Sudeep Pharma Private Limited, a leading manufacturer of calcium-based pharmaceutical excipients, food, and feed ingredients since 1989, is hiring for multiple Quality Control (QC) and In-Process Quality Control (IPQC) positions at our ISO 9001:2015-certified facility in Nandesari, Vadodara, Gujarat. With a global reach across 30 countries and a 10,000 MT annual capacity, we are committed to delivering Products That Matter. Join our team of 300+ professionals to ensure regulatory compliance and quality excellence in the pharmaceutical industry.
Application Details
- Location: 129/1/A, GIDC, Nandesari, Vadodara, Gujarat 391340
- Application Method: Email your updated CV to hr@sudeeppharma.com with the subject line “[Position Applied For] – Vadodara” (e.g., “Asst. Manager QC RM/PM – Vadodara”)
- Application Deadline: May 15, 2025
- Contact Email: hr@sudeeppharma.com
- Website: www.sudeeppharma.com
Notes:
- Mandatory: Candidates must have experience in pharmaceutical quality control, preferably in excipient or mineral actives manufacturing.
- Submit an updated CV, academic certificates (B.Sc/M.Sc), experience letters, last 4 months’ payslips, and valid ID proof (Aadhaar, PAN).
- Immediate joiners are preferred.
- Fraud Alert: Sudeep Pharma does not charge recruitment fees. Verify opportunities via www.sudeeppharma.com.
- Apply via the QR code in the job posting or email your resume if unable to scan.
Why Join Sudeep Pharma Limited?
Founded in 1989, Sudeep Pharma is a pioneer in calcium phosphates and calcium carbonate, serving 750+ customers worldwide. Our Nandesari facility complies with GMP, EXCiPACT, FSSC 22000, Kosher, and Halal standards, ensuring top-tier quality for pharma, food, and feed ingredients.
Rated 3.3/5 for career growth on AmbitionBox based on 40+ reviews, employees praise the “continuous learning opportunities” and “supportive colleagues,” though some note HR process improvements are needed. With a 3.1/5 work-life balance rating, Sudeep offers competitive salaries (₹4–8 Lakhs per annum for similar roles) and a chance to grow in a dynamic, export-driven company.
Available Job Positions
We are hiring for Quality Control and In-Process Quality Control roles at our Nandesari, Vadodara facility, focusing on raw materials, packaging materials, stability testing, and finished goods.
1. Assistant Manager – QC (Raw Materials/Packaging Materials)
- Openings: 1
- Qualification: B.Sc / M.Sc (Chemistry)
- Experience: Minimum 7 years in pharmaceutical QC
- Responsibilities:
- Oversee quality control testing of raw materials (e.g., calcium-based excipients) and packaging materials using techniques like ICP-MS, GC, and wet chemistry
- Ensure compliance with GMP, ISO, and FDA regulations, including documentation for audits
- Manage QC teams, optimize lab equipment usage, and resolve quality issues
- Skills:
- Proficiency in QC instruments (ICP-MS, GC, HPLC) and regulatory standards
- Strong leadership, analytical, and documentation skills
- Experience with USFDA/EDQM audits preferred
2. Assistant Manager – QC (Stability)
- Openings: 1
- Qualification: B.Sc / M.Sc (Chemistry)
- Experience: Minimum 7 years in stability testing
- Responsibilities:
- Lead stability testing programs per ICH Q1A and FDA guidelines for excipients and actives
- Analyze stability data, prepare regulatory reports, and ensure compliance with GMP/ISO standards
- Coordinate team activities and maintain lab compliance for regulatory inspections
- Skills:
- Expertise in stability protocols, HPLC, and data interpretation
- Knowledge of ICH, FDA, and WHO GMP guidelines
- Leadership and multitasking abilities
3. Senior Executive – QC (Stability)
- Openings: 1
- Qualification: B.Sc / M.Sc (Chemistry)
- Experience: 4–6 years in stability testing
- Responsibilities:
- Conduct stability testing (accelerated, long-term) and manage documentation per ICH/FDA protocols
- Operate lab instruments (HPLC, GC, UV) and ensure timely reporting of stability results
- Collaborate with QC teams to support regulatory compliance and audit readiness
