Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Pharmiweb.com RSS Feed PharmiWeb Candidate Blog

Pharmiweb.com RSS Feed PharmiWeb Client Blog

Job Details

Graduate Trainees - Program Management & Regulatory Documentation

Company: Roche
Location:
Reference: 3397869302
Closing Date: 26 Feb 17
Type: Full Time
Salary (£): On Application
Benefits:

Top Job

Job Summary:

We are currently seeking two exceptional Graduates to join our successful 2-year program based in our award winning offices in Welwyn Garden City, Hertfordshire, UK.   There are two Graduate Trainee opportunities within the Product Development Regulatory Group, one in Program Management and the other in Regulatory Documentation. ...

Requirements:

We are currently seeking two exceptional Graduates to join our successful 2-year program based in our award winning offices in Welwyn Garden City, Hertfordshire, UK.

 

There are two Graduate Trainee opportunities within the Product Development Regulatory Group, one in Program Management and the other in Regulatory Documentation.

For both roles, the Graduate Program is a two year program that offers you the opportunity to get hands on work experience including assignments to your own discrete tasks and responsibilities. You will gain insight into the work of Regulatory professionals who are responsible for providing the Regulatory input and leadership throughout the lifecycle of the product, from initial first-in-man studies all the way to the point at which the product lifecycle comes to an end.

The projects you will work on are real and you will be generating genuine added value.

To broaden your experience across the development value chain you will also have the opportunity to go for a six month rotation in another Product Development function.

 

Program Management

You will be providing support to Global Regulatory Leaders and Regulatory Managers responsible for EU and Rest of the World area by working on various regulatory activities across the whole development value chain from clinical trial applications through to license applications and maintenance.

Regulatory Documentation

You will be working with global drug development teams to bring novel pharmaceutical products to patients worldwide through planning and preparing a broad range of regulatory documents, developing your scientific writing skills and knowledge of regulations. You will have the opportunity to work on many document types, different therapy areas and all stages of product development.

Who you are

You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.

You have at least a BSc in life or pharmaceutical sciences, or a similar scientific qualification.

Some relevant work experience (up to 1 year) or training would be an advantage. However, if you already work within a Regulatory environment this would not be the right role for you.

Strong team-work is one of your strengths, and you are able to work under pressure and to deadlines. As we are working in a very dynamic environment, you are expected to demonstrate flexibility, good organisational skills and strong written and verbal communication. Furthermore you are someone who learns quickly and who has very good English skills.

 

Application process

Please ensure you include a covering letter and a copy of your CV with your application. As part of your cover letter, Roche is keen to understand your motivation in applying for one of these positions. As such, you should provide responses to the following questions:

• The role you wish to be considered for – Program Management or Regulatory Documentation

• What is your key motivation for applying for this role at Roche?

• What skills and experience will you bring to the role?

• What personal qualities will you bring to the role?

• What skills or abilities do you expect to develop through this role?

• What interests and activities do you have outside of work and study?

Your cover letter should not exceed one page.

Following a screening process, we will invite successful candidates to attend an assessment centre on 24th April 2017, all day. Please note that we would be unable to accommodate candidates who would not be available to attend this date.

 

We would aim for the successful applicant to join Roche in June or July 2017 although there is a degree of flexibility.

 

Who we are

Our UK Pharmaceutical head office is situated in Welwyn garden City, Hertfordshire, with beautiful country side surrounding the area. Supported by major motorways & airports as well as being a 30 minute train ride to London, access is easy. With over 1400 people occupying our site in Welwyn, you can expect opportunities in Early Development (pRED), Product Development (PD), Commercial (Rx) and of course our corporate function.

Roche is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.

Apply for this job: Graduate Trainees - Program Management & Regulatory Documentation

Contact Information:

Address:  UK Head Office
P.O. Box 8, Welwyn Garden City, Hertfordshire, United Kingdom
AL7 3AY
England
Tel:  +44 1707 36 6000
Fax:  +44 1707 33 8297
Website:  Visit Our Web Site

Advertising
Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.