Alembic Pharmaceuticals Ltd

Supervises staff to produce manufactured products, and organizes and monitors workflow. Accomplishes manufacturing results by communicating job expectations; planning, monitoring, and appraising job results; coaching, counseling, and disciplining employees; and initiating, coordinating, and enforcing systems, policies, and procedures. Recruits, selects, onboards, trains, and mentors employees. M

Alembic Pharmaceuticals Limited (APL) is a renowned Indian pharmaceutical company that has a rich history dating back over 100 years. It was established in 1907 with the aim of developing and transforming the pharmaceutical and drug industry in the Indian subcontinent. Over the years, APL has become one of the leading pharmaceutical companies in India and has made significant contributions to the i

Roles and Responsibilities: • Build a talent pipeline of candidates through sourcing, networking, industry mapping, and headhunting among others. • Source relevant profiles from job portals, social media platforms, job boards, and professional networks. • Conduct an initial preliminary evaluation of the candidates through a telephonic/virtual interaction. • Conduct thorough pre-employment check

Alembic Pharma Jobs - Careers at Alembic Pharmaceuticals Company for both Freshers and experienced, Grab this careers opportunity in Alembic. Alembic Pharma Posting New jobs Vacancy frequently as per availability of vacant post, Here you can check eligibility criteria and qualification, experience required for the position, and Apply Online or Offline or by scheduled walk-in interview for these Pha

Alembic Pharmaceuticals Ltd (APL) has a history spanning more than a century. Alembic Pharmaceuticals Ltd was founded in 1907 with the goal of expanding and revolutionising the pharmaceutical and drug industry in the Indian subcontinent. It is now one of the top pharmaceutical firms in India.

Alembic Pharmaceuticals - Walk-In for Freshers Alembic Pharmaceuticals Limited, with an established presence in the Indian pharma industry has a proud, historical track record going back one hundred years. With a turnover in excess of Rs. 3000 crores today, Alembic Pharmaceuticals Limited is one of the leading API & Formulations manufacturing and marketing pharmaceutical company. We continue to

Description: Formulating and developing new long term and short term strategies for new and existing products. To develop creative and innovative promotional inputs to improve sales. Responsible for training and development of field staff and to impart technical knowledge to the field staff. To conduct market research activities and new product launches. Designing promotional inputs. Sales

Responsible to manage entire corrugation plant operation end-to-end. Knowledge in similar industry preferably from Paper/ Paper Board / Printing / Packaging industry/Auto-corrugation industry.

Your responsibilities and tasks: To be familiar with, and act in accordance with, all relevant health & safety management, legislation and company quality system rules, regulations and policies. Follow the Company's Quality Management System / Procedures / Processes in line with ISO 9001:2015 Quality Standards. To maintain a formalized set of procedures, work instructions / Procedures / SOPs and

Job Duties: Develops project objectives by reviewing project proposals and plans; conferring with management/Consultants Determines/Develops project specifications by studying design, requirements, and performance standards; completing technical studies; preparing cost estimates Provides timely engineering solutions to problems associated with project assignments Assist with Technical evaluat

Manage PPAP and quality process analysis for launch, cost reduction, quality improvement activities and efficiency improvement. Create and implement a HACCP plan and modify the GMP's used in the food production. Assist manufacturing processes and assure compliance to internal and/or external specifications and standards such as GMP and ISO regulations. Maintain inspection and test methods consis

A quality assurance documentation specialist reviews and verifies document records to ensure the documentation complies with regulations and internal quality control practices. As a quality assurance documentation specialist, your primary job is to maintain record archives, reviewing them for accuracy and relevance.

Candidates should have Knowledge in HPLC, GC with HS, UV, IR, Wet Lab analysis and other lab Instruments.

Roles and Responsibilities: Media receipt, preparation and reconciliation. Perform Microbial Limit Test of Product and Water. Water Sampling and Chemical analysis of Water. Perform Environment monitoring by active and passive method. Calibration of instrument of Microbiology section. Preparation of Trend data. Bacterial endotoxin test by Gel Clot Method and by Nexgen-pts. Perform method v

Perform visual inspections of finished products. Compile laboratory test data and perform appropriate analyses. Complete documentation needed to support testing procedures, including data capture forms, equipment logbooks, or inventory forms. Calibrate, validate, or maintain laboratory equipment. Participate in out-of-specification and failure investigations and recommend corrective actions. S

Equipment handling-Reactors, centrifuges, dryers, filters .ANFD · Batch Processing as per BMR. BMR / BPR filing during process area. · Maintaining Compliance as per GMP requirements. · Exposure in handling shift Operations. · Initiation, completion and filling of batch production records. · Ensuring the cleanliness of the manufacturing equipment as mentioned in the batch production

Switch on equipment at the start of shifts and switch off equipment at the end of shifts. • Initiate assign production task. • Schedule regular equipment and tool maintenance and schedule repairs when needed. • Order materials needed for production. • Evaluate staff performance and organize training as needed. • Evaluate the quality of end products. • Ensure that the workspace is clean and ne

Description: Preparation and review the dossier of as per current prescribed guidelines of the respective regulatory authority. Well versed with the guidelines of ICH and other regulatory. Preparation of documents for license application. Preparation of documents for COPP, FSC, and other legal documents including product permission Preparation of registration documents as per ACTD , CTD , co

Roles and Responsibilities Person should have knowledge in API synthesis. Exploratory Studies / Synthesis on Milligram to Gram scale level. Good Analytical interpretation skills. Scale-up activity for the developed molecules. Planning and assigning the work to the team members and ensuring the completeness regarding cGMP. Co-ordination with analytical department for the analysis.

Knowledge in Analytical Method Development and Characterisation using HPLC, GC, LCMS, GCMS, NMR , DSC, TGA, Raman Spectroscopy and XRD in drug substance and drug products. Knowledge in analytical method validations in GMP environment . Good knowledge of different guidelines and regulatory requirements, versed in different protocol and report preparations