MSc EU Regulatory Affairs
Executive Regulatory Affairs
Wilshire Laboratories (Pvt.) Ltd.
124 Kotlakhpat Quaid e azam Industrial Area, 54000 Lahore (Pakistan)
▪ Compilation of Dossiers by gathering, evaluating, organizing, managing and collating information in a variety of formats. Specific focus on stability data and validation reports. Worked with Ac td and CTD format according to FDA, ICH and WHO guidelines.
▪ Participation in arranging documents such as COPP, Free Sales, GMP & DML certificates.
▪ Participation in attaining ISO certificates.
▪ Participation in the preparation of WHO inspections.
Before you fill out our registration form, we feel it necessary to pass on some important information.
After completing our registration process your details are checked over by our Validation Team. Their task is to upload suitable submissions or delete.
Registrations that pass validation automatically produce an online CV Profile. Due to the popularity of our website profiles are widely seen by prospective employers. On a daily basis we receive many Profile enquiries.
By following our guidelines your profile will pass our validation process.
Key points to note
Your aim should be to produce a fantastic online CV Profile.
Our task is to find you meaningful employment.