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Manager Aseptic Processing Jobs in Virginia (NOW HIRING)

RLS Radiopharmacies

Pharmacy Technician

Sterling, VA · On-site

$17.25 - $21/hr

As an RLS Pharmacy Technician, you will gain experience in areas such as aseptic processes ... Manage and maintain facility inventory * Perform disinfection task in the cleanroom, and stocking ...

RLS Radiopharmacies

Pharmacy Technician

Sterling, VA

$17.25 - $21/hr

As an RLS Pharmacy Technician, you will gain experience in areas such as aseptic processes ... Manage and maintain facility inventory * Perform disinfection task in the cleanroom, and stocking ...

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Manager Aseptic Processing information

Can you make 6 figures as a sterile processing technician?

Sterile processing technicians typically earn salaries below six figures, with most earning between $40,000 and $60,000 annually. Achieving a six-figure income usually requires advancing to supervisory or managerial roles, gaining specialized certifications, or increasing experience in the field. The Manager Aseptic Processing role often offers higher salaries, but entry-level sterile processing technicians generally do not reach six-figure earnings.

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 is the highest salary for a sterile tech?

A sterile processing technician's highest salaries can reach around $50,000 to $60,000 annually, depending on experience, certifications, and location. Advanced roles or those with specialized skills may earn higher wages, especially in healthcare settings with demanding schedules or regulatory requirements.

What are 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 some common challenges faced by a Manager in 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 does a sterile processing manager do?

A sterile processing manager oversees the sterilization and proper handling of surgical instruments and medical equipment in healthcare settings. They ensure compliance with safety standards, manage staff, and maintain sterilization equipment to prevent infections. Certification in sterile processing or central sterile services is often required.

What are the key skills and qualifications needed to thrive as a Manager Aseptic Processing, and why are they important?

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.

Will AI replace sterile processing techs?

AI is unlikely to fully replace sterile processing technicians, as their role requires hands-on skills, attention to detail, and adherence to strict sterilization protocols. While automation and AI can assist with inventory management and process monitoring, human oversight remains essential for ensuring patient safety and compliance with industry standards. Sterile processing techs will continue to be vital in healthcare environments, often working alongside automated systems.
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Manager Aseptic Processing jobs near you
Senior Product Development Engineer

Senior Product Development Engineer

Contraline, Inc.

Charlottesville, VA • On-site

Full-time

Posted 20 days ago

Job description

About Contraline Inc.
Contraline is a venture-backed medical device company based in Charlottesville, Virginia. The company's lead product is ADAM™, the world's first injectable hydrogel designed to provide long-lasting, non-hormonal, and reversible contraception for men. The company aims to use its hydrogel platform technology to address global reproductive health challenges with no solutions and significant unmet needs. The company is well recognized in the field of Contraception and positioned for success.
About the role
The Senior Product Development Engineer will support the design and development of Class II and Class III medical devices and their associated delivery systems. This role requires strong analytical and technical skills, adherence to Quality System Regulations, and the ability to operate independently in a fast-paced, hands-on environment. This is a full-time, on-site position.
What you'll do
  • Assist with the design and development of polymer implantable devices and delivery device tools through design development to manufacturing, consistent with medical devices regulatory and quality requirements.
  • Own development and execution of V&V strategies, including protocol authorship, design traceability, and establishment of clear, testable acceptance criteria.
  • Design and execute experimental benchtop studies and statistical analyses (e.g., DOE, capability studies) to assess the impact of processing parameters on product performance and variability.
  • Interpret data and communicate findings to cross-functional teams.
  • Lead design transfer activities from R&D into manufacturing environments, including preclinical and clinical builds, with a focus on aseptic/sterile processing and process consistency.
  • Collaborate with Operations, Quality, and external partners to ensure robust, scalable processes.
  • Contribute to design controls and risk management activities, including verification, validation, and FMEAs.
  • Manage relevant vendor relationships, including component vendors and external testing.
  • Continuously monitor compliance with FDA, ISO 13485, and design control requirements.

Qualifications
  • B.S., M.S., or Ph.D. in Biomedical, Mechanical, Chemical Engineering, or related field
  • 5+ years in Class II/III medical device product development or manufacturing
  • Experience with:
    • Process development & validation (IQ/OQ/PQ)
    • Design Controls and DHF documentation
    • Verification & Validation testing and protocol development
    • Applied statistics (DOE, regression, capability analysis)
    • Risk analysis (FMEA, hazard analysis, fault tree)
    • Manufacturing transfer and supplier interaction
    • ISO 13485 and FDA QMSR
    • Design transfer for sterile/aseptic processes (preferred)
    • Class II/III implantable devices or combination products (preferred)
  • Strong communication, documentation rigor, and cross-functional collaboration
  • Self-starter with strong problem-solving skills
  • Ability to work on-site in lab and controlled manufacturing environments (PPE/cleanroom gowning, hands-on work, lifting up to 25 lbs.)

Applicants must be authorized to work in the United States.
Contraline is a Charlottesville-based company working at the forefront of reproductive medicine. We believe that we go further when we go together. We are dedicated to building a diverse, inclusive and authentic workplace. If you're excited about this role but your past experience doesn't align perfectly with every qualification in the job description, we encourage you to apply anyways. All backgrounds, identities, and voices are welcomed!

Apply