Bioprocessing Associate I
King of Prussia, PA
Full Time
Entry Level
SKPT pharmteco (SKPT, the Corporation) is a U.S.-based global Contract Development and Manufacturing Organization (CDMO) that consolidates the operations of sites worldwide – Korea, France, Ireland, and the United States (CA and PA). Built on over 75 years of experience, SK pharmteco is a trusted partner specializing in the manufacture of small molecule APIs and intermediates, viral vectors for gene therapies, cell therapies, registered starting materials and analytical services for the pharmaceutical industry worldwide.
We are seeking a motivated Bioprocessing Associate I to support cGMP manufacturing operations for advanced therapeutics. This role is responsible for performing hands-on upstream and downstream manufacturing activities in a cleanroom environment while ensuring compliance with cGMP standards and company procedures.
Key Responsibilities
SK pharmteco Inc., is an equal opportunity employer who prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants.
We are seeking a motivated Bioprocessing Associate I to support cGMP manufacturing operations for advanced therapeutics. This role is responsible for performing hands-on upstream and downstream manufacturing activities in a cleanroom environment while ensuring compliance with cGMP standards and company procedures.
Key Responsibilities
- Perform hands-on manufacturing activities in support of upstream and downstream processing operations
- Operate production equipment for adherent and suspension systems
- Maintain compliance with cGMP standards, SOPs, batch records, and controlled documentation
- Support inspection readiness and maintain the cGMP status of the manufacturing facility
- Assist with investigations related to manufacturing deviations and non-conformances
- Support validation and qualification activities for manufacturing processes, equipment, and facility suites
- Follow all applicable safety policies, procedures, and regulatory requirements
- High school diploma required; bachelor’s degree in Biological Sciences, Engineering, or related field preferred
- 0–2 years of experience in cGMP biologics or pharmaceutical manufacturing preferred
- General understanding of cGMP regulations and cleanroom operations
- Experience working in a Biological Safety Cabinet (BSC) preferred
- Familiarity with cell expansion vessels and purification equipment is a plus
- Willingness to learn and operate manufacturing equipment
- Ability to work flexible schedules based on business needs
- Strong attention to detail and documentation practices
- Ability to follow procedures and work safely in a regulated environment
- Team-oriented with strong communication skills
- Adaptable and eager to learn new processes and technologies
- Ability to stand for periods of time working in the laboratory.
- Ability to lift up to 55 lbs at times.
SK pharmteco Inc., is an equal opportunity employer who prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants.
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