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Urgent Requirements in Glenmark Pithampur
1. Production Manufacturing (Granulation/Compression/Capsule Filling ) officers
2. Primary Packing Officer in bottle Line
3. Hicart Operator
4. Compression Operator
For all positions, interview mode will be virtual.
Experience: 3 to 6 yrs
Min. Qualification: Diploma for Operators & B Pharma for officer
Send cv on naveen.sharma@glenmarkpharma.com with following details
Current CTC
Min. Expected CTC
Notice Period
How soon u can join us
Interview date: 7th Jan & 8th Jan 2021
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Roles and Responsibilities
In this role, you are required to solve routine problems, largely through precedent and referral to general guidelines
Your expected interactions are within your team and direct supervisor
You will be provided detailed to a moderate level of instruction on daily work tasks and detailed instruction on new assignments and the decisions that you make that would impact your work
You will need to be well versed with basic statistics and terms involved in the day to day business and use it while discussing with stakeholders
You will be required to help in the overall team's workload by managing your deliverables and help the team when required
You will be an individual contributor as a part of a team, with a predetermined focused scope of work.
Qualifications
BE/BCA/Bachelor of Pharmacy/Master of Pharmacy/Bachelors of Information Technology
TO APPLY CLICK HERE
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Walk In drive for Quality Assurance Department in Formulation Division on 09.01.2021 (Saturday).
Vacancies: Jr. Executive - Trainee| Executive - Trainee
Qualification:
B.Pharm | M.Pharm (Fresher's 2019 and 2020 Passed out Candidates only)
Only Male Candidates
Interview Date: 09.01.2021 (Saturday)
Interview Time: 09:00 AM to 12:00 Noon.
Venue Details:
MSN Laboratories Pvt. Ltd| Formulation Unit -2 |Sy. No 1277&1319 -1324 |Nandigama|Rangareddy| Telangana - 509216.
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Dear All,
Greetings of the Day !!!
Walk-in Drive......
Dated: 09.01.2021@ Saturday...
Looking for Production professionals for Natco Pharma Limited (formulations - OSD & Injectables)
Work location: Kothur, near shadnagar, R.R District, Telangana
Exp: 0 - 5 years
Qualification; (B.Sc (Chemistry)/M.Sc/B.Pharmacy/M.Pharmacy
Freshers: 2018, 2019 & 2020 passed outs
Department: Production
Preferences: Only male candidates
Desired candidates shall attend the interview along with their updated CV at our Corporate Office..
Dated: 09.01.2021@ Saturday...
Timings: 9:00 AM to 1:00 PM
Venue:
Natco House,
Road No: 02,
Banjara Hills,
Hyderabad.
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Job Purpose
Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines
Accountabilities
I. Collate, review and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner
II. Review Master Validation protocol and report for timely execution of validation batches and timely submission of documents in order to response for deficiencies
III. Review annual product quality review report at units for completeness and data correctness to ensure compliance to cGMP requirements and audit readiness
IV. Review, upkeep and issue regulated market technical agreements at site for execution of batches as per customer requirement
V. Receive and distribute approval certificate, dossiers (TDP & RAP) and development report at unit for execution of new products smoothly
VI. Coordinate with auditors and site teams for regulatory and customer inspection/ audit at site to meet regulatory expectation and acquire GMP approvals
VII. Prepare final draft of compliance to audit observation and check whether it is in line with cGMP requirement to avoid regulatory action and continual improvements
VIII. Collect, compile and review raw data and finalise the same for timely submission of MHRA, UK interim update document to corporate as per agency requirement by tracking interim updates at a site level, for risk based inspection planning
IX. Drive continuous improvement initiatives in CQA to facilitate adherence to cGMP
X. Execute on time and errorless submissions by reviewing product license, all certificates for product registration and tender , staff approvals and other applications to adhere to legal requirements
XI. Support in CDSCO and state FDA inspection to be GMP compliant and getting product licence, FDA stall approvals by ensuring cross functional interaction
Education Qualification
B. Pharma/ M.Sc
Relevant Work Experience
2 years of experience in quality assurance department
TO APPLY CLICK HERE
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PRIMARY JOB FUNCTION:
Responsible for the process and systems related to the review of global advertising and promotional material across all of EPD and responsible for ensuring the accurate and detailed medical reviews of worldwide commercial advertising and promotional materials against supporting documentation including digital and social media material.
