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Manufacturing Associate II

  • ... Posted on: Mar 26, 2026
  • ... Aequor
  • ... Swiftwater, Pennsylvania
  • ... Salary: Not Available
  • ... Full-time

Manufacturing Associate II   

Job Title :

Manufacturing Associate II

Job Type :

Full-time

Job Location :

Swiftwater Pennsylvania United States

Remote :

No

Jobcon Logo Job Description :

Title:- Manufacturing Associate II, 1st ShiftLocation: Swiftwater, PA Duration: Contract until April 2027 (Possible extension) Job ID:- SNFIJP00010982JD:- Continuous Improvement professional with 3–5 years of experience in pharmaceutical manufacturing and strong knowledge of cGMP environments, particularly in formulation and filling operations. Ideal candidates will have hands on experience managing CAPA and Change Control activities, authoring technical documentation, and supporting cross functional teams including Quality, MSAT, Engineering, Operations, and Sterility Assurance. They should bring expertise in Lean/Six Sigma methodologies, equipment qualification, OEE improvement, and electronic systems such as eBR, Opstrakker, and Qualipso. Strong candidates excel in communication, technical writing, project management, and influencing across teams. Proficiency with Microsoft Office and familiarity with ERP systems (iShift preferred) are important. Candidates must be adaptable, detail oriented, and capable of driving continuous improvement in a fast paced, regulated environment.Thanks MINAKSHI SANGWAN Recruiting Lead - US Recruitment O 732-339-3518 E W

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Jobcon Logo Position Details

Posted:

Mar 26, 2026

Reference Number:

10440_4390285163

Employment:

Full-time

Salary:

Not Available

City:

Swiftwater

Job Origin:

APPCAST_CPC

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Title:- Manufacturing Associate II, 1st ShiftLocation: Swiftwater, PA Duration: Contract until April 2027 (Possible extension) Job ID:- SNFIJP00010982JD:- Continuous Improvement professional with 3–5 years of experience in pharmaceutical manufacturing and strong knowledge of cGMP environments, particularly in formulation and filling operations. Ideal candidates will have hands on experience managing CAPA and Change Control activities, authoring technical documentation, and supporting cross functional teams including Quality, MSAT, Engineering, Operations, and Sterility Assurance. They should bring expertise in Lean/Six Sigma methodologies, equipment qualification, OEE improvement, and electronic systems such as eBR, Opstrakker, and Qualipso. Strong candidates excel in communication, technical writing, project management, and influencing across teams. Proficiency with Microsoft Office and familiarity with ERP systems (iShift preferred) are important. Candidates must be adaptable, detail oriented, and capable of driving continuous improvement in a fast paced, regulated environment.Thanks MINAKSHI SANGWAN Recruiting Lead - US Recruitment O 732-339-3518 E W

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