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 the global leader in supplying Active Pharmaceutical Ingredients (APIs), with an extensive portfolio of over 350 API products. TAPI serves 80% of the top 50 global pharmaceutical companies and is renowned for its reliability and expertise in the generic API industry, spanning more than 80 years. We are committed to providing high-quality APIs and excellent customer service. With production facilities across Italy, Hungary, Israel, Mexico, India, and more, TAPI employs over 4,000 professionals and continues to lead the industry with cutting-edge research and development.

How You’ll Spend Your Day

As a Quality Control Technician II, you will be involved in various laboratory tasks to ensure the highest quality and regulatory standards. Your responsibilities will include:

Audit Readiness & Compliance:
- Maintain 24x7 audit readiness to meet internal, external, and regulatory audit requirements.
- Participate in audits and ensure full compliance with all quality control guidelines.
Investigations & Reporting:
- Lead investigations on Laboratory Incident Reports (LIR), Out of Specification (OOS), Out of Trend (OOT), and borderline results.
- Report findings to the in-charge and ensure proper documentation of results.
Sampling & Testing:
- Perform sampling and analysis of raw materials (RM), finished goods (FG), intermediates, and cleaning samples as required.
- Ensure accurate entry of test results in analytical sheets, QA forms, LIMS, and other online documentation, following data integrity norms.
- Conduct analytical tests in accordance with monographs and Standard Operating Procedures (SOPs).
Instrument Calibration & Maintenance:
- Calibrate and verify laboratory instruments, ensuring their proper functioning.
- Maintain reserved sample rooms, chambers, autoclaves, and incubators in compliance with quality standards.
Documentation & Coordination:
- Assist with the preparation and updating of departmental documents, such as Standard Test Procedures (STPs) and SOPs.
- Manage the sampling and dispatch of finished products, raw materials, and intermediates to external laboratories for analysis.
- Maintain chemical stock records and reconcile standards.
Team Coordination & Safety:
- Support team priorities based on the plant’s needs and coordinate with the team leader/manager.
- Adhere 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:
- A minimum of 3 years of experience in a Quality Control laboratory, with expertise in wet chemistry.
Skills & Knowledge:
- Strong knowledge of laboratory techniques, testing, and equipment calibration.
- Familiarity with cGMP, GLP, and safety standards in laboratory environments.
- Excellent documentation and analytical skills.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is an equal opportunity employer. We are committed to providing equal employment opportunities without discrimination based on age, race, gender, disability, or any other protected status under applicable laws. We foster a diverse and inclusive workplace. If you need accommodations during the recruitment process, please inform us, and we will treat all information confidentially to provide an accessible candidate experience.

If you are looking to be part of a dynamic team committed to high-quality standards in the pharmaceutical industry, apply now!

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Quality Control Technician Ii

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