Highly creative and experienced Graphic Designer. With a strong portfolio of packaging, promotional materials, digital media, and branding projects. Seeking Designing Pharma industry candidate. hrd@stedmanpharma.com / 9786920463
Role & responsibilities : Prepare and review documentation such as SOPs, BMRs, and logs with attention to detail and good command of English. SHARE RESUME TO hrd@stedmanpharma.com / 9786920463 Preferred candidate profile : Education: B.Pharm / M.Pharm / M.Sc. (Chemistry, Biotechnology, Microbiology) / B.Tech or B.E. in Chemical Engineering or related fields. Freshers or recent graduates looking to start their career in pharmaceutical production Basic understanding of GMP , manufacturing processes, and safety protocols Good written and verbal communication skills in English (especially for documentation purposes) Attention to detail, willingness to learn, and ability to work in a team Open to working in production environments and learning practical applications Available for a full-time, 6-month paid internship
Handling statutory audit. Handling tax audit. TDS. MIS Reports. Handing IT assessments, Appeals & IAT related works. Forex remittance - Documents processing. share your Resume to -hrd@stedmanpharma.com / 7904827192, 9786920463.
Role & responsibilities : Assist in the preparation, review, and submission of regulatory documents Help maintain regulatory files and records Support in compiling dossiers for product registrations and renewals Research regulatory requirements and updates from national/international authorities Coordinate with cross-functional teams for required data or documents Share your resume to hrd@stedmanpharma.com / 9786920463 Preferred candidate profile : This internship is ideal for students or recent graduates looking to gain hands-on experience in the field of Regulatory Affairs within the pharmaceutical industry. The intern will work closely with the RA team and assist with documentation, compliance tasks, and regulatory submissions.
Stedman Pharmaceuticals is looking for a dynamic and experienced candidate for the Quality Control (QC) department with hands-on experience in Analytical Method Validation for various dosage forms. Resume to hrd@stedmanpharma.com / 9786920463
Experienced QA Manager to oversee&manage QA operations our pharmaceutical manufacturing unit.Ideal candidate will ensure compliance with GMP, WHO other regulatory standard,while developing &maintaining QMS Share your Resume to hrd@stedmanpharma.com
We are seeking Purchase Executive to manage the packing materials.Candidate should have prior experience in sourcing packaging materials pharma industry. Resume to hrd@stedmanpharma.com
New product development Be updated on regulations/notification/advisories issued by FSSAI FSSAI license documentation Ensure compliance on statutory requirements for FSSAI license TM search for new products resume to hrd@stedmanpharma.com
Experienced in preparation,execution&review of process/cleaning validation,equipment qualification,calibration, preventive maintenance, and validation schedules. Ensures effective implementation validation master file. resume to hrd@stedmanpharma.com
We are looking for skilled committed Production Operators.candidate will be responsible for operating production machinery,maintaining production line efficiency,ensuring quality compliance cGMP environment. share resume to hrd@stedmanpharma.com
Invoicing and Dispatching stocks. Payment collection. Transport Coordination. Billing. Responsible for verification of Chennai C&F – TN stockiest expiry replacement details by way of replacement MRP to MRP. share resume to hrd@stedmanpharma.com
Ensuring timely dispatch of important documents, samples, or deliveries as per company requirements. Helping with photocopying, scanning, and filing of documents Assisting with organizing and maintaining office files and records ensuring refreshments
Prepare training slides, visual aids, and leave-behinds for new/existing products. Support with scientific references. Must have good communication skills. Email your resume to hrd@stedmanpharma.com
Looking for R&D Trainee (Fresher). Role includes product development, lab trials, SOP preparation, literature survey & coordination with analytical team, Good in subject knowledge. Share resume to hrd@stedmanpharma.com
QA Manager OSD/Liquid formulation background.Must have experience in BMR, batch release,validations,qualifications,SOPs,GMP,audits,QMS(Deviation,OOS, OOT, CAPA), tech transfer. Analytical exposure is an added advantage Resume to hrd@stedmanpharma.com
Role & responsibilities Provide first-level technical support to office employees (hardware, software, and network issues). Assist in installation, configuration, and maintenance of desktops, laptops, printers, and other IT equipment. Support IT team in managing LAN/WAN, internet connectivity, and system security. Help in troubleshooting email, MS Office, and other software applications. Assist with system updates, backups, and antivirus management. Document IT support activities, troubleshooting steps, and resolutions. Coordinate with vendors/service providers for IT-related requirements. Learn and support IT projects, such as ERP, cloud systems, or data management, as assigned. Preferred candidate profile Recently completed B.Sc. (Computer Science/IT), BCA, B.Tech (IT/CS), M.Sc. (Computer Science/IT), or MCA . Basic knowledge of Windows/Linux OS, networking, and troubleshooting . Familiarity with MS Office, email configuration, and antivirus tools . Strong problem-solving skills with a willingness to learn new technologies. Good communication skills and ability to work in a team environment. Candidates available for full-time internship (6 months) will be given preference. Share resume to hrd@stedmanpharma.com
Responsible for assisting in the receipt, storage, dispensing, and stock management of products and related supplies. Maintaining accurate inventory levels, and supporting the dispensing process.
Handling statutory audit. Handling tax audit. TDS. MIS Reports. Handing IT assessments, Appeals & IAT related works. Forex remittance - Documents processing. share your Resume to -hrd@stedmanpharma.com
Review & approval of Specification&STP against Monograph BMR&QMS Review of COA and analytical work record of RM, PM, FP & Stability Review of audit trials Review of Analytical Method development Share resume to hrd@stedmanpharma.com, call 7904827192
Experienced in preparation,execution&review of process/cleaning validation,equipment qualification,calibration, preventive maintenance, and validation schedules. Ensures effective implementation validation master file. resume to hrd@stedmanpharma.com
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