Therapiva Private Limited - Mega Walk-In Drive for Production | QC | Microbiology | AR&D on 15th Feb' 2020 - PHARMA WISDOM

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Friday, 14 February 2020

Therapiva Private Limited - Mega Walk-In Drive for Production | QC | Microbiology | AR&D on 15th Feb' 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     

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  or

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