Deskripsi Pekerjaan
Lloyd Laboratories, Inc., a premier pharmaceutical manufacturer in Malolos City, Bulacan, is seeking a dedicated and detail-oriented Process Lead to join our dynamic team. In this critical role, you will be the cornerstone of our production quality, ensuring that every process aligns with the highest standards of Good Manufacturing Practice (GMP), International Organization for Standardization (ISO), and Pharmaceutical Inspection Co-operation Scheme (PIC/S) requirements.
As a Process Lead, you will serve as the primary point of contact for all compliance-related queries on the production floor. You will collaborate closely with Quality Assurance, Regulatory Affairs, and Engineering teams to resolve deviations, implement corrective actions (CAPA), and streamline operational workflows.
Your role involves meticulous oversight of batch records, standard operating procedures (SOPs), and training logs. You will be responsible for developing and conducting training sessions to ensure all team members are current with evolving regulatory standards. Leadership is key; you will motivate your team to achieve production targets without compromising quality or safety.
We are looking for a leader who thrives in a regulated environment, possesses an eagle eye for detail, and has a proven track record of implementing robust quality systems. If you are passionate about maintaining the integrity of pharmaceutical manufacturing and possess strong technical writing skills for documentation, this is the perfect opportunity to advance your career with an industry leader.
We pride ourselves on fostering a culture of continuous improvement and professional growth. As a Process Lead, you will have access to ongoing training and development programs to sharpen your skills. If you are ready to take on a challenging yet rewarding role where your expertise directly contributes to public health, we encourage you to apply.
Join Lloyd Laboratories and play a vital role in delivering high-quality healthcare solutions to the Filipino people. Your commitment to excellence will help us maintain our reputation for quality, safety, and innovation.
Tanggung Jawab
- Strictly monitor and enforce company rules and regulations regarding GMP, ISO, and PIC/S compliance on the production floor.
- Lead, mentor, and supervise a team of production operators and technicians to ensure adherence to established protocols.
- Oversee and maintain accurate documentation processes, including batch records, logbooks, and standard operating procedures (SOPs).
- Conduct regular internal audits and inspections to identify areas for improvement and ensure continuous compliance.
- Investigate and resolve process deviations, non-conformances, and quality incidents, implementing effective corrective and preventive actions (CAPA).
- Collaborate with cross-functional teams (QA, QC, Engineering, Regulatory) to optimize manufacturing processes and enhance operational efficiency.
- Prepare and present detailed reports on production performance, compliance metrics, and process improvements to management.
- Develop and deliver training programs for staff to ensure comprehensive understanding of quality systems and safety protocols.
Kualifikasi
- Bachelor's degree in Pharmacy, Chemical Engineering, Chemistry, or any related Life Sciences field.
- At least 3-5 years of experience in a supervisory or lead role within a pharmaceutical, medical device, or highly regulated manufacturing environment.
- Comprehensive knowledge and hands-on experience with GMP, ISO 9001, ISO 13485, and PIC/S guidelines.
- Strong background in documentation, technical writing, and records management.
- Excellent leadership, communication, and interpersonal skills to effectively manage a diverse team.
- Proficient in conducting internal audits and root cause analysis investigations.
- Certification in Quality Management Systems or Lean Six Sigma is a strong advantage.
- Must be willing to work in Malolos City, Bulacan, and amenable to shifting schedules if required.