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Qc Technician - Controlled Area

2+ years
Not Disclosed
10 Dec. 6, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Quality Control Technician

Job ID: 15075
Location: Manufacturing Site (fully site-based)


About Boehringer Ingelheim

Boehringer Ingelheim is a research-driven pharmaceutical company with a history of over 130 years, dedicated to improving lives through innovative therapies. With 52,000 employees globally, we foster a diverse, collaborative, and inclusive culture. We believe that talented and passionate people have no limits, and we work every day to make a meaningful impact.


The Position

As a Quality Control Technician, you will play a key role in supporting the Quality Control Department in the testing and release of raw materials, intermediates, and final products at our manufacturing site. This is a fully site-based role focused on ensuring product quality and regulatory compliance.


Tasks & Responsibilities

  • Sampling and Testing: Perform sampling and testing of incoming raw materials and release them to production.

  • Stability Testing Support: Support the vaccine stability testing program, including all related in-vivo testing.

  • Final Product Testing: Conduct final product testing and collaborate with third-party testing facilities.

  • QC QMS Support: Support with quality control processes like Out of Specification (OOS) investigations, deviations, CAPA (Corrective and Preventive Actions), and change controls.

  • SOPs and Specifications: Write and update relevant SOPs, material specifications, and release forms.

  • Validation Activities: Assist with validation activities.

  • GMP & HSE Standards: Carry out duties in accordance with Good Manufacturing Practices (GMP), site Health, Safety & Environmental (HSE) standards, and Biosafety standards.

  • Environmental Testing: Support with site utilities and environmental testing programs.


Requirements

  • Experience: Some experience working in a regulated analytical laboratory is desirable.

  • Knowledge: Familiarity with GxP (Good Laboratory and Manufacturing Practices) quality systems is preferred.

  • Skills: Proficiency in Microsoft Office applications.

  • Attributes: Strong team player, with the ability to meet deadlines and work efficiently under pressure.


Why This Is a Great Place to Work

Boehringer Ingelheim has been recognized as a Top Employer in the UK for our commitment to fostering a positive work environment and excellent HR policies. Learn more about why Boehringer Ingelheim is a great place to work: Top Employer Recognition.


About Boehringer Ingelheim

We are a family-owned company with a vision to improve the lives of both humans and animals. Our employees are committed to making a difference through innovation, collaboration, and growth.

  • Growth & Collaboration: Work in a respectful global environment that values innovation and personal development.

  • Inclusive Culture: We foster a diverse culture and embrace different perspectives to drive success.

  • Impact: Your work will contribute to improving lives across the world.


For more details, visit: Boehringer Ingelheim Careers.