Careers
Career with Us
Would you like to be a part of an organization that is devoted to excellence in quality and uncompromising integrity in its service? If yes, read on. In our fervor to realize our vision, we are looking for talented, experienced professionals who have a taste for excellence and who never want to stop learning. As a multi disciplinary scientific organization, Jansat gives its people an experience in a variety of scientific fields. We encourage our people to constantly improve their knowledge and skills and to this end we conduct ongoing training programs in various ways. Jansat Labs is an equal opportunity employer and provides excellent working environment with competitive salaries commensurate with experience and education.
Jansat Labs is an equal opportunity employer and provides excellent working environment with competitive salaries commensurate with experience and education.
Our current career opportunities:
Do you have experience of Method Development and Validation using LC/MS?
Would you like to work for a growing Pharmaceutical company?We are a leading pharmaceutical analytical organisation in Hyderabad, with a friendly and high performing analytical team.
Working as part of the ARD team the Sr. Research Associate / Research Associate - Pharmaceuticals will perform a key laboratory based role in the chemical analysis of raw materials, intermediates and finished pharmaceutical products according to GMP / GLP standards.
In addition the Sr. Research Associate / Research Associate - Pharmaceuticals will undertake regular method development and method validation to GMP and ICH guidelines.
In this role you will work closely with the Quality Assurance department to ensure ongoing product quality and adherence to FDA/MHRA guidelines and the internal Quality Management System.
The role of Sr. Research Associate / Research Associate - Pharmaceuticals will involve a variety of tasks including: Analysis of samples using HPLC, LCMS, IC, UV/VIS, GC and other analytical chemistry test methodologies. Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting.
Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols.
Training and development of less experienced analytical staff as and when required.
To be considered you must have the following skills and experience.
Previous experience of working within a GMP or GLP pharmaceutical analytical chemistry laboratory.
Previous experience of running analytical techniques such as HPLC, LC, LC/MS and IC with the ability to extract and prep various samples in a variety of forms.
A BSc, B.Pharm, M.Pharm, MSc a relevant chemical science (or have equivalent laboratory experience).
As this role involves liaising with other departments on a regular basis, you will need good communication skills and the ability to work effectively as part of a team.
Interested Candidates can drop your CV at info@jansatlabs.comThe Systems Administrator is responsible for the administration of laboratory system software to meet end-user needs and regulatory expectations (21 CFR Part 11 and cGMP), and established SOP’s
To perform this position successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required:
⦁ Shall adhere to all applicable regulatory requirements, including FDA, EPA, OSHA, and related safety, health and environmental procedures, policies and practices.
⦁ Consistent support and practice of all Jansat Labs mission, vision, and values.
⦁ Identify and protect the original technical information as part of the company property.
KEY RESPONSIBILITIES.1. Perform all duties as administrator, on-going configuration and improvements, develop custom reports, troubleshooting, and maintenance in conjunction with QA.
2. Administer analytical laboratory software systems, including the Empower3 FR4, for GC, HPLC, and Analyst for LCMS systems and other softwares for back-up and archiving of analytical data.
3. Collaborate with vendors on upgrades and improvements. Install and validate new software revisions as they are released. Partner with the AS laboratory staff for troubleshooting.
4. Lead and coordinate technical issue investigations and manage technology resolution implementations.
5. Actively participate on change control by following procedures and work instructions.
6. Develop SOP’s and policies for laboratory computers and IT.
7. Stay up to date on advances in the software and technology; provide appropriate training to new and current employees as needed.
Qualifications1. Diploma/Bachelor’s degree in Chemistry or life sciences. A minor in computer sciences is helpful.
2. Three (3) to five (5) years’ experience in laboratory operations, LIMS administration, chromatography data systems, or equivalent training and experience.
3. Knowledge of cGMP, 21 CFR Part 11, and computer system validation (GAMP) is a plus.
JOB COMPETENCIES1. Excellent written and oral communication. Present and train relevant information to all levels within the company.
2. Ability to adapt to and thrive in a dynamic work environment and cooperate with employees and clients from a broad range of disciplines and subject-level expertise.
3. Proficiency in computer applications (Microsoft Office, ERP, etc.)
Interested Candidates can drop your CV at info@jansatlabs.com