Thursday, October 6, 2022

Vacancy- Cognizant- Process Executive- M.Pharm, MSc, B.Pharm apply

 Post : Process Executive - Voice

Job Description
• Provide documentation coverage for a set of healthcare providers, which involves listening to audio recordings of patient clinic visits and leveraging technology to summarize medical facts in professional clinical reports (History of Present Illness, Physical Exam, Results, Assessment & Plan).
• Achieve proficiency in navigating EHRs and enter clinical reports and data directly into customer EHRs, adhering to specific clinic guidelines and workflows.
• Maintain a high-quality standard and adhere to account-specific documentation which delineates documentation requirements for our customers.
• Collaborate with managers on feedback from providers and successfully resolve issues.


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Candidate Profile
•  BSc/MSc graduate (medical)
•  Bpharmacy/Mpharmacy
• Fresher required.
• Familiarity with medical terminology & medical summarization.
• Excellent English professional writing skills; including advanced proficiency in grammar and spelling.
• Excellent listening skills and ability to understand diverse accents and dialects of physicians, their staff, and patients.
• Ability to work independently in a secure and private location with a reliable high-speed internet connection.
• Ability to participate in live video chat and screen sharing sessions for training.
• Experience with the Microsoft Office 365 or other cloud-based productivity tools.
• Should be comfortable working for Night Shifts and work from office

Additional Information
Experience : Fresher
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc
Location : Pune, Maharashtra, India
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 30th October, 2022

Apply Online


IPCA Laboratories: Walk In Interview for QA / QC- 9th Oct’ 2022

 WALK- IN- INTERVIEW : Ipca Laboratories Limited

QC Department

        • Qualification:- B.Sc, B.Pharm, D.Pharm
        • Experience:- 1-7 years.
        • Job Responsibility:- HPLC, GC, GCMS, QMS, LCMS
QA Department
        • Qualification :- B.Sc, B.Pharm, D.Pharm
        • Experience:- 1-7 years.
        • Job Responsibility:- QMS, IPQA & QA Documentation.


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Venue:

Hotel Woodland , N.H. No.48, Near Tejpal Motors, Balitha, Vapi-396195.

All Vacancies are for shift duty, so only male candidates are preferred

Intas Pharmaceuticals Limited: Walk In Interview M.Sc / D.Pharm / B.Pharm / Diploma / ITI Candidates on 10th Oct’ 2022

 Walk-In Interview for Tablet Packing Department


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Job Description in Details: 

Technician:

  • Positions : Machine Operator / Technician – Tablet Packing Jockey for Blister Primary / Secondary / Secondary Bottle Packing Line Area)
  • Qualification: ITI / Diploma Engineering / Diploma Pharmacy
  • Experience: 2-6 Years
  • Job area :Experience in Sticker labelling machine, Track and trace system, Oursertor placement machine, Autocolator (Shrink bundling machine) Blister Packing machine CAM (nMX)Automatic Cartoning Machine (HV1), Track and trace system, Check weiger Machine.
  • To do the online documentation in logbook and BPCR, Perform in process checks online without any error.
Staff:
  • Positions : Officer/ Executive- Tablet Packing (Primary / Secondary bottle packing line / QMS Area
  • Qualification: B.Pharm / M.Sc
  • Experience: 2-8 Years
  • Job area :

  1. Experience in Primary / Secondary Tablet Packing Area.
  2. Should have good knowledge in Sticker Labelling,
  3. Track and Trace system, Oursertor placement machine , Autocolator (Shrink bundling machine)
  4. Tablet / capsule counting and filling machine, TIS inspection system, Check weigher with metal detector system, capping machine, Induction sealing machine.
  5. Should have good knowledge in CAPA, Deviation, Change Control,
  6. Prepare SOP and another cGMP documents.

Date: 10th October 2022 (Monday)

Time: 09.00 a.m. to 03.00 p.m.

Job Location: Intas, Pharmez, Ahmedabad

Interview Venue: Plot No 5 to14, Pharmez, Nr. Village Matoda, Sarkhej Bavla National Highway No. 8-A, Taluka Sanand, Dist Ahmedabad 382213 Gujarat.

Candidates who had appeared for an interview in Last 6 Months need not to apply.

Candidate having pharma experience in regulated plant like USFDA, MHRA should apply.

Due to Covid-19 all candidates are requested to follow social distancing, masking and sanitizing while appearing for an interview. All covid-19 regulations will be followed strictly.

