Marksans Pharma Hiring for Senior Executive / Assistant Manager – Packing at Goa Full Time

Full Job Description
Supervision and monitoring of Bulk packing (CVC packing line),Blister packing (BQS,BMax,B45,230XT and packing line to achieve plan.
Reviewing and complying batch packing record and Monitoring of cleaning and operation of all rooms and equipment of packing as per the GMP and completion of checklist and logs.
Training and reviewing reports with respect to SOP, Compliance, maintenance of DATA integrity and improvements with packing operation.
Maintaining log book and all controlled document.
Ensuring periodical calibration and daily verification of balance.
Checking and completion of in process records for various physical parameters of all the products in packing the area.
Planning and implementing preventing maintenance schedules without affecting productivity.
Review of sops and analyses the gap.
Ensuring the establishment and maintenance of area for “All Time Audit Readiness”
Role:Production Manager / Supervisor
Salary: 7,00,000 – 10,00,000 P.A.
Industry:Pharmaceutical & Life Sciences
Functional Area:Production, Manufacturing & Engineering
Role Category:Operations, Maintenance & Support
Employment Type:Full Time, Permanent

Key Skills
CVC
bulk packingusfdaBottle lineshift incharge
Skills highlighted with ‘‘ are preferred keyskills

Education

UG:B.Pharma in Any Specialization

Company Profile

marksans Pharma Ltd

The essence of our culture is built on meeting global standards in every aspect of our business.”

These envisioned words of Mr. Mark Saldanha, our Chairman and Managing Director, reflect the extreme passion and enthusiasm that drives the organization.

Marksans Pharma, headquartered at Mumbai (India) is a global pharmaceutical company. We are actively engaged in R&D and offer CRAMS to global pharmaceutical companies.

ur key focus areas lie in the OTC & prescription drugs that have wide-ranging applications across fields like Oncology, Gastroenterology, Antidiabetic, Antibiotics, Cardiovascular, Pain Management, Gynaecology, among others.

We have established world-class manufacturing facilities by leveraging state-of-the-art technology, incorporating best practices and adhering to stringent regulatory compliances. Our plants are approved by prestigious US FDA, UK MHRA, Australian TGA and other foreign health authorities.

Our R&D capabilities include dossier development, chemical synthesis, process optimization, formulation development, analytical development and conducting stability studies. We have a team of over 50 experienced scientists specializing in formulation development and analytical development.

We possess end-to-end capabilities from Lab scale development to Pilot scale up and from commercializing the product for large scale manufacturing to marketing globally.

The company has achieved global recognition within a very short span of time and has major global expansion plans for the near future.