Quality Specialist TRD GCS

Vor 2 Tagen

Basel, Basel-Stadt, Schweiz RM Group (Switzerland) Vollzeit

Quality Specialist TRD GCS
vacancy for our Basel based client in the Pharma sector.

Your tasks:

  • Support a discipline and/or provide a service individually or within a team of associates.
  • May provide functional expertise to Line Unit and other QA Units in area of responsibility.
  • Write and review GMP-relevant deliverables and/or related tools as per area of responsibility in order to ensure compliance with cGMP and project quality deliverables.

Support project related activities (e.g. TRD product portfolio, development of new tools, processes, Quality initiatives, Quality Manual implementation, Quality Plans, Quality Risk Assessments, training activities, qualification and facility upgrade activities, IT validation projects) as per area of responsibility.
- Comply with internal and external guidelines regarding quality and safety (Quality Manual, regulatory cGMP guidelines, Health Authority guidance's, SOPs etc.).
- List individual specific activities (e.g.: as described in SOP TRD QA Approval and Release responsibilities/authorities).
- Receives incoming documents (e.g. executed batch records, vendor labels, etc.).
- Support the timely release of GMP batches of labels, primary packed materials and Investigational Medical Products.
- Scan, file and archive documents owned by QA. (e.g. Certificate of Compliance, Batch Record Review Checklists).
- Each associate is allowed to perform an assigned task only after completion of the related trainings.

Your experience/knowledge:

  • Technician with a minimum of 5 years' experience or Bachelor with at least 3 years' experience.
  • Scientific, technical and regulatory knowledge in a specific area.
  • Detailed knowledge of cGMP and basic knowledge of drug development.
  • Communication skills to sufficiently address GMP and logistic related questions with line unit experts.
  • Scientific, technical and regulatory knowledge in a specific area.
  • Basic knowledge of drug development.
  • Detailed knowledge of cGMP, working knowledge of safety and environmental regulations and guidelines.
  • Good organizational skills.
  • Language skills: English - fluent

Location:
Basel, Switzerland

Work setting:
Hybrid

Sector:
Pharma

Start:
01/2026

Duration:
6+ months

Workload:
100%

Ref.Nr.:
BH 23758

Take the next step and send us your resume along with a daytime phone number where we can reach you.

Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens, and current work-permit holders for Switzerland.

We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application.

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