Friday, 29 March 2019

Urgent requirement In Omgreek Job Placement Service for Multiple Department -QA /QC/MFG/ Production / Micro Department @ Near Daman and Vapi

Urgent requirement For QC
Gender:- Male / Female
Job Profile :- Sr. Executive Officer/ Production Manager /.Factory Manager
Qualification :- B.Sc/ M.Sc (Chemistry) / B. E or B. Tech Chemical Engineer
Experience :- 2~15 years
Package :- As per Company Norms
Job Profile :- Sr. Executive Officer
Qualification :- B.Sc/ M.Sc (Microbiology)
Experience :- 0~4 years
Package :- As per Company norms
Qualification : Any Graduate
Job Profile :- Store Officer / Store Manager
Experience :- 2 ~15 Years
Package:- As per Company norms

Job location:- Daman and Vapi(Gujarat)
Interview Date :- 30/03/19 to 04/04/19
Candidate should have good knowledge. In communication skill.
Contact:-
send your resume on my 📧mail I'd :- omgreek@yahoo.com
☎me on +917802847663
or 📝 me on what's app at +917802847663

Walk-In Interviews for Freshers on 1st April 2019 @ Jodas Expoim Pvt. Ltd, Hyderabad


Troikaa Pharmaceuticals - Walk-In Interviews on 30th March 1st & 2nd Apr' 2019 @ Ahmedabad


AUROBINDO PHARMA LTD - Walk-In Interview for B.Sc Computers Freshers & Experienced Candidates on 31st March 19


Mylan Laboratories - Walk-In Interviews for QA & Production on 31st March 2019 @ GOA


Walk-in Interview at Goa on 31st March 2019

Job Location: Bangalore
Walk in date: 31st March, 2019 (Sunday)
Timings: 9am - 5pm
Venue:  THE FERN KESARVAL
Verna Plateau Kesarval
Cortalim Goa 403710
Tel: 0832 - 2783344
Qualification: B. Pharma / M. Pharma / M.Sc.
Experience: 2-6 years
Department: Quality Assurance
Must have knowledge in- 
  • Injectable experience in-process QA, 
  • Sterility assurance, 
  • Document management, 
  • Quality Management Systems, 
  • Risk assessments, 
  • Batch Release, 
  • Product Quality Reviews, Process / Cleaning validation and Training 
Department: Production
Must have knowledge in -
  • Vial washing & Depyrogenation, 
  • Bulk compounding, 
  • Autoclave sterilization, 
  • Aseptic filling processing, 
  • Lyophilization, 
  • SAP Operations, 
  • QMS relat e d activities, regulatory & cGMP requirements and validations
Note: Present working experience in Injectables is mandatory 
In case you are unable to attend the interview please email your resume tocareers@mylan.in, Contact no. 080-39254819 / 080-39254912 

Monday, 18 March 2019

Apollo Pharmacy - Campus Drive for B.Pharm, M.Pharm, Pharm.D, Pharm.D(PB) Freshers on 23rd March 2019


Maithili Life Sciences - Walk-In Interviews for Warehouse, Electrical, RO Plant & Account Dept. on 22nd March 2019


Job Openings in Bioanalytical Research / Clinical Research Departments @ Veeda Clinical Research



Zydus Cadila - Walk-Ins for Multiple Positions - QC, QA, Micro, Manufacturing, Packing, Stores, Warehouse, Engineering on 24th March 19

