Job Opportunity: Associate / Senior Associate – Drug Product Manufacturing
Job Description:
- Responsible Operations: Manage DP facility manufacturing activities including operating isolators and associated equipment for cartridges, vials, and pre-filled syringes.
- Commissioning and Qualification: Assist in installation, commissioning, and qualification activities such as IQ, OQ, and PQ of Filling lines.
- Quality Management: Ensure compliance with QMS in qualification and manufacturing activities, and validate equipment and areas along with aseptic media fill.
- GMP Compliance: Identify and implement manufacturing procedures adhering to current GMP requirements.
- Maintenance and Safety: Oversee daily cleaning, disinfectant preparation, workplace safety procedures, and SAT of equipment.
- SOPs and Protocols: Prepare SOPs and protocols related to equipment and drug product facility.
- Timely Initiatives: Initiate QMS elements promptly and complete SAP-related transactions as applicable.
Candidate Profile:
- Education: M.Sc/M.Pharma
- Experience: 2-8 Years in relevant field.
Additional Information:
- Experience: 2-8 Years
- Qualification: M.Sc/M.Pharma
- Location: Doddaballapura, Bengaluru, India
- Industry Type: Pharma/Healthcare/Clinical research
- Functional Area: Manufacturing
- End Date: 30th April 2024
Email your resume to: J.DhanaVignesh@stelis.com | Email subject: DP manufacturing – Stelis
