Pharma Jobs

Greetings from Unichem! We are looking for qualified and experienced candidates for our facility based at  Ghaziabad, Uttar Pradesh  (USFDA approved). Candidates possessing good communication skills and exposure in Quality Control Department are invited for interviews. Position: Officer/ Sr. Officer / Executive / Asst. Manager - Quality Control Position Overview: Knowledge of QC instruments like HPLC & GC). To Implement Good Laboratory Practices. Exposure of USFDA, MHRA, TGA, audits. Preparation of SOP & STP Exposure of LIMS, & ERP Software Experience: 5-10n yrs Location: Ghaziabad Qualification: M.Sc (Chemistry) or B Pharma If interested, then kindly share your resume on  manisha.upadhyay @unichemlabs.com We are looking for qualified and experienced candidates for our facility based at  Pithampur (Indore) . Candidates possessing good exposure of  API Facility  are invited for interviews. Officer - Quality Assurance Experience: 2-5 Years in API manufacturin

Greetings from Hetero!!! We are having an opening for the R&D Unit in multiple Departments. Department: Formulation Research Development (FR&D) Designation: T.RA/ Jr. RA Experience: 1-4 Years Qualification: M.Pharmacy (Pharmaceutics) Department: Packaging Development Designation: Asst. Manager/ Deputy Manager Experience: 08-12 years. Department: DQA (Formulation) Designation: Sr.Executive / Executive Experience: 05- 06 years. Note: QA formulation also Eligible Candidates who are interested can share their  CV's to the below-mentioned Mail id:  pavankumar.p@heterodrugs.com .

| WE ARE HIRING | AIXIAL is hiring and looking for different profiles for a permanent contract in several countries: 1.       Clinical Data Managers 2.       Regulatory Affairs Specialists 3.       Clinical Research Associates Don't hesitate to contact our teams and send us your resume at    drh@aixial.com

Greetings of the KRISHNAVENI PHARMA CONSULTANCY Jobs...!!! Immediate Openings for Departments: QC / QA / Production / R&D Location: Around Hyderabad Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc Experience: Freshers / 1-2 yrs No. of Vacancies:  45 Interested persons contact on Below Details Mobile: 9652169734, 9640950679, 8885637856, 9550606504, 9581679067, 040-48530335. Mail ID:  krishnavenipharmaconsultancy@gmail.com

An opportunity for B.Sc. / M.Sc. / B. Pharm / M. Pharm qualified candidates to join our State-of-art Manufacturing Sites (OSD) for the position of Officer / Senior Officer / Executive / Senior Executive. QC - HPLC Analyst B.Sc. / M.Sc. / B. Pharm / M. Pharm with 3 to 6 years hands-on experience of HPLC Handling, Qualification of Working Standard on HPLC, Calibration of HPLC. QC - LIMS Operation B.Sc. / M.Sc. / B. Pharm / M. Pharm with 3 to 6 years hands-on experience of LIMS Operation Handling, Master and Worksheet Creation. QC - Sampling B.Sc. / M.Sc. / B. Pharm / M. Pharm with 2 to 4 years of hands-on experience of Raw Material and Packing Material Sampling. QC - Stability Sample Management B.Sc. / M.Sc. / B. Pharm / M. Pharm with 4 to 7 years hands-on experience of Sample Management, Sample Withdrawal, Preparation Reports, Protocols, and Data Logger. For the positions, candidates should also have sound knowledge of cGMP documentation. Interested candidate

Fresher openings for Clinical Data Coordinators. Company: Imaging Endpoints Location: Multiple EDUCATION AND EXPERIENCE: Working knowledge and competence in using MS Office and internet applications required High school diploma required; Coordinator’s Degree preferred Data entry experience/competence required; exposure to electronic data capture for clinical trials preferred Working knowledge of medical terminology preferred Knowledge of clinical trials and/or healthcare industries preferred SKILLS: Must have great attention to detail and excellent oral and written communication skills Ability to excel in a team environment Must have the ability to multitask and work under pressure Must have strong time management and organizational skills. Prioritizing workload to the changing needs of the day to day business is a critical skill. Able to quickly and accurately assess the importance of a phone call, email, or document and take appropriate action to involve

