Production - Chemist / Officer (API) - Jubilant Biosys - Mysore

Jubilant Pharmova

Mysuru

On-site

INR 250,000 - 400,000

Full time

14 days+

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Job summary

Jubilant Biosys Limited in Mysuru, Karnataka, seeks a Chemist/Officer - Production to manage intermediate/API production within a clean room, ensuring calibration and maintainance of documentation. The role covers material handling, SRP duties, and strict SOP adherence in a GMP environment.

Ideal candidates have 1 to 6 years of API industry experience and will work at the Nanjangud, Mysore site, performing various manufacturing and documentation tasks with diligence and teamwork.

Qualifications

Degree in Science / Graduate Engineers / MSc - Chemical/Diploma in Chemical Engineering.
Experience in API industry preferred.

Responsibilities

Producing Intermediates/API/Solvent Recovery according to pre-approved instructions and to record the same in respective BPR/documents.
To perform the cleaning activity as per the procedure and to record the same in respective BCR/documents.
Maintaining the Intermediate/Pharma/SRP and equipment clean and well appropriately disinfected.
To ensure that the respective equipment is calibrated
Maintaining the respective equipment /Area in clean condition.
Online updating of equipment status boards w.r.t to equipment status.
Identifying /Labelling of accessories and storing the same in designated place.
Identify abnormalities associated risk and objectives by cross verifying interlocks in equipment.
To ensure the availability of utilities and to maintain the same by requesting utility department whenever required.
Receiving the raw material from the stores and storage of raw materials in the designated place
Identification and storage of intermediates/ APIs in the designated place.
Maintaining the RM/ intermediate/ rejected material storage area clean and when appropriate disinfected.
To maintain the accessories per respective SOP.
To indent, receive and issue the required documents with in timeline according to pre-approved instructions.
To ensure that documents being recorded contemporaneously.
To ensure the records are updating contemporaneously and to facilitate the required documents.
To ensure the availability of calibration documents where ever required.
To ensure that those documents are completed and signed.
To ensure the online entries of status board, log books and daily updating documents.
To ensure the accessories are properly maintained/ destructed as per the respective SOP and it is properly documented.
To submit the completed documents with in the timeline as per respective SOP
On line monitoring of the environment conditions in process area

Education

Degree in Science / Graduate Engineers / MSc - Chemical/Diploma in Chemical Engineering

Job description

Introduction:

Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S. Bhartia and Mr. Hari S. Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research & Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Group has global presence employing around 42,000 people across the globe with over 2,400 in North America.

Jubilant Biosys Limited

Jubilant Biosys Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses.

In the Radiopharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Companys Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectables business offers manufacturing services including sterile fill and finish injectables (both liquid and lyophilization), full-service ophthalmic offer (liquids, ointments & creams) and ampoules.

The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies.

Find out more about us at www.jubilantpharmova.com.

The Position

Organization : Jubilant Biosys Limited

Designation : Chemist / Officer - Production

Work Location : Nanjangud, Mysore

Key Responsibilities.

Intermediate/Clean room/SRP:

Producing Intermediates/API/Solvent Recovery according to pre-approved instructions and to record the same in respective BPR/documents.
To perform the cleaning activity as per the procedure and to record the same in respective BCR/documents.
Maintaining the Intermediate/Pharma/SRP and equipment clean and well appropriately disinfected.
To ensure that the respective equipment is calibrated
Maintaining the respective equipment /Area in clean condition.
Online updating of equipment status boards w.r.t to equipment status.
Identifying /Labelling of accessories (e.g. Scoop /Scrapper/Hose pipe/Filter bags/ AHU filters / micron filter cartridges) and storing the same in designated place.
Identify the abnormalities associated risk and objectives by cross verifying the interlocks in equipment.
To ensure the availability of utilities and to maintain the same by requesting utility department whenever required.

Material Handling:

Receiving the raw material from the stores and storage of raw materials in the designated place
Identification and storage of intermediates/ APIs in the designated place.
Maintaining the RM/ intermediate/ rejected material storage area clean and when appropriate disinfected.
To maintain the accessories per respective SOP.

Documentation:

To indent, receive and issue the required documents with in timeline according to pre-approved instructions.
To ensure that documents being recorded contemporaneously.
To ensure the records are updating contemporaneously and to facilitate the required documents.
To ensure the availability of calibration documents where ever required.
To ensure that those documents are completed and signed.
To ensure the online entries of status board, log books and daily updating documents.
To ensure the accessories are properly maintained/ destructed as per the respective SOP and it is properly documented.
To submit the completed documents with in the timeline as per respective SOP

Safety, health and environment: