On-Site QA Lead at Biopharmaceutical

Position: On-Site QA Lead at Biopharmaceutical Company
Elevate quality standards as an On-Site QA Lead with Smart Work flexibility. This senior role focuses on managing QA procedures and supporting team training and compliance.

As a QA Lead, your leadership will streamline QA systems while ensuring regulatory compliance for biopharmaceutical manufacturing. Utilize your advanced problem-solving abilities, mentoring skills, and knowledge of cGMP standards to guide the team effectively. Your expertise will play a crucial role in ensuring the integrity of early-phase clinical products and facilitate successful audits and inspections.

Key Responsibilities:

• Maintain and revise QA procedures as necessary

• Provide training in Quality matters for team members

• Support GxP oversight for site functions

• Perform QA batch record reviews and approvals

• Investigate non-conformities and manage Change Controls

Requirements:

• B.S. degree in relevant scientific field

• 10–12 years in Quality Assurance/Control

• Experience with regulatory inspections

• Strong leadership and communication skills

• Familiarity with Office software and regulatory requirements

Drive compliance and elevate quality processes with your expertise in biopharmaceutical QA.
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