Biopharma Process Operator - GMP Manufacturing & Quality

Artech Information System LLC; Malvern (Chester County); On-site; USD 60,000 - 80,000; Full time

Job summary

A biopharmaceutical company is seeking an individual responsible for manufacturing procedures and maintaining compliance in a CGMP environment. The role involves executing processes per Standard Operating Procedures, ensuring documentation accuracy, and demonstrating a commitment to safety and teamwork. Candidates must possess a college degree or HS diploma along with 5+ years of relevant experience in the biopharmaceutical industry, ideally with a background in Manufacturing Execution Systems. Strong communication and mechanical aptitude are preferred.

Qualifications

• 5+ years of experience in the biopharmaceutical industry.
• Experience with Standard Operating Procedures (SOPs).
• Knowledge of testing and sampling methods.

Responsibilities

• Execute manufacturing processes according to standards.
• Complete documentation accurately in SOPs and logbooks.
• Maintain compliance with safety regulations.
• Support ongoing production schedules.

Skills

Manufacturing Execution System (MES)

Mechanical aptitude

Process flow understanding

Interpersonal skills

Communication skills

Education

College degree or HS Diploma with 5+ years experience

Job description

A biopharmaceutical company is seeking an individual responsible for manufacturing procedures and maintaining compliance in a CGMP environment. The role involves executing processes per Standard Operating Procedures, ensuring documentation accuracy, and demonstrating a commitment to safety and teamwork. Candidates must possess a college degree or HS diploma along with 5+ years of relevant experience in the biopharmaceutical industry, ideally with a background in Manufacturing Execution Systems. Strong communication and mechanical aptitude are preferred.