- Skills:
- Hands-on experience with stability chambers and analytical instruments
- Familiarity with GMP, ICH, and FDA documentation standards
- Strong organizational and teamwork skills
4. Assistant Manager – IPQC (Finished Goods)
- Openings: 1
- Qualification: B.Sc / M.Sc (Chemistry)
- Experience: Minimum 7 years in IPQC for finished goods
- Responsibilities:
- Manage in-process quality control and inspections for finished goods (e.g., calcium phosphates, carbonates)
- Ensure compliance with GMP, ISO, and FDA standards during production
- Lead IPQC teams and coordinate with production and QA departments for quality assurance
- Skills:
- Expertise in in-process testing, BMR/BPR review, and regulatory compliance
- Strong leadership and interdepartmental coordination skills
- Experience with WHO GMP and Schedule M guidelines
5. Senior Executive – IPQC (Finished Goods)
- Openings: 3
- Qualification: B.Sc / M.Sc (Chemistry)
- Experience: 4–6 years in IPQC for finished goods
- Responsibilities:
- Conduct in-process quality control checks and product inspections during manufacturing
- Follow GMP, ISO, and FDA standards, ensuring accurate documentation
- Identify and resolve quality issues, collaborating with production teams
- Skills:
- Proficiency in IPQC processes, physical testing, and BMR/BPR documentation
- Knowledge of GMP, ISO, and FDA regulations
- Problem-solving and teamwork abilities
Required Skills and Qualifications
| Category | Details |
|---|---|
| Education | B.Sc / M.Sc (Chemistry) |
| Experience | Asst. Manager: 7+ years; Sr. Executive: 4–6 years in pharma QC/IPQC |
| Technical Skills | QC: HPLC, GC, ICP-MS, stability testing; IPQC: In-process checks, BMR/BPR |
| Regulatory Knowledge | GMP, ISO 9001:2015, FDA, ICH, WHO GMP, Schedule M |
| Soft Skills | Leadership (Asst. Manager), teamwork, analytical, and documentation skills |
| Preferred Expertise | USFDA/EDQM audits, excipient testing, stability protocols |
Why These Roles?
- Global Impact: Ensure quality for products exported to 30+ countries, enhancing health and nutrition.
- Career Development: Rated 3.3/5 for promotions, Sudeep offers learning opportunities in a GMP-compliant facility.
- Specialized Expertise: Work on calcium-based excipients, a niche segment, with advanced instruments like ICP-MS.
- Supportive Team: Join a collaborative environment with “excellent team members,” as noted by 52% of AmbitionBox reviewers.
How to Apply
To apply for any of the listed positions, follow these steps:
- Prepare Your Documents: Update your CV, highlighting your QC/IPQC experience in pharmaceuticals, and gather academic certificates (B.Sc/M.Sc), experience letters, payslips (last 4 months), and ID proof (Aadhaar, PAN).
- Email Your Application: Send your documents to hr@sudeeppharma.com with the subject “[Position Applied For] – Vadodara.”
- Include Key Details: Mention your total experience, current CTC, expected CTC, and notice period.
- Research Sudeep Pharma: Visit www.sudeeppharma.com to understand our expertise in excipients and regulatory compliance.
- Prepare for the Interview: Be ready to discuss stability testing, ICH guidelines, IPQC processes, or GMP audit experiences.
Why Vadodara, Gujarat?
Vadodara, a pharmaceutical hub with over 300 companies, is home to Sudeep Pharma’s Nandesari facility, strategically located in GIDC for excellent connectivity. The city offers a vibrant lifestyle, affordable living, and a thriving chemical industry, making it ideal for pharma professionals. Learn more about Vadodara’s economy.
Contact Information
For inquiries or to apply, reach out to:
- Email: hr@sudeeppharma.com
- Office Address: Sudeep Pharma Pvt. Ltd., 129/1/A, GIDC, Nandesari, Vadodara, Gujarat 391340
- Website: www.sudeeppharma.com
- LinkedIn: Sudeep Pharma Private Limited
Don’t miss this chance to join Sudeep Pharma Limited and contribute to Delivering Products That Matter. Apply by May 15, 2025, and advance your career in Vadodara’s thriving pharma sector!