Quality Assurance – API with Rusan Pharma Ltd – Ankleshwar location

Quality Assurance – API with Rusan Pharma Ltd – Ankleshwar location

There is an opening for Manager  – Quality Assurance(API only)  Role.

Job Location Ankleshwar

Exp : 10 + Years from API Background
Please carry all your current company documents and your qualification certificate at the time of interview.
Visit the website : www.rusanpharma.com (Manufacturing of Pain and De- Addiction Medicine)
Narcotics and Psychotropics manufacturing Unit)
Job Role :
i.    The medicinal products are designed and developed in away that take account of the requirements of GMP and GLP (Good laboratories Practice).
ii.    Production and control operations are clearly specified and GMP doted.
iii.    Arrangements are made for the manufacture, supply and use of correct starting and packaging arrangements.
iv.    All necessary controls on intermediate products and any other in process controls and validations are carried out.
v.    The finished product is correctly processed and checked, according to the defined procedure.
vi.    Medicinal products are not sold or supplied before a QA Manager or his designated has certified that each production batch has been produced and controlled in accordance with the requirements of the marketing authorization and other regulations relevant to the production, control and release of medicinal products.
vii.    Satisfactory arrangements exist to ensure, as far as possible, that the medicinal products are stored, distributed and subsequently handled so that quality is maintained throughout their shelf life.
viii.    There is a procedure for self-inspection and / or quality audit, which regularly appraises the effectiveness and applicability of the QA system.
2.    He is independent of everybody in the organization and he is directly answerable to Plant Head / Corporate QA Head.  However in day to day working he may work ion consultation with Plant Manager / Corporate QA Head.
3.    All the departmental head and assistants of organization are answerable to Quality Assurance Head at Corporate Office/ his designated.
4.    He is responsible to all day in and day out activities of organization and it should be reported or intimated to him.
5.    Quality Control Department should report to him all day to day activities and problems and take his opinion as a final verdict.
6.    Production Department is also to report to him all the activities of the department.

Send updated CV to

singhvipriti@gmail.com / priti.singhvi@rusanpharma.com

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