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JOB TITLE - Executive : Production, Chemistry JOB PURPOSE Generic Purpose of this job is to co-ordinate and organize API manufacturing activities in shifts adhering to cGMP / HSE norms/ standards with optimum utilization…
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Full-time
Posted 3d ago
~40 hrs/week
Responsibilities
Oversee daily maintenance services for plant and utility equipment, ensuring timely compliance and preventive maintenance. Manage regulatory documentation for audits and coordinate with inter-departmental teams for materials and services.
Requirements
Requires expertise in mechanical and utility maintenance, failure analysis, and energy conservation. Must be proficient in maintaining documentation according to cGMP, GDP, and various ISO standards for regulatory audits.
Full job description
Maintenance Services
To distribute the daily work to Engineers / Section wise in-charge as per plant & Utility job & ensure timely compliance.
To co-ordinate with electrical, instrument and Utility person for job related work.
To communicate and maintain check list of mechanical & utility equipment’s & carryout preventive maintenance as per schedule.
To proper coordination with project department for plant modification and building maintenance work.
To prepare daily / monthly maintenance report.
To review & ensure timely compliance of plant maintenance & Utility services to plant operation.
To evaluate the breakdown of the equipment’s by failure analysis & implementation of corrective & preventive measures
For Technical Problem & Supporting for engineering activities supposed to visit on Unit-II.
To maintain the housekeeping work and scrap removal as per process on daily basis.
Coordination with Electrical & instrument Dept engineers on daily basis.
Energy Conservation
To inspect the functioning of instruments regularly to avoid malfunctioning & energy loss.
To ensure the optimization usage of resources for reduction of waste on daily basis.
To ensure & timely rectification of leakages / spillages to save energy in entire plant.
Safety
To comply & maintain the safety guidelines & procedures in the maintenance function
With coordination to all engineers.
To ensure & maintain the safety interlocks & guarding of mechanical system.
To comply and maintain the statutory inspection/legasis with records.
Materials & Service Management
To prepare Min / Max list of spares & consumables & maintain the inventory in respective plant.
To verify the measurement and proceed the bills, to prepare purchase & service requisition of spares, consumables and services.
To carryout inspection of received material for quality & specification with coordination to Engg. Store.
To make the RGP and NRGP of preparation, record & analysis & maintained the records.
Documentation
To prepare and maintain USFDA, all regulatory audits, customer audits, Internal audits, ISO 9001, ISO 14001 & OHSAS system documentation with proper record.
To prepare and maintain the documentation record as per GDP & cGMP.
To ensure compliance regulatory documents & proper record of the same.
To face the audits in absence of Documentation engineer.
Inter departmental co ordination
To co-ordinate with purchase department for timely availability of materials & services.
To co-ordinate with finance department for timely concurrence of indent.
To support for engineering activities to CPL-2.
To work as a second line of Engg Dept & responsible for all type of engineering activities.
Founded by Shri I.A. Modi, Cadila Pharmaceuticals Ltd. is one of the largest privately held pharmaceutical companies in India, headquartered at Ahmedabad, in the State of Gujarat. Over the last seven decades, the company has been developing and manufacturing pharmaceutical products in India and selling and distributing these in over hundred other countries around the world.
Focused strongly on Innovation and Research, the company is present in more than forty-five therapeutic areas spread across twelve specialities, including cardiovascular, gastrointestinal, analgesics, haematinics, anti-infectives and antibiotics, respiratory agents, antidiabetics and immunologicals.
At Cadila Pharmaceuticals, Research and Development is at the core of all its initiatives, be it Biotechnology, APIs, Formulations, Plant Tissue Culture or Phytochemistry.
More than 300 scientists in its various Research and Development setups reinforce the competitiveness of research in the therapeutic areas which have high unmet medical needs.
Cadila Pharmaceuticals Excellence in manufacturing facilities is central to Cadila Pharmaceuticals. The company’s formulations manufacturing plant at Dholka near Ahmedabad, Gujarat is spread over hundred acres of land. This state-of-the- art facility is not only impressive in size, but is also USFDA approved.
The second formulations manufacturing facility is located at Samba in Jammu and Kashmir. The facility meets most of the stringent quality standards across the globe to produce tablets, capsules, soft and hard gelatin capsules, liquids and orals.
Two Active Pharmaceutical Ingredient (API) manufacturing units at Ankleshwar, Gujarat manufacture a wide range of APIs and intermediates including many USFDA-certified products.
The company has strong foothold in the African continent through its formulation manufacturing facility at Addis Ababa in Ethiopia.
For more information visit: https://www.cadilapharma.com/
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