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Quality Control Technician - Analytical Lab

2+ years
Not Disclosed
10 Nov. 30, 2024
Job Description
Job Type: Full Time Education: B.Sc/B.Pharm/MLO+ / HBO Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Quality Control Technician - Analytical Lab

Location: Haarlem, Netherlands
Company: Teva Pharmaceuticals
Job ID: 36306
Date Posted: November 25, 2024


About Teva

Teva Pharmaceuticals is a global leader in the pharmaceutical industry and the largest producer of generic medicines worldwide. With operations in over 80 countries, Teva’s diverse portfolio impacts the lives of 200 million people daily. As we advance innovative solutions, expand our product pipeline, and invest in R&D, we are on a mission to improve global health and empower people to lead healthier lives.


Your Responsibilities

As a Quality Control Technician at Teva's Haarlem production site, your duties will include:

  • Conducting routine testing of finished products and in-process control samples according to SOPs and timelines.

  • Managing quality systems, including handling deviations and investigating Out of Specification (OOS) results (Phase 1 investigations).

  • Writing, reviewing, and approving test results.

  • Ensuring compliance with corporate policies and regulatory standards.

  • Engaging in advanced problem-solving, root cause analysis, and troubleshooting of quality issues.

  • Performing first-line troubleshooting for laboratory equipment.

  • Working within a 24/7 shift pattern.


Your Profile

Education and Experience:

  • MLO+ / HBO / Bachelor’s degree in analytical chemistry, pharmacy, or equivalent experience.

  • Familiarity with Pharmacopoeia methods and pharmaceutical quality systems.

  • Experience in a pharmaceutical environment, especially with analytical techniques like UPLC/HPLC, TOC, PSD, etc.

Knowledge and Skills:

  • Strong analytical mindset with a results-oriented approach.

  • Familiarity with regulatory environments, including inspections like EU cGMP, US-FDA, and ANVISA.

  • Effective problem-solving and decision-making abilities.

Personal Attributes:

  • Team-oriented mindset and ability to collaborate effectively.

  • Strong "can-do" mentality.


Function

Department: Quality
Sub-Function: Manufacturing Quality Control


Teva’s Commitment to Equal Opportunities

Teva is committed to fostering an inclusive workplace that values diversity. Employment opportunities are open to all, regardless of age, race, gender, religion, disability, or any legally recognized status entitled to protection under applicable laws.


Pre-Employment Screening

Teva conducts appropriate verification and legally permitted vetting as part of the hiring process. Details will be shared at the relevant stage.


Apply today to join Teva's journey to deliver health solutions that make a global impact!