37 Job openings found

4 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
Documentation review and reconciliation. Responsible and ensuring following GMP. Granulation Process Management: Oversee all aspects of the granulation process, including equipment setup, operation, and troubleshooting. Ensure that granulation activities are carried out efficiently and in compliance with standard operating procedures (SOPs) and regulatory requirements. Team Leadership: Lead and supervise a team of granulation operators, ...
10 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
Documentation review and reconciliation. Responsible and ensuring following GMP. Granulation Process Management: Oversee all aspects of the granulation process, including equipment setup, operation, and troubleshooting. Ensure that granulation activities are carried out efficiently and in compliance with standard operating procedures (SOPs) and regulatory requirements. Team Leadership: Lead and supervise a team of granulation operators, ...
4 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
Documentation review and reconciliation. Responsible and ensuring following GMP. Granulation Process Management: Oversee all aspects of the granulation process, including equipment setup, operation, and troubleshooting. Ensure that granulation activities are carried out efficiently and in compliance with standard operating procedures (SOPs) and regulatory requirements. Team Leadership: Lead and supervise a team of granulation operators, ...
1 Opening(s)
0 To 1.0 Year(s)
1.80 LPA TO 1.80 LPA
Job Description   27.04.26 131943 HPS/2026/361 Trainee Production/Quality Male 3 0 to 1 B.Pharma/M.Pharma Masat Job Summary We are looking for enthusiastic and detail-oriented freshers or candidates with up to 1 year of experience to join our Production and Quality departments as Trainees. The role offers hands-on exposure to pharmaceutical manufacturing processes and quality systems in a regulated environment. Key Responsibilities Production: Assist in manufacturing ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
Analysis of Raw Materials (RM), Packing Materials (PM), In-Process (IP), Finished Goods (FG), Returns, and Recall samples; preparation of approved/rejected test reports as per SOP/STP. Perform sampling of gases, powders, granules, liquids, and semi-solid materials safely and accurately. Ensure proper batch numbering, packing, labeling, sealing, and sample management procedures. Maintain QC analytical data ...
4 Opening(s)
2.0 Year(s) To 5.0 Year(s)
1.80 LPA TO 3.60 LPA
A Chemist (SID/Raw Material) in the steel/mineral industry conducts chemical analyses of raw materials (iron ore, coal, coke, limestone) and finished products (sponge iron, pig iron, slag) to ensure quality standards. They perform wet chemical analysis, operate instruments like proximate analyzers, and maintain lab safety in a plant setting.  Key Responsibilities Chemical Analysis: Perform ...
1 Opening(s)
12.0 Year(s) To 25.0 Year(s)
12.00 LPA TO 18.00 LPA
Hiring for the upcoming plant in Aurangabad MH of Manufacturing  Edible Oils, Refineries, Coconut Oil Post: Plant Head Level: Manager / Senior Manager Job Details: - Planning, organizing, directing and running optimum day-to-day operations to exceed customers- expectations - Increasing production, assets capacity and flexibility while minimizing unnecessary costs and maintaining current quality ...
1 Opening(s)
4.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 6.00 LPA
Job summery objective:We want candidates with experience in the production department who are sharp, good at numbers, proactive, passionate about production, will stay long term, have a problem solving approach, good decision making skills, and managerial skills, and will always have a desire to improve the process with innovation.The person ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
  Key Responsibilities: Operate and maintain Ion Chromatography instruments (e.g., Metrohm, Dionex, Thermo Scientific). Prepare and analyze samples for cations and anions in various matrices (e.g., water, pharmaceuticals, food). Develop, validate, and optimize IC methods in accordance with internal SOPs and regulatory requirements. Perform system suitability testing, calibration, and routine maintenance of IC equipment. Troubleshoot ...
1 Opening(s)
0.5 Year(s) To 2.0 Year(s)
1.44 LPA TO 2.50 LPA
Documentation & Compliance: Maintain accurate and complete laboratory records in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Prepare and review Certificates of Analysis (CoAs), test reports, and deviation reports. Ensure compliance with company SOPs, safety protocols, and regulatory requirements (e.g., FDA, EPA, ISO). Process Validation & Improvement: Participate in validation of ...

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