WALK-IN INTERVIEW FOR CADILA HEALTHCARE LTD., SEZ UNIT, AHMEDABAD
OFFICER / EXECUTIVE / SENIOR EXECUTIVE
Quality
Quality Control (Oral Solid Dosage): 
B.Sc. /B.Pharm/ M.Sc. /M. Pharm. with 1-5 years of hands-on experience in handling HPLC, GC, dissolution apparatus and UV-visible spectrometer. Should also have knowledge of weight analysis and stability studies for oral solid dosage forms.
Quality Control (Microbiology): 
B.Sc/M.Sc Microbiology with 1-5 years of hands-on experience in Environment Monitoring, analysis of water sampling & testing, TOC, MLT.
Quality Assurance (Oral Solid Dosage: B.Pharm / M.Sc. / M.Pharm with 1 -4 years of relevant exposure to IPQA activities /QA in QC in an oral solid dosage manufacturing facility. Should have knowledge of operating Trackwise, packaging, manufacturing IPQA, warehouse IPQA, BPR review, process validation, cleaning validation and packaging validation.
QA in QC / Analytical Lab (Oral Solid Dosage): 
B.Pharm / M.Sc. / M.Pharm with 1 -4 years of relevant exposure in QA in QC. Should have knowledge of Trackwise software, operation of QC instruments, handling deviations, laboratory incidents, OOS investigation and operation of Minitab software.
Manufacturing
Manufacturing of Tablet / Capsule / Dispensing / Inspection/ Pellets: 
B.Pharm / M.Pharm with 1- 4 years of relevant experience in supervision, operation monitoring and related documentation.
Manufacturing QMS (Tablet / Capsule / Dispensing / Inspection): 
B.Pharm /M.Pharm with 3-6 years of Handling of various QMS documents like change controls, CAPA, deviations, failure investigations(OOS/OOT) and risk assessment etc. for system compliance 
Packing Tablet / Capsule: 
B.Sc. / B.Pharm /M. Sc. / M.Pharm with 1 -5 years of experience in supervision, operation monitoring and related documentation.
Stores / Warehouse: Any graduate with 2- 10 years of relevant experience in raw material / packing material dispensing of oral solid dosage, online documentation & reconciliations of materials. Should have knowledge of receipt of raw materials, storage & packaging materials and experience in handling physical stocks verification & its reconciliation and QMS documentation for warehouse. Experience in auto storage retrieval system (ASRS) is preferable.
TECHNICAL ASSISTANT/ OPERATOR
Tablet/ Capsule - Pellet/ Coating/ Wurster/ Inspection/ Compression/ Imprinting:
ITI/ Diploma Engineer/ D. Pharm with 2 - 8 years of experience in operating pharmaceutical machines in Granulation/Compression/ Coating/ Wurster/ Pellets/ Capsule filling. Should have exposure to pharma machines like HSG/ FBP/ FBE/ FETTE/ MG2 etc., and expertise in handling sophisticated technology including PLC/SCADA system. Candidates must have exposure to handling inspection machines like Sensum, Viswill, Enclony etc and hands-on experience in dispensing activities.
Packing: 
ITI/ Diploma Engineer / D. Pharm with 2 - 8 years of experience in handling CVC, Countec, IMA or any bottle packaging line. Should have knowledge of 21CFR, track & trace system (exposure in handling packing machines like capping machine, labeling machine). Expertise in handling sophisticated technology including PLC/SCADA system.
Stores / Warehouse: ITI /Any diploma with 2- 10 years of relevant experience in raw material/ packing material dispensing of oral solid dosage & reconciliations of materials. Should have knowledge of receipt of raw materials, storage & packaging materials and experience in handling physical stocks verification & its reconciliation.
SENIOR EXECUTIVE / ASSISTANT MANAGER
ENGINEERING
B.E. / B.TECH/ Diploma (Mechanical / Electrical/ Instrumentation) with 3 - 10 years pharmaceuticals (OSD) Maintenance, Operation and Maintenance of HVAC Exposure to ERP system for plant maintenance activity are essential. Experience in QMS documentation, equipment installation qualification will be added advantage. 
TECHNICIAN/ OPERATOR
ENGINEERING
ITI (Fitter/ Electrician/ Instrument Technician) with 3 - 10 years pharmaceuticals (OSD) plant maintenance experience only.
ITI (Fitter/ Electrician) with 3 - 10 years in water system, plant operation and maintenance.
ITI (Fitter) for Utility (chiller, cooling tower, Air Compressor with HOC dryer & BMS) with 3 - 10 years plant operation and maintenance.
For all the positions, candidate having exposure to regulatory requirement of documentation, cGMP/GLP having worked in regulated plants shall be preferred.
Interested candidates may Walk-in for an interview along-with their updated CVs, a passport sized photograph & Salary Slips/ Latest Increment Letter and relevant documents as per the below schedule.
Interested candidates may also email their resume toparesh.patel@zyduscadila.com
Date : 24th March 2019, Sunday
Timings : 09.00 AM 04.00 PM
Location : Ahmedabad
Venue :
Hotel Nami Residency
Opp. V S Hospital,
Ellisbridge, Ashram Road,
Ahmedabad, Gujarat 380006

Thursday, 14 March 2019

SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF MERCURY

SOP for ESTIMATION OF BORON




SOP for BIOASSAY METHOD



SOP for DETERMINATION OF THE TOTAL WATER SOLUBLE SALTS

SOP for DETERMINATION OF ACUTE TOXICITY OF WASTE WATER AND INDUSTRIAL EFFLUENTS

SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF SODIUM



SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF NICKEL



SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF IRON

SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF MANGANESE




PRINCIPLE:
         
The Manganese content of the sample is determined by AAS. For dissolved Manganese, the filtrated sample is directly aspirated to the atomizer. For total recoverable
Manganese an acid digestion procedure is done prior to aspiration of the sample.

