Document processor Offres d'emploi - Vaughan, ON
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Document processor • vaughan on
Dernière mise à jour : il y a 4 jours
Permanent Full-Time Production Supervisor.Working hours from 09:00 to 17:00.Health benefits, Financial benefits, Other benefits.Secondary (high) school graduation certificate.Work must be completed...Voir plusDernière mise à jour : il y a plus de 30 jours
Job Title: Personal Support Worker (PSW) – Live-in Shift*.Location: Richmond Hill, ON, L4C 0Z3*.We are seeking a compassionate, reliable, and physically capable Personal Support Worker (PSW) for a ...Voir plusDernière mise à jour : il y a 13 jours
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Great Benefits – Full Time Permanent position.Install, calibrate, and maintain a wide range of instruments and control systems.Troubleshoot and repair electrical and mechanical issues in instrument...Voir plusDernière mise à jour : il y a plus de 30 jours
Our Center of Expertise and Major Projects division brings together the exceptional expertise and remarkable achievements of our Building and Civil & Mining divisions.This new entity embodies our p...Voir plusDernière mise à jour : il y a 4 jours
This Volunteer Placement is located in:.Open to Canadian Citizens and Permanent Residents of Canada only.Cuso International is on the lookout for a passionate individual eager to join the Volunteer...Voir plusDernière mise à jour : il y a 6 jours
Secondary (high) school graduation certificate.Read and interpret engineering drawings, blueprints, charts and tables.Repair machine tools and parts.Set up and adjust production machineries/tools.F...Voir plusDernière mise à jour : il y a 23 jours
Adecco is currently hiring a full-time.Distribution Centre and plant environment for our client in Bolton, ON.In this role, you will perform preventive and corrective maintenance on powered lift tr...Voir plusDernière mise à jour : il y a 4 jours
AFIMAC is a global leader in providing elite security, crisis management, and investigative solutions to a wide range of industries.We specialize in delivering reliable and cost-effective services,...Voir plusDernière mise à jour : il y a plus de 30 jours
A Better Life for Those at Home.We help people stay in their homes for as long as they choose, and our real talent is helping people Make Each Day Count.We are a company that puts People First and ...Voir plusDernière mise à jour : il y a plus de 30 jours This Volunteer Placement is located in:.Open to Canadian Citizens and Permanent Residents of Canada only.Cuso International is on the lookout for a passionate individual eager to join the Volunteer...Voir plusDernière mise à jour : il y a 6 jours 
Are you looking for a role that provides challenge, growth and developmental opportunities? Are you looking to support managing a multi-million dollar project? Take the leap and make your mark at P...Voir plusDernière mise à jour : il y a plus de 30 jours
HireArt is helping our client find an IT Operations Specialist to support the Technical Operations (TechOps) function within a real-time Fusion Center environment in Scottsdale, AZ.In this role, yo...Voir plusDernière mise à jour : il y a 9 jours
Heures de travail: 35 to 40 hours per week.Develop and implement a strategic blueprint to follow when deploying databases within their organization.Develop and maintain computer databases.Enact mea...Voir plusDernière mise à jour : il y a 13 jours
Production Supervisor
AX Pharmaceutical CorpVaughan, Ontario, CanadaTemps plein +1
Quick Apply
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Production Supervisor
AX Pharmaceutical CorpVaughan, Ontario, CanadaIl y a plus de 30 jours
Type de contrat
- Temps plein
- Permanent
- Quick Apply
Description de poste
Experience:
Additional information:
Transportation/travel information:
Work conditions and physical capabilities:
Personal suitability:
Benefits:
Financial benefits:
Other benefits:
Position: Permanent Full-Time Production Supervisor.
On site.
Salary: $42.50 hourly/40 hours per week.
Starts as soon as possible.
Working hours from 09:00 to 17:00.
Benefits: Health benefits, Financial benefits, Other benefits.
1 vacancy.
Overview:
On site.
Salary: $42.50 hourly/40 hours per week.
Starts as soon as possible.
Working hours from 09:00 to 17:00.
Benefits: Health benefits, Financial benefits, Other benefits.
1 vacancy.
Overview:
Languages: English.
Education:
- Secondary (high) school graduation certificate.
Experience:
2 years to less than 3 years.
On site.
Work must be completed at the physical location. There is no option to work remotely.
Responsibilities:
Tasks:
- Recommend measures to improve productivity.
- Resolve work problems, provide technical advice and recommend measures to improve productivity and product quality.
- Investigate deviations in yield associated with critical process steps , determine their impact or potential impact on the result quality of affected batches.
- Supervise, co-ordinate and schedule (and possibly review) activities of workers.
- Establish work schedules.
- Prepare production and other reports.
- Recommend measures to improve productivity and product quality.
- Provide information for maintenance plans to ensure that maintenance and production objectives are met.
- Co-ordinate work activities with other departments, including but not limited to:
- Review Batch Production Record, deviation, investigation and OOS reports before the batch is released by quality team.
- In charge of production documents control before quality team review and Health authorities on site audit.
- Coordinate with quality control team to qualify hoods and cleanrooms based on SOP, put air samples into cleanrooms, mapping the worst and best spot for microbial sampling.
- Train staff/workers in job duties, safety procedures and company policies, including but not limited to:
- Train and supervise operators to clean the hoods and cleanrooms based on approved and validated cleaning procedures from quality assurance team and document it.
- Train and supervise operators to sample from specific batch and document it into master batch record.
- Supervise operators for daily calibration of standard weights, scales and document it.
- Requisition or order materials, equipment and supplies.
- Set up machines and equipment.
- Good Manufacturing Practices (GMP), including but not limited to:
- Good knowledge of different APIs chemical structurer , density, particle size to determine the primary and secondary packing size.
- Knowledge of licensing regulations, including but not limited to:
- Proficient in ICH guidelines Q7 for Active Pharmaceutical Ingredients ( APIs ).
- Proficient in FDA eCFR 21 regulations for APIs.
- Proficient in Health Canada Drug Establishment License requirement for APIs sampling, re-labelling and re-packaging activities.
- Label, file and retrieve documents, including but not limited to:
- Verify all the critical information from master batch record during the re-packaging process.
- Document and report deviations from specifications and tolerances.
- Supervise and investigate any label damages, package damages, APIs spillage, document it and report to quality team for review.
Supervision:
- 3-4 people.
Additional information:
Security and safety:
- Criminal record check.
Transportation/travel information:
- Valid driver's licence.
Work conditions and physical capabilities:
- Attention to detail.
Personal suitability:
- Organized.
- Team player.
Benefits:
Health benefits:
- Dental plan.
- Health care plan.
Financial benefits:
- Registered Retirement Savings Plan (RRSP).
Other benefits:
- Deferred Profit Sharing Plan (DPSP).
- Free parking available.