Manufacturing Operator – Compression – USA

City:  New York, USA

Location: Central Islip, NY

Experience: 2 – 20 Years

Salary: As per Industry Standards.

Job Description

Job Summary:

This position is a Production Operator assigned to support Compression.  This is an hourly labourer 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.

The person should be able to operate Sejong & Cadmach compression machines independently (PREFERRED)

There are positions open for Compression, and these will be in either Morning Shifts or Evening Shift.
Morning Shift (7am – 3.30pm)
Evening shift (3pm – 11.30pm)

Job Responsibilities:

  • Persons 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 labelling as per BMR.
  • Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating the process.
  • Able to operate applicable equipment independently as per the 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 maintaining 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 a manufacturing schedule when needed.
  • Should maintain discipline and comply with company policies and procedures.
  • Should perform entire duties as communicated from 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/descent 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.

About the client:

The client is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, client has strengthened our leadership in India’s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.  The client employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Client’s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

Manufacturing Operator-Coating – USA

Location: New York, USA.

City: Central Islip, NY

Experience: 2 – 10 Years

Salary: As per Industry Standards.

Job Description:

Job Summary:

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 2 positions open for Evening shift (3pm – 11.30pm)

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.

About the client:

The client is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, client has strengthened our leadership in India’s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.  Client employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Client’s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

 

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Sr. Solution Architect- Java Microservice – USA

Location: Brentwood TN, USA

Experience: 12 – 15 Years

Salary: 
As per Industry Standards.

Key Skill: Java 8, Microservices.

Mandatory Skills: Java 8, Spring boot, Spring core, Hibernate, Microservices, Google Cloud Platform.

Desired Skills: Docker, Google Kubernetes Engine, Cloud DataFlow, Cloud Spanner, Kafka, Elastic search, Jenkins, GIT, JIRA.

Job Description:

  • 12+ years of professional experience in Java technology based application/product development with good solid understanding of Application Migration to Google Cloud platform.
  • Solid hands-on experience using Spring Boot, Spring Core, Spring Boot, Spring Cloud, Spring Integration, Hibernate, and Microservices.
  • Should have experience in writing & consuming REST API.
  • Good understanding with NoSQL such as Cassandra, Couchbase, Realm.
  • Experience in Design patterns, microservices.
  • Experience with Kafka, streaming.
  • Experience in multithreading and data structures.
  • Experience working on Docker containers.
  • Should be able to provide technical solutions to problems raised / arised in a product development.
  • Should be able to probe the technical solutions suggested and vet the aptness of the solution from a holistic perspective.
  • Play a senior role on the team to facilitate code reviews, interact effectively with senior Java team mates at Client slide.
  • A combination of Google certifications desired – Google Associate Cloud Engineer; Google Professional Cloud Architect.
  • Hands-on experience in Application Migration to Google Cloud Platform is preferred.
  • Need to have excellent communication skills (including English conversation skills), demonstrate excellent problem solving and critical thinking skills.
  • Agile product development experience is required.
  • Excellent team player with strong communication, interpersonal, presentation skills.
  • Experience in working with multi-location and offshore teams.
  • Good understanding of US HC, especially on RCM (revenue cycle management), clinicals (medications, orders, labs, etc) will be an added advantage.

About the Client:

The client has played a deep and meaningful role in accelerating technology innovation and shaping the way healthcare is delivered to patients. The Client is a specialist provider of healthcare technology services and solutions, with a strong presence across the globe. The client focuses on multiple areas of digital technology, such as Business Intelligence, mobility & IoT, Big Data, cloud computing, predictive analytics & data science. The client has won several awards such as the 2019 Innovators Award for the Best Value-Based Care Solution.

 

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