeneca we are now looking for candidates for a 12 month consultant assignment as a Regulatory CMC Associate, CMC Regulatory Compliance & Stability, Operations Quality. You will be employed by Dfind and this will be your first assignment. As our consultant you get a secure employment with collective agreements (Almega), fixed monthly salary and benefits such as healthcare, occupational health insurance, insurance, ITP pension and health care allowance.

Dfind Science & Engineering is a consulting and recruitment company specialized in science and technology skills. We arrange various events and training courses for our consultants that enable exchange of experience, networking and insight into working in different roles and companies. With us, you get a consultant manager who is committed to your assignment and career development.



About AstraZeneca

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration.

CMC Regulatory Compliance & Stability is a global function that manages all Chemistry, Manufacturing and Controls (CMC) post-approval regulatory activities across the global supply chain.

The role

The Regulatory CMC Associate generates CMC documentation presented in the required format to the agreed timetable, for worldwide submissions. You will work with colleagues and other functions within AstraZeneca to obtain information that supports the generation of regulatory documentation.

You may also coordinate assembly of submission-ready documents to support lifecycle submissions.

You will keep business wide electronic systems up to date to be consistent with regulatory submissions and commitments.

The role will be based in Södertälje, Sweden, and you will work in a team of 8-10 people.

Minimum Requirements - Education and Experience

• Degree in Chemistry or Pharmacy or Chemical Engineering

• Fluently spoken and written English and Swedish

• Experience in Pharmaceutical Production or Quality Assurance or Quality Control or Product Maintenance or Regulatory Affairs

• Experience in Post Approval Regulatory CMC including CMC documentation authoring is desirable

Skills and Capabilities

• Able to work collaboratively with customers and colleagues to achieve optimum outcomes

• Ability to work with short and/ or changing timelines

• Attention to details, highly organized, able to plan and control own workload effectively and manage expectation of others

• Good communication skills

• Knowledge of information and document management technology and electronic/paper publishing software

• IT software skills

Business: Dfind Science & Engineering

City: Södertälje

Job type: Full time

Deadline for applications: 2017-12-22

More information: Sofie Önnestam, sofie.onnestam@dfind.se, 073 343 99 61

Please send your application in English.

We encourage you to send your application as soon as possible, since interviews and candidate selection are done continuously! We put great emphasis on personal suitability for this role.

Organization/Business description:

Dfind Science & Engineering is part of Randstad, one of the Nordic region's largest specialists within staffing, recruitment and outplacement.

Dfind Science& Engineering is specialized in recruitment and consulting providing competences within Life Science, Science and Engineering and is a company where people make all the difference. At Dfind Science & Engineering specialists are recruiting specialists!

All our recruitment consultants , consultants and sourcing managers have a technical or scientific background, combined with extensive networks within relevant communities and expertise within recruitment and HR. We understand our customers specific requirements and know how to find the best candidates. Through our passionate commitment and high degree of attentiveness we help people and businesses to grow and be competitive in a changing world.

Kontaktpersoner på detta företaget

Camilla Wern

Linda Nord
073 343 46 54
Ulrica Marklund

Stefan Grip

Camilla Wern

Johanna Wagrell

Kristin Bolund

Ulrika Bäckman
073-343 45 31
Carina Almquist

Britta Granath
073-3434624

Sammanfattning

Besöksadress

Styrmansgatan 2
None

Postadress

Styrmansgatan 2
Malmö, 21118

Liknande jobb


Postdoktor inom medicinsk teknologi

Postdoktor inom medicinsk teknologi

5 oktober 2023