JOB DETAILS

Chemist

CompanyiolchemicaP2
LocationIndia
Work ModeOn Site
PostedMay 10, 2026
About The Company
Company was established in 1986 IOLCP is Indias one of the leading generic pharmaceutical company and is significant player in the Organic chemicals space. IOLCP has wide presence across various therapeutic categories like Pain Management Anti-diabetic Anti hypertensive Anti Convulsants etc. Our capabilities are nurtured by pursuing implementing the high standards of excellence in our operations. By delivering consistent results quality we have earned the admiration of customers and stakeholders. Innovative Strengths Strong Growth have made us the market leaders. We have built up our expertise responding to diverse customer requirements Our products cater to the key industrial sectors of Pharmaceutical Flexible Packaging Paint Lamination Ink Pesticides etc. Efficient teamwork strong associations have guided us to success. Accolades for our environmental policies have come from the highest levels of power. Through an unwavering focus on Quality Commitment Delivery we have charted our way to success in our operations and have won the admiration of our customers. Our success is built on the strong pillars of innovation quality dedicated customer service. By incorporating these other business strengths we have boosted our capabilities to maintain the leading edge in the industry earn the loyalty of our customers.
About the Role

1.             To maintain the systems as per applicable standard operating procedures in the department.

2.             To take the round of production area on routine basis for the cGMP compliance.

3.       To ensure the calibrations are performed and records are updated accordingly at site.

 

4.             To monitor the critical process parameters of respective BPCR’s on routine basis at shop floor.

5.             To do the label printing, reconciliation of labels and maintenance of the records.

6.             To perform final products sampling and sealing activity.

7.             To participate in the activities related to retention sample verification and destruction.

8.          To ensure the placement and checking of the retention samples of all products on daily basis and maintain temperature records of the retention sample form.

9.             To inspect the intermediate/ Powder processing area for IPQA audits and maintain the records are maintained accordingly.

10.          To participate/review of dispatch activities (like vehicle inspection, material allocation, loading activities) for products dispatch outside of company premises.

11.         To issue/retrieval of the protocols, BPCRs, packing detail, logbooks, formats, etc. to all departments.

12.         To review the submitted Batch Production Control Record and data punching of the same as required for APQR.

13.         To ensure the line clearance in P.P Area and Intermediate area.

14.         To inspect ISO tanks before dispatch.

15.         To issue and maintain the record of controlled documents for other departments in absence of issuance team.

16.         To do the work described in the job responsibility of Officer/Executive-QA in absence of them.

17.      In case of absence job delegation will be assigned to Chemist/Technical trainee - QA.

18.         To ensure the physical cleanliness of PP Area.

19.         Environment Health & Safety (EHS)

19.1          Supervising personnel for effective implementation of the EHS program into the work process.

19.2          Ensure Labels of all containers of hazardous materials in plants.

19.3          To review the Implementation of specific standard operating procedures in the workplace.

19.4          Informing his / her superiors about the safety requirements (equipment’s etc.)

19.5          Ensure that EHS rules/regulations are followed fully during work processes.

Key Skills
cGMP ComplianceQuality AssuranceSamplingCalibrationDocumentationEHS ImplementationIPQA AuditsLine ClearanceBatch Production Control RecordsHazardous Materials Handling
Categories
Science & ResearchManufacturingSecurity & Safety
Job Information
📋Core Responsibilities
The Chemist is responsible for maintaining quality assurance systems, monitoring critical process parameters on the shop floor, and ensuring cGMP compliance. Key duties include performing product sampling, managing controlled documents, and overseeing EHS regulations within the production area.
📋Job Type
full time
📊Experience Level
0-2
💼Company Size
7
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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