Knowledge and skill
Technical skills:
Basic knowledge of pharmaceutical industries, machines cleaning operation and maintenance.
Understand workplace safety and related procedures (First aid)
Basic Knowledge on Pharmaceutical industries and its standards.
Good communication skills.
Knowledge on basic trouble shooting.
Standards, Process and policies:
Basic understanding of cGMP, global quality standard and data Integrity.
Behavioral/ any Other skills:
Attention to details
Willingness to take direction and adhere to procedures
Basis understanding of hygiene, Clean room work culture.
Proper utilization of personal protective equipment during activities.
Responsibilities
Equipment installation and qualification:
Participate in the installation, site acceptance test, Installation qualification, operation qualification, Process qualification and Re-qualification of equipment in the respective functional area.
Participate in the execution of equipment qualification, performance verification and process validation
Ongoing Operation
Maintain personnel hygiene while coming to office and entering in working area.
Beware of and always adhere to change room procedures
Check for proper housekeeping in his/ her area and follow all time audit readiness practices.
Receive and maintain the daily consumables.
Achieve the desired output in lines as per shift, week, monthly and yearly target assigned.
Error to be escalated to higher authorities immediately when identified.
Accountable for area and equipment upkeep.
Accountable for the cleaning and sanitization of area and equipment as per procedures
Hand over the shift at the end of shift and to take charge of the shift
Coordinate with cross functional department and participate in preventive and breakdown maintenance of equipment and machines.
Attend shift Communication meetings and Improvement projects meeting.
Generate new idea for workplace improvement and lockout on implementation.
Active involvement in increase in Efficiency and effectiveness programs in departments.
Follow procedure for proper material movement from SFG area to Inspection area and from inspection area to SFG/FG area with proper status label
Handling of rejects generated in process with proper status labelling.
Attend office as per shift schedule and maintain attendance as per requirement, leave shall be preapproved (Except and medical issue or emergency)
Ensure qualification status.
Complete all trainings site specific and global training assign in to do list as per requirement.
Follow proper material and product movement in area pre-inspection and post inspection.
Part of continuous improvement meetings and add necessary inputs for improving efficiency and compliance.
Quality management and Compliance
Follow cGMP and safety at all stages of manufacturing activity.
Compliance to Pfizer integrity principles at all stages of manufacturing.
Participate in internal and external (Regulatory and Non-regulatory) audits.
Documentation
Prepare the daily activity report. Complete the documents online as per cGMP and GDP.
Preparation of user requirement specification (URS), standard operating procedures, change controls forms and corrective action and preventative action and support investigation.
Responsible for protocols preparation execution, completion, review and submission and retrieval to document cell and validation as per requirement.
Training
To Attend training for all the applicable procedures as per the schedule before performing the job.
Should be able to provide training to the trainees.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Manufacturing
#LI-PFE
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