We are seeking to hire a Supervisor to join our Quality Assurance team…

If any of the below describes you, we would love to meet you!

JOB SUMMARY

The Quality Assurance Supervisor is responsible for leading and developing the team of Quality Assurance personnel assigned to the manufacturing floor. This role ensures that production operations comply with cGMP, company policies, and regulatory requirements. The QA Supervisor acts as a key liaison between Quality and Operations, supporting real-time quality decision-making and fostering a strong culture of compliance and continuous improvement.

RESPONSIBILITIES AND LEARNING OPPORTUNITIES

• Ensure QA presence on the manufacturing floor to support in-process checks, line clearance, and real-time quality decisions.
• Oversee routine QA floor activities such as batch record review, deviation identification, and verification of manufacturing operations.
• Escalate and coordinate responses to deviations and other quality events.
• Serve as a point of contact for Operations, offering guidance to maintain compliance during manufacturing activities.
• Supervise, mentor, and schedule QA floor personnel to ensure adequate coverage across all shifts and production areas.
• Ensure manufacturing floor activities are conducted in accordance with SOPs, batch records, and cGMP regulations.
• Support timely and accurate completion of production and quality documentation.
• Collaborate with QA management to identify and implement process improvements to enhance compliance and efficiency.
• Foster a culture of accountability, teamwork, and continuous learning among the QA team.
• Partner with Production, Engineering, and other functions to address quality-related issues in a timely manner.
• Communicate quality trends and metrics to management and recommend corrective/preventive actions.
• Assist in developing or revising SOPs and work instructions related to floor QA activities.
• Support onboarding and ongoing training of QA associates on procedures, cGMP expectations, and company values.
• Prepare Trend reports
• Implement CAPAs, as needed.
• Approve SOP revisions, protocols, reports, master batch records, analytical method and specifications, COA, COC, finished product release for distribution.

REQUIRED SKILLS AND QUALIFICATIONS

• Bachelor’s Degree with 3+ years or High school diploma with 10+ years’ experience in Quality Assurance, with previous supervisory experience in the pharmaceutical industry preferred.
• Strong leadership, interpersonal, and coaching skills.
• Ability to make timely, sound decisions in a fast-paced manufacturing environment.
• Excellent verbal and written communication skills.
• Detail-oriented with strong organizational and problem-solving skills.
• Comfortable working in cleanroom and manufacturing floor environments
• Strong knowledge of GMP/CFR/ICH, and industry standards.
• Prior experience in conducting/approving manufacturing investigations is preferred.
• Ability to set priorities and manage multiple tasks.
• Effective interpersonal skills.
• Experience with Electronic quality management system is desirable.

Adare Pharma is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status.

PRINCIPALS ONLY
NO AGENCIES OR THIRD PARTIES