1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: Manager/Sr. Manager - R&D
Location: Vadodara
Experience: 10 - 15 Years
Industries: Pharma
Responsibilities:
Project & Team Management
Lead and manage multiple API development projects across various stages (Route scouting, lab development, scale-up, validation).
Plan and allocate resources effectively among chemists and analysts.
Mentor and guide junior ...
9 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 3.60 LPA
Job Description: Production Executive
We are looking for a Production Executive with hands-on experience in API manufacturing to join our dynamic production team. The ideal candidate will be responsible for supervising daily production activities, ensuring batch operations run smoothly, and maintaining compliance with safety and quality standards.
Key Responsibilities:
Execute and monitor day-to-day ...
10 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 7.00 LPA
Industry: Pharma Formulation
Openings: 10Experience: 3–7 YearsPreference: Male Candidates only / Gujarati-speaking
Key Responsibilities:
Perform testing of Raw Materials (RM) & Packaging Materials (PM) as per pharmacopoeial standards.
Ensure timely release of materials with accurate documentation.
Follow cGMP, GLP, and regulatory compliance in QC lab.
Maintain records, calibration logs, and SOP adherence.
Coordinate with QA, Production, and Warehouse for smooth operations.
Requirements:
B.Sc./M.Sc. ...
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 ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Housekeeping & Facility Management
Supervised daily housekeeping across GMP/non-GMP areas, washrooms, corridors, pest control, horticulture, waste disposal, and audits as per pharma hygiene & EHS standards.
Maintenance & Repairs
Coordinated preventive maintenance, civil/electrical/plumbing/carpentry repairs, and maintained documentation for audit readiness.
Inventory & Vendor Management
Managed consumables inventory, vendor manpower, schedules, compliance, and invoice processing.
Audit & ...