1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
Responsibilities:
Operate and monitor capsule filling machines as per SOPs.
Perform line clearance, changeover, and basic machine maintenance.
Ensure accurate capsule weight, sealing, and batch output.
Maintain GMP compliance, documentation, and safety standards.
Coordinate with QA/QC for in-process checks.
Requirements:
ITI/Diploma/Graduate with 2–5 years’ experience in pharma capsule filling.
Knowledge of cGMP, SOPs, and machine troubleshooting.
Attention to detail ...
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)
2.0 Year(s) To 3.0 Year(s)
Not Disclosed by Recruiter
Support OE Head in driving Operational Excellence and site performance.
Facilitate manufacturing excellence initiatives across all departments.
Identify process improvement opportunities to enhance Productivity, Quality, Cost, Delivery & Safety.
Lead Focused Improvement & Daily Management Teams; deliver KPI improvements.
Train teams on structured problem-solving techniques.
Implement daily management tools (Fishbone, Pareto, 5 Why, FMEA); build ...
10 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
Key Responsibilities:
Conduct routine microbiological testing (water, environment, raw materials, in-process & finished products).
Perform environmental monitoring of cleanrooms, utilities, and aseptic areas.
Support media fill, sterility testing, endotoxin testing, and microbial limits testing.
Ensure compliance with cGMP, SOPs, and regulatory guidelines (USFDA, EU, WHO, etc.).
Review and document microbiological data, deviations, and OOS/OOT investigations.
Participate ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: QC Executive (Reviewer)
Location: Vapi
Experience: 4 - 6 Years
Industries: Pharma
Responsibilities:
Experience in Method Validation.
Experience in Stability Study.
Experience of review Electronic data review and backup systems.
Expert in Qualification of analytical instruments like HPLC, GC, AAS, FTIR, UV etc.
Expert in Calibration of analytical instruments like HPLC, GC, ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
To ensure the work allocation All Quality control person.
To ensure the quality of raw material, packing material and finished product are compliant with the approved specification and GMP/GLP
Maintains accurate, complete, and timely documentation (analytical reports, logbook).
Ensure compliance with cGMP, GLP and regulatory standards. participate in internal audits, external regulatory inspection ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 6.00 LPA
The ideal candidate will be responsible for overseeing formulation and production processes while ensuring compliance with Batch Manufacturing Records (BMR) and regulatory standards. This role requires a detail-oriented individual with strong organizational and communication skills to manage production activities efficiently
Job Responsibilities:
Develop and establish product formulations based on industry trends, market ...
1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
18.00 LPA TO 20.00 LPA
Position: Maintenance Manager
Location: Vapi
Experience: 12 - 15 Years
Industries: Pharma
Responsibilities:
Planning and execution of maintenance activities.
Utility Log sheet monitoring.
Co- ordination with all departments pertaining to maintenance activity.
Review utility consumption report on daily / monthly basis.
Preventive maintenance of all the equipment monitoring.
Ensure calibration of ...
5 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
System Operation & Monitoring:
Operate, monitor, and troubleshoot purified water, water for injection (WFI), and pure steam generation systems, including but not limited to, reverse osmosis (RO) units, deionization (DI) units, multi-effect stills, and clean steam generators.
Monitor critical parameters such as temperature, pressure, flow rate, conductivity, TOC (Total Organic Carbon), and ...
2 Opening(s)
10.0 Year(s) To 15.0 Year(s)
Not Disclosed by Recruiter
POSITION -Quality Control Manager
Location - Terre Haute. IN
Job description
The Quality Control Manager plays a crucial role in ensuring that SPI maintains high standards and consistently delivers quality products and services. This job description provides a comprehensive overview of the responsibilities and qualifications expected from the Manager of Quality Control. By effectively ...