Technicien laboratoire contrôle qualité GMP (H/F/X)

Ekkiden; Bern; Vor Ort; CHF 70.000 - 110.000; Vollzeit

Benefits dieser Stelle

Comprehensive health insurance

Meal vouchers

Zusammenfassung

Ekkiden is seeking a QC laboratory technician to support GMP-compliant quality control analyses of raw materials, intermediates, and finished products. You will work in a regulated, documentation-driven environment, collaborating with QC, QA, production and engineering teams.

The role requires a laboratory degree (CFC, BSc, or MSc) and 5–10 years of pharmaceutical QC experience, with GMP and GLP knowledge. German at operational level is requested, French is a plus, and a structured, autonomous

Qualifikationen

• Degree such as lab technician (CFC) or BSc/MSc in chemistry, biology, microbiology or pharmacy.
• Minimum 5–10 years of experience in a pharmaceutical QC laboratory.
• Significant GMP experience.
• Good laboratory practices (GLP) knowledge.
• Data integrity knowledge.
• Experience in managing OOS/OOT results.
• German at operational/intermediate level (French is a plus).
• Rigorous, autonomous and quality oriented profile.
• Ability to work in a regulated and documented environment.
• Good teamwork and communication skills.

Aufgaben

• Perform quality control analyses in compliance with GMP and internal procedures.
• Carry out physicochemical analyses on pharmaceutical samples.
• Perform or participate in microbiological analyses according to laboratory needs.
• Prepare samples, solutions, reagents and media required for analyses.
• Use and maintain laboratory equipment.
• Participate in investigations in case of atypical or out of specification results (OOS / OOT).
• Document analysis results in quality systems and files.
• Ensure traceability and data integrity in accordance with GMP / data integrity requirements.
• Participate in qualification, calibration and maintenance activities of laboratory equipment.
• Draft and/or update laboratory documents and procedures.
• Collaborate with QC, QA, production and engineering teams.

Kenntnisse

GMP knowledge

GLP knowledge

Data integrity

German language (operational)

Autonomous work style

Team collaboration

Ausbildung

Chemistry/Biology/Pharmacy degree

Jobbeschreibung

International consulting group founded in 2019, Ekkiden brings together an ecosystem of passionate and committed consultants who lead organizational, operational, and technological transformation projects in IT/Digital, Industry/R&D, and sustainability, for large corporations and SMEs, in France, Switzerland, Spain, and Germany.

The role:

As part of the strengthening of quality control activities within a pharmaceutical company, you will work as a QC laboratory technician in an environment subject to GMP requirements. You will carry out the analyses required to control raw materials, intermediate products and/or finished products, while ensuring compliance with procedures and regulatory requirements.

Responsibilities:

• Perform quality control analyses in compliance with GMP and internal procedures
• Carry out physicochemical analyses on pharmaceutical samples
• Perform or participate in microbiological analyses according to laboratory needs
• Prepare samples, solutions, reagents and media required for analyses
• Use and maintain laboratory equipment
• Participate in investigations in case of atypical or out of specification results (OOS / OOT)
• Document analysis results in quality systems and files
• Ensure traceability and data integrity in accordance with GMP / data integrity requirements
• Participate in qualification, calibration and maintenance activities of laboratory equipment
• Draft and/or update laboratory documents and procedures
• Collaborate with QC, QA, production and engineering teams

What we are looking for:

• Degree such as CFC laborantin(e), bachelor's/master's in chemistry, biology, microbiology, pharmacy or equivalent qualification
• Minimum 5 to 10 years of experience in a pharmaceutical QC laboratory
• Significant experience in a GMP environment
• Good command of good laboratory practices (GLP)
• Knowledge of data integrity requirements
• Experience in managing OOS/OOT results
• German at operational/intermediate level (french is a plus)
• Rigorous, autonomous and quality oriented profile
• Ability to work in a regulated and documented environment
• Good team spirit and good communication skills

What we offer:

• Join us at the right time to make your mark within a rapidly growing organization
• Varied assignments in a challenging environment that will let you have a real impact on the company
• The opportunity to work autonomously and take initiative to grow together
• A career path tailored to your personality, both in terms of role and location
• Demanding, ongoing training to unlock your full potential
• A performance-driven culture with great results-based bonuses
• Comprehensive health insurance (GEREP) and meal vouchers (Swile card)

What does the recruitment process look like at Ekkiden?
At Ekkiden, we are committed to providing a positive experience for every candidate.
First contact: Our recruitment team will reach out to discuss your motivations and expectations.
Interviews: You will have one or two interviews with our business managers, depending on the position you're applying for.
Meeting the client: Finally, you'll have the opportunity to meet the client.

While this is our standard process, we may adapt it depending on specific circumstances.