drjobs QA Associate I - Marken

QA Associate I - Marken

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

London - UK

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Before you apply to a job select your language preference from the options available at the top right of this page.

Explore your next opportunity at a Fortune Global 500 organization. Envision innovative possibilities experience our rewarding culture and work with talented teams that help you become better every day. We know what it takes to lead UPS into tomorrowpeople with a unique combination of skill passion. If you have the qualities and drive to lead yourself or teams there are roles ready to cultivate your skills and take you to the next level.

Job Description:

Main Purpose:

The Quality Assurance Associate I (QAA I) is responsible for the oversight and implementation of the Marken Quality Management System (QMS) Marken Standard Operating Procedures (SOPs) processes and policies. The QAA I also needs to ensure compliance with applicable regional and local regulations and requirements and customer requirements as appropriate but not limited to: current Good Manufacturing Practice (GMP) Good Distribution Practices (GDP) Good Clinical Practices (GCP) Good Storage Practices (GSP) ISO 13485 and ISO 9001.

Main Duties and Responsibilities

1. Implement communicate and maintain companys quality systems in compliance with Markens Global QMS requirements.

2. Interact with clients on Quality Assurance (QA)/ GxP related matters under management supervision.

3. Effectively interact with Marken Departments and stakeholders to maintain that all QA tasks are appropriately supported by QA.

4. Support on internal audits.

5. Support client audits and regulatory inspections including the preparation of appropriate materials required within those audits when applicable.

6. Responsible for the QTA process including ownership of the QTA from initiation of the QTA template through to final signatures and filing; assigning a QTA # and PRA # if applicable and assuring compliance to the SOP including ensuring a QTA is updated or retired appropriately.

7. Collate issues CAPA Risk Assessment Change Control and training metrics and identify quality improvement initiatives. Oversee activities that conclude on the appropriate close-out of all CAPA entries.

8. Identify relevant GxP/ Quality related training needs and deliver training where required.

9. Ensuring that the Marken Quality System and GxP Program are implemented and maintained.

10. Ensuring the accuracy and quality of records and documents.

11. Participate actively in all the internal Quality and/ or designated meetings.

General

1. Perform activities assigned by QA Management.

2. Travel as reasonably requested by the Line Manager to the performance of duties.

3. Support your line manager that a timely and effective communication and escalation process exists to raise quality issues to the appropriate levels of management.

4. Adhere to Good Manufacturing/ Distribution / Clinical Practices

5. Undertake any other reasonable duties at the request of the Line Manager

6. Adhere to company Policies at all times.


Employee Type:

Permanent


UPS is committed to providing a workplace free of discrimination harassment and retaliation.


Required Experience:

IC

Employment Type

Full-Time

Company Industry

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.