QA Advisor

QA Advisor
Centrient Pharmaceuticals Netherlands, Netherlands

Experience
1 Year
Salary
0 - 0
Job Type
Job Shift
Job Category
Traveling
No
Career Level
Telecommute
No
Qualification
As mentioned in job details
Total Vacancies
1 Job
Posted on
Aug 25, 2021
Last Date
Sep 25, 2021
Location(s)

Job Description

Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics, and a provider of next generation statins and anti-fungals. We produce and sell intermediates, active pharmaceutical ingredients and finished dosage forms.

We stand proudly at the centre of modern healthcare, as a maker of essential and life-saving medicines.

With our commitment to Quality, Reliability and Sustainability at the heart of everything we do, our over 2200 employees work continuously to meet our customers’ needs. We work towards a sustainable future by actively participating in the fight against antimicrobial resistance.

Founded 150 years ago as the ‘Nederlandsche Gist- en Spiritusfabriek’, our company was known as Gist Brocades. Headquartered in Rotterdam (Netherlands), we have production facilities and sales offices in China, India, the Netherlands, Spain,the United States and Mexico. Centrient Pharmaceuticals is wholly owned by Bain Capital Private Equity, a leading global private investment firm.

The Production department of the business Unit EMENA has a vacancy in its Delft offices, for the following position:

QA Advisor

The Position

Support to the QA manager, acting according to c-GMP’s guidelines and promoting compliance.

The main activities and responsibilities

  • Manage documentation, reports and systems related to c-GMP of manufacturing products.
  • Keep SOP’s up to date.
  • Manage and participate to staff GMP’s training program for all departments.
  • Contribute Deviation Investigations and change procedure in relation to c-GMP.
  • Contribute to qualification and validation activities.
  • Contribute to the execution of stability studies.
  • Achieve objectives related to the standards of GMP and Good Housekeeping.
  • Inspect shipments.
  • Manage internal quality audits and housekeeping.
  • Contribute to annual product reviews according to the products manufactured.
  • Key user’s SAP and others IT quality systems (Quality environment).
  • Participate on project, committees and subcommittees
  • Release or reject raw materials, intermediates and final products based on the analytical results and the review of incident reports.
  • Act as Quality Manager if he/she is not present.
  • Participate in audits.
  • Keep all supporting systems up to date related to DI’s, audits and documentation.
  • Release or reject raw materials, intermediates and final products based on the analytical results and the review of incident reports.
  • Act as Quality Manager if he/she is not present.
  • Participate in audits.
  • Keep all supporting systems up to date related to DI’s, audits and documentation.

The Ideal Candidate

  • Affinity with a production environment.
  • Minimum 3 years of relevant experience in pharmaceutical industry or similar industry.
  • Bachelor degree in a technical, process technical or analytical field of study.
  • Dutch and English verbally and writing.
  • Knowledge of c GMP.
  • Knowledge of audit procedures.
  • Knowledge of production processes.
  • Result Orientation.
  • Good communication and interpersonal skills.
  • Able to work in multidisciplinary teams.

Terms and reward

We offer a local contract in a challenging, comprehensive, operational environment, with many opportunities for personal input and growth and plenty of discussions with other professionals. The organization is very flat. You have a lot of freedom and responsibility in an open, direct and informal atmosphere.

The Procedure

Please submit your application before September 10, 2021 via the 'apply' button and upload your CV amp; cover letter in English. We also ask you to include information on your current remuneration. Only applications with CV and Cover Letter will be considered.

For more detailed information about the role feel and about the Recruitment amp; Selection process you can contact us via . We invite you to visit our website www.centrient.com for information about our company.

Reference check procedures are part of the Centrient Recruitment amp; Selection Process. You will be contacted when a reference check is required.

Acquisition in regard to this vacancy is not appreciated

Job Specification

Job Rewards and Benefits

Centrient Pharmaceuticals Netherlands

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