job description
Join ManpowerGroup in a pivotal leadership role as the Quality Assurance Site Head for a global pharmaceutical company. This position offers a unique opportunity to oversee QA/QC operations in Bali, ensuring compliance with international standards while driving operational excellence. Based in key locations such as Canggu, Ubud, or Denpasar, you will lead a team dedicated to maintaining the highest quality benchmarks in pharmaceutical manufacturing.
As a global leader in workforce solutions, ManpowerGroup partners with top-tier pharmaceutical firms to deliver cutting-edge quality assurance strategies. This role is ideal for a seasoned QA professional seeking to make a significant impact in a dynamic, fast-growing market.
Enjoy a competitive salary range of $16,700 – $25,000 per month, along with opportunities for career advancement in a globally recognized organization.
Responsibility
- Lead and manage the QA/QC team to ensure adherence to GMP, GLP, and other regulatory standards.
- Develop and implement quality assurance policies, procedures, and systems for pharmaceutical manufacturing.
- Conduct regular audits and inspections to maintain compliance with local and international regulations.
- Collaborate with cross-functional teams to resolve quality-related issues and drive continuous improvement.
- Oversee documentation and reporting processes to ensure accuracy and regulatory compliance.
- Train and mentor staff on quality assurance best practices and regulatory requirements.
- Monitor and analyze quality metrics to identify trends and implement corrective actions.
- Represent the site in regulatory inspections and audits, ensuring successful outcomes.
Qualifications
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, or a related field.
- Minimum of 8 years of experience in QA/QC within the pharmaceutical industry, with at least 3 years in a leadership role.
- In-depth knowledge of GMP, GLP, ISO, and other relevant regulatory standards.
- Proven experience in managing regulatory inspections and audits.
- Strong analytical and problem-solving skills with a focus on continuous improvement.
- Excellent communication and interpersonal skills to lead and collaborate with diverse teams.
- Familiarity with quality management systems (QMS) and documentation practices.
- Ability to work in a fast-paced environment and adapt to changing regulatory requirements.