Team HR Contact Number :- 2717619783


Sun Pharmaceutical Industries: Walk In Interview on 9th Oct’ 2022

 Sun Pharmaceutical Laboratories Limited – Sikkim

WALK IN DRIVE – Process Development / Tech Transfer – Oral Solid

  • Department: Process Development & Technology Transfer ( Oral Solid)
  • Role : Executive / Sr Executive
  • Job location : Sikkim & Guwahati
  • Qualification : B.Pharm or M.Pharm
  • Experience : 3- 7 years in PDL & Tech Transfer OR Production (Granulation, Compression and Coating)
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Job Description:

1. Process development for new immediate release and modified release solid oral dosage to facilitate technology transfer.
2. Plan scale-up / down batches in manufacturing area and oversee the batch executions with the responsible project scientists / mfg team.
3. May lead and/or Collaborates with multidisciplinary teams to resolve complex product / process development issues and respond to internal and external audits.
4. Generate accurate, reliable data by following established procedures and practices. Record, tabulate, summarize, interpret, report and publish study results.
5. Develop and maintain department standard operating procedures.
6. Co-ordination with QA/QC/Store/Eng./manufacturing department for smooth functioning of MSTG activities.
7. To do the documentation as per cGMP/SOP/BMR/Qualifications as per GDP.

Date : Sunday, 9th October 2022 | Time : 9.30 am – 2.00 pm
Venue of Interview : Venue : Sun Pharma Guest House, (Within Sun Pharma Colony), Ranipool – SIKKIM

Piramal Pharma Limited: multiple openings Walk in drive on 8th and 9th October

Mega Vacancy- Walk in drive for multiple openings

EDUCATION & RELATED EXPERIENCE:

  • M.Sc. (Organic Chemistry), M.Pharm (Pharmaceuticals Chemistry /Medicinal Chemistry), Ph.D. (Organic Chemistry / Natural Product Synthesis)
  • 2 to 10 years of relevant experience with CRO industry. Fresh PhDs or Post Docs, are also eligible.
  • Experience to safely and effectively carry out routine synthetic organic chemistry techniques (Reactions, recrystallizations, chromatography).
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Job Location 
Ahmedabad, Gujarat  : CRO,R & D medchem

Walk in date & time
08/10/22 – 08:00 AM to 06:00 PM
09/10/22 – 08:00 AM to 06:00 PM

Venue for Interview
Park Ascent Hotel l 126, Opp. IIM Lucknow – Noida Campus, Sector-62, Noida – 201309, U.P.

Register yourself at below portal

Torrent Pharmaceuticals: Walk-In Interviews


WALK-IN INTERVIEW on  8th Oct’ 2022 @ Torrent Pharmaceuticals Limited, R&D Centre, Gandhinagar


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Date: 08/10/2022
Time: 10.00 AM – 5.00 PM
Venue for Interview: Torrent Pharmaceuticals Limited, Village-Bhat, Kanoriya Hospital, R&D Centre, Gandhinagar

Department: Bioanalytical / Pharmacokinetic

  • Exp: 2 to 8 Yrs
  • Qualification: M.Sc / M.Pharm
  • Position: Executive (SCI-II)VILSHA SHAH- Contact: Mr. Vishal Shah 6359621127 / vilshashah@torrentpharma.com

    Note: Read all instructions carefully provided in advertisement.

Wednesday, October 5, 2022

Assoc, Quality Control - QMSBaxter International Inc.


Assoc, Quality Control - QMS at Baxter International Inc. Ahmedabad, Gujarat, India.
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

  • To review, update, report and inform Supervisor as & when deviation is initiated.
  • To ensure that the recording of NCR is done in line with standard operating procedure
  • To investigate Lab incidences, OOS.OOT and OOL.
  • To prepare investigation reports.
  • To ensure the implementation of GMP, GDP practices and review of issues and impact of the same, if any, & take corrective actions.
  • To carry out GLP rounds in the Quality Control lab.
  • To work as a Good Manufacturing Practice (GMP) inspector in the plant
  • To train/update the team members on various regulatory guidelines
  • To identify, monitor the deviation/abnormalities in process/documents/systems are captured and resolve them according to Quality management System.
  • To ensure that all the deviations and OOS are reported to QA within required time frame.
  • To prepare, review, Implement and update SOP’s according to current regulations systems.
  • To conduct Technical committee meeting on CCN impact assessment.
  • To conduct monthly corrective and Preventive Action Meeting.
  • To review the CAPA summary report and ensure that all CAPA are closed within time frame.
  • To review Change Control Note and NCR report before sending to Quality Committee for final closure and ensure the timely closure of Change Control Note and NCR
  • To train/update the personnel for the various aspect of current Good Manufacturing Practices.
  • To investigate and close the QMS elements in timely manner.

Preferred Educational Qualification:
  • Bachelor or Master in science (Chemistry) with 3 - 6 yrs of relevant experience (Pharma Industry)Seniority level

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