Limit of Detection: 0.04 mg/L

REAGENTS:

  1. Hydrochloric Acid – Concentrated
  1. Nitric Acid: Concentrated
  1. Nitric Acid: (1:499)
  1. Manganese Stock Solution: Merck 1000 mg/L NIST Certified Reference Material or Dissolve 1.0 gm of Manganese Metal in 10 ml conc. HCl mixed with 1 ml conc. HNO3 Dilute to 1000 ml with water (1 ml = 1 mg of Mn)

PROCEDURE:

Preparation of Standard solution: Prepare a regent blank and a series of 100 ml standards containing 0.04, 0.08, 0.12, 0.16 and 0.20 mg/L of manganese by diluting a
Suitable volume of the standard solution with dilute nitric acid.

Sample Preparation: To 100 ml portion of the acidified sample add 0.5 ml of nitric acid
If total recoverable Manganese is to be determined, add 5 ml of concentrated HCl and
Filter the sample through acid washed filter paper. Make up to 100 ml in a volumetric flask.

Analysis: Operate the instrument as per SOP. Aspirate nitric acid
(1:499) as blank. Then aspirate series of standards and then aspirate the sample solution.
Read the concentration in mg/L of Manganese directly.



REFRENCE: APHA 22nd Edition 3111 B/ IS 3025 (Part 59) - 2003                     


SOP for ESTIMATION OF CYANIDE

SOP for ESTIMATION OF BERYLLIUM

SOP for ESTIMATION OF IODINE




SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF CALCIUM

SOP for ESTIMATION OF SULPHITE



SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF CHROMIUM

SOP for ESTIMATION OF SLUDGE VOLUME INDEX


SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF ZINC

SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF LEAD

SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF MAGNESIUM

SOP for ESTIMATION OF SODIUM AND POTASSIUM BY AAS

SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF COPPER



SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF CADMIUM

SOP for STANDARD WORKING PROCEDURE FOR ESTIMATION OF ARSENIC

SOP for ESTIMATION OF HEXAVALENT CHROMIUM



PRINCIPLE:
The hexavalent chromium is determined calorimetrically by reaction with diphenylcarbazide in 
acid solution. A red-violet colored complex of unknown composition is produced. The reaction
 is very sensitive, the molar absorptivity based on chromium being about 40000 Lg –1 cm-1 
at 540 nm.

MINIMUM DETECTION LIMIT:    0.05 mg/l


REAGENTS:

1.        Stock chromium solution: Dissolve 141.4 mg K2Cr2O7 water and dilute to 100 ml; 
1.00 ml = 500 µg Cr.
2.        Standard chromium solution: Dissolve 1.00 ml stock chromium solution to 100 ml; 
1.00 ml = 500 µg Cr.
3.        Phosphoric acid, H3PO, conc.
4.        Diphenylcarbazide solution: Dissolve 250 mg 1,5- diphenylcarbazide 
(1,5-diphenylcarbazide) in 50 ml acetone. Store in a brown bottle. Discard when solution
 becomes discolored. Chromium solution (5 mg/L) ranging from 2.00 to 20.0 ml, to give 
standards for 10 to 100 µg Cr, into 250-ml beakers or conical flasks. Proceed with 
subsequent treatment

PROCEDURE:

Preparation of calibration curve: To compensate for possible slight losses of  
chromium during digestion or other analytical operations, treat standards by the 
same procedure as the sample. Accordingly, pipette measured volumes of standard
 of standards as if they were samples, also carrying out cupferron treatment of standards 
if this is required for samples. Develop color as for samples, transfer a suitable portion of 
each colored solution to a 1-cm absorption cell, and measure absorbance at 540 nm, 
using reagent water as reference. Correct absorbance readings of standards by 
subtracting absorbance of a reagent blank carried through the method.

Color development and measurement: Add 0.25 ml (5 drops) H3PO4. Use 0.2 N 
H2SO  and a pH meter to adjust solution to pH 1.0 ± 0.3 the matter of pH range is 
currently being considered by standard methods. Transfer solution to a 100-ml volumetric 
flask, dilute to 100 ml, and mix. Add 2.0 ml diphenylcarbazide solution, mix, and let stand 
5 to 10 min for full color development. Transfer an appropriate portion to a 1-cm 
absorption cell and measure its absorbance at 540 nm, using reagent water as reference. 
Correct absorbance reading of sample by subtracting absorbance of a blank through 
the method. From the corrected absorbance, determine micrograms chromium 
present by reference to the calibration curve.


