URGENT OPENINGS IN USA MARKET FOR PHARMA/ BIO-TECHNOLOGY/ CLINICAL RESEARCH INDUSTRIES.....

CONTACT ON---- amlendubhushan1982@gmail.com, amlendubhushan2@gmail.com MOBILE-------- +91-8404957878 Please check the below requirements for US Market urgent positions. Regards. HAVE ALSO ATTACHED A SHEET THAT NEEDS TO BE FILLED AND SHARED ALONG WITH THE RESUME Kindly find the JD for the profile. Kindly Make sure that no details ( company name, Salary etc) of the position should be uploaded on the social networking sites because these positions are very confidential. These instructions should be strictly followed as told by our client. The time limit for sharing the CV will for 3-4 Working days. REQUIREMENT 1 Please find JD for Encapsulation Operator - CAPSULE FILLING Experience: 2-10 Year Work Location: Central islip, New York, USA Supplier Commission : 400USD Qualification: Graduate Domain: Pharmaceuticals/Biotechnology/Clinical Research Positions: 3 Openings 4.ONLY US citizens/ Green Card holders will be processed. 5. NO POACH with Torrent Pharma. JD: This position is a Production Operator assigned to support capsule filling. This is an hourly laborer and individual contributor role that will report to a Front-Line Supervisor. This position may be based at the Company’s manufacturing units in Hauppauge or Central Islip, New York. Person should be able to operate AF90T & ZRO200 from ACG PAM independently There are 3 positions open for Encapsulation. 1 positions open for the Morning Shift (7am - 3.30pm) 2 positions open for the Evening shift (3pm - 11.30pm) Please confirm and mention what shift is preferred. Job Responsibilities: Person should be able to operate AF90T & ZRO200 from ACG PAM independently Execute manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements. Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time. Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms. Ensure line clearance before initiating manufacturing activities in each area. Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR. Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating process. Able to operate applicable equipment independently as per area of operation. Troubleshoot and make appropriate adjustments to equipment to maintain product/BMR specifications. Ensure adherence to quality standards during all stages of the manufacturing process. Complete manufacturing documents on time, ensuring accuracy and completeness. Responsible for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process. Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals. Flexible to work extended hours, to achieve manufacturing schedule when needed. Should maintain discipline and comply with company policies and procedures. Should perform entire duties as communicated time to time by department management/designee. Minimum Requirements: Solid mechanical aptitude. Minimum of 2 years of experience working in industrial environments such as pharmaceutical manufacturing and related settings. Must have excellent communication skills. Must be able to clearly communicate in English (verbally and in writing). Positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors. Must be able to work different shifts as per organizational requirement and should be flexible for working additional hours such as overtime and weekends. Physical Requirements Should not have any restriction to work with powder containing active pharmaceutical ingredients. This position requires the ability to do heavy lifting / bending frequently. Long periods of standing up/walking during the working hours; ability to ascent/decent ladders; and able to lift to 35 pounds. Must be able to move pallets/equipment weighing about 200 – 300 kgs using suitable moving equipment like pallet jacks. REQUIREMENT 2 Please find JD for Manufacturing Operator - COATINGS Experience: 2-10 Year Work Location: Central islip, New York, USA Supplier Commission : 200USD Qualification: Graduate Domain: Pharmaceuticals/Biotechnology/Clinical Research Positions: 6 Openings 4.ONLY US citizens/ Green Card holders will be processed. 5. NO POACH with Torrent Pharma. JD: This position is a Production Operator assigned to support coating. This is an hourly laborer and individual contributor role that will report to a Front-Line Supervisor. This position may be based at the Company’s manufacturing units in Hauppauge or Central Islip, New York. Person should be able to operate Neocota, Xiaolun coating pans independently There are 6 positions open for Coating 4 positions open for the Morning Shift (7am - 3.30pm) 2 positions open for the Evening shift (3pm - 11.30pm) Please confirm and mention what shift is preferred. Job Responsibilities: • Person should be able to operate Neocota, Xiaolun coating pans independently • Execute manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements. • Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time. • Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms. • Ensure line clearance before initiating manufacturing activities in each area. • Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR. • Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating process. • Able to operate applicable equipment independently as per area of operation. • Troubleshoot and make appropriate adjustments to equipment to maintain product/BMR specifications. • Ensure adherence to quality standards during all stages of the manufacturing process. • Complete manufacturing documents on time, ensuring accuracy and completeness. • Responsible for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process. • Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals. • Flexible to work extended hours, to achieve manufacturing schedule when needed. • Should maintain discipline and comply with company policies and procedures. • Should perform entire duties as communicated time to time by department management/designee. Minimum Requirements: • Solid mechanical aptitude. • Minimum of 2 years of experience working in industrial environments such as pharmaceutical manufacturing and related settings. • Must have excellent communication skills. • Must be able to clearly communicate in English (verbally and in writing). • Positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors. • Must be able to work different shifts as per organizational requirement and should be flexible for working additional hours such as overtime and weekends. Physical Requirements • Should not have any restriction to work with powder containing active pharmaceutical ingredients. • This position requires the ability to do heavy lifting / bending frequently. • Long periods of standing up/walking during the working hours; ability to ascent/decent ladders; and able to lift to 35 pounds. • Must be able to move pallets/equipment weighing about 200 – 300 kgs using suitable moving equipment like pallet jacks. REQUIREMENT 3 Please find JD for Manufacturing Operator - COMPRESSION Experience: 2-20 Year Work Location: Central islip, New York, USA Supplier Commission : 300USD Qualification: Graduate Domain: Pharmaceuticals/Biotechnology/Clinical Research Positions: 16 Openings 4.ONLY US citizens/ Green Card holders will be processed. 5. NO POACH with Torrent Pharma. JD: This position is a Production Operator assigned to support Compression. This is an hourly laborer and individual contributor role that will report to a Front-Line Supervisor. This position may be based at the Company’s manufacturing units in Hauppauge or Central Islip, New York. Person should be able to operate Sejong&Cadmach compression machines independently (PREFERRED) There are 16 positions open for Compression, and these will be in either Morning Shifts. 8 positions open for the Morning Shift (7am - 3.30pm) 8 positions open for the Evening shift (3pm - 11.30pm) Please confirm and mention what shift is preferred. Also mention which facility is preferred. Job Responsibilities: Person should be able to operate Sejong&Cadmach compression machines independently (PREFERRED) Execute manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements. Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time. Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms. Ensure line clearance before initiating manufacturing activities in each area. Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR. Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating process. Able to operate applicable equipment independently as per area of operation. Troubleshoot and make appropriate adjustments to equipment to maintain product/BMR specifications. Ensure adherence to quality standards during all stages of the manufacturing process. Complete manufacturing documents on time, ensuring accuracy and completeness. Responsible for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process. Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals. Flexible to work extended hours, to achieve manufacturing schedule when needed. Should maintain discipline and comply with company policies and procedures. Should perform entire duties as communicated time to time by department management/designee. Minimum Requirements: Solid mechanical aptitude. Minimum of 2 years of experience working in industrial environments such as pharmaceutical manufacturing and related settings. Must have excellent communication skills. Must be able to clearly communicate in English (verbally and in writing). Positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors. Must be able to work different shifts as per organizational requirement and should be flexible for working additional hours such as overtime and weekends. Physical Requirements: Should not have any restriction to work with powder containing active pharmaceutical ingredients. This position requires the ability to do heavy lifting / bending frequently. Long periods of standing up/walking during the working hours; ability to ascent/decent ladders; and able to lift to 35 pounds. Must be able to move pallets/equipment weighing about 200 – 300 kgs using suitable moving equipment like pallet jacks. Attachments area AMLENDU BHUSHAN 9:41 PM (11 minutes ago) These all are permanent positions not contractual one.