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India’s API pharmaceutical industry continues to grow rapidly, creating strong demand for experienced Quality Control (QC) professionals. Regulatory-driven manufacturing environments such as USFDA- and MHRM-approved API plants require skilled QC officers who can ensure data integrity, analytical accuracy, and compliance.
In this context, Sahaj Pharma is inviting applications for the position of QC Officer at its Vadodara facility. This opportunity is ideal for professionals with 2–3 years of experience in API quality control, especially those with hands-on expertise in HPLC analysis and GMP-compliant systems.
Sahaj Pharma is a reputed API pharmaceutical manufacturing company engaged in the development and production of high-quality Active Pharmaceutical Ingredients for regulated and semi-regulated markets.
Company Name: Sahaj Pharma
Industry: API Pharmaceutical Manufacturing
Headquarters: Gujarat, India
Manufacturing Facility: Vadodara, Gujarat
Established: 2010
Employees Strength: Approx. 150–250 professionals
Regulatory Approvals: USFDA, MHRM, GMP
The company focuses on quality-driven manufacturing, regulatory compliance, and continuous improvement in analytical and quality systems. Sahaj Pharma supplies APIs to domestic and international markets while maintaining strict adherence to global quality standards.
The QC Officer role at Sahaj Pharma is a critical position within the Quality Control department. The selected candidate will be responsible for routine and non-routine testing of API samples, handling analytical instruments, and ensuring compliance with USFDA, MHRM, and GMP guidelines.
This role offers hands-on exposure to regulated API manufacturing operations, audit readiness activities, and compliance-driven quality control systems, making it a strong career opportunity for experienced QC professionals.
Job Title: QC Officer
Company: Sahaj Pharma
Industry: API Pharmaceutical Manufacturing
Job Location: Vadodara, Gujarat
Employment Type: Full-Time
Experience Required: 2–3 Years
Qualification: B.Sc / M.Sc (Science or relevant discipline)
As a QC Officer, the candidate will play a key role in ensuring analytical quality and regulatory compliance. Major responsibilities include:
Performing routine and non-routine quality control analysis of API samples
Operating, handling, and troubleshooting HPLC systems
Ensuring compliance with USFDA, MHRM, and GMP guidelines
Maintaining accurate analytical records, logbooks, and test reports
Supporting method validation, calibration, and stability studies
Assisting during internal and external audits
Participating in investigations, deviations, and CAPA activities
Following SOPs, data integrity principles, and laboratory best practices
This role demands precision, documentation accuracy, and a strong compliance mindset.
B.Sc or M.Sc in Chemistry, Pharmaceutical Sciences, or a relevant discipline
2–3 years of experience in API pharmaceutical QC laboratories
Candidates from USFDA- and MHRM-approved manufacturing units are strongly preferred
To succeed in this role, candidates should possess the following skills:
Strong hands-on experience with HPLC analysis
Working knowledge of GMP, GLP, and regulatory compliance
Understanding of API analytical testing procedures
Excellent documentation and data integrity practices
Familiarity with analytical instruments used in API QC labs
Ability to work in audit-ready and compliance-focused environments
Attention to detail and problem-solving approach
Estimated CTC Range: ₹3,00,000 – ₹5,00,000 per annum
Salary will depend on experience, technical expertise, and interview performance
Regulated API companies often provide steady annual increments and long-term growth
Interview Mode: HR screening followed by a technical interview
Interview Type: Telephonic / Face-to-Face (as per company decision)
Shortlisting: Candidates will be contacted after resume screening
Candidates may be asked to carry or submit the following documents during the interview or joining:
Updated resume / CV
Educational qualification certificates
Experience certificates or appointment letters
Government ID proof
Passport-size photographs
📍 Vadodara, Gujarat
Vadodara is one of India’s major pharmaceutical and chemical manufacturing hubs, offering excellent career growth opportunities for API professionals.
Interested and eligible candidates can apply by email:
📧 Email ID: hrm5@sahajpharma.com
👉 Send your updated resume with relevant QC and HPLC experience clearly mentioned.
Yes, hands-on HPLC experience is strongly required for the QC Officer position.
No, this role requires 2–3 years of API QC experience.
Yes, Sahaj Pharma operates USFDA- and MHRM-approved manufacturing facilities.
The role involves quality control testing of Active Pharmaceutical Ingredients (APIs).
The QC Officer vacancy at Sahaj Pharma, Vadodara, is a strong opportunity for professionals seeking stability, regulatory exposure, and long-term growth in the API pharmaceutical sector. With USFDA-compliant operations, hands-on HPLC work, and audit exposure, this role can significantly enhance your career profile in pharmaceutical quality control.
Note: Pharma Duniya does not charge any money for job information.
Candidates are advised to verify details from the official company website.
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