Head Quality Operations job at Dei BioPharma | Apply Now

• Bachelor’s degree in pharmacy, Chemistry, Biochemistry, Microbiology, or related field.

• A master’s degree in quality management, Industrial Pharmacy, or related discipline is an added advantage.

• Minimum of 8–10 years of experience in a GMP-regulated pharmaceutical or biopharmaceutical environment.

• Proven experience in supervisory or managerial roles within Quality Assurance or Quality Control.

• Strong understanding of GMP, GLP, GDP, and ISO quality standards.

• Demonstrated ability to manage audits and regulatory inspections.

• Excellent analytical, problem-solving, and leadership skills.

• Strong communication and report-writing abilities.

• High integrity, attention to detail, and commitment to product quality and patient safety.

Experience:

• Minimum of 8–10 years of progressive experience in Quality Assurance, Quality Control, or related functions within a GMP-regulated pharmaceutical or biopharmaceutical environment.

• Experience in managing or supervising QA/QC teams and coordinating regulatory inspections and audits.

• Proven track record in establishing, maintaining, and improving Quality Management Systems (QMS).

• Familiarity with validation, qualification, and product release processes in a biopharma setting is highly desirable.

JOB KNOWLEDGE

• The incumbent should possess comprehensive knowledge of:

• Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Distribution Practices (GDP).

• Quality Management Systems (QMS) and documentation control processes.

• Regulatory requirements and inspection readiness (e.g., NDA, WHO, ISO, FDA).

• Pharmaceutical manufacturing processes, validation, and product lifecycle management.

• Root Cause Analysis, CAPA systems, and risk-based quality management.

• Laboratory operations and analytical testing methods.

• Quality metrics, deviation handling, and change control management.

• Leadership, supervision, and performance management within quality teams.

• Continuous improvement and quality culture development.

• EVALUATIONS:

• (This may be tested)

• LANGUAGE:

• English Level IV (Advanced Knowledge) — Reading, Writing, and Speaking are required.

Skills and abilities:

• Strong leadership and supervisory skills.

• Excellent understanding of GMP, GDP, and quality compliance systems.

• Exceptional analytical and problem-solving abilities.

• Effective communication and report-writing skills.

• Proficiency in QMS and laboratory information systems (LIMS).

• High attention to detail and commitment to documentation accuracy.

• Ability to conduct and manage audits and inspections.

• Team collaboration and cross-departmental coordination.

• Strategic thinking and decision-making under pressure.

• Commitment to continuous learning and improvement.

• Qualifications: All applicants under consideration will be required to pass medical and security certifications.

EQUAL OPPORTUNITY EMPLOYER: Dei BioPharma Ltd. provides equal opportunity and fair and equitable treatment in employment to all people without regard to race, color, religion, sex, national origin, age, disability, political affiliation, marital status, or sexual orientation.