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Production Supervisor
3 weeks ago
Fredericton, New Brunswick, Canada SUN PHARMA Full timeJob SummaryAs 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 individual will be responsible for managing and documenting manufacturing and packaging operations, as well as supervising team leads and operators. The ideal candidate will have a strong...
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Production Supervisor
3 weeks ago
Fredericton, New Brunswick, Canada SUN PHARMA Full timeJob SummaryAs 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 individual will be responsible for managing and documenting manufacturing and packaging operations, as well as overseeing the work of Team Leads and Operators. The successful candidate...
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Production Supervisor
3 weeks ago
Fredericton, New Brunswick, Canada SUN PHARMA Full timeJob SummaryAs 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...
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Production Supervisor
3 weeks ago
Fredericton, New Brunswick, Canada Baie Ste Anne Seafoods (2014) Inc. Full timeJob Title: Production Supervisor - Fish PlantJob Summary: We are seeking a highly skilled Production Supervisor to join our team at Baie Ste Anne Seafoods (2014) Inc. The successful candidate will be responsible for supervising and coordinating the activities of workers in the fish plant, ensuring the efficient production of high-quality products.Key...
Production Supervisor
2 months ago
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 carried out 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 adherence to batch records, SOPs, and protocols to meet quality specifications.
- Oversee scale-up, exhibit, characterization, and validation batch execution, as well as cleaning verification/validation protocols.
- Initiate event/investigations and 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.
- Collaborate with the work team to provide suggestions for solutions that contain the appropriate level of risk.
- Effectively build alignment on difficult issues.
- Follow DEA Controlled Substance SOPs and report any violations to the Manager.
The ideal candidate will be comfortable working in a manufacturing/production/laboratory environment, with exposure to various environmental conditions, including noise, fumes, odors, gases, and dust.
Physical RequirementsThe physical demands of this role include standing, walking, sitting, stooping, kneeling, crouching, crawling, pushing, and bending. The ability to lift, move, and/or carry up to approximately pounds is also required.
Education and Qualifications- Minimum of High School/Trade School/Vocational School Diploma, GED, or equivalent; B.S. in a related field preferred.
- Extensive knowledge of granulation, blending/mixing, compression (AWC machines), coating, encapsulation equipment.
- Able to work extended hours to achieve manufacturing schedules 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).
- Minimum of four years of pharmaceutical manufacturing experience required.
- 2-3+ years of experience, and a Master's Degree in Science or Engineering considered.