Chemical Technologist

Phil. United Pharma Corporation; Cavite City; On-site; PHP 279,000 - 446,400; Full time

Benefits offered by this job

Performance bonus

Employee of the Month Award

Scholarship Program

Maternity & Paternity Leave

Leave benefits

Job summary

Phil. United Pharma Corporation is seeking a qualified pharmaceutical professional for an on-site position in Cavite. The role requires 1–3 years of experience, a Bachelor’s degree, and readiness to work full-time in a pharmaceutical manufacturing environment.

Responsibilities include conducting laboratory testing, maintaining quality documentation, and ensuring compliance with GMP/FDA regulations. The candidate should possess solid knowledge of lab testing procedures and quality control

Qualifications

• Experience with laboratory testing procedures in a pharmaceutical setting.
• Knowledge of GMP, FDA regulations and quality standards.
• Ability to maintain accurate laboratory documentation and support validation efforts.

Responsibilities

• Conduct physical, chemical, and analytical testing of materials and products.
• Maintain and update laboratory documentation and records.
• Ensure compliance with GMP and regulatory requirements; investigate out-of-spec results.
• Support validation or stability studies as needed.

Skills

Laboratory procedures

Quality control

GMP/FDA knowledge

Education

Pharmacy

Chemistry

Chemical Engineering

Medical Technology

Job description

On-site - Cavite 1-3 Yrs Exp Bachelor Full-time

Job Description

Employee Recognition and Rewards

Performance Bonus, Employee of the Month Award, Employee Recognition Program, Holiday Gifts, Incentives

Government Mandated Benefits

Employee Discount, Parking Space, Sleeping Quarters

Professional Development

Employee Assistance Program, Job Training, Scholarship Program

Maternity & Paternity Leave, Sick Leave, Vacation Leave

The role requires a competent professional with pharmaceutical industry experience to ensure that raw materials, in-process products, and finished goods meet strict quality standards and regulatory requirements. Key duties and responsibilities include conducting physical, chemical, and analytical testing, preparing and maintaining laboratory documentation, ensuring compliance with GMP, FDA regulations, and company quality standards, investigating out-of-specification results, and supporting validation or stability studies. To qualify, candidates must be a graduate of Pharmacy, Chemistry, Chemical Engineering, Medical Technology, or a related course, possess experience in a pharmaceutical manufacturing company, and have a solid knowledge of laboratory testing procedures and quality control standards.

Working Location

9005 Phinma Compound, 72C5+QVM, Kaong, Silang, Cavite, Philippines