Instagram
youtube
Facebook

Quality Control Technician I

3+ years
Not Disclosed
10 Dec. 27, 2024
Job Description
Job Type: Full Time Education: MSc. 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 Analyst
Company: TAPI (Teva Active Pharmaceutical Ingredients)

Company Overview:
TAPI is a global leader in the supply of active pharmaceutical ingredients (APIs), offering the industry's broadest portfolio of over 350 API products. Serving 80% of the top 50 global pharmaceutical companies, TAPI has built a reputation as one of the most trusted API suppliers, with over 80 years of experience. With state-of-the-art production facilities across several countries, TAPI continues to drive innovation and ensure the timely introduction of new products to the market.

Role Overview:
As a Quality Control Analyst at TAPI, you will be responsible for performing critical tasks related to the operation, maintenance, and validation of laboratory instruments and equipment. This includes handling HPLC/GC, GCMS, and other instruments, ensuring compliance with safety and regulatory procedures, and performing investigations of deviations and analytical errors. You will be a key contributor to ensuring high-quality standards and compliance with data integrity requirements in the laboratory environment.

Key Responsibilities:

  1. Operate and maintain HPLC/GC and GCMS MS, ICMS instruments.
  2. Perform method transfer and validation for analytical procedures.
  3. Calibrate and validate instruments/equipment such as pH meters and analytical balances.
  4. Investigate deviations, out-of-specification (OOS), out-of-trend (OOT), alert limits, action limits, and atypical analytical test results.
  5. Handle daily calibration of laboratory instruments and equipment.
  6. Be skilled in handling regulatory inspections and ensuring laboratory compliance.
  7. Follow defined safety procedures during day-to-day laboratory activities.
  8. Maintain spares and accessories for all laboratory instruments and equipment.
  9. Report deviations, chromatographic errors, and Laboratory Incident Reports (LIRs).
  10. Ensure compliance with data integrity policies and maintain relevant registers and logbooks.
  11. Contribute to any additional tasks assigned by the Manager of Quality Control.

Qualifications and Experience:

  • Education: M.Sc. in a relevant scientific field.
  • Experience: 3+ years of experience in quality control or laboratory testing within the pharmaceutical industry, with hands-on experience in handling HPLC/GC, GCMS, and other laboratory instruments.

Teva’s Equal Employment Opportunity Commitment:
Teva is committed to providing equal employment opportunities to all candidates, regardless of age, race, gender, disability, or other legally protected statuses. We value diversity and inclusivity and strive to provide accommodations throughout the recruitment and selection process to ensure an accessible candidate experience.

Join TAPI in contributing to the global success of Teva's active pharmaceutical ingredients and making a meaningful impact on the healthcare industry!