R&D Technician IV

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

• Good technical acumen in the area of manufacturing process of solid oral dosage forms
• Understand the critical attributes of manufacturing process.
• Should have in-depth knowledge of pharmaceutical manufacturing equipment's and its working principals.
• Should have understanding of current cGMP requirements prescribed by local government authority.
• Should be able to support the drafting of SOPs and procedures for pilot plant area
• Should be able to identify the challenges associated with manufacturing process and suggest the mitigation proposal
• Co-ordinate with the team and keep area/equipment ready for the timely execution of pilot batches.
• Should be aware of IQ/OQ/PQ/Preventive Maintenace/routine calibration for the equipment's available in pilot plant
• Align the day-to-day activities of the pilot plant
• Assist the formulation scientist in execution of batches in pilot plant.
• Should be able to take care of activities related to development lab area as per organization requirement as and when required.
• Demonstrate personal accountability and effective work habits, viz. working productively & act responsibly, and learn from mistakes

How you’ll spend your day

• Area and equipment management of pilot plant.
• Responsible for day-to-day activity planning for pilot plant.
• Support to formulation scientist for the execution of batches in area.
• Responsible for Maintenace of Logbooks/Calibration/ Validation/Preventive Maintenace logs for pilot area equipment's.
• Monitoring of AMC of equipment's of Pilot plant.
• Coordination with engineering for resolving any Maintenace related requirements.
• Responsible for SOP preparation and working procedure establishment
• Ensure the compliance to cGMP requirements
• Should highlight any deviation/change from SOP during routine working
• To comply the EHS requirements as per company EHS policy.

Your experience and qualifications

• Bachelors in Pharmaceutical Sciences with 5 Yrs. +/ M.Pharm with 3yrs+ from reputed universities
• Experience in working in a high-performance manufacturing team with exposure to batch manufacturing for regulated countries like US/EU/CANADA
• Should be approved manufacturing chemist for tablet and capsule from Maharashtra FDA/State licensing authority.

 

Technical Skills

• Indepth knowledge of different manufacturing processes for solid oral dosage form,
• Should have good know how of different equipment's used in solid oral manufacturing
• Good learning acumen
• Good understanding of cGMP and local regulatory body requirements for GMP batches manufacturing

Skills and Specific Knowledge Required

People Skills

• Must be confident, able to work in the team and a good team player
• Stable and calm, Supports functional colleagues
• Has the ability to take comprehend facts and data to help the decision making.
• Shows respect, listens effectively, show caring & be compliant with the core values of TEVA
• Demonstrates timeliness

 

Interpersonal Skills

• Collaborates with team within functional area and cross functional teams.
• Good technical communication applied locally and contributor to local and/or global project teams.
• Delivers technical presentations.
• Ability to work with very little supervision, work with junior staff
• Ability to work with internal and external partners.

Reports To

Manager/Sr. Manager/ Associate Director, Generic R&D

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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.