Sanofi Hiring Content Editor – Omnichannel in Hyderabad | Pharma Digital Marketing Job 2026 (Sanofi Hiring Content Editor – Omnichannel in Hyderabad) If you are a Life Sciences or Pharmacy professional with experience in medico-marketing content and pharmaceutical digital campaigns, here is a premium opportunity from one of the world’s leading pharmaceutical companies. Sanofi is inviting applications for the position of Content Editor – Omnichannel at its Hyderabad Hub. This is a permanent, full-time pharma digital marketing job designed for professionals with 2–4 years of experience in Omnichannel campaign execution, SEO-optimized healthcare content, and MLR-compliant scientific communication. With pharmaceutical companies increasingly investing in AI-enabled content frameworks and global go-to-market transformation strategies, this role offers strong career growth in the pharma marketing and digital transformation domain. Introduction The pharmaceutical industry is rapidly s...
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Swiss Parenterals Ltd has announced a major recruitment drive for experienced pharmaceutical professionals across multiple departments related to sterile injectable manufacturing. This hiring initiative presents an excellent opportunity for candidates seeking to establish a long-term and stable career in a regulated pharmaceutical environment that complies with US FDA and EU-GMP standards.
The openings are available at the company’s GIDC Bavla manufacturing facility in Ahmedabad, which is one of Gujarat’s most prominent pharmaceutical hubs. Positions are open for Officers, Senior Executives, Executives, and Managers, depending on experience and expertise.
About the Company – Swiss Parenterals Ltd
Swiss Parenterals Ltd is a well-established Indian pharmaceutical company specializing in sterile injectable formulations. The company is known for its strong presence in regulated international markets and its focus on quality-driven manufacturing practices.
Global Presence: Exports to multiple regulated and semi-regulated markets
Swiss Parenterals has consistently invested in advanced manufacturing technology, quality systems, and employee development, making it a preferred employer in the injectable pharma segment.
Job Overview Summary
This recruitment drive covers multiple technical and managerial roles across Production, Quality Assurance, Quality Control, Microbiology, Engineering, Packing, and Analytical Development Laboratory (ADL). The company is seeking professionals with hands-on injectable experience, strong GMP/QMS knowledge, and the ability to work in a regulated manufacturing environment.
These roles are ideal for candidates aiming for career stability, regulatory exposure, and professional growth in the injectable pharmaceutical industry.
Vacancy Details (Official)
1️⃣ Production – Injectable
Experience: 2 to 6 Years
Designation: Officer to Senior Executive
Key Areas:
QMS documentation
Autoclave operations
Injectable manufacturing
Washing, filling & dry powder filling
2️⃣ Quality Assurance – Stability
Experience: 1 to 5 Years
Designation: Officer to Senior Officer
Key Areas:
Stability studies
QMS compliance
Regulatory documentation
3️⃣ Quality Control (Chemical / PV)
Experience: 2 to 6 Years
Designation: Officer to Senior Executive
Key Areas:
HPLC analysis
Stability testing
QMS & pharmacovigilance support
4️⃣ Engineering
Experience: 8 to 12 Years
Designation: Manager
Key Areas:
Utility & maintenance operations
Qualification & validation
EHS & GPCB compliance
QMS activities
5️⃣ Packing – Injectable
Experience: 1 to 4 Years
Designation: Officer to Senior Officer
Key Areas:
Line clearance & reconciliation
Injectable packing (vials, ampoules, PFS)
Deviation handling & audit support
6️⃣ Quality Control – Microbiology
Experience: 1 to 4 Years
Designation: Officer to Senior Officer
Key Areas:
Environmental Monitoring (EM)
BET, MLT
Water testing & validation
⚠ Note: Only male candidates (as per operational requirements)
7️⃣ Analytical Development Laboratory (ADL)
Experience: 4 to 8 Years
Designation: Executive to Senior Executive
Key Areas:
Analytical method development & validation
Method transfer
QMS compliance
Responsibility Explanation
Selected candidates will be responsible for executing day-to-day departmental activities while ensuring strict compliance with GMP, QMS, and regulatory guidelines. The roles require active participation in documentation, audits, validation activities, deviation handling, and continuous improvement initiatives. Senior roles will also involve team coordination, technical decision-making, and regulatory readiness.
Q1. Is injectable experience mandatory? Yes, hands-on injectable manufacturing experience is required.
Q2. Are freshers eligible? No, this hiring is for experienced professionals only.
Q3. Is this a regulatory-approved facility? Yes, the plant follows USFDA and EU-GMP standards.
Q4. Can female candidates apply? Yes, except for QC Microbiology (male only as specified).
Q5. Is relocation assistance provided? Details will be discussed during the interview process.
Final Conclusion
Swiss Parenterals Ltd offers an excellent opportunity for pharmaceutical professionals seeking career growth in sterile injectable manufacturing. With strong regulatory exposure, competitive salary, and a stable work environment, this hiring drive is ideal for candidates aiming to grow in the regulated pharma sector.
Disclaimer
This job information is shared based on official sources and public notifications. Candidates are advised to verify all details before applying.
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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