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Manager Aseptic Processing Jobs in Fall River, MA

Jobtailor

Principal Engineer - R&D

Bridgewater, MA · On-site

$150 - $190/hr

Support the aseptic late differentiation technology development. * Drive the development of processes and manage the planning and execution in accordance with the project brief. * Coach junior ...

Amgen, Inc.

Associate Manufacturing I

West Greenwich, RI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... aseptic processing, etc. * Knowledge of Single-use Systems * CFR and Regulatory knowledge ... Able to demonstrate project management skills and presentation skills * Ability to understand ...

Amgen

Associate Manufacturing - Nights

West Greenwich, RI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... aseptic processing, etc. * Knowledge of Single-use-Systems * CFR and Regulatory knowledge ... Able to demonstrate project management skills and presentation skills * Ability to understand ...

Amgen, Inc.

Associate Mfg I

West Greenwich, RI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... aseptic processing, etc. * Knowledge of Single-use-Systems * CFR and Regulatory knowledge ... Able to demonstrate project management skills and presentation skills * Ability to understand ...

Amgen, Inc.

Associate Mfg I

West Greenwich, RI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... aseptic processing, etc. * Knowledge of Single-use-Systems * CFR and Regulatory knowledge ... Able to demonstrate project management skills and presentation skills * Ability to understand ...

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All JobsAseptic Processing JobsManager Aseptic Processing JobsManager Aseptic Processing Jobs in Fall River, MA

Manager Aseptic Processing information

What is a manager aseptic processing?

A Manager of Aseptic Processing oversees the sterile production environments in pharmaceutical or biotechnology manufacturing. They are responsible for ensuring that products are processed and packaged without contamination, following strict regulatory and safety standards. Their role includes supervising staff, maintaining compliance with Good Manufacturing Practices (GMP), conducting risk assessments, and implementing process improvements. They also play a key part in training employees and managing documentation to ensure product quality and patient safety.

What are the key skills and qualifications needed to thrive as a manager aseptic processing?

To thrive as a Manager Aseptic Processing, you need a strong background in microbiology, pharmaceutical manufacturing, quality assurance, and regulatory compliance, often supported by a relevant degree and experience in sterile production environments. Familiarity with Good Manufacturing Practices (GMP), cleanroom management systems, and environmental monitoring tools is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and ensuring strict adherence to protocols. These skills and qualities are vital to maintain product sterility, meet regulatory standards, and ensure patient safety in pharmaceutical operations.

What are some common challenges faced by a manager aseptic processing, and how can they be addressed?

Managers in Aseptic Processing often face challenges related to ensuring strict compliance with regulatory standards, maintaining a contamination-free environment, and leading cross-functional teams in high-pressure situations. Addressing these challenges requires staying updated on evolving industry guidelines, fostering a culture of continuous training, and implementing robust monitoring systems. Effective communication and collaboration with Quality Assurance, Maintenance, and Production teams are also crucial for swiftly resolving issues and upholding product safety.

What is the difference between Manager Aseptic Processing vs Aseptic Processing Technician?

AspectManager Aseptic ProcessingAseptic Processing Technician
CredentialsBachelor's degree in life sciences or related field, GMP training, leadership experienceHigh school diploma or associate degree, GMP training
Work EnvironmentSupervisory role overseeing aseptic processes in pharmaceutical manufacturingHands-on role operating aseptic equipment in cleanroom settings
ResponsibilitiesManaging teams, ensuring compliance, process optimizationPerforming aseptic procedures, equipment setup, documentation

The Manager Aseptic Processing oversees the aseptic manufacturing process, focusing on team management and compliance, while the Aseptic Processing Technician handles the direct operation of aseptic equipment. Both roles require GMP training and work in sterile environments, but the manager has additional leadership and oversight responsibilities.

What cities near Fall River, MA are hiring for Manager Aseptic Processing jobs?

Cities near Fall River, MA with the most Manager Aseptic Processing job openings:

Manager Aseptic Processing jobs near you

Sterile Manufacturing Technician

TekWissen LLC

Plainville, MA • On-site

$20 - $26/hr

Temporary

Re-posted 10 days ago

Job description

Overview:      
     
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands.   
   
Position:           Sterile Manufacturing Technician
Location:          Plainville, MA - 02762
Duration:         12 Months   
Job Type:         Temporary Assignment   
Work Type:     Onsite   
Shift:                Day Shift
 
Training Schedule:             Monday–Friday, 7:00 AM – 3:30 PM (approximately 2–3 months)
Post-Training Schedule:    2-2-3 shift, 7:00 AM – 7:00 PM (12-hour shifts)
                   
 
Summary
 
This is a Formulation Technician II / Sterile Manufacturing Technician to support the site. This client site in Plainville, MA supports sterile pharmaceutical manufacturing operations, including formulation, filtration, aseptic processing, visual inspection, and other GMP-regulated activities. This role is responsible for independently performing sterile manufacturing operations while ensuring compliance with cGMP regulations, quality standards, and safety requirements. The ideal candidate will have hands-on GMP manufacturing experience and the ability to work in a fast-paced, highly regulated environment.
 
Responsibilities
  • Perform sterile manufacturing operations, including formulation, filtration, and aseptic filling.
  • Handle materials, perform line clearance, prepare equipment, and support manufacturing operations.
  • Operate, monitor, and troubleshoot manufacturing equipment and automated systems.
  • Execute weight and dispense activities, solution preparation, autoclave operations, visual inspections, and material transactions.
  • Ensure compliance with cGMP regulations, Good Documentation Practices (GDP), and data integrity standards.
  • Monitor manufacturing processes and identify opportunities to improve safety, quality, and operational efficiency.
  • Support investigations, deviations, change controls, and corrective and preventive actions (CAPA).
  • Assist with equipment qualification, validation, and continuous improvement initiatives.
  • Cross-train across multiple manufacturing functions to support production needs.
  • Maintain a safe and compliant work environment while following all site procedures and PPE requirements.
​​​​​​ Required Skills:
  • Associate's or Bachelor's degree in Life Sciences, Engineering, or a related field preferred.
  • Relevant GMP manufacturing experience may be considered in place of a degree.
  • Minimum 2 years of GMP manufacturing or related technical experience.
  • Experience working in sterile manufacturing or pharmaceutical production is preferred.
  • Working knowledge of cGMP manufacturing operations.
  • Experience operating and troubleshooting manufacturing equipment.
  • Familiarity with sterile manufacturing processes, including formulation, filtration, and aseptic filling.
  • Strong documentation skills with knowledge of Good Documentation Practices (GDP).
  • Excellent problem-solving and troubleshooting abilities.
  • Ability to work across multiple manufacturing processes and adapt to changing production priorities.
  • Strong verbal and written communication skills.
  • Ability to work in cleanroom environments while following gowning and PPE requirements.
  • Ability to stand, walk, bend frequently, and occasionally lift up to 25 lbs.
  • Willingness to work non-standard hours as required.
TekWissen® Group is an equal opportunity employer supporting workforce diversity. 

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

TekWissen logo

About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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