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@ Actalent
  • Post Date : Jun 25, 2025
  • Apply Before : Jul 25, 2025
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Job Detail

  • Offered Salary 0
  • Commitment Full Time
  • Compensation Paid
  • Required education level High SchoolAssociate degree

Job Description

Job Description

The Biomanufacturing Associate I is a vital part of the gene therapy manufacturing team, utilizing biological, bioprocess, manufacturing, and mechanical principles in a cGMP and GLP environment to ensure the production and release of high-quality products according to client specifications. This role involves performing various routine and semi-routine tasks, requiring judgment to resolve issues or make recommendations, with guidance when necessary, in order to effectively execute manufacturing protocols within a regulated setting.

Responsibilities

  • Apply and adhere to SOPs, cGMP, GLP, Quality, and basic Safety requirements under guidance.
  • Perform routine and semi-routine tasks according to SOPs in areas such as upstream activities, downstream activities, and fill-finish activities.
  • Follow verbal and written instructions in alignment with the batch record during planned manufacturing activities.
  • Utilize basic quality documents and apply Good Documentation Practices with guidance.
  • Document, review, and check work accurately to prevent errors prior to submission.
  • Identify, record, and report observed process variances/deviations in real time.
  • Operate equipment and complete process tasks by following SOPs, safety guidelines, and manufacturing instructions.
  • Prepare, clean, and maintain equipment and tools.
  • Recognize common safety issues and report incidents immediately.
  • Adhere to safe working practices and comply with site-based guidelines, including cleanroom and aseptic procedures, PPE and gowning requirements, and safe handling of biological specimens and hazardous materials.
  • Ensure 100% on-time completion of the training plan.
  • Be punctual and flexible with work schedule to support business demands.
  • Perform other responsibilities as required.

Essential Skills

  • Experience with cGMP, GLP, and SOPs.
  • Knowledge of aliquoting, cell culture, chromatography, Tangential Flow Filtration (TFF), fill finish, and GDP.
  • Strong attention to detail and ability to recognize deviations.
  • Good analytical, critical thinking, and problem-solving skills.
  • Proficiency in MS Word, Excel, Teams, and databases.

Additional Skills & Qualifications

  • High School Diploma or equivalent with high grades in science courses and 2 years of related experience, or an A.S. with 1 year, or a degree in biology/life sciences, bioengineering, or related discipline with 0-1 years of related experience.
  • Ability to work in accordance with established values and as a team player.
  • Positive attitude, professional tone, and effective collaboration skills.
  • Willingness to continuously learn and improve.
  • Pass/maintain aseptic/gowning qualifications & media fill activities.
  • Ability to work in a cleanroom for at least 4 hours/day.
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