Nitika Pharmaceutical Specialities Pvt. Ltd., a global leader in pharmaceutical excipients, invites talented professionals to join our growing team at our facilities in Waddhamna and Butibori, Nagpur. Since 1991, we’ve been a trusted name, exporting to over 90 countries and earning accolades like the Best Manufacturing Enterprise in MSME (2016) from Hon.

Prime Minister Shri Narendra Modi. With a mission to positively impact human lives, we are hiring for multiple roles to drive innovation in excipient manufacturing. Apply now to advance your career with a WHO-GMP and US-DMF certified organization!

Why Join Nitika Pharmaceutical Specialities?

Nitika is among the top 15 global excipient manufacturers, producing high-quality products like Magnesium Stearate and Sodium Stearyl Fumarate for clients like Pfizer, Novartis, and Cipla. Our Nagpur facilities, located near the MIHAN cargo hub, offer a dynamic environment for professional growth.

With certifications like WHO-GMP, ISO 9001:2000, and 14 DMFs, we are committed to quality and innovation. Join our 300+ employee team to contribute to global healthcare solutions.

Open Positions at Nitika Pharmaceutical Specialities

We are hiring for various roles across our Waddhamna and Butibori facilities. Candidates must have relevant qualifications and experience in the pharmaceutical industry. Below is a detailed overview of the open positions.

R&D Head (Waddhamna)

Lead research and development efforts for innovative excipient solutions.

Responsibilities:

Develop new excipients and optimize formulations.
Oversee R&D projects and ensure regulatory compliance.
Collaborate with global clients for product development.
Manage documentation for US-DMF and EDMF filings.

Qualifications:

M.Pharm or M.Sc. in Chemistry or related field.
10+ years of experience in pharmaceutical R&D.
Expertise in excipient development and cGMP.

Senior Executive – QA (Waddhamna)

Ensure quality assurance processes align with cGMP and regulatory standards.

Responsibilities:

Conduct quality audits and manage CAPA, deviations, and OOS.
Review BMRs, BPRs, and SOPs for compliance.
Support USFDA and WHO-GMP inspections.
Train staff on quality protocols.

Qualifications:

B.Pharm or M.Pharm.
4+ years of experience in API or excipient QA.
Knowledge of cGMP, GLP, and regulatory audits.

Assistant Manager – Account Operation (Civil Lines)

Manage financial operations and ensure efficient accounting processes.

Responsibilities:

Oversee accounts payable/receivable and financial reporting.
Ensure compliance with tax and audit requirements.
Coordinate with vendors and manage budgets.
Support ERP-based accounting systems.

Qualifications:

M.Com, CA Intern, or MBA.
4-6 years of experience in accounts management.
Proficiency in financial software and MS Office.

Vendor Development Executive (Civil Lines)

Develop and manage vendor relationships for raw material procurement.

Responsibilities:

Identify and onboard new vendors for excipient raw materials.
Negotiate contracts and ensure timely supply.
Maintain vendor database and quality records.
Ensure compliance with procurement SOPs.

Qualifications:

B.Sc. in Chemistry or related field.
3+ years of experience in vendor management.
Strong negotiation and communication skills.

Purchase Executive (Butibori)

Handle procurement activities for the Butibori facility.

Responsibilities:

Procure raw materials and equipment for excipient production.
Manage purchase orders and supplier coordination.
Ensure cost-effective and timely procurement.
Maintain documentation as per cGMP standards.

Qualifications:

BE in Mechanical Engineering.
3+ years of experience in pharmaceutical procurement.
Knowledge of supply chain and ERP systems.

Senior Chemist – Reviewer (Waddhamna)

Review analytical data and ensure quality compliance for excipients.

Responsibilities:

Review analytical results from HPLC, GC, and FTIR testing.
Ensure compliance with IP, BP, USP, and Ph.Eur standards.
Support validation and stability studies.
Maintain GLP-compliant documentation.

Qualifications:

B.Sc. or M.Sc. in Chemistry.
4-6 years of experience in analytical chemistry.
Expertise in analytical method validation.

Operators (Waddhamna/Butibori)

Support production operations for excipient manufacturing.

Responsibilities:

Operate equipment like granulators, blenders, and dryers.
Perform equipment cleaning and area sanitization.
Follow SOPs and cGMP guidelines.
Maintain production logs and batch records.

