Technischer Mitarbeiter QC (m/w/d)

AveThera; Braunschweig; On-site; EUR 42,000 - 56,000; Full time

Benefits offered by this job

30 days vacation

Deutschlandticket subsidy

Company pension scheme

Regular team events and lunches

Job summary

AveThera in Braunschweig, Germany, seeks a meticulous laboratory professional for GMP-regulated analytics, focusing on protein analysis via HPLC and related techniques, and testing for process-related impurities.

You will contribute to endotoxin and microbiological assays, maintain GMP records, and help develop SOPs and specifications. A BTA/CTA/PTA training and strong MS Office skills are essential.

Qualifications

• Experience with protein analysis methods (HPLC, capillary electrophoresis, ELISA).
• Proficiency in MS Office.
• Ability to work independently, precisely, in a structured and goal-oriented manner.

Responsibilities

• Perform protein analysis methods (e.g., HPLC, capillary gel electrophoresis, ELISAs).
• Execute methods for the analysis of process-related impurities (ELISAs).
• Conduct pharmacopoeial methods (e.g., endotoxin assays, microbiological testing).
• Ensure GMP-compliant documentation.
• Develop SOPs and specifications in a GMP-regulated environment.
• Assist with the validation of analytical methods.
• Conduct qualification of analytical instruments.
• Perform maintenance of quality control equipment.
• Execute and evaluate stability studies in accordance with ICH guidelines.
• Implement current GMP and safety requirements.
• Assist with the documentation of deviations and OOX results.

Skills

Protein analysis methods

HPLC

Capillary electrophoresis

ELISA

MS Office

Independent & precise work

Teamwork & communication

Education

BTA/CTA/PTA training

Job description

Your mission

• Perform protein analysis methods (e.g., HPLC, capillary gel electrophoresis, bioassays such as cell-based assays)
• Execute methods for the analysis of process-related impurities (e.g., ELISAs)
• Conduct pharmacopoeial methods (e.g., endotoxin assays, microbiological testing of samples)
• Ensure GMP-compliant documentation
• Develop standard operating procedures and specifications in a GMP-regulated environment
• Assist with the validation of analytical methods
• Conduct qualification of analytical instruments
• Perform maintenance of quality control equipment
• Execute and evaluate stability studies in accordance with ICH guidelines
• Implement current GMP and safety requirements
• Assist with the documentation of deviations and OOX results

Your profile

• Completed training (BTA, CTA, or PTA)
• Experience with protein analysis methods (e.g., HPLC, capillary gel electrophoresis, ELISA)
• Proficiency with MS Office
• Ability to work independently, precisely, in a structured and goal-oriented manner
• High flexibility
• Ability to work well in a team, strong interpersonal skills, and excellent communication skills
• German: Native speaker or at least B1 level; English: at least B1 level (or equivalent)

Why us?

• Opportunity to work in an innovative and growing biopharmaceutical environment
• Exposure to advanced manufacturing technologies and GMP processes
• Collaborative and international team culture
• Long-term development and career growth potential
• Competitive compensation package
• Modern on-site facilities
• 30 days of vacation
• 2 additional days off on Deccember 24 and 31
• Deutschlandticket subsidy
• Company pension scheme
• Regular team events and lunches

We welcome applicantions from candidates regardless of gender, gender identity, disability, nationality, ethnic or social background, religion, age and sexual orientation.We firmly believe that diverse perspectives, experiences and backgrounds strengthen our teams and contribute to better innovation and busienss success.