Quality Assurance Specialist

2 semanas atrás

Oeiras, Lisboa, Portugal MSD Tempo inteiro

Job Description

Are you eager to expand your expertise in Quality Assurance within a leading pharmaceutical company? We are seeking a motivated early-career Pharmacist with a passion for excellence, meticulous attention to detail, and a strong commitment to high quality standards. In this role, you will help ensure full compliance with Good Distribution Practices in Portugal while collaborating closely with our local team to drive continuous improvement and operational rigor.

If you thrive in structured, high‑standards environments and are ready to contribute to a dynamic team, we would be delighted to hear from you.

What you will do: 

Bring energy, knowledge and innovation to carry out the following:

  • Review and approve Quality documentation for all incoming goods and for activities related to re-packaging.
  • Verify transportation conditions from the manufacturing site to the customer.
  • Ensure the quality and accuracy of documentation and records retention in accordance with Good Documentation Practices.
  • Manage and track internal deviations, CAPA, change controls, customer qualification requests, returned goods, and other Quality System activities.
  • Prepare Quality Metrics, contribute to the Quality System Review, and participate in 3PL compliance monitoring.
  • Execute quality activities required by Good Distribution Practices, Corporate Policies, and applicable EU regulatory requirements for products marketed by our company Portugal.

What skills you will need:

In order to excel in this role, you will more than likely have:

  • One year of experience in Quality Assurance (GDP) within Pharma industry
  • Knowledge of EU quality related pharmaceutical regulations
  • Designs clear SOPs and micro-training that raise compliance and cut documentation errors
  • Technical and scientific knowledge
  • Quality management system principles
  • Fluency in English
  • Good communicator
  • Ethics and integrity

Required Skills:

Accountability, Accountability, Aseptic Manufacturing, Audits Compliance, Authorizations, Corrective and Preventive Action (CAPA), Detail-Oriented, Documentation Review, Driving Continuous Improvement, GMP Compliance, IS Audit, Pharmacy, Pharmacy Laws, Pharmacy Practice, Pharmacy Regulation, Production Operations, Quality Assurance (QA), Quality Assurance Tools, Quality Auditing, Quality Control Management, Quality Management, Quality Management Systems (QMS), Quality Standards, Regulatory Compliance, Repackaging {+ 2 more}

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

11/18/2025

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID:R372873

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