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Softgel Healthcare Pvt. Ltd., a leading CDMO specializing in soft gelatin capsules for pharmaceuticals and nutraceuticals, is hosting a walk-in interview for its USFDA and EU-GMP approved facility in Puducherry.
An associate of Madras Pharmaceuticals, Softgel has over 20 years of expertise, exporting to 60+ countries with a focus on Rx, OTC, and nutraceutical products. Rated 3.0/5 on AmbitionBox for overall employee experience, we invite professionals to join our team of ~300 employees to drive innovation in softgel manufacturing.
Walk-In Interview Details
- Date: Sunday, July 6, 2025
- Time: 9:00 AM to 2:00 PM
- Venue: Hotel Annamalai International, 479, Kamaraj Salai, Sakthi Nagar, Saram, Puducherry – 605013
- Work Location: Softgel Healthcare Pvt. Ltd., Survey No. 20/1, Vandalur – Kelambakkam Road, Pudupakkam Village, Chengalpattu District, Tamil Nadu – 603103
- Pre-Registration: Scan the QR code provided in the original job posting to register.
- Contact:
- Email resumes to career@softgelhealthcare.com, pna@softgelhealthcare.com, hrqms@softgelhealthcare.com, or hr@softgelhealthcare.com
- Call/WhatsApp: +91 89399 88984 or +91 86083 96077
Required Documents:
- Updated resume (2 copies)
- Original and photocopies of educational certificates (B.Sc/M.Sc/B.Pharm/M.Pharm/Diploma/ITI)
- Last 3 months’ payslips and latest increment letter
- Relieving and service certificates from previous organizations
- Aadhar card and PAN card
- Passport-size photographs (2)
Note:
- Candidates must have experience in soft gelatin capsule manufacturing or regulated plants (USFDA, EU-GMP).
- Candidates interviewed at Softgel in the last 6 months are ineligible.
- Willingness to work in shift operations is required.
- Spot offers may be provided subject to document verification.
Open Positions
Production (Manufacturing)
- Designation: Operator / Technical Assistant / Executive
- Qualification: ITI / Diploma / B.Sc / B.Pharm / M.Pharm
- Experience: 2–6 years (preferred, based on previous Softgel postings)
Responsibilities:
- Operate soft gelatin encapsulation machines, mixers, and gelatin preparation equipment.
- Perform line setup, cleaning, and changeovers per SOPs.
- Ensure cGMP compliance and maintain BMR/BPR documentation.
- Support regulatory audits (USFDA, EU-GMP).
Key Skills:
- Hands-on experience in softgel manufacturing.
- Knowledge of cGMP, SOPs, and regulatory compliance.
Production (Packing)
- Designation: Operator / Technical Assistant / Executive
- Qualification: ITI / Diploma / B.Sc / B.Pharm
- Experience: 2–6 years (preferred, based on previous Softgel postings)
Responsibilities:
- Manage primary and secondary packing (blister, bulk, bottling) for softgel capsules.
- Perform labeling, cartoning, and track & trace operations.
- Ensure cGMP compliance and accurate batch documentation.
Key Skills:
- Experience in softgel packing operations.
- Familiarity with cGMP and regulatory standards.
Quality Assurance (QA)
- Designation: Officer / Executive / Senior Executive
- Qualification: B.Pharm / M.Pharm / M.Sc
- Experience: 2–6 years (preferred, based on previous Softgel postings)
Responsibilities:
- Conduct IPQA, line clearance, and audit trail checks for softgel production.
- Review BMR/BPR, manage QMS (deviations, CAPA, change control).
- Ensure compliance with cGMP and regulatory standards (USFDA, EU-GMP).
Key Skills:
- Expertise in IPQA, QMS, and regulatory documentation.
- Strong coordination with production and QC teams.
Quality Control (QC)
- Designation: Chemist / Senior Chemist / Executive
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
- Experience: 2–6 years (preferred, based on previous Softgel postings)
Responsibilities:
- Perform HPLC, GC, FTIR, and UV analysis for raw materials, stability, and finished softgel products.
