Zydus Cadila - Walk-In Interviews for Multiple Positions on 12th & 13th January 2019

Walk-In Interview – Officer / Operator – OSD / Injectables /Packing

Walk-In Date: 12th & 13th January, 2019 (Saturday & Sunday)
Officer/Executive Compression, Granulation &CoatingEducation: B.Pharm
Experience: 2 to 6 years
Should have experience in working with regulatory environment. Co-ordinate the activities of subordinates, maintain working as per cGMP requirements and supervision of related activities of granulation, compression, coating area. 
Operator Compression, Granulation & Coating
Education: Diploma/ITI
Experience 4 to 6 years.
Should have experience in working with regulatory environment. Must have experience to operating mentioned machines like, Korsch XL -400, Fette compression, Glatt RMG, Tapasya RMG, GEA Granulation Machine, Fluid bed processor, PAM Glatt, Glatt Coater.
Wruster/Pellet Coating - Officer/ Executive Qualification: B.Pharm / B.Sc 
Experience 2-5 years. 
Co-ordinate the activities of subordinates, maintain working as per cGMP requirements and supervision of related activities in department. To monitor the issuance of raw materials. To complete all manufacturing records with recipe management system. Supervision of related activities in department. Review of BMR of all stages and other QMS document.
Wruster/Pellet Coating - Operator Qualification: Diploma
Experience 4 -6 Years. 
To operate and to clean equipment as per the cleaning and operating procedure of the laid down SOPs. To check and to fill sequential log card, cleaning check list, temperature and % RH record and BMR. 
OSD Packing Supervisor - Officer/ExecutiveEducation: B.Pharm/B.Sc - 2 to 5 years experience
Relevant experience to supervise packing line (Oral Solid Dosage form), recording in BPR/logbook etc, Review of filled BPR. Awareness about track and trace system. Achieving daily packaging targets.
OSD Packing OperatorEducation: Diploma / ITI 
Experience 4 to 6 years
Experience of operating Hi-cart and BQS Machine with camera systems. To operate machine as per SOP. To maintain sequential log entry. To maintain status labelling of respective machine/area. 
Designation: Officer/Executive/Senior ExecutiveEducation: B.Pharm
Department: Injectable / Parenteral
Experience: 2 6 years relevant experience in, supervision, monitoring & documentation of Injectable / Parenteral area. Experience with Aseptic area is preferred. 
Designation: OperatorEducation: ITI / Diploma
Department: Injectable / Parenteral 
Experience: 2-6 years relevant experience in Injectable Production, ensure the department work discipline and maintain GMP, clean respective area during clearance and remove previous product material, perform activity allotted by supervisor.
Venue: - Zydus cadila, Sarkhej Bavla NH No 8A, Moraiya, 
Near Modern Denims Dist: Ahmedabad 382210
Timings: - 9:30 AM to 3:30 PM

Aspiro Pharma Limited - Walk-In Interviews on 11th January 2019 for AR&D / FR&D / Microbiology

Urgent Openings for B.Sc Chemistry Freshers & Experienced Candidates @ Sahithi Drugs & Intermediates Pvt. Ltd

UMEDICA LABORATORIES - Walk-In Interviews for QC (Analyst / Reviewer) on 13th January 2019 @ Vapi

BIOCLINICA - Freshers Walk-In for Pharmacovigilance on 8th & 9th January 2019 @ Mysore

Freshers Walk-in for Pharmacovigilance on 8th & 9th Jan @ Mysore

PLEASE NOTE : BIOCLINICA IS CONDUCTING THIS WALK-IN INDEPENDENTLY AND NOT WITH PARTNERSHIP WITH CONSULTANCIES.

Bioclinica invites you for an opportunity to be part of our PHARMACOVIGILANCE team.

Meet us on 8th or 9th Jan 2019  between  9 AM to 1 PM at the below address:

Venue Details:

Bioclinica India Pvt Ltd
Silver Spirit Tech Park
317 (P), (PII) 318, Hebbal Industrial Area,
Mysore-16
JOB TITLE: DRUG SAFETY ASSOCIATE
WORK LOCATION: MYSORE
YEARS OF EXPERIENCE: 0 TO 2 YEARS
EDUCATION:  M PHARMACY, PHARM D, BDS, MDS, MSc / BSc (Nursing)
ROLES & RESPONSIBILITIES
As Case Intake Member : 

·         Responsible for case intake, duplicate check , and registration

·         Maintain log of source documents and other communications

As Case Processor :

·         Responsible for data entry of individual case safety reports into the safety database.

·         Review and evaluate AE case information to determine required action based on and following internal policies and procedures

·         Process all incoming cases in order to meet timelines 

·         Full data entry including medical coding and safety narrative

As Medical Coder :

·         Responsible for coding all medical history, events, drugs /procedures/indications and laboratory tests according to the appropriate dictionary (For e.g. MedDRA, Company Product Dictionary, WHO-DD)

As Narrative Writer :

·         Responsible for writing medically relevant safety narrative of cases and checking the completeness and accuracy of the data entered in the various fields.

As Literature Review Specialist :

·         Ensure effective and accurate collection, recording, review and reporting of literature searches conducted. 

·         Review of literature articles to identify case safety reports.

·         Responsible for operational Pharmacovigilance activities for assigned developmental and/or marketed products.

·         Assist in signal generation and safety analysis activities.

·         Ensure quality of literature searches and reporting.

·         Review of local/global literature reports to determine regional reportability.

·         Create/maintain study summary documents.

·         Assist with narrative writing for periodic/ad hoc submissions.

·         Assist with ad hoc or routine safety monitoring activities.