Quality
Assurance - API with Rusan Pharma Ltd - Ankleshwar location
Hello,
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.
With Best Regards,
Priti Singhvi
singhvipriti@gmail.com / priti.singhvi@rusanpharma.com
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