- Effectively demonstrates understanding of GMPs and how they apply to specific responsibilities.
- Practices safe work habits and adhere to TScan's safety procedures and guidelines.
- Follows verbal and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentation.
- Maintains cleanliness and orderliness of process area.
- Ensures production area is stocked with supplies.
- Performs batch record review, procedure revisions, and work order generation.
- Utilizes manufacturing knowledge to improve process operations and affect positive change.
- Supports in and or leads in Commissioning and Validation activities.
- Assists in the creation and revision of manufacturing documentation by providing input to technical composition of document.
- Maintain equipment operation through responsive troubleshooting, repairs and following operations guidelines.
- Document all production efforts in appropriate logs, forms, reports and databases.
- Maintains safe and clean work environment by following current good manufacturing practices (cGMP), and standard operating procedures; complying with legal regulations; monitoring environment.
- Enhance organizational reputation by striving to meet and exceed performance expectations.
- Identifies and assists in the corrective actions of processing related issues.
- Performs other related duties as assigned to meet departmental and Company objectives.
- Assists in the identification and implementation of continuous improvement opportunities.
- Uses ability to complete tasks in a compliant and safe manner.
- Adheres to all cGMPs, compliance/regulatory mandates and quality requirements.
- Associate's degree in science or BS in science
- MINIMUM of 5 years of experience in cleanrooms or manufacturing setting is required.
- Must be able to read, write and speak English fluently.
- Experience in reviewing and creating controlled documents.
- After safety training, must be able to perform required tasks in fully compliant manner.
- Must possess strong documentation and communication skills.
- Must be able to lift and transport (using carts or wheelies) packages weighing up to 5O pounds.
- Extensive walking throughout the facility will be required.
- Must be able to use a companyissued computer and have at least intermediate skills in Microsoft Word, Excel, Outlook, and PowerPoint programs needed to perform job.
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
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Lab Technician - Waltham, United States - Actalent
Description
:Responsibilities:
cell therapy, t cell, GMP, batch record, batch record review, biologics, tcr, validation, manufacturing technician, Lab Technician, Laboratory Technician, cell biology, flow cytometry
Top Skills Details:
cell therapy,t cell,GMP,batch record,batch record review,biologics,tcr,validation,manufacturing technician,Lab Technician,Laboratory Technician
Additional Skills & Qualifications:
Requirements:
Intermediate Level
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions.
We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market.
With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people.
DE&I are embedded into our culture through:
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
