2 Opening(s)
0 To 2.0 Year(s)
1.00 LPA TO 2.40 LPA
We are hiring a QA/QC Executive in Ahmedabad.
Key Responsibilities
• Raw materials, in-process aur finished products ki quality checking karna• Production process monitoring aur quality standards maintain karna• Lab testing, sample verification aur product inspection me support karna• QA / QC documentation aur reports maintain karna• SOPs aur GMP guidelines follow ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
5.00 LPA TO 7.00 LPA
Description
Position: Sr. Executive/Asst. Manager - Projects
Location: Ahmedabad
Experience: 3 - 7 Years
Industries: Pharma
Responsibilities
Executed construction activities as per approved drawings and specifications
Coordinated with contractors, consultants, and internal teams for smooth project flow
Monitored site progress, quality, and timelines, resolving issues proactively
Assisted in project planning, scheduling, and ...
2 Opening(s)
0 To 3.0 Year(s)
2.16 LPA TO 3.00 LPA
We are looking for a highly skilled and detail-oriented QA Officer to oversee quality assurance operations. The QA in charge will be responsible for implementing quality control procedures, ensuring compliance with industry standards, and maintaining product/service quality. The ideal candidate should have strong leadership skills, a keen eye for detail, ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 15.00 LPA
Position: Asst. Manager - QA
Location: Daman
Experience: 8 - 15 Years
Industries: Pharma
Responsibilities:
To maintain a robust Quality Management System (QMS) aligned with regulatory expectations.
To handle internal, external, and regulatory inspections, ensuring successful outcomes and continuous compliance readiness.
To handle compliance of deviation management, change control, Market Complaint Recall, ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.40 LPA TO 3.60 LPA
A "FACT Chemist" (often referring to a Formulation, Analytical, Compliance, and Technology Chemist or simply a specialized Manufacturing Chemist) in a personal care products company is responsible for developing, testing, and ensuring the quality of cosmetic products such as lotions, shampoos, and skincare items. They bridge the gap between R&D and mass production, ensuring products are ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: EHS Manager
Location: Vapi
Experience: 10 - 12 Years
Industries: Pharma - API
Responsibilities:
Ensure compliance with EHS regulations, Factory Act, GPCB, and Pollution Control Board requirements.
Manage statutory approvals, hazardous waste disposal, and EHS documentation.
Conduct risk assessments (HAZOP/HIRA), incident investigations, and implement CAPA.
Handle GMP, regulatory, safety, and customer audits and ensure ...
1 Opening(s)
0 To 2.0 Year(s)
1.20 LPA TO 1.80 LPA
Designation: QA/QCExperience: 0-2 yearsLocation:Palghar
Department: QA & QC
Role Summary: The QA & QC – Junior will handle daily IQC, PQC & OQC Of Material and FG Products. Also Manage Quality Related Documents.Key Responsibilities:•Perform incoming inspection of raw materials•Conduct in-process inspections during manufacturing•Perform final inspection of finished Product•Use measuring instruments (vernier caliper, ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
24.00 LPA TO 25.00 LPA
Description:
Position: Sr. Manager - Manufacture & Operation
Location: Ahmedabad
Experience: 15 - 20 Years
Industries: Pharma
Responsibilities:
Develop and implement corporate manufacturing strategies aligned with business goals.
Monitor production performance across multiple manufacturing sites.
Support plant leadership teams to achieve productivity and efficiency targets.
Drive continuous improvement ...
2 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 3.50 LPA
Urgent Opening -Chemist / Officer
Experience - 1 Year to 5 years of experiencelocation - Kodadara Jolwa , suratRotational Shift Time - 6am to 2pm2pm to 10pm10pm to 6amGeneral shift - 9am to 6pmCanteen facilityDepartment - Production Department
Operate and monitor production equipment under supervision Follow GMP/GLP guidelines and other industry regulations ...
2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
IPQA activities, Plant round, Online BMR review, Line clearance, Samplingof APIs, Analytical data review, Batch release, APQR preparation. People who have faced regulatory audits like EDQM would be givenpreference.
Process & cleaning validation, including cleaning matrix preparation
QMS documentation management; SOP preparation, review, and training
IPQA activities
to ensure GMP compliance during manufacturing.
Regulatory inspection exposure ...