CALCULATION

HEXAVALENT CHROMIUM (mg/l)   =   ABS / SLOPE

REFERENCE:  APHA – 3500 Cr - B  Colorimetric Method

SOP for ESTIMATION OF SOLIDS


PRINCIPLE:

TOTAL SOLIDS (TS) – The sample is evaporated in a weighed dish on a steam
 bath and is dried to a constant mass in an oven either at 103 – 105°C or 
179 to 181°C. Total residue is calculated from increase in mass.

TOTAL DISSOLVED SOLIDS (TDS) – the sample is filtered and the filtrate 
evaporated in tared dish on steam bath. The residue after evaporation is dried
 to constant mass at 103 – 105°C.

MINIMUM DETECTION LIMIT(TDS): 5.0 mg/l

REQUIRMENT:

Filtration apparatus: Any one of the following can be used.

1.      Membrane filter funnel
2.      Gooch crucible, 25 ml to 40 ml capacity with Gooch crucible adapter.
3.      Filtration apparatus with reservoir and coarse (40 – 60 mm) fritted disk as filter support.
4.      Suction flask of sufficient capacity for sample size selected.
5.      Drying oven for operation at 180 ± 2 °C.
 
PROCEDURE:

PREPARATION:

Clean & thoroughly wash all the glassware’s with dilute Sulphuric acid. 
Rinse the glassware’s several times with distilled water. Dry the glassware’s in oven 
at 180oC for 1 hour. Keep them in desiccators for cooling. Weigh the cooled 
evaporating dishes (two nos.) initially. Note down the reading A (dish for TS) &
 B (dish for TDS).
Sample testing: Select volume of the sample, which has residue, contains 
approximately 100 to 200 mg. This value may be calculated from values of 
specific conductance. To obtain measurable residue if necessary, add successive
 sample portions to the same dish after evaporation.

Pipette this sample to previously weighed evaporating dish A (for TS). Filter the sample 
(20 ml /25 ml) using 0.45 m m membrane filter. Collect the filtrate in a clean beaker. 
Measure 10 ml or suitable aliquot of filtrate & transfer it to second evaporating
 dish B. Evaporate the water content completely using water bath / oven. If oven is used 
adjust the temp 103 – 105 oC. Cool the dishes in desiccators.

Weigh the cooled dishes. Again heat the samples at temperature 105oC for one hour 
and check the weight loss. If there is considerable difference in first observation and 
second one then repeat the heating till weight of dried sample remains constant 
in two consecutive observations & note down the reading (C-for without filtration & 
D-for filtrate).


OBSERVATIONS:

 1. Initial weight of evaporating
    dish for sample without filtration -------(A)   =                      g 
 2. Initial weight of evaporating
     dish for sample with filtration---------(B)     =                      g
 3. Final weight of evaporating
    dish for sample without filtration ------- (C)  =                     g
 4. Final weight of evaporating
     dish for sample with filtration ---------- (D)   =                    g

CALCULATIONS:
 
Total Solids (TS)
                                             C - A                 
                     mg/L  = ----------------------------- x 1000  x  1000
                                      ml of sample taken                            

Total Dissolved Solids (TDS)

                                              D - B
                TDS        = --------------------------------- x 1000  x  1000
                                     ml of sample taken

Total Suspended Solids (TSS) mg / l = TS mg / l – TDS mg / l

REFERANCE: IS : 3025 (Part 15 & 16) – 1984

DRY RESIDUE, DVS AND TVS


PROCEDURE:

After noting down the final weights of TS and TDS, keep the samples in muffled 
furnace at temperature 550oC for one hour.
Note down the final weights of the evaporating dishes.

OBSERVATION:

Final weight of TS evaporating dish        (E)       =                    g 
Final weight of TDS evaporating dish     (F)       =                     g


CALCULATIONS: 
1.    TVS
                                                                (C - A) - E
                        TVS mg/L       = -----------------------------------  x 1000 x 1000         
                                                            ml of sample taken

2.    DVS
                                                                  (D - B) - F
                        DVS mg/L      = ------------------------------------- x 1000 x 1000        
                                                            ml of sample taken


REFERENCE:  APHA –2540 Std. Methods for water and wastewater analysis

requirement of Q.C in Daman

  We have requirement of Q.C Working area : Daman/Dalwada Exp: Fresher Gender: Male Qualification: Any Graduated Interested Person Call On t...