What positions are currently available at Arch 24 HR Tech Factory?

Arch 24 HR Tech Factory is currently hiring for Specialist Quality Assurance - Pharmaceutical Industry. These positions offer competitive employment opportunities for qualified candidates.

How can I apply for positions at Arch 24 HR Tech Factory?

Interested candidates should prepare their complete application including updated CV, educational certificates, experience documents, CNIC copy, and recent photographs. Submit through the specified application method before the deadline mentioned in the job advertisement.

What documents are required when applying to Arch 24 HR Tech Factory?

Required documents for application to Arch 24 HR Tech Factory typically include: Updated CV/Resume, CNIC/National Identity Card copy, all educational certificates and transcripts, professional experience certificates, recent passport-sized photographs, domicile certificate, and any other position-specific documents mentioned in the application requirements.

What is the selection process at Arch 24 HR Tech Factory?

The selection process at Arch 24 HR Tech Factory typically involves multiple stages: Initial application screening and document verification, written tests or skill assessments for certain positions, personal interviews with the selection committee, final document verification, and official appointment. Only shortlisted candidates will be contacted for subsequent stages.

What is the application deadline for positions at Arch 24 HR Tech Factory?

The application deadline for current positions at Arch 24 HR Tech Factory is December 19, 2026. Applications must be submitted before this date to be considered for the selection process.

Where are the job locations for Arch 24 HR Tech Factory positions?

The job locations for Arch 24 HR Tech Factory positions are primarily in Chiasso. Specific location details for each position are provided in the detailed job advertisement.

Specialist Quality Assurance - Pharmaceutical Industry

Embark on a fulfilling career as a Quality Assurance Specialist within the dynamic chemical-pharmaceutical sector.

This exciting opportunity offers the chance to contribute to critical product release processes and ensure adherence to stringent global standards.

If you possess a strong scientific background and a keen eye for detail, this role provides excellent professional growth within a reputable organization.

Private

temporary

Switzerland

Jobs Date Posted:	04 November, 2026
Jobs Last Date to Apply:	19 December, 2026
Industry:	Pharmaceuticals
Jobs Industry Type:	Private
Job Hiring Organization:	Arch 24 HR Tech Factory
Experience Required (In months):	36
Occupational Category:	Research and Development
Employment Type:	temporary
Advertisement Source:	Eurojobs
Job Location:	Chiasso
Address Region:	Tessin
Country of Appointment:	Switzerland

🎓 Qualifications Required

📌 Job Positions:

Specialista Quality Assurance

Further Details

We are seeking a dedicated Quality Assurance Specialist for a leading chemical-pharmaceutical company based in Lugano, Switzerland. This position is crucial for maintaining product integrity and compliance with Good Manufacturing Practices (GMP). It's an ideal role for professionals aiming to advance their careers in pharmaceutical quality assurance.

Quality Assurance Specialist Role in Pharmaceutical Sector

A prominent chemical-pharmaceutical company located in the Lugano region is actively seeking a skilled Quality Assurance Specialist. This role is pivotal in ensuring the highest standards of product quality and regulatory compliance, making it a significant opportunity for career advancement.

The ideal candidate will be instrumental in managing deviations, reviewing batch records, and updating crucial operational procedures. This position offers a chance to work within a key industry and contribute to impactful pharmaceutical operations.

Job Title: Specialist Quality Assurance
Industry: Chemical-Pharmaceutical
Location: Chiasso, Switzerland
Experience: Minimum 3 years in Pharmaceutical QA
Qualifications: Degree in scientific disciplines (Chemistry, Pharmacy, Biology) or equivalent
Key Responsibilities: Deviation Management, Batch Record Review, SOP Updates, Internal Audits, GMP Training
Language Proficiency: Excellent Italian and English

Skills

Proficiency in managing production deviations and CAPA implementation
Expertise in reviewing and approving Batch Records for product release
Ability to update and maintain Standard Operating Procedures (SOPs)
Experience conducting internal audits of production departments
Skill in organizing and delivering GMP training to operational staff
Strong analytical and ethical rigor
Excellent teamwork and inter-functional collaboration skills

Duties and Responsibilities:

Manage production deviations, investigate root causes, and define corrective/preventive actions (CAPA)
Review and approve Batch Records for final product release
Draft, revise, and continuously update company Standard Operating Procedures (SOPs) in compliance with regulations
Conduct periodic internal inspections and audits in production areas to ensure guideline adherence
Organize and deliver internal training sessions for operational staff on GMP compliance