Walk-In for HPLC Analyst - Quality Control Date & Time:  16th March - 21st March, 9 AM onwards Venue: Zenara Pharma Pvt. Ltd #83/B, 84 & 87-96, Phase III IDA Cherlapally Hyderabad-51, Near Indian Oil Corporation Key Responsibilities and Accountabilities: ·           Instrument Handling: Candidate should have exposure in handling HPLC, RS by HPLC and other instruments Experience:  2-3 years Must hold a regular degree in  M.Sc/ M.Pharm/ B.Pharm  from a reputed university Should have actively faced regulatory audits Timings:  9:00 AM to 3:00 PM Contact No. :  9701990968, 9701112983 Please carry your updated Resume, Passport size photograph, Aadhar copy and kindly share among your network of friends/colleagues

Statistical Programmer Job Description Your responsibilities: Your responsibilities include, but are not limited to: 1. Provide input as required at all meetings, discussions, and activities covering aspects of Statistical Reporting on trial level activities. 2. As required, make certain that documents and specifications are consistent and comply with company standards for specifications of analysis datasets, listings, summaries, figures and tables for phase I – IV clinical trials. 3. The program, according to specifications, analysis datasets, listings, tables, and figures for phase I-IV clinical trials and/or apply standard statistical methods (as Reporting Statistician in Phase I) to standardized PK study designs. 4. Track clinical trial milestones for ONC Biometrics deliverables. 5. Maintain records for all assigned deliverables including archiving of trial analysis and associated documentation. Comply with pre-defined project/study standards and s

Role: Clinical SAS Programmer Domain: Life Science Preferred Educational Qualification for the role: Graduate/Postgraduates/Bachelor’s or Master’s degree or equivalent in statistics, mathematics, engineering or computer-related subject Work Location: Mumbai Experience: 0 to 2 years’ relevant experience in SAS Programming in the clinical domain Good knowledge of Base SAS, SAS / STAT, SAS /Graph modules Experience and understanding of ICH GCP principles and clinical drug development process Exposure to macro development  knowledge of CDISC SDTM data mapping Good communication and presentation skills Responsibilities: Develop SAS® programs for tasks assigned by Lead Statistical Programmer. Perform development and validation of datasets, tables, listings, and figures. Prepare data derivation specifications as per the defined/ standards guidelines. Maintain a full understanding of study documentation. Understand and comply with ICH-GCP guidelines, core

Opening at Otsuka Pharmaceuticals India Pvt. Ltd, Ahmedabad (Large Volume Parenteral experience preferable) 1) For Production Manager  (only Large Volume Parenteral [LVP] experienced candidate will be preferred) Experience: 12 to 15 years Qualification:  B.Sc./M.Sc/D.Pharm./B.Pharm./M.Pharm. 2) For Production Executive  (only Large Volume Parenteral [LVP] experienced candidate will be preferred) Experience: 5 to 8 years Qualification:  B.Sc./M.Sc/D.Pharm./B.Pharm./M.Pharm . Interested candidates can share their resumes on  pooja.sharma@otsukapharma.in Thanks and regards, Team HRM

Openings for Fresher’s Company: Aspiro Pharma!!! Department: DQA (Developmental Quality Assurance) Qualification: B.Pharmacy/M.Sc-Chemistry Year of Pass: 2017, 18, 19 Date: 12th March 2020(Thursday) Time: 10AM-12PM Venue: Aspiro Pharma Limited Plot No-23, Survey No-321, Biotech Park Phase-III, Karakapatla(Vil) Markook(Mndl), Siddipet(Dist), Hyderabad. Regards, Vijay-HR

We have openings for experienced people in the Production department. Experience: 2 - 5 Years, Qualification: B. Pharmacy, M. Pharmacy, Work Location: Goa. Interested one can share profiles with their basic details (Total Experience, Present CTC, Expected CTC & Notice Period) to Eswar.r@glenmarkpharma.com