•To follow the safety rules in the premises according to the company norms.
•Timely completion of SOPs training and On the job trainings related to visual inspection and packing
area.
•Monitoring of DP, RH and temperature area in their visual inspection and packing area.
•Responsible for Maintenance of cleaning in visual inspection and packing area.
•To maintain the BMRs and other log books in the visual inspection and packing area as per cGMP and
SOP.
•Operation and cleaning of dynamic pass box.
•Responsible to perform the in process checks during operation.
•Responsible for Operation and Cleaning of Wrap around labeling machine, Autocartonator machine,
Online check weigher, track and trace system, Bopp taping machine with weighing balance and PFS
packing area machines.
•Responsible for labeling and packing of products as per BPR.
•Operation and cleaning of visual inspection table and Operation of Lux meter.
•Responsible for Operation and cleaning of Automatic visual inspection machine and X-RAY inspection
machine.
•Responsible to perform visual inspection of the products /media filled vials or PFS as per the sop.
•Responsible for the co-ordination with cross functional departments like QA,QC, warehouse Engineering
,HR and administration for the day to day activities.
•Responsible for timely completion of calibrations and validations in coordination with EN and QA related
to visual inspection and packing area.
•Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by
following HODs instructions and guidance.
•To prepare BMR and BPR.
•Preparation and periodic revision of SOPs related to QMS area.
•Responsible for intra and inter coordination with different functions.
•To participate in Regulatory & Customer Audits.
•To perform Gap analysis of defined procedures in Batch Manufacturing Record / Batch Packing Record /
Standard Operating Procedure / Protocol and initiation of corrective actions.
•To prepare and review of Standard Operating Procedures / Protocols.
•To perform risk analysis for different process or procedures and implement necessessory mitigation plans
through Quality Risk Management (QRM).
•To prepare Failure Investigation Reports against Quality impacting deviations, Out-of- Specifications and
Non-Conformances.
Education:
Experience:
Specialized Knowledge: Licenses: Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.
Amneal (NASDAQ: AMRX) is rapidly becoming one of the most dynamic, purpose-driven pharmaceutical companies delivering more affordable access to essential medicines. Our family delivers for yours through a robust U.S. generics business, a growing branded business and deepening portfolios in injectables, biosimilars and select international markets. We’ve bolstered our world-class scientific rigor, production capabilities and commercial infrastructure. And we invest substantially in our people through leadership development and employee well-being programs – all so we can deliver even more value. We are Amneal and We make healthy possible.
Content is for informational purposes only and 3rd party content does not reflect Amneal’s opinions.
Amneal has the right to remove comments that violate another’s copyright or intellectual property, mention an Amneal product, use profanity or are defamatory, promote and solicit for third-party sites, initiatives, or products, or are factually inaccurate or misleading or spam.
Amneal recommends that you consult with your healthcare provider regarding personal health matters. To report a product complaint or adverse event related to an Amneal product, contact Drug Safety at 877-835-5472, option 3 or drugsafety@amneal.com. If you are currently experiencing a life-threatening event, please immediately contact 911.
