Ipca Laboratories

Responsibilities 1. Roles & responsibilities are as a QC-Reviewer in chemical analysis section. 2. Review of followings but not limited to: Analytical Data of Raw material, In-process, Intermediates, Finished Products and Stability, Certificate of Analysis (COA), Analytical Method Transfer and Analytical Method Verification Data, Calibration records, Working standard qualification document

Requirements: Sound Knowledge and understanding regarding ICH Guidelines Sound Knowledge and understanding regarding Regulatory Guidelines for new DMF filings and DMF variations Knowledge in preparing NEW DMF , handling customer queries, responding to Agency queries on DMF Knowledge in technical documentation and customer support for DMF related activities Sound Knowledge and underst

Responsibilities 1. Roles & responsibilities are as a QC-officer in chemical analysis section during shift. 2. Sampling of Raw material,Intermediate and Finished Products. 3. Wet/ chemical analysis of In-process & intermediate samples received during shift. Also chemical analysis of Raw materials, Packaging materials, stability product and Finished Products after successful completion of t

Job description: Visual Inspection of incoming packing materials as per shade card or Master sample. Sampling of all kind of packing materials (primary, Secondary & tertiary) as per sampling plan at the time of arrival at factory. Testing / Inspection of PM as per Company approved SOP. Testing / Inspection of consumer Gift Items (CPI). Responsible to maintain raw data of tested PM and report

Job Responsibilities: Create quality measurements to track improvement in products Execute quality improvement testing and activities Develop quality assurance standards and company processes Adhere to industry quality and safety standards Ensure products meet customer expectations and demand Create reports documenting errors and issues for fixing Work closely with the developm

1 Preparing Preventive maintenance of plant equipment and carry out as per schedule. 2 To attain routine maintenance of plant as well as break down maintenance during shift. 3 Training of fitter ,utility operator as per schedule . 4 Manpower planning & Control. 5 Check and review SOP as per cGMP Requirement. 6 Preparing shift scheduled for Fitter Utility Operator & DM Water operator.

Responsibilities : Reports to the department Incharge. To transcribe the reports dictated. Ensuring quality of output with marginal or zero errors. Ensuring the documents is submitted on time to the consultant for signatures. To coordinate with the technicians if urgent reports are received. To give appointments for EEG/EMG. To coordinate with JMS if dictation required help in interpretat

Job Description: • Preparation, execution, compilation & review of Qualification re-qualification protocols. • Handling of master documents & Issuance of controlled documents i.e. Qualification/ re-qualification Documents, Cleaning Validation documents, Hold time study of drug products • Checking & Execution of documents/ activities i.e.,URS, DQ, FAT & SAT, Installation & operational qualificati

Job Responsibilities: Assess clients needs and present suitable promoted products Present product information and deliver product samples Communicate with and persuade targeted doctors to prescribe our products utilizing effective selling skills and performing cost-benefit analysis Attend sales meetings, conference calls, training sessions and symposium circuits Keep detailed records of all

Supervise and conduct research on various microbiological activities on a regular basis. • Maintain knowledge on various research methods and perform all manual operations on various supplies. • Develop and maintain validation in all protocols for various environmental controls. • Perform laboratory analysis on all materials after appropriate sterilization. • Perform tests on component samples

Job Description: Communication skills handle and greet visitors handling calls basic knowledge of computer problem solving skills

Key Responsibilities : • Ensuring timely submission of Travel and Hotel invoices. • Checking and processing the Travel and Hotel invoices as per defined guidelines. • Coordination with Field Staff, Booking Team, Accounts. • Punching Travel and Hotel invoices through SCM system. • Arrangement for necessary approvals as per defined protocol. • Ensuring timely payment to vendors. • Handling q

Responsibilities 1. Roles & responsibilities are as a QC-Reviewer in chemical analysis section. 2. Review of followings but not limited to: Analytical Data of Raw material, In-process, Intermediates, Finished Products and Stability, Certificate of Analysis (COA), Analytical Method Transfer and Analytical Method Verification Data, Calibration records, Working standard qualification document

Job description: Assisting in aggregated data reports preparation (periodic safety update reports (PSUR), addendum to clinical overview (ACO), risk management plans (RMPs). Maintain tracking systems and documentation for various pharmacovigilance processes and archiving as per Bluefish SOPs. Candidate Specifications Bachelor s degree in any life sciences or pharmaceutical sciences Knowledge

Responsibilities 1. Roles & responsibilities are as a QC-officer in chemical analysis section during shift. 2. Sampling of Raw material,Intermediate and Finished Products. 3. Wet/ chemical analysis of In-process & intermediate samples received during shift. Also chemical analysis of Raw materials, Packaging materials, stability product and Finished Products after successful completion of t