Therapiva Private Limited Mega Walk-in for API - Production / Quality Control / Analytical R&D 15th February 2020
Mega Walk-in for API - Production / Quality Control /
Analytical R&D
Walk- In at Therapiva Private Limited for API- Production /
Quality Control / Analytical
Method Development & Validations.
Date: 15th February 2020
Time: 9:30 AM to 3:00 PM
Venue :
Hotel Delicacy
Adj. JNTU Metro Station Nizampet X Roads,
Kukatpally, Hyderabad,
Telangana 500085
Production
Job Role: Executive / Sr. Executive
Experience: 1 to 5 yrs
Location: Hyderabad
Qualification: B.Sc/M.Sc
Key Responsibilities:
· Responsible
for day to day shift activities and report to Executive (or) Shift In charge.
· Responsible
to maintain Good housekeeping in production block and surrounding areas of the
production area.
· All
documents like batch manufacturing and control records, cleaning records,
equipment log books, housekeeping and weighing balance checklists etc to be
maintained online.
·
Manufacturing the drug products as per Batch Production and Control
Records (BPCR) and performing process operations as per standard operation
procedure.
· To check all
the labels before batch charging.
· Any
deviation (or) abnormality observed to be intimated to the executive (or) shift
in charge.
· Responsible
to follow safety instructions given in batch manufacturing and control records.
· Responsible
to attend cGMP, Safety and other trainings conducted.
· Responsible
to guide casual helpers to get the work in safe manner.
· Candidates
should have regulatory audit exposure, Good communication and Documentation
skills
Quality Control & Quality Control-Microbiology
Job Role: Executive / Sr. Executive
Experience: 1 to 5 years
Location: Hyderabad
Qualification: M.Sc.(Chemistry)
Key Responsibilities :
· Monitoring
of work allocation and previous day output review,
· Ensure
current and relevant specifications, testing procedures and standard operating
procedures are available in the laboratory to carry out the testing,
· To ensure
required Reference standards, Columns, working standards, Microbiological
media, etc. are available for testing,
· Release and Rejection of Raw materials, In
process, Finished products and Packaging materials.
· Expertise in
analyzed & handle finished products, in process samples, packing material,
stability samples,
· Responsible
for completion of activities such as OOS, OOT, CAPA, Calibration and
maintenance of all Q.C related instruments,
· Analytical
support to all Process Validation activities, QC Documentation Control
(Preparation, review & updating of QC SOPs ), standard testing procedure
and specification,
· Knowledge of
method development, impurity profiling, method validation technology transfer,
validation, establishing specifications for new launch products
· Competent in
establishing QC lab as per cGMP/ cGLP requirement,
· Strong
exposure in regulatory / customer audit expectations, audit compliance report
and response to regulatory agencies queries
·
Co-ordination with internal customer departments, along with Lab support
team which covers Calibrations of all QC instruments, Internal /External Audit
& Compliance.
· Preparation
& maintenance of working standards, Primary standards, Reference standards,
Formation & Stability cell & handling of all stability study related
activities,
Instrument / Equipment Qualification activities.
· Candidates
should have regulatory audit exposure, Good communication and Documentation
skills
API Analytical Method Development & Validations :
Job Role: Research Associate / Scientist / Sr.Scientist
Experience: 1 to 8 years
Location: Hyderabad
Qualification: M.Sc (Analytical Chemistry)
Key Responsibilities:
Candidate should be working in reputed API Manufacturer
having 1-6 yrs of experience.
Having the Knowledge of Analytical method development and
method validations by HPLC / GC / LC-MS. Also should have experience in force
degradation studies.
Should have good knowledge in wet chemistry techniques.
Having the Knowledge of Data integrity and Audit trails
compliance handling with Empower 3.0 Software.
Having the knowledge of Cleaning validations, Technology
transfer activity, with good documentation skills.
Positive and confident individual with strong work ethics.
Team player and good communications skills.
Interested candidates can send their updated resume to
ranjit.nalbothu@therapiva.net or
hr@therapiva.net
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