Production Supervisor

2 days ago

Fredericton, New Brunswick, Canada SUN PHARMA Full time
Job Summary

As a key member of our production team, you will play a critical role in ensuring the smooth operation of our manufacturing facility. Your primary responsibility will be to oversee and manage the production operations, ensuring that all processes are followed in accordance with cGMP and SOP requirements.

Key Responsibilities
  • Coordinate and supervise daily/weekly manufacturing activities of production staff in assigned areas.
  • Work closely with other supervisors to set priorities and ensure task completion.
  • Prepare and train employees on manufacturing-related SOPs.
  • Ensure that processes and procedures are followed as per batch records, SOPs, and protocols, and quality specifications are met.
  • Oversee scale-up, exhibit, characterization, and validation batch execution, as well as cleaning verification/validation protocols.
  • Initiate events and investigations, and implement change controls as needed.
  • Apply expertise to solve standard and non-standard problems within the manufacturing area.
  • Work within budgetary/financial objectives, applying knowledge of profit drivers to work processes.
  • Resolve day-to-day or routine manufacturing problems using defined processes.
  • Work with the team to brainstorm solutions that contain the appropriate level of risk, and ensure that the team understands and supports the focus on operational excellence.
  • Effectively build alignment on difficult issues.
  • Follow DEA Controlled Substance SOPs and report any violations to management.
Work Environment

The ideal candidate will be able to work in a fast-paced manufacturing environment, with exposure to various chemicals, equipment, and processes. The physical demands of this role include standing, walking, sitting, and stooping, as well as the ability to lift and move up to approximately pounds.

Requirements
  • Minimum of four years of pharmaceutical manufacturing experience required.
  • 2-3+ years of experience, and a Master's Degree in Science or Engineering considered.
  • Extensive knowledge of granulation, blending/mixing, compression (AWC machines), coating, encapsulation equipment.
  • Able to work extended hours to achieve manufacturing schedule when required.
  • Builds confidence and respect of others through a positive and energizing style.
  • Demonstrated proficiency with MS Office applications.
  • Ability to work under pressure and meet tight deadlines.
  • Good problem-solving and decision-making skills.
  • Sound knowledge of cGMP's, SOP's, FDA guidelines, and safety regulations.
  • Demonstrated excellent communication: verbal, written, and presentation skills.
  • A self-starter with a hands-on approach and a can-do attitude.
  • The requirement for English language proficiency for this role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).

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