Instagram
youtube
Facebook

Quality Control Technician Ii

3+ years
Not Disclosed
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 (TAPI)


Who We Are

Teva Active Pharmaceutical Ingredients (TAPI) is the leading international supplier of Active Pharmaceutical Ingredients (APIs) and one of the most trusted names in the generic API industry, with over 350 products in our portfolio. Serving 80% of the top 50 global pharmaceutical companies, we are proud of our rich 80-year history and commitment to innovation and exceptional customer service. With production facilities across Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India, TAPI employs over 4,000 professionals worldwide and continues to lead the industry through experience, technology, and cutting-edge R&D.


The Opportunity

As a Quality Control Technician II, you will be responsible for ensuring the highest standards of quality and compliance in the laboratory. Key responsibilities include:

  • Audit Readiness & Compliance:

    • Ensure 24x7 audit readiness.

    • Participate in internal, external, and regulatory audits to maintain laboratory compliance.

    • Ensure 100% participation in training related to Corrective and Preventive Actions (CAPA).

  • 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 ensure proper documentation.

  • Sampling & Testing:

    • Perform sampling and analysis of raw materials (RM), finished goods (FG), intermediates, and cleaning samples according to specifications.

    • Enter test results in analytical sheets, QA forms, LIMS (Laboratory Information Management System), and other online documentation, ensuring data integrity.

    • Perform analytical tests according to monographs and Standard Operating Procedures (SOP).

  • Instrument Calibration & Maintenance:

    • Ensure the calibration and verification of laboratory instruments.

    • Maintain reserved sample rooms, chambers, autoclaves, and incubators.

  • Documentation & Coordination:

    • Assist in preparing and updating departmental documents such as STPs (Standard Test Procedures) and SOPs.

    • Support in sending samples to external laboratories for analysis and ensure proper documentation.

    • Maintain accurate records for chemical stock and reconcile standards.

  • Team Coordination:

    • Coordinate team priorities with the plant’s needs and work closely with the team leader/manager to ensure smooth operations.

    • Follow housekeeping, cGMP, GLP, and safety guidelines within the laboratory.


Your Experience and Qualifications

  • Educational Requirements:

    • Bachelor’s or Master’s degree in Science, preferably in Chemistry.

  • Experience:

    • A minimum of 3 years of experience in a Quality Control laboratory setting, preferably with wet chemistry experience.

  • Skills & Knowledge:

    • In-depth knowledge of laboratory practices, testing, and analysis.

    • Familiarity with cGMP, GLP, and safety regulations.

    • Strong record-keeping and analytical skills.

    • Ability to perform troubleshooting, calibration, and maintenance of instruments.


Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to fostering an inclusive and diverse workplace. We provide equal employment opportunities to all individuals without regard to race, gender, disability, or other legally protected status. If you need accommodations during the recruitment process, we are happy to provide them.


If you're passionate about quality control in the pharmaceutical industry and want to join a global leader, we encourage you to apply!