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(Strides Pharma Walk-In Drive 2025) |
If you are a pharma professional looking to grow your career with a globally recognised pharmaceutical company, then this opportunity is for you.
Strides Pharma Science Limited is conducting a Walk-In Interview for experienced candidates across the Production, Packing, Quality Control (QC), Quality Assurance (QA), and Formulation & Development (F&D) departments.
This hiring drive is ideal for professionals with experience in OSD manufacturing, quality systems, analytical testing, and formulation development who want to work in a regulated, innovation-driven environment.
Strides Pharma Science Limited is a leading global pharmaceutical company headquartered in Bengaluru, India, with manufacturing and R&D facilities across India and abroad.
The company operates in 100+ countries and is well known for:
High-quality generic formulations
Strong compliance with global regulatory standards
Robust R&D and formulation expertise
Employee-friendly and growth-oriented work culture
Strides focuses on Oral Solid Dosage (OSD), APIs, and complex generics, making it a preferred employer for pharma professionals seeking long-term career growth.
Key Responsibilities:
Granulation, compression, coating, and capsule filling
Equipment operation as per SOPs
Handling deviations, change controls, and CAPA
Batch Manufacturing Record (BMR) documentation
Compliance with GMP and safety standards
✅ Best suited for candidates with hands-on OSD production experience.
Key Responsibilities:
Bottle and blister packing operations
Handling BQS and CVC systems
Review of Batch Packing Records (BPR)
Packing line optimisation and compliance
Ensuring data integrity and GMP adherence
✅ Ideal for professionals experienced in pharma packing operations.
Key Responsibilities:
Analytical testing using HPLC, GC, UV, IR, KF, FTIR, and Dissolution
Routine analysis of raw materials, in-process samples, and finished products
GLP compliance and documentation
LIMS usage and data accuracy
✅ Perfect opportunity for QC analysts with strong analytical skills.
Key Responsibilities:
In-process quality checks on the shop floor
BMR/BPR review and line clearance
Validation activities and deviation handling
Ensuring GMP compliance across operations
✅ Suitable for professionals experienced in IPQA and pharma QMS.
Key Responsibilities:
Lab-scale formulation trials and optimisation
DOE (Design of Experiments)
Stability study protocols and execution
Development documentation and scale-up support
✅ Ideal role for candidates seeking R&D and formulation development careers.
B.Pharm
M.Pharm
M.Sc (Relevant Specialisation)
2 to 7 years in relevant pharma departments
Strong understanding of OSD manufacturing / QC / QA / F&D
Knowledge of GMP, QMS, GLP, and regulatory guidelines
Hands-on experience in documentation and audits
Based on department and requirement, selected candidates may be placed at:
Chennai
Bangalore
Pondicherry
π Date: 23rd December 2025
⏰ Time: 10:00 AM – 3:00 PM
Hotel Ravila Grand
Plot No. 9, Mumbai Highway Road
Opposite Pranaam Hospital Lane
Sri Durga Colony, Madeenaguda
Hyderabad, Telangana
Candidates must bring:
Updated Resume
Valid ID Proof (Aadhar / PAN)
Educational Certificates
Experience Letters
Last 3 Months Payslips
Appointment Letter (if applicable)
Siva Shankar Mohanty
π§ Email: Sivashankar.Mohanty@arcolab.com
π 22nd December 2025
π Candidates are advised to attend the walk-in before the deadline with complete documents.
✔ Global exposure and regulated work environment
✔ Strong learning and career growth opportunities
✔ Employee-friendly company culture
✔ Work with advanced pharma technologies
✔ Long-term stability in a reputed organisation
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