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Job Title: Manufacturing AssociateJob Description

This role involves optimizing bioprocesses for the production of biologics, including cell culture, fermentation, purification, and lyophilization processes. The ideal candidate will have hands-on experience in biotech manufacturing, a solid understanding of bioprocess engineering, and a commitment to maintaining high-quality standards. Experience working under GMP is preferred. In addition to manufacturing duties, the candidate will support process development in executing production processes for new synthetic biology-based cellular medicines. Other duties include process scale-up and carrying out in-process analytical tests, including flow cytometry and colony-forming unit (CFU) assays.

Responsibilities

+ Operate and monitor upstream bioprocess equipment, including independently setting up and executing bioreactors, scale-up fermentation, concentration, drying, and associated systems.

+ Perform cell culture, media preparation, and fermentation processes as per standard operating procedures (SOPs).

+ Optimize process parameters to maximize yield, productivity, and product quality.

+ Maintain accurate and detailed records of all manufacturing activities, including batch records, process parameters, and deviations.

+ Ensure compliance with Good Manufacturing Practices (GMP), regulatory requirements, and internal quality standards.

+ Work closely with cross-functional teams, including Quality Assurance, Quality Control, and R&D, to ensure seamless integration and execution of manufacturing processes.

+ Communicate process changes, updates, and issues effectively to stakeholders.

+ Present data at internal meetings, work with research groups, and author scientific reports for internal documentation, as required.

+ Participate in process improvement initiatives and contribute to the development of new technologies and methodologies.

+ Stay current with industry trends and advancements to enhance manufacturing practices.

Essential Skills

+ Strong understanding of bioprocess principles, equipment operation, and troubleshooting.

+ Excellent problem-solving skills and attention to detail.

+ Proficiency in using process control systems and laboratory equipment.

+ Strong organizational and communication skills.

Additional Skills & Qualifications

+ Bachelor’s degree in Biotechnology, Biochemistry, Chemical Engineering, or a related field.

+ Minimum of 1-2 years of experience in upstream biomanufacturing, including hands-on experience with cell culture and fermentation processes.

+ Ability to work in a fast-paced, dynamic environment.

Work Environment

The role is based in a GMP environment and lab environment, working within a small collaborative team focused on initiatives to develop treatments for immunity and cancer. The team is developing new technology for delivering medicine through capsules, offering more convenience for patients compared to traditional IV infusion centers.

Pay and Benefits

The pay range for this position is $30.00 - $35.10/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Rockville,MD.

Application Deadline

This position is anticipated to close on Jun 16, 2025.

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.

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.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.