Qualifications:

12th or ITI certification.
1+ year of experience in pharmaceutical production.
Familiarity with cGMP and safety protocols.

Analytical Chemist (Waddhamna)

Conduct analytical testing for excipient quality control.

Responsibilities:

Perform testing using HPLC, GC, and UV-Vis spectroscopy.
Conduct raw material and finished product analysis.
Ensure compliance with cGMP and GLP standards.
Prepare analytical reports for audits.

Qualifications:

M.Sc. in Chemistry.
1-3 years of experience in analytical chemistry.
Proficiency in analytical instruments.

Analytical Chemist – Raw Materials (Waddhamna)

Focus on quality testing of raw materials for excipient production.

Responsibilities:

Test raw materials for compliance with IP, BP, USP standards.
Perform impurity profiling and stability testing.
Maintain GLP-compliant documentation.
Support supplier qualification processes.

Qualifications:

B.Sc. or M.Sc. in Chemistry.
2+ years of experience in raw material testing.
Knowledge of cGMP and analytical techniques.

IPQA Chemist (Waddhamna/Butibori)

Ensure in-process quality assurance during excipient manufacturing.

Responsibilities:

Conduct in-process quality checks and line clearances.
Monitor compliance with cGMP and SOPs.
Handle deviations, OOS, and CAPA processes.
Support batch release and audit readiness.

Qualifications:

B.Pharm, D.Pharm, or B.Sc.
1+ year of experience in IPQA.
Knowledge of cGMP and quality assurance.

PPIC Executive (Waddhamna)

Manage production planning and inventory control for efficient operations.

Responsibilities:

Plan production schedules and monitor inventory levels.
Coordinate with production and procurement teams.
Ensure timely availability of raw materials.
Maintain PPIC documentation as per cGMP.

Qualifications:

Any graduate degree.
2+ years of experience in PPIC.
Proficiency in ERP systems and MS Office.

Skills Required for All Roles

To succeed at Nitika, candidates must demonstrate expertise in the following areas:

Skill	Description
cGMP Compliance	Adherence to Good Manufacturing Practices and SOPs
Analytical Testing	Proficiency in HPLC, GC, FTIR, and UV-Vis techniques
Equipment Operation	Knowledge of production equipment like granulators
Documentation	Accurate record-keeping for audits and compliance
Communication Skills	Strong interpersonal skills for team collaboration
Regulatory Knowledge	Familiarity with USFDA, WHO-GMP, and IP/BP/USP standards

Why Work with Nitika Pharmaceutical Specialities?

Nitika is a WHO-GMP and ISO-certified company with 14 DMFs, including USFDA and European filings. Our Nagpur facilities produce high-quality excipients like Tablube (Magnesium Stearate) and Novalube (Sodium Stearyl Fumarate), serving clients in over 90 countries.

We offer a challenging work environment with a focus on skill development (rated 3.1/5) and opportunities to work with cutting-edge technology in a globally recognized organization.

How to Apply

Interested candidates can email their resumes to sarita.paswan@nitikapharma.com or contact 7798801060 for application details. Please include your updated resume, academic certificates, and CTC proof.

Nitika Pharmaceuticals – Urgent Openings for B.Sc, M.Sc, B.Pharm, M.Pharm, D.Pharm, M.Com, MBA, 12th, ITI, Any Graduates

For more information about our company and mission, visit www.nitikapharma.com. Immediate joiners are preferred.

Location and Contact Information

Work Locations:

Plot No. J-21, J-21/1, Butibori Industrial Area, Nagpur, Maharashtra 441122
Block No. 03, Plot No. 1296, 1297/08, Waddhamna, Tah-Hingna, Amravati Road, Nagpur, Maharashtra 440023

Email: sarita.paswan@nitikapharma.com
Contact: 7798801060
Website: www.nitikapharma.com

Join Our Mission to Impact Lives

Nitika Pharmaceutical Specialities is dedicated to delivering high-quality excipients to the global pharmaceutical industry. Whether you’re an R&D Head, QA Executive, Chemist, Operator, or PPIC professional, your contributions will drive our success.

Apply today to join a team committed to innovation, quality, and positively impacting human lives through pharmaceutical excellence!