- Conduct method validation and stability studies.
- Use e-LIMS for data management and ensure GLP compliance.
Key Skills:
- Proficiency in HPLC, GC, and analytical testing.
- Knowledge of cGMP, GLP, and regulatory audits.
Warehouse
- Designation: Technician / Officer
- Qualification: Diploma / B.Sc / Graduate
- Experience: 2–5 years (preferred, based on previous Softgel postings)
Responsibilities:
- Manage raw materials, packing materials, and finished goods inventory.
- Handle dispensing, storage, and SAP-based inventory tracking.
- Ensure cGMP compliance in warehouse operations.
Key Skills:
- Experience in pharmaceutical warehouse operations and SAP.
- Knowledge of cGMP and regulatory standards.
Technology Transfer
- Designation: Executive / Senior Executive
- Qualification: B.Pharm / M.Pharm
- Experience: 3–6 years (preferred, based on previous Softgel postings)
Responsibilities:
- Prepare BMRs, BPRs, and protocols for trial, scale-up, and validation batches.
- Coordinate and execute process validation and technology transfer for softgel products.
- Review departmental SOPs and support regulatory audits.
Key Skills:
- Expertise in technology transfer and cGMP documentation.
- Familiarity with USFDA/EU-GMP requirements.
Engineering
- Designation: Technician / Officer / Executive
- Qualification: ITI / Diploma / B.Tech (Mechanical/Electrical/Instrumentation)
- Experience: 2–6 years (preferred, based on previous Softgel postings)
Responsibilities:
- Perform preventive and breakdown maintenance of softgel encapsulation machines, HVAC, and utilities.
- Conduct equipment qualification and maintain calibration records.
- Ensure cGMP compliance and support regulatory audits.
Key Skills:
- Expertise in pharmaceutical equipment maintenance (e.g., encapsulators, HVAC).
- Knowledge of cGMP and regulatory compliance.
Why Join Softgel Healthcare?
- Global Reach: Contribute to a CDMO exporting to 60+ countries, producing over 3 billion softgel capsules annually with 100+ B2B partners.
- Regulatory Excellence: Work in a USFDA and EU-GMP approved facility, designed for stringent regulatory audits.
- Innovative Environment: Join a state-of-the-art Puducherry plant with advanced encapsulation technology, backed by Madras Pharmaceuticals’ 25+ years of WHO-GMP expertise.
- Challenges to Note: Employee reviews indicate moderate satisfaction (3.0/5), with low ratings for salary (2.5/5) and career growth (2.4/5), suggesting potential challenges in compensation and appraisals.
How to Apply
- Walk-In: Attend the interview on July 6, 2025, at Hotel Annamalai International, Puducherry, with all required documents. Pre-register using the QR code for faster processing.
- For Those Unable to Attend: Email your updated CV to career@softgelhealthcare.com, pna@softgelhealthcare.com, hrqms@softgelhealthcare.com, or hr@softgelhealthcare.com, mentioning the specific role and department (e.g., “Production Operator” or “QC Executive”) in the subject line. Include total experience, current CTC, expected CTC, and notice period.
Note: Candidates with softgel manufacturing experience or exposure to USFDA/EU-GMP plants are preferred.
About Softgel Healthcare
Founded in 2003, Softgel Healthcare Pvt. Ltd., headquartered in Chennai, is a leading CDMO specializing in soft gelatin capsules for pharmaceuticals, OTC, and nutraceuticals. An associate of Madras Pharmaceuticals, the Puducherry facility is equipped with advanced encapsulation technology, producing over 3 billion capsules annually.
Acquired by Bioriginal Food & Science in 2023, Softgel exports to 60+ countries, supported by a workforce of ~300 and a revenue of ₹150–250 crore. Learn more at www.softgelhealthcare.com.
Important Disclaimer
Softgel Healthcare Pvt. Ltd. does not charge any fees for recruitment or authorize agencies to collect payments. Report suspicious job offers to hr@softgelhealthcare.com.
Join Softgel Healthcare and contribute to high-quality softgel manufacturing in a globally compliant facility!