Pharma Manufacturing Process Technician (Contract)

Pioneer Data Systems

Malvern (Chester County)

On-site

USD 45,000 - 65,000

Full time

3 days ago
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Benefits offered by this job

Group medical insurance with dental &视
Dental coverage
Vision coverage

Job summary

SmartRecruiters, Inc. is seeking a Temporary Biotechnician (Scientific Process Operator) in Malvern, PA, for a 06-month contract with potential extension up to 24 months.

The role reports to Manufacturing Supervisor in Technical Operations and focuses on CGMP downstream manufacturing processes. Responsibilities include executing manufacturing procedures, documenting parameters, analyzing process data, and maintaining high compliance with SOPs, batch records and safety regulations.

Qualifications

  • College degree or HS Diploma with ≥5 years industrial experience.
  • Biotech/Pharmaceutical industry background or SOP documentation experience preferred.
  • Experience with SOPs, batch records and GMP documentation advantageous.
  • Knowledge of MES systems and manufacturing software is a plus.

Responsibilities

  • Execute manufacturing processes according to SOPs and procedures.
  • Verify and enter production parameters in Batch Records.
  • Analyze trend charts and process data for quality control.
  • Complete GMP documentation in logbooks and SOPs.
  • Maintain compliance with FDA, EPA and OSHA regulations.
  • Operate with PPE and maintain a safe working environment.
  • Support the production schedule and attend required meetings.

Education

College degree or HS Diploma with +5 years industrial experience

Tools

SAP Production
Werum MES
Compliance-Kaplan Wire
MS Office
MS Word
MS Excel

Job description

SmartRecruiters, Inc. is seeking a Temporary Biotechnician (Scientific Process Operator) in Malvern, PA, for a 06-month contract with potential extension up to 24 months.

The role reports to Manufacturing Supervisor in Technical Operations and focuses on CGMP downstream manufacturing processes. Responsibilities include executing manufacturing procedures, documenting parameters, analyzing process data, and maintaining high compliance with SOPs, batch records and safety regulations.

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