Biopharma GMP Process Operator

Integrated Resources Inc.; Malvern (Chester County); On-site; USD 45,000 - 65,000; Full time

Job summary

A leading staffing firm is seeking a skilled manufacturing professional for a contract position in a CGMP environment. This role emphasizes quality and compliance in daily operations and requires significant experience in the biopharmaceutical industry. Ideal candidates will possess strong technical knowledge and excellent documentation skills.

Qualifications

• Must have formal documentation experience in a biopharmaceutical setting.
• Previous experience with manufacturing equipment is preferred.
• +5 years experience required.

Responsibilities

• Execute manufacturing processes per established SOPs.
• Maintain compliance with all regulations.
• Complete documentation accurately in GMP formats.

Skills

Good interpersonal and communication skills

Autonomy

Technical Knowledge

Ability to follow SOPs

Education

College degree or HS Diploma with +5 years biopharmaceutical industry experience

Tools

MS Office

SAP Production

Werum MES

Job description

A leading staffing firm is seeking a skilled manufacturing professional for a contract position in a CGMP environment. This role emphasizes quality and compliance in daily operations and requires significant experience in the biopharmaceutical industry. Ideal candidates will possess strong technical knowledge and excellent documentation skills.