Analytical Chemist

Nitika Pharmaceutical Specialities Pvt. Ltd; Nagpur District; On-site; INR 250,000 - 400,000; Full time

Job summary

Nitika Pharmaceutical Specialities Pvt. Ltd in Nagpur, Maharashtra, India, is seeking a QC-focused laboratory professional for a full-time position.

The role requires 1-3 years of QC experience and adherence to GLP, with responsibilities spanning testing, documentation, equipment maintenance, and safety oversight. You will perform routine and non-routine analyses on in-process materials, raw materials, and finished products, ensuring compliance with approved procedures and protocols.

Qualifications

• Minimum 1–3 years of QC experience in pharma/biotech labs.
• Familiarity with GLP and lab safety standards.
• Ability to maintain accurate documentation and records.

Responsibilities

• Follow QC procedures with compliance and maintain cleanliness and safety standards.
• Perform tests as per established procedures and specifications.
• Complete documentation to support testing procedures (data capture, logs, inventory).
• Calibrate, validate, or maintain laboratory equipment as required.
• Prepare solutions and reagents for analyses.
• Inspect finished products visually and report deviations or incidents.
• Respond to incidents such as OOS/OOT and investigations.
• Attend QC SOP training and adhere to SOPs.
• Ensure safety in all work activities and report any hazards.
• Perform analyses on in-process, raw materials, R&D samples, finished products, and stability samples per MOA/Protocol.

Skills

Quality control

Lab safety

Documentation

Analytical testing

Job description

Nitika Pharmaceutical Specialities Pvt. Ltd | Full time

• Industry Pharma/Biotech/Clinical Research
• Date Opened 07/09/2026
• Work Experience 1-3 years
• Job Type Full time
• City Nagpur
• State/Province Maharashtra
• Country India

Job Description

JobResponsibilities:

• 1. Following the QC laiddown procedures with compliance.
• 2. Ensure that lab cleanliness and safety standardsare maintained
• 3. Perform the tests as per testing procedures andensure that all tests are performed according to established itemspecifications, standard test methods, or protocols.
• 4. Complete documentation needed to support testingprocedures including data capture forms, equipment logbooks, or inventoryforms.
• 5. Calibrate, validate, or maintain laboratoryequipment.
• 6. Perform all the laboratory analytical documents,protocol, investigations and lab instrument logs.
• 7. Following the GLP
• 8. Conduct routine and non-routine analyses ofin-process materials, raw materials, R&D samples, finished products, andstability samples.
• 9. Preparation of volumetric solutions and reagents
• 1. Perform visual inspectionsof finished products.
• 1. Reporting andinvestigation of Incident, OOS, OOT and deviation.
• 1. Attending the training program for QC-SOP’s and another relevantSOP’s.
• 1. Ensuringand Reporting safety in work activities in work environment.
• Perform analysis of finishedproducts, in-process samples, cleaning samples, and analytical methods validation and stability samples etc as per thespecifications/MOA/Protocol etc.