Arshad Mulla Email & Phone Number

Hyderabad, In

Ikp Knowledge Park- Hyderabad- Telengana

• Conducts laboratory tests and performs tasks related to product formulation & analysis.• Record test results and identify inconsistencies.• Collaborate with other teams at the lab.• Maintain inventory and reorder items required for routine lab activities.• Assisting set up of equipment and liaison with vendors for repairs as required.• Ensure compliance to site EHS requirements.• Provide key insights to project teams during product development & evaluation.

Singapore

GMP & abiding and ensuring compliance to the Health, Safety & Environment policy. Ensure compliance with Pharmacopoeia/Group. Requirements /local and International authorities. Completion of all trainings assigned to individuals role. To ensure the integrity of data at workplace. To follow current Good Manufacturing Practices and Good Documentation Practice.Follow Standard Operating Procedures of Manufacturing and their documents. Maintain cleanliness in the work area, equipment and Machine. To allot & follow up of work as per plan. Co-ordination with cross-functional department. Provide training to new joining associate.Follow the procedure of miscellaneous material at the time receiving and handling the material. To supervise the work as per allocated job in respective department as per Production norms and Quality norms adhering to Good Manufacturing Practices. Plan & procure the material as per daily production requirement. Executing Electronic Batch Manufacturing records MES Maintain the shop floor records; carry out in process checks and record. Co-ordination with engineering department for various maintenance activities. To maintain & ensure compliance at shop floor. To handle associates in the shift, their work allocation & target allocation for the shift. To prepare protocol reports for deviations, quality events & for track wise actions. To conduct trainings of associates at shop floor.Change control, Quality Event and deviation handling as per SOP. To raise CR and Deviation in track wise and support in investigation and implementation of CAPA.

Mumbai, Maharashtra, India

Plan, organize and oversee all activities related to the manufacturing of tablets and capsules to include delivery, in-process, and finished product samples in a defined schedule.Provide daily supervision and support to the operators in regarding day-to-day production activities such as trouble shooting and other work tasks.Manage performance and train assigned employees using Company systems, procedures, policies, practices, and other tools to meet established performance standards, productivity targets, and overall business requirements.Review and compile the documents generated during production like batch manufacturing records and validation protocols.Initiate and review written procedures such as standard operating procedures (SOPs), operating instructions, cleaning procedures, safety procedures, and other work procedures as needed.Ensure compliance with safety, quality, productivity, and established job performance standards.Effective implementation of current good manufacturing practices (cGMP) and safety practices.Coordinate with departments such as Quality Assurance (QA), Quality Control (QC), Research & Development (R&D), Maintenance & Engineering, Supply Chain and Warehousing, Human Resources, and other internal functional partners to ensure the completion of work and achieving production targets and objectives.Work with Integrated Product Development (IPD)/R&D on the execution of bio-batches (abbreviated new drug applications - ANDA) and validation batches.Perform any other work or job assignments as allocated and required by management.

Navi Mumbai

Execute production activities in a shift by managing available resources to achieve production target.Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality.Prepare manufacturing records and update online documentation to meet production and cGMP requirements.Follow safe work processes and ensure safety appliances are utilized during production activities in shifts to create a safe working environment.

Navi Mumbai, Maharashtra, India

Supervise Granulation & Compression activities.

Navi Mumbai, Maharashtra, India

Supervise Ointment manufacturing activities.

Bachelor Of Pharmacy - Bpharm, Pharmacy, First Class

Education record