Laborant in der Qualitätskontrolle (m/w/d) - Schwerpunkt Methodenetablierung

KVP Pharma+Vet. Produkte GmbH; Kiel; Vor Ort; EUR 36.000 - 48.000; Vollzeit

Benefits dieser Stelle

Attractive salary according to tariff

13th month salary

Holiday pay

Pension scheme

37.5-hour week

30 days vacation

Hansefit membership

Job ticket subsidy

Free parking

Employee share program

Zusammenfassung

KVP Pharma+Vet. Produkte GmbH in Kiel, Germany is seeking a Laboratory Assistant in Quality Control (m/f/d) for a two-year limited contract. You will perform CG/LC analyses and ensure GMP-compliant documentation, aligning methods with pharmacopoeial standards.

You will establish and verify analytical methods per EP/USP, optimize procedures, and participate in CAPA-driven improvements. Proficiency in HPLC/GC, spectroscopy, and SAP/Empower will support cross-functional quality operations.

Qualifikationen

• Training as chemical laboratory assistant (CTA) or equivalent, with 2+ years pharma QC experience.
• In-depth instrumental analysis knowledge (HPLC, GC, spectroscopy) and EP/USP application.
• Fluent German and good English for international pharmacopoeia.

Aufgaben

• Perform wide-ranging analysis using chromatographic and wet chemical methods for QC, documenting in GMP-compliant records.
• Independently establish and verify analytical methods per EP/USP monographs and conduct verifications.
• Investigate and optimize analytical procedures; implement CAPA to improve robustness.
• Carry out method validations and verifications for new products and feedstocks.
• Develop best practices for analytics and record them in supplementary audit regulations (APVs) to ensure consistency.

Kenntnisse

HPLC

GC

Spectroscopy

EP/USP knowledge

MS Office

Empower

SAP

German language

English language

Ausbildung

Chemical laboratory assistant (CTA) or equivalent

Tools

Empower

SAP

Jobbeschreibung

Your role: Laboratory Assistant in Quality Control (m/f/d)

The position is initially limited to 2 years.

Your Responsibilities:

• Wide-ranging analysis: You will apply chromatographic (HPLC, GC) and wet chemical methods to ensure precise quality control, maintaining data integrity through GMP-compliant documentation and modern laboratory standards (e.g., 5S).


• Pharmacopoeia compliance: You will independently establish and verify analytical methods according to applicable monographs (e.g. EP, USP) and carry out verifications in regulatory revisions.


• Method optimization & CAPA management: You will experimentally investigate and optimize analytical procedures in the context of deviations and CAPA measures to sustainably increase methodological robustness.


• Conducting validation studies: You will carry out method validations and verifications for new products and feedstocks practically on the device and strictly comply with GMP requirements.


• Securing method transfer (APVs): You will develop "best practices" for analytics and record them in supplementary audit regulations (APVs) to ensure consistent application of the methods across the team.

What You Need to Succeed (minimum qualifications):

• Education: You have completed training as a chemical laboratory assistant (m/f/d), CTA (m/f/d) or a comparable qualification and 2+ years relevant professional experience in pharmaceutical quality control.


• Expertise: You have in-depth, field-tested knowledge in instrumental analysis (HPLC, GC, spectroscopy) as well as in the application of international pharmacopoeia (EP, USP).


• Languages: Fluent German and good English skills for working with international pharmacopoeia.

What Will Give You a Competitive Edge (Preferred Qualifications)

• Methodological competence: Experience in the practical processing of methodological issues in the context of CAPA processes and in the implementation of method validations.


• Way of working: High level of technical understanding of laboratory processes, work reliably in the implementation of complex monographs and passion for working directly in the laboratory.


• IT affinity: Experience with MS Office and chromatography data systems (e.g. Empower) and SAP.

What we offer you – Why Elanco?

• Attractive salary according to the chemical tariff (MTV), full 13th month salary (Christmas bonus) and 40 € holiday pay per day. Plus: employer-financed pension scheme\\..


• Work-life balance: 37.5-hour week and 30 days of vacation. On top of that, there's the \"future amount\" (up to 5 extra days off or cash), overtime? Are recorded and compensated for by free time\\..


• Well-being: Hansefit membership, annual events (our employee party is legendary!) and preventive care offers directly on site.


• Convenient commute: Subsidy for the job ticket and free parking.


• Benefits: Employee share purchase program and corporate benefits platform.

Additional Information:

• Location: Kiel, Germany - On-site Work Environment


• Travel: 0%


• Position: Limited contract of 2 years.