Responsible for providing medical and scientific writing for the support of Established Pharmaceutical Division (EPD) Global Products including global regulatory and safety documents; advertising and promotional review; and global medical information.
Serves as a conduit and facilitator of communication between Medical Affairs and Commercial, Global PV, Global Regulatory, and affiliate medical departments with respect to assigned brands and therapies.
Manage the development, approval, and maintenance of medical and technical information on EPD products. Provide medical information responses to unsolicited requests from internal (medical affairs, affiliates, and other global scientific colleagues) or external customers (healthcare professionals and consumers).
Drives timely medical assessments and due-diligence feedback for concrete in-licensing and acquisition opportunities.
Provides training to affiliates and other colleagues on medical information and medical review skills to support their business objectives.
Maintains systems and SharePoint sites related to global medical services activities.
Takes ownership of medical knowledge management across all geographies and levels in EPD.
Drives and manages the maintenance and further development of the Medical Knowledge Centre.
CORE JOB RESPONSIBILITIES:
Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
Performs timely and accurate medical review of advertising and promotional materials for designated complex therapeutic areas within EPD in accordance with established corporate, departmental, and regulatory guidelines, with recognition of legal ramifications.
Independently handles the interpretation of complex medical data and recommends and implements changes to cross-functional projects. Disseminates pertinent information to appropriate areas.
Accountable for providing medical and scientific opinion and reviews for regulatory and safety documents, in particular for requests from health care authorities. The deliverables, recommendations, actions, and decisions made by the incumbent are critical to assuring compliance with applicable regulatory standards as well as to safeguard Abbott’s marketed products.
Develops and reviews medical and technical responses on EPD products that summarize pertinent clinical information from multiple sources in an accurate and concise manner.
Serves as a conduit and facilitator of communication between Medical Affairs and Commercial, Global PV, Global Regulatory, and affiliate medical departments with respect to assigned brands.
Has solid understanding of adverse event reporting requirements and the impact of medical information and promotional review activities on Pharmacovigilance.
Provides on-boarding and training to new GMS team members on EPD products and GMS processes.
Independently handles the interpretation of complex medical data and recommends and implements changes to cross-functional projects.
Disseminates pertinent information to appropriate areas.
MINIMUM EDUCATION: Degree in Medicine, or Health Sciences Field, or Pharmacy Degree or equivalent
TO APPLY CLICK HERE
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Amneal Pharmaceuticals Walk in Interview on 10th January 2021(Sunday) for Manufacturing(OSD)
Requirement for Granulation & Encapsulation only
We are looking for competent, dynamic and motivated candidates for suitable positions in Manufacturing OSD (oral solid dosage) unit for our Ahmedabad SEZ Matoda Plant.
Note:
Date: 10th January,2021 (Sunday)
Timing: 8:30 AM to 2:00 PM
Venue:
Amneal Pharmaceuticals Pvt. Ltd.
Plot No 15,16,17 Pharmez
Village: Matoda
Sarkhej Bavla Road, Abad
Please find the Job details below :
For Manufacturing (OSD Encapsulation & Granulation)
Designation: For Officer/Sr. Officer/Executive/Operators
Qualification: B.Pharm/B.Sc/Diploma/ITI
Experience: 02 to 05 years
Desired profile:
Required Candidate profile
The candidate with good communication and inter personal skills, computer knowledge and exposure to cGMP/ GLP Knowledge and understanding of regulatory requirement is essential.
Note:
If you are unable to attend interview you can share cv on chandanid@amnealindia.com
With Regards
Chandani Daswani
Human Resources
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OPENINGS FOR B.TECH (CHEMICAL), M.SC (ORGANIC / ANALYTICAL) & B.PHARMACY
Dear Candidates,
Greetings from Hetero Labs Limited,
We have openings for B.Tech (chemical), M.Sc (Organic/Analytical) & B.Pharmacy Freshers.
Candidate should have good communication skills and also should have basic knowledge on Technical Services.
Candidate who are pass out in 2018/2019/2020 year only eligible.
Interested candidate can share their resumes to prasanth.v@heterodrugs.com
Preferable: Male Candidates Only, Age Limit : Below 27 Years. Applicable only Andhra Pradesh & Telangana Candidates
Job Location: Nakkapally-Visakhapatnam
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