Sanofi Pharma Production Specialist Vacancy - Apply Online

Sanofi Pharma Production Specialist Vacancy – Apply Online

Sanofi Job. Career at Sanofi. Chemistry Candidates with a Master’s degree are encouraged to apply online at Sanofi for Production Specialist vacancies that are available. Sanofi is hiring Chemistry & Pharma candidates for Specialist vacancies. Interested candidates may apply online. Check out all the details on the same below:

Job Title: Production Specialist

Location: Toopran Mandal

Qualifications

  • A minimum of Bachelor Degree in Science / Pharmacy.
  • 2-3 years of relevant experience in visual inspection and packing.
  • Relevant working experience in the Pharmaceutical industry

Requirements of the job

  • This position requires the incumbent to work in shifts.
  • This position requires to maintain positive working relationships with all the stakeholders to meet the supply chain requirements

Knowledge, Skills & Competencies / Language

  • Demonstrated capacity to efficiently prioritize work and timely inform supervisor on the progress
  • Excellent verbal and written communication skills in English are required.
  • Knowledge of soft skills like MS Office is required

Duties & Responsibilities

Visual inspection and packing

  • Will be responsible for troubleshooting in visual inspection and packing related machines.
  • Will be responsible for effective installation, commissioning and qualification of the equipment’s in Inspection and Packing area.
  • Will be responsible for the operation of machines in visual inspection and packing area.
  • Perform manual inspection of cartridges and loading/unloading of cartridges.
  • Perform execution of in-process checks as per current SOP’s and BMR’s.
  • Accountable for handling and transfer of secondary packaging materials.
  • Ensure maintenance and validation activities for visual inspection and packaging equipment in compliance with the current GMP practices and support in failure investigations.
  • Execute the actions described in the SOP’s and BMR’s includes cleaning and line clearance of visual control and packing machines.
  • Support in continuous improvement of industrial performance in visual inspection and packaging area.
  • It is required to operate and troubleshoot the visual inspection and packing related equipment (automatic inspection machine, labelling machine, blister packing machine, carbonator machine etc)- hence maintenance and troubleshooting experience of automatic VI & P machines is required
  • Excellent verbal and written communication skills in English are required.
  • Knowledge of soft skills like MS Office is required.
  • Knowledge on GXP and technical skills involved in relevant manufacturing activities.
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Medical device packing

  • To ensure GMP and GDP is followed at all levels of medical device packing activities and relevant activities.
  • To ensure adherence to ISO 13485 and laid down standards, Laws & Acts.
  • Will be responsible for troubleshooting in medical device packing related machines.
  • Will be responsible for the operation of machines in medical device packing.
  • Supervise manual packing of medical device and document the activities performed.
  • Perform execution of in-process checks as per current SOP’s and BR’s.
  • Accountable for handling and transfer of secondary packaging materials.
  • Ensure maintenance and validation activities for medical device packing in compliance with the current GMP practices and escalate the Non-compliance and non-conformance.
  • Ensure the actions described in the SOP’s and BR’s includes cleaning and line clearance of medical device packing area.

Training and Documentation

  • Responsible to training and qualification of the people in the team.
  • Complete the assigned training and maintain the training file updated.
  • Accountable for online entries of batch records, record sheet template, log books etc. for the operation of visual inspection and packing area and medical device packing.Support
  • for preparation of production operations and SOPs, batch production records, record sheet template, logbooks, etc.
  • Working in teams and Inspection readiness
  • Ensure the compliance of area/activity for various regulatory inspections/ audits and GMP compliance.
  • Create good working relationships within the team and cross-functional teams.
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Health, safety and environment

  • To identify, correct and promptly report unsafe conditions, behaviours, or potentially hazardous situations.
  • To animate a strong, proactive culture oriented towards promoting positive behaviours at all levels of the organization.

Apply Online

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1 COMMENT

  1. Sir, I HV completed B.pharma 2019.i want to join in pharmaceutical company plzzz inform me if any company requires for fresher candidate

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