Project Manager for QC Method Implementation

Posted 11 January 2022
SalaryNegotiable
LocationHaarlem
Job type Temporary
DisciplineLife sciences careersProject/Program Management
ReferenceBBBH506250_1641910631

For our client, a Pharmaceutical company in Haarlem, we are looking for a Project Manager for QC Method Implementation.

The Role

The Project Manager is responsible for planning, organizing, monitoring and completing project activities being successfully executed within the Method Implementation & Transfer group and implemented in the Quality Control department. Examples are analytical method transfers, validations, quality improvement projects, monitoring CAPAs, investigating and implementing new techniques. The company is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.

Responsibilities

  • Develop project plans by collecting relevant information regarding the project; checking registrations files, drafting transfer plans.
  • Develop and execute activity planning. Provide management reports on status of the (QC)-project activities
  • Establish and maintain network within all interested organizational units so that relevant information is available in an efficient and effective
    way and that it is shared appropriately with all stakeholders.
  • If necessary, assemble, organize and lead the multidisciplinary project team, consisting of participants from the different departments within QC,
    in such a way that results, deliverables and information are delivered in a timely and complete manner.
  • Implement project results in routine QC production processes.
  • Support and guide analysts in analytical challenges, in advance problem solving, trouble shooting.


Requirements

  • Bachelor/Masters/PhD in life sciences, or equivalent experience
  • Min 3 years of experience in pharmaceutical industry
  • Project management experience with strong analytical chemistry background
  • Good knowledge of analytical method validation/transfer and pharmacopeia methods
  • Excellent communication and organizational skills and a strong analytical oriented mindset
  • Good knowledge of Pharmaceutical quality systems and production processes
  • Good scientific analytical attitude


Important details

  • Full time position (40h/week)
  • Requires atleast 50% onsite (Haarlem facilities)


Contact Hajar Amagir at:
T: +31 626326600
Email:
When interested please react through the application process with your English resume.

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