Production Supervisor

4 weeks ago

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

As a key member of the SUN PHARMA team, the Production Supervisor will play a critical role in ensuring the smooth operation of our manufacturing facility. This position requires a strong leader who can manage and document manufacturing and packaging operations in accordance with cGMP and SOP requirements. The successful candidate will be responsible for supervising team leads and operators, conducting regular checks on documents, and taking corrective actions to prevent deviations. Additionally, they will ensure that target production numbers are met on a daily basis and cGMP documents are completed in a timely manner.

Responsibilities

Coordinate and supervise daily/weekly manufacturing activities of production staff in assigned areas
Coordinate work activities with other supervisors and set priorities for the team to ensure task completion
Prepare and train employees on manufacturing-related SOPs
Ensure 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/investigations and change controls
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/brainstorm with the work team and provide suggestions for solutions that contain the appropriate level of risk; ensure the work 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 the Manager

Work Conditions

Manufacturing/production/laboratory environment
Environmental conditions related to manufacturing/production/laboratory environments:
Noise: sufficient noise to cause marked distraction or possible injury to the sense of hearing
Fumes: smoky or vaporous emissions, usually odorous, thrown off as the result of combustion or chemical reaction
Odors: unpleasant smells
Gases: examples include carbon monoxide and helium
Dust: airborne particles of any kind, such as textile dust, wood, and silica
Hazards: conditions where there is danger to life, health, or bodily injury, such as closeness to moving mechanical parts; working on scaffolding and high places; exposure to burns, radiant energy, explosives, toxic chemicals, and electric shock

Physical Requirements

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job
While performing the duties of this job, the employee is regularly required to use hands to handle or feel and talk or hear
The employee is frequently required to stand, walk, sit, and stoop, kneel, crouch, crawl, push, and bend
Must be capable of bending and lifting, moving and/or carrying up to approximately 50-75 pounds
Must have the ability to navigate office, lab, warehouse, and/or plant floor working environments, stand, ambulate, and reach
Must have the ability to wear applicable personal protective equipment utilized at the site, including but not limited to respirators, safety glasses/goggles, and safety shoes

Travel Estimate

Up to 0%

Education and Job Qualification

Minimum of High School/Trade School/Vocational School Diploma, GED, or equivalent; B.S. in related field preferred
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 job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR)

Experience

Minimum of four years of pharmaceutical manufacturing experience required
2-3+ years of experience, and a Master's Degree in Science or Engineering considered

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