Abbott D Pharma Job

Abbott D Pharma Job – Apply For Production Officer

Abbott is a renowned pharmaceutical company that specializes in the production and development of various healthcare products. With a strong commitment to innovation and quality, Abbott strives to improve the lives of people around the world.


LOCATION: India > Village Mauza: Baddi

CATEGORY: Operations

Experience Required

Diploma in Engineering/D.Pharm with 4-5 years of experience in the core granulation area & exposure to ISOLATOR & GEA BLENDER. Candidates with expertise in negative isolators & in granulation department exposure in machine installation & qualification activity and exposure to regulatory audits such as MHRA, USFDA, etc., are preferred. Persons working in a CONTAINMENT FACILITY are preferred.


  • Responsible for Operation, cleaning and primary maintenance of negative isolators, sifters & GEA dry granulation line equipments.
  • Competent for (entry) recording of activity in logbooks, Batch manufacturing record & Responsible for completing documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP’s and good documentation practices.
  • To perform all in-process checks and monitoring of all intermediate processes in granulation to prepare new recipes set process parameters in PLC/SCADA in blender HMI & ensure its correctness before blender revolution.
  • Issuance, utilization, cleaning, and retrieval of sieves, valves & proper handling of machine change parts with its inventory. Responsible for set up, changeover, and operation of various manufacturing equipment’s but not limited to granulation department.
  • Ability to read, write and communicate in English, Strong work ethic, professional approach, and ownership of lines production performance.
  • Ability to read & understand SOP’s, Batch Records, training documents & Basic computer knowledge.
  • Ensures accurate and timely completion of all equipment logs and documentation. Understands and adheres to all cGMP and FDA regulations.
  • Responsible for reporting and/or escalating any conditions or problems that may affect the quality or integrity of product to supervisor and HOD production.
  • Responsible for maintaining a neat, clean and safe working environment at all times and notifies supervisor immediately of any safety concerns, accidents or injuries are observed.
  • Understands and adheres to all Company policies, procedures, SOPs and Safety regulations.
  • Willingness to do overtime as needed & responsible for performing additional task, related duties as assigned.
  • To ensure all in-process checks and monitoring of all intermediate processes, To check set process parameters in PLC/SCADA as per BMR before machine run in granulation area.

Click here to apply online

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