3 – 6 years
Not Disclosed
Jaipur,Rajasthan
Time and Venue
28 December – 29 December , 9.30 AM – 5.30 PM
F-118, PHARLADPURA , RIICO industrial Area , Sanganer , Jaipur ( Rajasthan) 302022 (View on map)
Contact – SANJAY PUROHIT ( 9871579672 )
Job description
Post – HPLC Operator/Chemist
Job Responsibilities & Description:
1. The successful candidate will have experience in high-performance liquid chromatography, and other associated techniques. In addition, responsibilities include analytical method development, cGMP method validation, method transfers, and method verifications. He/she must be able to independently design and perform experimental work on i- series HPLC 2050.
2. Independently perform hands-on experimental work utilizing high performance liquid and gas chromatography, and other associated analytical techniques
3. Develop, validate, and document analytical methods and operating procedures according to specific sample or testing requirements.
4. Prepare reagents, solutions, and standards as required.
5. Conduct routine performance qualification and maintenance of chromatography and other laboratory instrumentation as necessary to assure proper performance.
6. Participate in troubleshooting of analytical test methods and laboratory instruments.
7. Perform data analysis and interpretation and prepare well-written scientific reports.
8. Maintain appropriate documentation (records and lab notebooks) as required by SOPs.
9. Comply with all cGMP and safety requirements, laboratory SOPs, and company policies and procedures.
10. Qualify new instruments (IQ/OQ/PQ) and participate in software validation as necessary.
Job Qualifications:
B.SC./M.Sc. in Analytical Chemistry /organic/Inorganic/Food Tech/Food Science with Five to ten years of professional pharmaceutical chemistry/Ayurvedic/Food & supplements.
Significant experience in HPLC method development will be given preference.
The ability to self-motivate to a high level of productivity.
Excellent interpersonal, verbal, managerial, and written communication skills.
Proven analytical and chromatographic background in a method validation and method development role.
The ability to organize and coordinate a variety of complex tasks to achieve consistent and efficient production and delivery of high-quality laboratory work.
. • Experience with Good Manufacturing Practices (cGMP) and a regulated environment.
Critical thinking, problem solving and troubleshooting capabilities.
Experience with Experience in qualifying HPLC units for GMP analysis and software validations is mandatory.Role & responsibilities
Role: Pharmaceutical & Biotechnology – Other
Industry Type: Fitness & Wellness
Department: Research & Development
Employment Type: Full Time, Permanent
Role Category: Pharmaceutical & Biotechnology
Education
UG: BAMS in Ayurveda
PG: MS/M.Sc(Science) in Bio-Chemistry, Chemistry, Medical-MS/MD in Ayurveda
