1 Opening(s)
4.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 6.00 LPA
A Quality Assurance (QA) Assistant Manager for a starch powder or pharmaceutical/food-grade starch active/derivative manufacturing plant in the Dhule/Dondaicha MIDC region oversees cGMP compliance, QMS documentation, process validation, and regulatory audits for specialized grades (IP, BP, USP).
Job Profile & Core Details
Position Title: Assistant Manager - Quality Assurance (QA)
Industry Segment: ...
1 Opening(s)
3.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 4.50 LPA
📌 Key Responsibilities
Handle day-to-day API production operations as per BMR/BPR and SOPs.
Operate and monitor reactors, centrifuges, dryers, filters and other process equipment.
Execute batch manufacturing activities as per approved procedures.
Monitor critical process parameters and ensure batch yield and quality.
Maintain proper production documentation and ensure ALCOA+ compliance.
Follow cGMP, SOP, EHS and safety ...
3 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Position: officer, lab chemistNo. of Openings: 3Industry: Pharma Intermediate / API ManufacturingGender: Male Candidates OnlyQualification: B.Sc. / M.Sc. (Chemistry)
Experience:- 2+ Yrs Pharma API industry Qualifications:-/Bsc/Msc/ Location: DAHEJ
Job Requirements:
Candidates must have experience in Pharma Intermediate or API manufacturing.
Hands-on experience in R&D activities, process development, process optimization, scale-up, and documentation.
Major Skill Required:
1) carry out reaction process as per ...
3 Opening(s)
4.0 Year(s) To 6.0 Year(s)
3.50 LPA TO 4.00 LPA
Hiring for Starch powder, liquid Glucose Manufacturing Industry
Position:- Production Assistant Manager & Supervisor
(Products - liquid Glucose, Sorbital, DMH, DAH, M alto Destine)
Education: - B.E chemical / Bcs Chemistry
Experience: - Min 2 to 8 Years in a chemical factory, Food Industry, and Pharma Industry
Job Description:
Plan and execute production plan to meet marketing requirements following ...
5 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Key Responsibilities:
Documentation Management:
Review, approve, and control various quality documents, including Standard Operating Procedures (SOPs), Batch Manufacturing Records (BMRs), Batch Packing Records (BPRs), Specifications, Test Procedures (STPs), and other quality-related documentation.
Ensure proper archiving, retrieval, and revision control of all controlled documents.
Participate in the preparation and review of site master files (SMF), ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
12.00 LPA TO 15.00 LPA
To understand, communicate and prepare a system to meet the desired production of each product as per the plan agreed by SCM team.
To manufacture all products of high quality by complying with CGMP and safety systems at Udaipur Plants.
To Plan and set production targets and ensure achieving the same for ...
5 Opening(s)
1.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
Responsibilities
Perform and supervise In-Process Quality Assurance (IPQA) OR QA checks during API manufacturing operations.
Conduct on-line review of Batch Production Records (BPR) and ensure adherence to approved procedures.
Ensure sampling, line clearance, and process compliance as per GMP/cGMP norms.
Identify, record, and support resolution of deviations, non-conformances, and quality incidents during manufacturing.
Support quality investigations and prepare required ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Job Description:
We are seeking a skilled and experienced microbiology professional to lead microbial testing and environmental monitoring activities in an API manufacturing setup. The Assistant Manager will ensure compliance with regulatory standards, supervise microbiological operations, and support quality systems in the microbiology lab.
Key Responsibilities:
Oversee routine microbiological testing of raw materials, ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
Job Description:
We are seeking a dedicated QMS professional to oversee and maintain the Quality Management System in compliance with cGMP and regulatory requirements. The role involves managing documentation, handling quality events, and supporting internal and external audits in an API manufacturing environment.
Key Responsibilities:
Implement and maintain QMS processes in line with ...
13 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 6.00 LPA
Key Responsibilities
1. Quality System Management and Compliance:
Implement, maintain, and monitor the company's Quality Management System (QMS) as it relates to API manufacturing.
Ensure all processes, procedures, and documentation comply with cGMP, regulatory guidelines, and corporate policies.
Conduct routine inspections and on-line process checks to ensure adherence to standard operating procedures (SOPs) and ...