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R&D Technician II - Granulation

Date: Sep 15, 2022

Location: Goa, IN, 403722

Company: Teva Pharmaceuticals

Who are we?

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

  • Responsible for execution of manufacturing activities in Granulation area in Production (PDL).
  • Set up, operation, cleaning, line clearance and maintenance of all equipment’s in the Granulation area.
  • Monitoring and recording of environmental conditions in the department.
  • Calibration and handling of IPQA instruments.
  • Cleaning and housekeeping of Granulation area.
  • To provide support for equipment qualification. 
  • To perform the cleaning activities in wash area as per current SOP.
  • Handling of material storage area as per current SOP.
  • Handling of all change parts, spares and tools used in Granulation area.
  • To perform on-line documentation for all activities.
  • To follow BMR instructions during batch manufacturing.
  • Ensure Standard Operating Procedure compliance.
  • To comply with the cGMP practices.
  • Undergoing the training as per the identified training needs.
  • To follow the normal safety precautions in production department.
  • To keep the department audit worthy at any point of time.
  • Executions of daily production activities as per the target production plan.
  • To support for achieving the monthly production target of Pre Exhibit and Exhibit batches.
  • To ensure compliance to data integrity as per laid down system and procedure.

Qualifications

Diploma in engineering/Pharmacy or ITI with 4 to 6 years experience in handling of automated HSMG and FBE (Preferred Glatt).

Function

Research & Development

Sub Function

Drug Analysis and Formulation

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided 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.