Manufacturing Associates II (Day & Second Shift)

requirements. Assist with deviation investigations, CAPAs, non‑conformance reports, and OOS documentation by gathering information and completing assigned actions under supervision. Identify and report process issues, equipment concerns, or conflicts to the Lead, Supervisor, or Manager in a timely manner. Adhere to company policies, GMP

requirements, and safety standards while consistently maintaining quality and compliance. Perform other assigned duties consistent with training and role level. EDUCATION AND EXPERIENCE: Associate degree or higher and/or a Biotech Program certificate from an accredited college, or equivalent industry experience in a relevant technical discipline such as biology, chemistry, pharmaceutical sciences, biochemistry, biotechnology, molecular biology, chemical or bioengineering. Minimum 2 years of experience working in pharmaceutical/biotechnology industry. First-hand understanding/ experience with cell culture (preferably adherent mammalian culture) and composing/supplementing media required. Working experience in cleanroom (ISO 7 and 5), fibroblast, primary tissue culture, and iPSC cells preferred. Some trainer experience preferred. JOB SPECIFICATIONS: CMC Awareness: Basic understanding of CMC development and manufacturing concepts, with the ability to follow established procedures in a GMP manufacturing environment. Cell Culture Skills: Ability to perform routine manual and automated cell culture activities in accordance with approved protocols, GMP

requirements, and quality standards, with supervision. Regulatory Understanding: Foundational knowledge of GMP principles and awareness of ISO standards, Quality Systems, and FDA regulations applicable to manufacturing operations. Communication Skills: Effective verbal and written communication skills, with the ability to follow instructions, document work accurately, and communicate status or issues to team members and supervisors. Technical Skills: Basic computer skills, including use of Microsoft Office and other systems required for documentation and data entry. GMP & Aseptic Practices: Working knowledge of cleanroom behavior, aseptic techniques, safety practices, and documentation

requirements in a regulated environment; including working in a cleanroom environment while gowned for an extended period. Collaboration: Ability to work effectively as a member of a manufacturing team and coordinate with others to support assigned tasks and team objectives. Documentation: Ability to complete batch records, logs, and other manufacturing documentation accurately and in compliance with GMP expectations, with guidance as needed. Flexibility: Ability to work a flexible schedule to support manufacturing operations, including overtime, weekend, and holiday work as business needs require.​ WORKING CONDITIONS Office and Lab environment. While performing the duties of this Job, the employee is frequently exposed to toxic or caustic chemicals. This is an indoor position requiring the ability to perform experiments in the laboratory, and type and use a computer. May work in Cleanroom for an extended period of time. PHYSICAL DEMANDS While performing the duties of this Job, the employee is regularly required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms and talk or hear. Fine motor skills include eye/hand coordination, flexibility and balance are required. Employees must be able to gown and work in cleanroom environment. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision (especially the ability to distinguish different hues/shades of purple, red, pink, orange and yellow), peripheral vision, depth perception and ability to adjust focus. These work environmental characteristics are representative of the environment the job holder will encounter. Reasonable accommodation may be made to enable people with disabilities to perform the essential functions of the job. EEO and Employment Eligibility: Aspen Neuroscience is committed to providing equal employment opportunities to all employees and job applicants and prohibits discrimination and harassment of any type. We are committed to creating an inclusive environment for all employees. Aspen is not able to provide visa sponsorship for this role. Applicants must have valid work authorization that does not require employer sponsorship now or in the future. Total Rewards and Culture: Aspen Neuroscience, Inc., located in scenic Torrey Pines, is noted for its collaborative and learning focused culture where each person is valued for contributing their strengths and energy to building a world-class line of products for patients in need. The company offers a competitive total

compensation package, time-off in addition to Company observed holidays, Medical/Dental insurance

benefits, onsite gym, and other wellness

perks. The anticipated hourly range for candidates who will work in San Diego is $30-$33 hourly with a shift differential of 10% provided for the Second Shift. The final hourly rate offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the industry, education, etc. Aspen Neuroscience is multi-state employer, and this salary range may not reflect positions that work in other states. Apply for this job First name Last name Email address Location Phone number Resume Attach resume Attach another file Attach file Add another Are you willing to work weekends? Yes No What is the highest level of education you’ve obtained? No answer GED or Equivalent High School Some College College - Associates College - Bachelor of Arts College - Bachelor of Fine Arts College - Bachelor of Science College - Master of Arts College - Master of Science College - Master of Fine Arts College - Master of Business Administration College - Doctorate Medical Doctor Other This position will be on a Pitman schedule with a repeating 2-2-3 schedule. Which 12-hour shift would best fit your schedule? Do you have experience working with mammalian cell cultures and composing and supplementing media? Do you have experience working in a cleanroom environment? Linkedin url Should be {http://www.linkedin.com/pub/[member-name/]x/y/z} or {http://www.linkedin.com/in/string} © 2014-2026 TriNet Group, Inc. All rights reserved. Privacy Policy

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