Openings for Production, Packing, QC, QA, ADL at Stallion Laboratories

Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO CMP approved production facility and GLP qualified stringent quality control. The path of success lies in its belief of creativity and no negotiation with the quality of work. Stallion Laboratories Unit-ll a USFDA & UK-MHRA approved facility and proposed to be EU CMP approved plant. With its approval, Stallion aims to enter regulated markets.

Openings at Stallion Laboratories Pvt. Ltd. For following Positions at OSD Formulation facility - Unit-ll

Production
Qualification : M.Pharma / B.Pharm
Experience : 2 to 5 Years
Post : Officer/ Sr.Officer
Skill : Compression / Coating Capsule/Granulation/QMS

Packing
Qualification : M.Pharma / B.Pharm / M. Sc
Experience : 2 to 5 Years
Post : Sr.Officer/Officer
Skill : Primary / Secondary Packing

QC
Qualification : M.Pharma/ B.Pharm/M.Sc
Experience : 3 to 7 Years
Post : Sr.Officer/ Executive
Skill : HPLC Analyst

QC Micro
Qualification : B.Sc/ M.SC Micro
Experience : 0 to 2 Years
Post : Trainee Officer/ Officer
Skill : Microbiology Analyst (Only Male Candidate)

QA
Qualification : M.Pharma/ B.Pharm
Experience : 15 to 18 Years
Post : Manager
Skill : IPQA

ADL
Qualification : M.SC
Experience : 2 to 5 Years
Post : Officer/Sr. Officer
Skill : ADL

QA
Qualification : M.Pharma/ B.Pharm
Experience : 25+ Years
Post : DGM/GM
Skill : Quality Assurance oversight/ Regulatory Compliance & audit handling/ QMS implementation and continuous improvement