Quality Control Technician Ii

Teva Pharmaceuticals

3+ years

Not Disclosed

Gwalior

10 Nov. 30, 2024

Job Description

Job Type: Full Time Education: B.Sc./M.Sc. 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 II

Location: Gwalior, India, 477117
Company: Teva Pharmaceuticals
Job ID: 58748

Who We Are

Teva Active Pharmaceutical Ingredients (TAPI) is a global leader in supplying Active Pharmaceutical Ingredients (APIs). With an extensive portfolio of over 350 API products, TAPI is the trusted supplier to 80% of the top 50 global pharmaceutical companies. For over 80 years, TAPI has established itself as a reliable and innovative leader in the generic API industry. Our commitment to quality, technology, and exceptional customer service enables us to stay at the forefront of the industry. We employ over 4,000 professionals across 14 sites worldwide, with production facilities located in Italy, Hungary, Israel, Mexico, India, and more.

How You’ll Spend Your Day

As a Quality Control Technician II, you will be responsible for ensuring the highest quality control standards in the laboratory. Your daily responsibilities will include:

Audit Readiness & Compliance:
- Maintain 24x7 audit readiness for both internal and external audits, including regulatory audits.
- Participate in audit processes, ensuring compliance with quality standards.
Investigation & Reporting:
- Initiate and investigate Laboratory Incident Reports (LIR), Out of Specification (OOS), Out of Trend (OOT), and borderline results.
- Report findings to the in-charge and provide detailed documentation for investigations.
Sampling & Testing:
- Perform sampling and analysis of raw materials (RM), finished goods (FG), intermediates, and cleaning samples as required.
- Enter test results in analytical sheets, QA forms, LIMS, and online documentation while adhering to data integrity standards.
- Conduct analytical tests according to monographs and Standard Operating Procedures (SOPs).
Instrument Calibration & Maintenance:
- Ensure proper calibration and verification of laboratory instruments.
- Maintain the reserved sample room, chambers, autoclaves, and incubators according to established protocols.
Documentation & Coordination:
- Assist in preparing and updating department documents, such as Standard Test Procedures (STPs) and SOPs.
- Ensure proper handling and timely dispatch of finished products, raw materials, and intermediates for external laboratory analysis.
Stock Management:
- Maintain chemical stock records and ensure accurate reconciliation of standards and materials.
Team Support & Safety Compliance:
- Determine team priorities based on the plant's needs, coordinating with the team leader/manager.
- Ensure adherence to housekeeping, cGMP, GLP, and safety guidelines within the laboratory.

Your Experience and Qualifications

Educational Requirements:
- A Bachelor’s or Master’s degree in Chemistry or a related field.
Experience:
- At least 3 years of experience in a Quality Control laboratory, preferably with experience in wet chemistry.
Skills & Knowledge:
- Proficiency in laboratory testing techniques and instrument calibration.
- Strong knowledge of cGMP, GLP, and safety standards.
- Excellent documentation and communication skills.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to fostering a diverse and inclusive workplace. We provide equal employment opportunities without regard to age, race, religion, sex, disability, or any other legally protected status. We encourage applicants from all backgrounds to apply. If you require any accommodations during the recruitment process, please let us know, and we will make necessary arrangements to ensure an accessible experience.

If you are looking to contribute to a leading pharmaceutical company with a focus on quality and compliance, apply today!

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