Onsite QA on-the-Floor Specialist – Aseptic Pharma

FUSTIS LLC; Indianapolis (IN); On-site; USD 55,104 - 68,880; Full time

Job summary

A pharmaceutical contractor in Indianapolis is seeking a QA contractor for onsite support in aseptic drug product manufacturing. The role involves daily quality oversight, ensuring GMP compliance, reviewing batch records, and supporting investigations. Candidates must have a Bachelor’s degree in a scientific field, 5-7+ years of experience in cGMP pharmaceutical manufacturing, and strong communication and organizational skills. This position offers an hourly pay rate of $40/hr. (W2) or $50/hr. (1099).

Qualifications

• 5-7+ years of cGMP pharmaceutical manufacturing experience, preferably in Quality Assurance.
• Strong knowledge of manufacturing processes and quality systems.
• Ability to work independently in a fast-paced environment.

Responsibilities

• Maintain strong presence on the manufacturing floor and participate in QA walkthroughs.
• Review batch records, assess deviations, and support investigations.
• Escalate critical issues and act as quality liaison across teams.
• Coach operational teams to maintain GMP compliance.

Skills

Excellent communication

Problem-solving

Organizational skills

Knowledge of GMP documentation

Proficiency in Microsoft Office

Proficiency in QMS systems (e.g., Veeva Vault)

Education

Bachelor’s degree in a scientific field

Job description

A pharmaceutical contractor in Indianapolis is seeking a QA contractor for onsite support in aseptic drug product manufacturing. The role involves daily quality oversight, ensuring GMP compliance, reviewing batch records, and supporting investigations. Candidates must have a Bachelor’s degree in a scientific field, 5-7+ years of experience in cGMP pharmaceutical manufacturing, and strong communication and organizational skills. This position offers an hourly pay rate of $40/hr. (W2) or $50/hr. (1099).