Multiple Vacancies in STIVAPH Healthcare Pvt. Ltd | M.Pharm, MSc, B.Pharm

“STIVAPH PHARMA CHEM” is located in Ahmedabad, Gujarat, India. Our mission is to improve the health of community by introducing new innovative products with great value. “STIVAPH PHARMA CHEM” has been involved in sourcing and distribution of Pharmaceutical; Surgical; Cosmetic; Herbal; Chemical; Agro products and Dietary supplement products. We believe in quality and timely supply of superior medicines at an economical rate.

Purchase Manager
Any Graduate
• Candidate should have having Pharma Raw Purchase Experience
• Well versed with Active Pharmaceutical Ingredients classification as per the quality standards and GMP requirements

Marketing Manager (Domestic)
B.Pharm + M.B.A/M.S.C+ M.B.A/B.Pharm; Minimum 8 Years
• Candidate should have basic Pharmaceutical Loan License/Third Party Manufacturing Practices
• Should be capable to bring the commercials as per the goal defined by the management
• Preparation of Production Plan; Supply Plan and Sales Plan and regular tracking of the same

Marketing Manager (Export - LATIN AMERICA/AFRICA)
B.Pharm + M.B.A/M.S.C+ M.B.A/B.Pharm; Minimum 8 Years
• Candidate should have thorough knowledge of Pharmaceutical markets of the particular domain
• Should be capable to bring the commercials as per the goal defined by the management
• Should be Well aware for the Regulatory requirements of the particular market

Production Head
M.Pharm/B.Pharm; Minimum 15 Years
• Thorough Experience of Solid Oral Dosage form, Liquid Oral & Topical Dosage Form Manufacturing, Planning & Operation Management within Regulatory Work Environment.
• Scientific Knowledge of Modified and Niche Molecule formulations.
• Must have faced any of the GMP Audits from Europe/US FDA/ANVISA agencies.

Quality Assurance Head
M.Pharm/B.Pharm/M.S.C ; Minimum 15 Years
• To lead and manage the strategic and operational performance of the Quality department, ensuring the successful delivery of business strategy, Key Performance Indicators (KPIs) and objectives, whilst adhering to regulatory compliance and achieving commercial success.
• Implementing and monitoring all Quality Assurance systems to ensure compliance with EU Commission Directive 2003/94/EC, covering GMP for medicinal products for human use and investigational medicinal products (IMPs) for human use.
• Must have faced any of the GMP Audits from Europe/US FDA/ANVISA agencies.

Quality Control Head
M.Pharm/B.Pharm/M.S.C; Minimum 15 Years
• Well versed in operation, maintenance, calibration, trouble shooting of various instruments employed in QC laboratories - FIPLCs automated systems Spectrophotometers, Auto- titrators, GCs, dissolution testers, etc.
• Experience of Quality documentation systems and procedures aspercGMPnorms.
• Understand and align with Production, QA, RA related requirements
• Must have faced any of the GMP Audits from Europe/US FDA/ANVISA agencies.

Microbiology Manager
M.S.C (Microbiology); Minimum 8 Years
• Managing the validation/qualification of Microbiology test methods and test systems to support in process and commercial release testing.
• Knowledge of Microbiology processes and associated controls with respect to the potential for microbial, endotoxin and particulate contamination and drive improvements across the network.
• Must have faced any of the GMP Audits from Europe/US FDA/ANVISA agencies.

Production Officer/Executive
M.Pharm/B.Pharm; Minimum 3 Years
• Candidate should have thorough experience in handling of Granulation, Compression, Coater, Capsule filling, Liquid Manufacturing - Filling , Ointment Manufacturing - Filling and Blister Packing Machines.
• Basic knowledge of cGMP and EU GMP Guidance.

Quality Assurance IPQA/DOC-CELL Executive
M.Pharm/B.Pharm/M.S.C; Minimum 3 Years
• Preparation of departmental SOPs (writing, revising and approving), ensuring regulatory compliance in conjunction with being 'fit for purpose' operationally and commercially.
• Preparing, reviewing and approving Technical and Quality Agreements.

Quality Control Executive
M.Pharm/B.Pharm/M.S.C; Minimum 3 Years
• Candidate should have thorough experience in handling of HPLC, UV, Dissolution and other instruments in compliance with the GLP Practices.
• Should have knowledge Stability Study along with its regression analysis
• Preparation of different Standard Operating Procedures for Quality Control Laboratory
• Should be well versed with software linked to Instruments

Engineer
B.E. Electrical/Mechanical ; Minimum 10 Years
• Candidate should be capable to handle the Boiler, Chiller, Air Compressor, AHUs, Water System
• Well Versed with AUTOCAD Software
• Experience should be there for EU GMP Audits