PhD Pharmaceutical Sciences, Chemistry, Biochemistry a relevant branch of Engineering Industrial Experience min. 1 year in Formulation department of any Pharmaceutical company

M.Sc, M. Pharma, B. Pharma. Analytical methods validation, verification and methods transfer. Validation of cleaning methods. Handling HPLC, GC, DR and other instruments. Preparing method validation verification protocol and report. Reviewing analytical hard copy and electronics data.

Support Established Products technical functions in MEAP and APAC region for Abbott manufacturing facilities and TPMs. Provide technical support to cross-functional teams during test method development, validation, transfer, or problem solving for a given drug product primarily of Biosimilars & Injectables.

Environmental monitoring  Media fill visual inspection  Aseptic area monitoring  Handling of media fill activity  Aseptic area personal qualification

Effectively generate new business leads and opportunities from various sources and engage through proper prospecting, email campaigns, cold-calling and regular follow-ups

As an Associate Regulatory Affairs Director I, you will be a key contributor to regulatory submission strategy, identifying submission risks and opportunities. You will lead regulatory applications and manage procedures through approval.

Leading study setup, including TF design, database structure, specification, and obtaining and providing approvals as needed. Coordinating and documenting the receipt and processing of electronic or ancillary data received from outside sources

Applications are invited from the eligible candidates for filling up of various categories of posts in Urban Clinics/UPHCs under NUHM in Erstwhile Guntur District.

Vacancy for the post of Principal, Professor, Associate Professor, Assistant Professor, Lecturer and Lab Technician in Sardar Patel College of Pharmacy, Gorakhpur U.P.

Masters in Virology, Microbiology, Biotechnology , Biochemistry, Bioinformatics , Life Sciences, Genetics, Stem cell from a recognised institution with first class aggregate

Diploma in Integrated Pharmacy D.I.P Two years. For certificate issued by Government of Tamil nadu Only.

Masters in pharmaceutical analysis, analytical chemistry, medicinal chemistry, Biochemistry, Biotechnology or equivalent with at least one year of hands-on experience

Seasoned experience in handling of various EU procedure like DCP, MRP, National. National phase handling for EU procedures. Post approval variation compilation and filling to various EU agencies

Knowledge of microbial testing for injectable products and environmental monitoring for sterile manufacturing area. Knowledge of instruments & equipment, method validations, finished dosage and RM testing

Promptly notify and escalate to JAMP headquarters quality department any potential quality or regulatory issues that may affect product quality or regulatory compliance

Candidates with AR&D experience and are interested for QC Position will also be Consider. Candidates who has thorough knowledge in handling HPLC, GC instruments independently only should attend the interview.

Looking for candidates with relevant experience in OSD & Injectable regulated manufacturing plant

M.Pharm, B.Pharm, M.Sc, B.Sc; Responsible for accurate production and packaging changeovers as per packaging schedule. Maintain a clean work area and clean equipment before and after shift.