Job Description Summary
Technician required for manufacturing processJob Description
Delivery
a. To achieve the weekly plan schedule NLT 90%.
b. Responsible to perform the operation, machine setting, cleaning, in process checks, challenge test and Trouble shooting.
c. To ensure no machine functioning parameters/facility by passed.
d. Proper operation and setting of machines to minimize the spillage and rejection.
e. To maintain the machine, accessories, documents, area, materials, and all other things are in place. Ensure things are in their designed place and vice versa.
f. To maintain machine, area and accessories with minimum breakdown. PMP and spares management.
g. Involved in the dispensing of raw materials. Storage and material movement of dispensed materials.
h. Verification of dispensed materials and in process storage materials against the batch record.
i. Ensure and discuss with supervisor and above if any special precaution (Like staggering during breaks, sensitive product, new product, new PM, new market, offline activity, special/critical product, new manpower, machine issues etc.).
j. Preparation and storage of disinfectant solution and cleaning agents.
k. Issuance and integrity checking of sieves, screen, filter bags, hose pipes, silicon tubes etc...
l. Cleaning and checking of tools before and after completion of batch.
m. Cleaning and storage of Utensils and Production accessories.
n. Indenting, storage, issuance, usage, and destruction of silica gel.
o. Responsible to prevent the cross contamination during manufacturing.
p. Execution of necessary document during cleaning, line clearance and BMR.
q. Performance of in process check and challenge test as per BMR and if any abnormalities observed inform to the superior and QA.
r. Responsible to Monitoring of Environmental condition and reporting maintenance team if any abnormalities noticed.
s. Involved in the Equipment PMP activities along with engineering person.
t. Ensure the calibration of weighing balance & instruments as per the calibration schedule.
u. To give Training to junior level operators and newly joined persons.
v. Identification and initiation of improvement projects in manufacturing.
w. Based on requirements to carry out the activity whenever assigned by management.
Quality and Compliance:
a. cGMP Compliance in entire manufacturing area and SOP compliance on all aspects.
b. To ensure zero overdue on trainings.
c. Follow ALCOA++ and ready for any time inspection.
d. Responsible to face regulatory and customer audits.
e. Ensure to follow quality culture in organization.
Safety:
a. To follow and ensure 100% safe operation in manufacturing area.
b. Ensure all the necessary PPEs are available in production facility and were the proper PPEs during manufacturing.
c. Reporting the near miss and ensure their compliances.
d. Follow ISO 14001& 45001 practices.
e. To follow and maintain 5s in workplace.
What We Do
At Endo, our far-reaching vision is simple: to help everyone we serve live their best life. As a specialty pharmaceutical company, we’re motivated by a strong sense of purpose to find better ways to meet unique medical needs.
Our global team of passionate employees understands the importance of their work. We’re dedicated to supporting one another as we connect with communities and foster partnerships that elevate quality-of-life and bring the best treatments forward.
Our uncompromising commitment results in the delivery of life-enhancing therapies. From intelligent product selection to commercialization, we strive to make a meaningful, tangible impact to help everyone live their best life.
Endo has global headquarters in Malvern, Pennsylvania.
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