Nirlife, an ISO Standard cGMP approved, is the healthcare division of Nirma limited (Rs. 7000 crore conglomerate) founded with the objective to make high-quality healthcare products easily accessible to the masses. Nirlife has evolved as one of world’s largest manufacturer of Parenterals, Medical Devices and pharmaceutical formulations under one roof and has presence in more than 70 including semi-regulated and regulated markets. For further expansion of pharmaceutical business, we require professionals to fill multiple vacancies in the following areas:
Posts: in Various Departments like QA/QC, F&D, PMT, Production
QUALITY ASSURANCE / QUALITY CONTROL
Head - Quality Assurance: B.Sc/B.Pharm with Minimum 15 yrs of exp. He shall be responsible for all QA related activities for Parenterals,Injectables.Solid and Liquid Oral dosages. Formulation development and for Implementing and maintaining various Quality Assurance processes such as documentation, validation, internal & external audits, master documentation creations, handling customer complaints and other department related activities. Exposure to DQ, IQ, OQ, PQ & regulatory audits such as USFOA. MHRA, TGA. PICS& IN VISA is desirable. Sr. persons who retired from reputed pharma company having exposure of regulated & semi regulated markets may also apply.
Head Engineering: B.E./M.E (Mechanical/ Electrical/ Instrumentation) having minimum 15-20 yrs of exp in Pharmaceutical Industry. He shall be responsible for maintenance of all equipments/machines like filling, stoppering, sealing machine, Air Compressor, Sterilizer, Rotary Sterilizer, in line mixer, Homogenizer, Packing Belts, WFI plant, PS6 plant and AHU's. He shall be responsible to execute all preventive maintenance activities as per planned schedule. He has to assist QA and production department for all necessary validation activities. He is responsible for manpower planning of the department, coordination for procurement of spares and monitoring of performance of machines.
Head-Training Centre: Retired Principal/professor/faculty from reputed engineering/management/pharmacy college who can handle training activity for fresh graduates & engineers to make them capable to handle different functions within the department.
Sr.Consultants (QA QC, Production): Senior professionals who retired from reputed pharmaceutical company having exposure of regulated & semi regulated market.
Analytical development & Validation Associates: M.Pharm/ B.Pharm/M.Sc. with 3-6 yrs of exp in testing and documentation of HPLC/UV Spectroscopy/DissolutkwGC/AAS/IC etc. Should have knowledge with expertise on Comparative dissolution/impurity probation / Analytical method Validation & Verification1' Stable sample analysis/Stress Testing.
QA Officers: B.Sc/M.Sc/B.Pharm/M.Pharm with 1 to 7 yrs of relevant exp in QMS. Validation & Documentation.
QC Chemists: B.Sc/M.Sc/B.Pharm/M.Pharm with 1 to 7 yrs exp in stability studies, microbial monitoring, analysis of RM, FP/IP & validation samples. Exp in handling of HPLC. GC. UV& TOC shall be preferred.
FORMULATION & DEVELOPMENT
Formulation Development Associates: M.Pharm with 3-5 yrs exp in Solid/Injectable Dosage formulation & regulated market. Product development report/Optimization study protocol'Validation Protocol preparation & execution is mandatory.
Packing Development Officers: M Pharm/B.Pharm/B.Sc with 3-5 yrs of exp & knowledge of Pharma product (Solid-Injectable) packing, understanding the pharma stability concept VS packing requirement of product.
PRODUCT MANAGEMENT TEAM
Production/Packing Chemists: B.Sc/ M.Sc/ B.Pharm having 1-5 yrs of exp in production of priarma products like IV fluid injection (BFS and Glass). Tablets. Capsules. Powder Injection & Dry Syrup (preferably CEPHA'BETA) including knowledge of GMP. GDP & Regulatory audits.
Utility: Engineers/Technicians having minimum 2 yrs of exp in operating and maintenance of rotary equipment like screw compressor, chillers & RO/DM plant.
CPP: Engineers/Technicians having minimum 3 yrs of exp in operating'' maintenance of coal based middle size (8-10 MW) power plant Environment
Environment Engineering: B.E (Specialization in Environment Engineering) having 1-2 yrs of exp in waste water management and air pollution control, recycling, waste disposal, radiation protection, industrial hygiene, environmental sustain ability, and public health issues as well as knowledge of environmental engineering law.
PRODUCTION
Operators: ITI Fitter/Electrician/lnstrument with minimum 1 yr of exp in Operating and Maintenance of filling Machme(Glass line filling. Rommelag /BFS filling nVc. capsule filling nVc. Tablet compression & coating m/c. Blister strip nVc. Medical device m/c. Syringe & Needle assemble. Plastic moulding) including knowledge of GMP and GDP.
Technicians: ITI Fitter with minimum 2 yrs of exp in maintenance of all type of romelag /BFS machines & HVAC with maintenance cum operation of cooling tower. WFI plant chiller etc.
Legal: LLB with minimum 2 yrs of exp in Drafting & vetting of various Agreements. Contracts. Power of Attorney. Affidavit and other legal documents. Filing & handling trademark applications and visiting trademark office. Handling cases under Negotiable Instrument Act. 1881.
Production Planning & Control: Graduate with minimum 2 yrs of exp in production planning & control in pharmaceutical company.
Costing & MIS: M.Com/ ICWA having minimum 3 yrs of exp m costing of manufacturing sector preferably of pharma industry. Knowledge of SAP. MIS & MS Excel is must.
Studio: Diploma in Graphics Design having minimum 3 yrs of exp of designing Promotional & Packaging Material. Candidate should have sound knowledge of different printing techniques and capable of dealing with printers. Exp of Pharmaceutical Industry would be preferred.
Interested candidates may please mail their updated CV's at recruitment@aculife.co.in.
clearly indicating the position in the subject line tor which they have applied within 7 days
LAST DATE: 20/01/2016
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