Sudeep Nutrition Hiring Officer – Documentation (Production)

Officer – Documentation Jobs for B.Sc./M.Sc./B.Pharm/M.Pharm with 1–5 Years Experience | Vadodara

Apply now for Officer – Documentation (Production) roles at Sudeep Nutrition in Vadodara. B.Sc./M.Sc./B.Pharm/M.Pharm graduates with 1–5 years of experience are eligible.

Build Your Career with Sudeep Nutrition – Apply Now for Officer – Documentation (Production) Roles in Vadodara

If you’re a science or pharmacy graduate with a passion for precision, documentation, and pharmaceutical compliance, this is your chance to grow with one of the industry’s most trusted names. Sudeep Nutrition, located in Poicha (Rania), Vadodara, is inviting applications for Officer – Documentation (Production) positions. This role plays a critical part in ensuring the highest standards of Good Manufacturing Practices (GMP) and documentation compliance.

Why Choose Sudeep Nutrition?

With a vision to enrich health and empower life, Sudeep Nutrition is a fast-growing name in the pharmaceutical and nutraceutical manufacturing segment. They believe in innovation, compliance, and employee growth. As an Officer in Documentation, you will be at the heart of their compliance and production excellence strategy.

Job Overview: Officer – Documentation (Production)

Location: Poicha (Rania), Vadodara
Designation: Officer – Documentation (Production)
Experience Required: 1 to 5 years
Educational Background: B.Sc., M.Sc., B.Pharm, M.Pharm

Key Responsibilities

H3: Documentation Compliance & Records Management

• Prepare and update Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) as per daily production plans
• Maintain daily production line status and logs
• Ensure proper filing and storage of all GMP-related documents
• Keep accurate records of cleaning, calibration, temperature, RH, pressure, and hygiene as per regulatory standards
• Verify equipment cleaning and usage logs

H3: Quality Coordination & Audit Preparedness

• Maintain QMS-related documentation, supporting GMP audits
• Ensure timely completion of preventive maintenance and fogging schedules
• Coordinate documentation activities with Quality Assurance (QA) and Production teams
• Adhere to and promote Standard Operating Procedures (SOPs)

H3: Continuous Improvement & Support

• Identify and implement documentation improvements aligned with GMP and GDP (Good Documentation Practices)
• Assist in driving digital documentation where applicable
• Support compliance trainings and initiatives

Required Skills

• GDP (Good Documentation Practices)
• Hands-on with MS Office and digital record management tools
• Attention to detail and proactive documentation habits

Eligibility Criteria

H4: Educational Qualifications

Candidates must hold any of the following degrees:

• Bachelor of Science (B.Sc.)
• Master of Science (M.Sc.)
• Bachelor of Pharmacy (B.Pharm)
• Master of Pharmacy (M.Pharm)

These programs typically cover core areas such as Industrial Chemistry, Biotechnology, Microbiology, Pharmaceutics, Pharmaceutical Analysis, and Pharmaceutical Quality Assurance – all crucial for documentation roles in pharma production.

H4: Experience Required

• Minimum: 1 year
• Maximum: 5 years

Send your updated resume to: jobs@sudeepgroup.com
Contact: +91 9016134609

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