Responsible for the sanitation and organization of all equipment, machinery and utensils used in the production process as well as the cleanliness of the plant and external premises while providing hands-on leadership.
Compensation
Competitive Compensation, Health Benefits, & a generous flexible medical / Health spending account
RRSP matching program
Tuition reimbursement
Discount program that covers almost everything under the sun - Restaurants, gyms, shopping etc.
Responsibilities
Leads by example and fosters an environment of mutual respect and team work among Team Members
Understands and fulfills the duties of a leader of the following programs within the production area: Good Manufacturing Practices (GMP’s), All food safety programs, All health & safety programs, All FGF policies, programs or procedures
Leads, coaches, mentors and trains Sanitation Team Members
Coordinates all sanitation activities to accomplish sanitation practices according to Sanitation Standard Operating Procedures (SSOP’s)
Maintains daily, weekly, and monthly sanitation records
Safely manufactures high quality pharmaceutical products according to established schedules.
Responsibilities
Process/manufacture products in accordance with written processing orders
Prepare manufacturing areas and equipment for the production of pharmaceutical products
Clean processing equipment and rooms in accordance with written Standard Operating Procedures (SOPs) and established Good Manufacturing Practices (GMP)
Provide assistance and training to Processing Technologist I
Effectively troubleshoot equipment they are trained on
Requirements
High school diploma/General Educational Development (GED) Certificate
Safely manufactures high quality pharmaceutical products according to established schedules.
Responsibilities
Process/manufacture products in accordance with written processing orders
Prepare manufacturing areas and equipment for the production of pharmaceutical products
Clean processing equipment and rooms in accordance with written Standard Operating Procedures (SOPs) and established Good Manufacturing Practices (GMP)
Provide assistance and training to Processing Technologist I
Effectively troubleshoot equipment they are trained on
Lead device engineering activities ensuring medical devices and drug/device combination products meet intended function and regulatory compliance.
Compensation
The annual base salary for this position ranges from $82,700.00 to $137,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary.
Responsibilities
Partner with Systems engineers in defining product requirements
Develop test fixtures, methods, and perform Test Method Validation activities
Coordinate with internal and external partners to procure test samples and manage conditioning and accelerated aging studies
Ensure integrity and compliance of data according to Standard Operating Procedures
Develop Verification Plans including test strategy
The Lab Support Specialist Microbiologie QC plays a key role in the microbiological laboratory, ensuring daily activities are efficient, safe, and compliant with GMP guidelines, supporting microbiological analysts in timely analysis execution.
Compensation
Competitief salaris afhankelijk van je kennis en ervaring.
Responsibilities
Signaleren, registreren, onderzoeken en opvolgen van afwijkingen, inclusief het coördineren van benodigde acties conform GMP-procedures.
Ondersteunen bij het uitvoeren van root cause analyses en het implementeren van correctieve en preventieve maatregelen (CAPA’s).
Opstellen, bewaken en optimaliseren van de laboratoriumplanning om een tijdige uitvoering van microbiologische analyses te waarborgen.
Beheren van laboratoriumvoorraden en verzorgen van bestellingen van reagentia, verbruiksmaterialen en overige laboratoriumbenodigdheden.
Coördineren en ondersteunen van de dagelijkse operationele activiteiten binnen het microbiologisch laboratorium.
Requirements
afgeronde mbo-opleiding in microbiologie, laboratoriumtechniek of een vergelijkbare studie
The SSO Operations Specialist will provide hands on assistance for daily production activities while ensuring compliance with Safety & Environmental (S&E) and current Good Manufacturing Practices (cGMPs) requirements to meet SSO objectives and customer requirements.
Locations (3)
Rahway, New Jersey, United States
San Francisco, California, United States
Los Angeles, California, United States
Compensation
The salary range for the primary location of this role is: $71,900.00 - $113,200.00
Responsibilities
participate in equipment setups
raw material sampling and subdivisions
solution preparations
batch processing planning and execution at a pilot scale
Independently operate and maintain at least one process, equipment or systems following autonomous maintenance (AM) standards and use technical skills to improve line and/or system performance to meet business needs.
Compensation
The hourly wage for this position is $24.74/hr. In addition, this position offers an annual incentive program of a target of 5% of your salary.
Responsibilities
Operate and maintain production equipment(s) as per standard
Operate in line with the site HSE and Quality Assurance guidelines
Perform basic trouble shooting and problem solving after required training and qualification
Cleaning and maintenance of equipment while following all Good Manufacturing Practice principles
Requirements
High School diploma or equivalent
Nice to have: Experience in a manufacturing or food production environment
Operate and maintain production equipment to deliver on safety, quality, cost, delivery, sustainability and morale targets within a fast-paced manufacturing environment.
Locations (4)
Indianapolis, Indiana, United States
Toronto, Ontario, Canada
Montreal, Quebec, Canada
East Hanover, New Jersey, United States
Compensation
The hourly wage for this position is $24.74/hr. In addition, this position offers an annual incentive program of a target of 5% of your salary.
Responsibilities
Operate and maintain production equipment(s) as per standard
Operate in line with the site HSE and Quality Assurance guidelines
Lead and support new product development, product trials, specifications management, food safety compliance, and technical support within a fast-paced food manufacturing environment.
Responsibilities
Coordinate and manage product trials, including planning, scheduling, execution, and communication with customers and internal stakeholders.
Provide technical guidance and support to the New Product Development (NPD) team throughout the development process.
Develop, review, and maintain recipes, job cards, specifications, assembly sheets, and technical documentation.
Ensure all trial outcomes, validation requirements, yields, nutritional data, shelf-life testing, and process improvements are documented and incorporated into product development processes.
Associate in Applied Science (ideally in Process Technology)
higher degree in a relevant technical field of study
High School Diploma/GED plus at least four (4) years of relevant experience in Pharmaceutical, Chemical, Petrochemical or Food Processing/Manufacturing
Nice to have: Operations experience in pilot plant or manufacturing environment
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