Steribio Lifesciences Pvt. Ltd is at the forefront of innovation in pharmaceutical manufacturing, specializing in parenteral solutions. By combining imported technology with indigenously developed machinery, the company is revolutionizing the production of Large Volume Parenterals (LVP) to ensure safer, more sterile, and cost-effective processes. If you are a skilled professional with experience in aseptic manufacturing and injectable production, this Production Officer/Executive role offers a rewarding opportunity to contribute to cutting-edge sterile operations in a compliant environment.
Roles and Responsibilities
As a Production Officer/Executive, you will play a key role in executing and supervising LVP manufacturing operations. Your key responsibilities include:
- Executing and supervising manufacturing operations such as solution preparation, filtration, filling, sealing, sterilization (autoclave), and visual inspection.
- Ensuring all activities comply with approved Batch Manufacturing Records (BMRs), SOPs, and production schedules.
- Performing and monitoring aseptic operations in classified cleanroom areas (Grade A/B/C/D).
- Maintaining compliance with cGMP, cGLP, GDP, and data integrity standards.
- Conducting line clearance, equipment cleaning, CIP/SIP, and changeover activities.
- Monitoring critical process parameters (CPPs) and adhering to validated processes.
- Operating and performing routine checks on LVP equipment, including compounding vessels, filtration systems, filling and sealing machines, autoclaves, and terminal sterilizers.
- Maintaining accurate production documentation, including BMRs, logbooks, and cleaning records.
- Identifying and reporting deviations, OOS/OOT trends, and incidents, while supporting investigations.
- Participating in change control, CAPA, and continuous improvement initiatives.
- Coordinating with QA, QC, Engineering, and Microbiology teams for seamless operations.
- Adhering to EHS guidelines, gowning procedures, and aseptic behavior.
- Supporting regulatory audits (WHO-GMP, USFDA, EU-GMP, etc.).
Required Qualifications and Skills
To excel in this role, candidates should meet the following criteria:
- Experience: 2 to 6 years in injectable/LVP manufacturing.
- Qualification: B.Pharm, M.Pharm, B.Sc, or M.Sc in Pharma/Chemistry.
- Employment Type: Full-time, Permanent.
- Reporting To: Production Manager / Head – Production.
Key Skills & Competencies:
- Hands-on experience in injectable/LVP manufacturing.
- Strong knowledge of aseptic processing and cleanroom operations.
- Understanding of sterilization, filtration, and contamination control.
- Familiarity with validation, qualification, and regulatory requirements for sterile products.
- Excellent documentation, communication, and team coordination skills.
- Willingness to work in shifts if required.
Salary, Benefits, and How to Apply
The position offers a competitive salary in the range of INR 4,00,000 to 8,00,000 per annum, depending on experience and qualifications. Additional benefits include opportunities for professional growth in a innovative pharmaceutical environment, compliance with industry standards, and contribution to advanced sterile production technologies.
How to Apply: Interested candidates can send their updated CV via WhatsApp to 7710027685.
This is an excellent opportunity for pharma professionals seeking a stable career in sterile manufacturing with a forward-thinking company.
