Quality Control Technician Iii

3-4 years

Not Disclosed

Gwalior 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 III
Date: Jan 16, 2025
Location: Gwalior, India, 477117
Company: Teva Pharmaceuticals
Job Id: 59905

Company Overview:

TAPI (Teva Active Pharmaceutical Ingredients) is a global leader in supplying active pharmaceutical ingredients (APIs). With the industry’s broadest portfolio of over 350 API products, TAPI is the trusted global supplier supporting 80% of the top 50 global pharmaceutical companies. With a strong history of over 80 years in the generic API industry, TAPI leads through innovation, expertise, and exceptional customer service. The company’s state-of-the-art production facilities span across Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India, supported by more than 4,000 professionals globally.

Position Overview:

The Quality Control Technician III is responsible for ensuring that quality standards are met in the laboratory, supporting audits, investigating deviations, and performing routine sampling and analysis. This role involves working in different shifts and maintaining laboratory equipment and materials in compliance with regulatory requirements, company standards, and safety guidelines.

Key Responsibilities:

Audit Readiness:
- Maintain 24×7 audit readiness, ensuring all procedures are in compliance and supporting internal, external, and regulatory audits.
Wet Chemistry:
- Apply knowledge of wet chemistry techniques to perform various laboratory tests.
Shift Work:
- Work in different shifts as required by operational needs.
CAPA Training:
- Ensure 100% participation in training programs related to Corrective and Preventive Actions (CAPAs).
Deviation Investigation:
- Initiate and investigate Laboratory Investigation Reports (LIR), Out of Specification (OOS), Out of Trend (OOT), and borderline results, and report findings to the in-charge.
Documentation Support:
- Assist with providing required QC documents to Regulatory Affairs (RA) and other departments as needed.
Team Coordination:
- Coordinate with the team leader and manager to determine priorities according to plant needs.
Regulatory Compliance:
- Follow Good Laboratory Practice (GLP), current Good Manufacturing Practice (cGMP), and safety guidelines in the laboratory.
Sampling and Analysis:
- Perform sampling and analysis of raw materials (RM), finished goods (FG), intermediates, and cleaning samples, ensuring proper documentation in analytical sheets, QA forms, LIMS, and other systems in compliance with data integrity norms.
Analytical Testing:
- Conduct analytical tests according to specified monographs and Standard Operating Procedures (SOPs).
Calibration & Maintenance:
- Ensure calibration and verification of laboratory instruments are performed regularly.
Sample Storage:
- Manage and maintain the reserved samples room, chambers, autoclaves, and incubators.
Documentation Preparation:
- Assist in the preparation of documents related to department activities, such as Standard Testing Procedures (STPs) and SOPs.
Labeling & Documentation:
- Ensure timely sampling, approval, and rejection labeling of products and maintain accurate stock records of chemicals and standards.
External Laboratory Coordination:
- Manage the sampling of finished products, raw materials, and intermediates for analysis by external laboratories.

Experience & Qualifications:

Educational Requirements:
- Bachelor’s or Master’s degree in Chemistry or a related field.
Experience:
- Minimum of 3 years of experience in Quality Control within a pharmaceutical or related manufacturing environment.

Teva’s Equal Employment Opportunity Commitment:

Teva Pharmaceuticals is committed to providing equal employment opportunities to all employees and applicants, without regard to 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 throughout the recruitment and selection process, please inform us, and we will treat your information with the utmost confidentiality to provide an accessible candidate experience.

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

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