Quality Control Technician Ii

3-4 years

Not Disclosed

Chennai India

10 Feb. 12, 2025

Job Description

Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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
Date: Jan 30, 2025
Location: Chennai, India, 600113
Company: Teva Pharmaceuticals
Job Id: 60347

Company Overview:

Teva Pharmaceuticals is a global leader in the development and manufacturing of generic medicines, aiming to make good health more affordable and accessible. With a presence in nearly 60 countries, Teva's mission is to help millions of people around the world live healthier lives. As the world's leading generic medicine manufacturer, Teva produces a wide range of medications, including many on the World Health Organization’s Essential Medicines List. Today, at least 200 million people rely on Teva’s medicines daily.

Position Overview:

The Quality Control Technician II will be responsible for performing various analytical and validation tasks in the laboratory, ensuring compliance with current guidelines and internal standard operating procedures (SOPs). The position involves stability analysis, method validation, instrument calibration, and preparation of required documentation, including Method Transfer Protocols and validation reports. This role requires experience with stability testing and method transfer activities, and handling laboratory software such as LSCMS.

Key Responsibilities:

Stability Analysis:
- Perform stability testing and analysis of pharmaceutical products as per established protocols and regulatory requirements.
Method Transfer/Validation:
- Carry out method transfer and method validation analysis in accordance with current guidelines.
- Prepare Method Transfer Protocols (MTP), Method Transfer Reports (MTR), Methods of Analysis (MTH), Test Data Sheets (TDS), and other related documents.
Instrument Calibration & Validation:
- Perform calibration and validation of laboratory instruments and equipment, ensuring compliance with established standards.
Documentation:
- Prepare and maintain departmental SOPs, validation protocols, and other essential documentation in line with current regulatory requirements.
- Ensure accurate entry of stability sample results in the LIMS (Laboratory Information Management System) and SAP (Systems, Applications, and Products) platforms.
Software Handling:
- Work with and handle LSCMS (Liquid Chromatography Mass Spectrometry) software for data analysis and reporting.
Compliance:
- Ensure all activities are conducted in full compliance with the current industry guidelines and Teva’s internal standards.

Experience & Qualifications:

Educational Requirements:
- M.Sc. in Chemistry or a related field.
Experience:
- A minimum of 3 years of experience in a quality control or analytical role within the pharmaceutical industry.

Teva’s Equal Employment Opportunity Commitment:

Teva Pharmaceuticals is committed to providing equal employment opportunities to all employees and applicants, irrespective of age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally recognized status entitled to protection under applicable laws. Teva fosters a diverse and inclusive workplace. If you require any accommodations during the recruitment process, please inform us, and we will ensure an accessible candidate experience.

Interested candidates are encouraged to apply via Teva Pharmaceuticals’ career portal.

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