Curia (formerly AMRI) Job in United States – Supervisor, Shift; Manufacturing

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Job Description

Supervisor, Production; Manufacturing in Rensselaer, NY

Curia provides global research contracts and manufacturing services to the pharmaceutical and biotechnology industries.

The shift supervisor is responsible for manufacturing Bulk Chemicals/Pharmaceuticals and maintaining manufacturing equipment and facilities in accordance with cGMP guidelines and prescribed Standard Operating Procedures (SOP). The incumbent oversees the hourly production workforce ensuring strict compliance with manufacturing processes and work practices.

Join our talented workforce where a commitment to excellence and a customer-focused attitude is everything. We strive for excellence because our work has the power to improve patients’ lives with the pharmaceutical products we develop and manufacture.

Responsibilities

  • Oversees all appropriate shift personnel to meet business requirements.
  • Responsible for manufacturing all bulk chemical/pharmaceutical products described in the production schedule.
  • Develops work schedules for production technicians to meet production requirements.
  • Assists the construction supervisor in developing effective overtime plans to meet business needs.
  • Ensures that adequate supplies of raw materials, intermediates and factory supplies are available in the manufacturing area to meet requirementsof production. Responsible for the orderly storage and flow of materials within the manufacturing area.
  • Provides regular performance feedback to designated technicians and conducts annual performance reviews. Take corrective action when necessary.
  • Responsible for ensuring that the manufacturing area and production equipment are properly maintained.
  • Ensures all manufacturing operations are conducted in accordance with approved cGMPs, SOPs and manufacturing monographs.
  • Responsible for ensuring that all materials used in the manufacturing operation have been approved for use by authorized personnel and documented as such.
  • Assists in solving manufacturing problems and contributes to equipment operations when necessary.
  • Ensures all areas and equipment are cleaned and documented in accordance with existing SOP and factory policies.
  • Ensures that all documentation relating to the manufacturing operation (batch records, cleaning records, calibration records, equipment records, etc.) is complete and up to date.
  • Ensures all materials located in and out of manufacturing areas (raw materials, intermediates, finished products) are maintained, packaged, labeled in accordance with factory policies and that materials are properly weighed.
  • Ensures work practices in all areas of manufacturing are completed in accordance with factory health and safety policies. Maintain adequate supplies of safety equipment.
  • Responsible for complying with all government regulations, including safety regulations,environmental and FDA.
  • Reports and investigates unsafe practices/accidents at work.
  • Initiates and participates in hands-on training for technicians.
  • Manages the clauses of the current union/company contract.
  • Provides day-to-day leadership, enabling subordinates to communicate and effectively complete their tasks.
  • Communicates effectively at all levels within the company to ensure continuous operations, in relation to shift changes, pre-shift meeting, and effective written shift status reports.
  • Recommends and implements methods to increase the quality of products and/or services.
  • Participates in self-development activities and third-party training.
  • Completes the core production technician competency in the learning management system.
  • Displays safety awareness and safe work practices. Protect employees and visitors by maintaining a safe and clean work environment.

Qualifications

  • 5-10 years manufacturing experience required, preferably chemical or BioTech
  • Additional engineering degree but not required
  • Knowledge of SOP’s
  • Good leadership and communication skills

US employees of Curia Global Inc. and its subsidiaries (a “Company ”) must be fully vaccinated against the COVID-19 virus and provide the Company with proof of vaccination as a condition employment, except for US employees who apply for and qualify under the applicable disability law and religious accommodations of the COVID-19 vaccine mandate. a candidatethat receiving an offer of employment from the Company for a position as a US employee must provide proof of vaccination, or request and receive a disability or religious accommodation to which the applicant is entitled under applicable law, prior to the first day of work. or any earlier or later period specified by the Company in the offer letter. The Company is an equal opportunity employer and offers employment opportunities and makes employment decisions regardless of an individual’s disability or religion or on any other basis prohibited by applicable law.

All interested candidates must apply online. Curia is an equal opportunity employer, we value diversity and inclusion. Minorities/women/veterans/people with disabilities/sexual orientation/gender identity are encouraged to apply.


Company: Curia (formerly AMRI)

Vacancy Type: Full-time · Mid-Senior level 

Job Location: United States

Application Deadline: N/A

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